MBP0002
HYBRID MAPPING PANEL
Description:
NIGMS HUMAN/RODENT SOMATIC CELL HYBRID MAPPING PANEL #2 DNA
Aliquot Size:
50 µg each
Brief Description:
50 µg DNA from each of 24 human/rodent somatic cell hybrids and 100 µg DNA from each of three parental cell lines.
| Walker JA, Hedges DJ, Perodeau BP, Landry KE, Stoilova N, Laborde ME, Shewale J, Sinha SK, Batzer MA, Multiplex polymerase chain reaction for simultaneous quantitation of human nuclear, mitochondrial, and male Y-chromosome DNA: application in human identification. Anal Biochem337(1):89-97 2005 |
| PubMed ID: 15649380 |
| |
| Otieno AC, Carter AB, Hedges DJ, Walker JA, Ray DA, Garber RK, Anders BA, Stoilova N, Laborde ME, Fowlkes JD, Huang CH, Perodeau B, Batzer MA, Analysis of the human Alu Ya-lineage. J Mol Biol342(1):109-18 2004 |
| PubMed ID: 15313610 |
| |
| Bridgland L, Footz TK, Kardel MD, Riazi MA, McDermid HE, Three duplicons form a novel chimeric transcription unit in the pericentromeric region of chromosome 22q11. Hum Genet112(1):57-61 2003 |
| PubMed ID: 12483300 |
| |
| Butler MP, Iida S, Capello D, Rossi D, Rao PH, Nallasivam P, Louie DC, Chaganti S, Au T, Gascoyne RD, Gaidano G, Chaganti RS, Dalla-Favera R, Alternative translocation breakpoint cluster region 5' to BCL-6 in B-cell non-Hodgkin's lymphoma. Cancer Res62(14):4089-94 2002 |
| PubMed ID: 12124346 |
| |
| Marti, S.B., Cichon, S., Propping, P., and Nothen, M., Human metabotropic glutamate receptor 2 gene (GRM2): chromosomal sublocalization (3p21.1-p21.2) and genomic organization Am J Med Genet114(1):12-14 2002 |
| PubMed ID: 11840499 |
| |
| Ormestad M, Blixt A, Churchill A, Martinsson T, Enerback S, Carlsson P, Foxe3 haploinsufficiency in mice: a model for Peters' anomaly. Invest Ophthalmol Vis Sci43(5):1350-7 2002 |
| PubMed ID: 11980846 |
| |
| Delany NS, Hurle M, Facer P, Alnadaf T, Plumpton C, Kinghorn I, See CG, Costigan M, Anand P, Woolf CJ, Crowther D, Sanseau P, Tate SN, Identification and characterization of a novel human vanilloid receptor-like protein, VRL-2. Physiol Genomics4(3):165-74 2001 |
| PubMed ID: 11160995 |
| |
| Ghosh AK, Majumder M, Steele R, White RA, Ray RB, A novel 16-kilodalton cellular protein physically interacts with and antagonizes the functional activity of c-myc promoter-binding protein 1. Mol Cell Biol21(2):655-62 2001 |
| PubMed ID: 11134351 |
| |
| Watkins WS, Ricker CE, Bamshad MJ, Carroll ML, Nguyen SV, Batzer MA, Harpending HC, Rogers AR, Jorde LB, Patterns of ancestral human diversity: an analysis of Alu-insertion and restriction-site polymorphisms. Am J Hum Genet68(3):738-52 2001 |
| PubMed ID: 11179020 |
| |
| Knight SJ, Lese CM, Precht KS, Kuc J, Ning Y, Lucas S, Regan R, Brenan M, Nicod A, Lawrie NM, Cardy DL, Nguyen H, Hudson TJ, Riethman HC, Ledbetter DH, Flint J, An optimized set of human telomere clones for studying telomere integrity and architecture. Am J Hum Genet67(2):320-32 2000 |
| PubMed ID: 10869233 |
| |
| Provencio I, Rodriguez IR, Jiang G, Hayes WP, Moreira EF, Rollag MD, A novel human opsin in the inner retina. J Neurosci20(2):600-5 2000 |
| PubMed ID: 10632589 |
| |
| Brass N, Racz A, Bauer C, Heckel D, Sybrecht G, Meese E, Role of amplified genes in the production of autoantibodies. Blood93(7):2158-66 1999 |
| PubMed ID: 10090922 |
| |
| Franz T, Vingron M, Boehm T, Dear TN, Capn7: a highly divergent vertebrate calpain with a novel C-terminal domain. Mamm Genome10(3):318-21 1999 |
| PubMed ID: 10051333 |
| |
| Kimura M, Matsuda Y, Yoshioka T, Okano Y, Cell cycle-dependent expression and centrosome localization of a third human aurora/Ipl1-related protein kinase, AIK3. J Biol Chem274(11):7334-40 1999 |
| PubMed ID: 10066797 |
| |
| Lu R, Chan BS, Schuster VL, Cloning of the human kidney PAH transporter: narrow substrate specificity and regulation by protein kinase C. Am J Physiol276(2 Pt 2):F295-303 1999 |
| PubMed ID: 9950961 |
| |
| Somia NV, Schmitt MJ, Vetter DE, Van Antwerp D, Heinemann SF, Verma IM, LFG: an anti-apoptotic gene that provides protection from Fas-mediated cell death. Proc Natl Acad Sci U S A96(22):12667-72 1999 |
| PubMed ID: 10535980 |
| |
| Song YH, Naumova AK, Liebhaber SA, Cooke NE, Physical and meiotic mapping of the region of human chromosome 4q11-q13 encompassing the vitamin D binding protein DBP/Gc-globulin and albumin multigene cluster. Genome Res9(6):581-7 1999 |
| PubMed ID: 10400926 |
| |
| Wong J, Blanco P, Affara NA, An exon map of the AZFc male infertility region of the human Y chromosome. Mamm Genome10(1):57-61 1999 |
| PubMed ID: 9892735 |
| |
| Angrist M, Jing S, Bolk S, Bentley K, Nallasamy S, Halushka M, Fox GM, Chakravarti A, Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility. Genomics48:354-62 1998 |
| PubMed ID: 9545641 |
| |
| Bernard M, Sanseau P, Henry C, Couturier A, Prigent C, Cloning of STK13, a third human protein kinase related to Drosophila aurora and budding yeast Ipl1 that maps on chromosome 19q13.3-ter. Genomics53:406-9 1998 |
| PubMed ID: 9799611 |
| |
| Betz R, Gray SG, Ekstrom C, Larsson C, Ekstrom TJ, Human histone deacetylase 2, HDAC2 (Human RPD3), is localized to 6q21 by radiation hybrid mapping. Genomics52:245-6 1998 |
| PubMed ID: 9782097 |
| |
| Bischoff JR, Anderson L, Zhu Y, Mossie K, Ng L, Souza B, Schryver B, Flanagan P, Clairvoyant F, Ginther C, Chan CS, Novotny M, Slamon DJ, Plowman GD, A homologue of Drosophila aurora kinase is oncogenic and amplified in human colorectal cancers. EMBO J17(11):3052-65 1998 |
| PubMed ID: 9606188 |
| |
| Bonne S, van Hengel J, van Roy F, Chromosomal mapping of human armadillo genes belonging to the p120(ctn)/plakophilin subfamily. Genomics51:452-4 1998 |
| PubMed ID: 9721216 |
| |
| Cao Y, Traer E, Zimmerman GA, McIntyre TM, Prescott SM, Cloning, expression, and chromosomal localization of human long-chain fatty acid-CoA ligase 4 (FACL4). Genomics49:327-30 1998 |
| PubMed ID: 9598324 |
| |
| Chae YJ, Chung CE, Kim BJ, Lee MH, Lee H, The gene encoding guanidinoacetate methyltransferase (GAMT) maps to human chromosome 19 at band p13.3 and to mouse chromosome 10. Genomics49:162-4 1998 |
| PubMed ID: 9570966 |
| |
| Chidambaram A, Gerrard B, Hanson M, Dean M, Chromosomal localization of the human and murine orthologues of the Drosophila smoothened gene. Genomics53:416-7 1998 |
| PubMed ID: 9799615 |
| |
| Chou HH, Takematsu H, Diaz S, Iber J, Nickerson E, Wright KL, Muchmore EA, Nelson DL, Warren ST, Varki A, A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence. Proc Natl Acad Sci U S A95(20):11751-6 1998 |
| PubMed ID: 9751737 |
| |
| Ding H, Beckers MC, Plaisance S, Marynen P, Collen D, Belayew A, Characterization of a double homeodomain protein (DUX1) encoded by a cDNA homologous to 3.3 kb dispersed repeated elements. Hum Mol Genet7:1681-94 1998 |
| PubMed ID: 9736770 |
| |
| Eki T, Okumura K, Abe M, Kagotani K, Taguchi H, Murakami Y, Pan ZQ, Hanaoka F, Mapping of the human genes encoding cyclin H (CCNH) and the CDK- activating kinase (CAK) assembly factor MAT1 (MNAT1) to chromosome bands 5q13.3-q14 and 14q23, respectively. Genomics47:115-20 1998 |
| PubMed ID: 9465303 |
| |
| Garcia-Barcelo M, Tsui SKW, Chim SS, Fung KP, Lee CY, Waye MM, Mapping of the human cysteine-rich intestinal protein gene CRIP1 to the human chromosomal segment 7q11.23. Genomics47:419-22 1998 |
| PubMed ID: 9480758 |
| |
| Gondo Y, Okada T, Matsuyama N, Saitoh Y, Yanagisawa Y, Ikeda JE, Human megasatellite DNA RS447: copy-number polymorphisms and interspecies conservation. Genomics54:39-49 1998 |
| PubMed ID: 9806828 |
| |
| Hashida H, Goto J, Zhao N, Takahashi N, Hirai M, Kanazawa I, Sakaki Y, Cloning and mapping of ZNF231, a novel brain-specific gene encoding neuronal double zinc finger protein whose expression is enhanced in a neurodegenerative disorder, multiple system atrophy (MSA). Genomics54:50-8 1998 |
| PubMed ID: 9806829 |
| |
| Her C, Doggett NA, Cloning, structural characterization, and chromosomal localization of the human orthologue of saccharomyces cerevisiae MSH5 gene [In Process Citation] Genomics52:50-61 1998 |
| PubMed ID: 9740671 |
| |
| Her C, Wood TC, Eichler EE, Mohrenweiser HW, Ramagli LS, Siciliano MJ, Weinshilboum RM, Human hydroxysteroid sulfotransferase SULT2B1: two enzymes encoded by a single chromosome 19 gene. Genomics53:284-95 1998 |
| PubMed ID: 9799594 |
| |
| Hirohata S, Seldin MF, Apte SS, Chromosomal assignment of two ADAM genes, TACE (ADAM17) and MLTNB (ADAM19), to human chromosomes 2 and 5, respectively, and of Mltnb to mouse chromosome 11. Genomics54:178-9 1998 |
| PubMed ID: 9806848 |
| |
| Howe K, Williamson J, Boddy N, Sheer D, Freemont P, Solomon E, The ubiquitin-homology gene PIC1: characterization of mouse (Pic1) and human (UBL1) genes and pseudogenes. Genomics47:92-100 1998 |
| PubMed ID: 9465300 |
| |
| Ishii H, Kim DH, Fujita T, Endo Y, Saeki S, Yamamoto TT, cDNA cloning of a new low-density lipoprotein receptor-related protein and mapping of its gene (LRP3) to chromosome bands 19q12-q13. 2. Genomics51:132-5 1998 |
| PubMed ID: 9693042 |
| |
| Johnstone RW, Tommerup N, Hansen C, Vissing H, Shi Y, Mapping of the human PAWR (par-4) gene to chromosome 12q21. Genomics53:241-3 1998 |
| PubMed ID: 9790775 |
| |
| Kishino T, Wagstaff J, Genomic organization of the UBE3A/E6-AP gene and related pseudogenes. Genomics47:101-7 1998 |
| PubMed ID: 9465301 |
| |
| Kohno T, Kawanishi M, Inazawa J, Yokota J, Identification of CpG islands hypermethylated in human lung cancer by the arbitrarily primed-PCR method. Hum Genet102:258-64 1998 |
| PubMed ID: 9544836 |
| |
| Kremmidiotis G, Baker E, Crawford J, Eyre HJ, Nahmias J, Callen DF, Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity. Genomics49:467-71 1998 |
| PubMed ID: 9615235 |
| |
| Laurent AM, Puechberty J, Prades C, Roizes G, Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity. Genomics52:166-72 1998 |
| PubMed ID: 9782082 |
| |
| Lin RY, Vera JC, Chaganti RS, Golde DW, Human monocarboxylate transporter 2 (MCT2) is a high affinity pyruvate transporter. J Biol Chem273:28959-65 1998 |
| PubMed ID: 9786900 |
| |
| Lund EG, Kerr TA, Sakai J, Li WP, Russell DW, cDNA cloning of mouse and human cholesterol 25-hydroxylases, polytopic membrane proteins that synthesize a potent oxysterol regulator of lipid metabolism. J Biol Chem273(51):34316-27 1998 |
| PubMed ID: 9852097 |
| |
| Malkhosyan S, Yasuda J, Soto JL, Sekiya T, Yokota J, Perucho M, Molecular karyotype (amplotype) of metastatic colorectal cancer by unbiased arbitrarily primed PCR DNA fingerprinting. Proc Natl Acad Sci U S A95:10170-5 1998 |
| PubMed ID: 9707619 |
| |
| Matena K, Boehm T, Dear N, Genomic organization of mouse Capn5 and Capn6 genes confirms that they are a distinct calpain subfamily. Genomics48:117-20 1998 |
| PubMed ID: 9503024 |
| |
| Nomiyama H, Amano K, Kusuda J, Imai T, Miura R, Yoshie O, Matsuda Y, The human CC chemokine TECK (SCYA25) maps to chromosome 19p13.2. Genomics51:311-2 1998 |
| PubMed ID: 9722960 |
| |
| Nomiyama H, Osborne LR, Imai T, Kusuda J, Miura R, Tsui LC, Yoshie O, Assignment of the human CC chemokine MPIF-2/eotaxin-2 (SCYA24) to chromosome 7q11.23. Genomics49:339-40 1998 |
| PubMed ID: 9598329 |
| |
| O'Keefe DS, Su SL, Bacich DJ, Horiguchi Y, Luo Y, Powell CT, Zandvliet D, Russell PJ, Molloy PL, Nowak NJ, Shows TB, Mullins C, Vonder Haar RA, Fair WR, Heston WDW, Mapping, genomic organization and promoter analysis of the human prostate-specific membrane antigen gene [In Process Citation] Biochim Biophys Acta1443:113-27 1998 |
| PubMed ID: 9838072 |
| |
| Pelletier GJ, Brody SL, Liapis H, White RA, Hackett BP, A human forkhead/winged-helix transcription factor expressed in developing pulmonary and renal epithelium. Am J Physiol274:L351-9 1998 |
| PubMed ID: 9530170 |
| |
| Peyrard M, Parveneh S, Lagercrantz S, Ekman M, Fransson I, Sahlen S, DumanskiJP, Cloning, expression pattern, and chromosomal assignment to 16q23 of the human
gamma-adaptin gene (ADTG). Genomics50(2):275-80 1998 |
| PubMed ID: 9653655 |
| |
| Porcellati F, Hlaing T, Togawa M, Stevens MJ, Larkin DD, Hosaka Y, Glover TW, Henry DN, Greene DA, Killen PD, Human Na(+)-myo-inositol cotransporter gene: alternate splicing generates diverse transcripts. Am J Physiol274(5 Pt 1):C1215-25 1998 |
| PubMed ID: 9612208 |
| |
| Rouquier S, Friedman C, Delettre C, van den Engh G, Blancher A, Crouau-Roy B,
Trask BJ, Giorgi D., A gene recently inactivated in human defines a new olfactory receptor family in
mammals. Hum Mol Genet7(9):1337-45 1998 |
| PubMed ID: 9700185 |
| |
| Saupe S, Roizes G, Peter M, Boyle S, Gardiner K, De Sario A, Molecular cloning of a human cDNA IGSF3 encoding an immunoglobulin-like membrane protein: expression and mapping to chromosome band 1p13. Genomics52:305-11 1998 |
| PubMed ID: 9790749 |
| |
| Seifarth W, Baust C, Murr A, Skladny H, Krieg-Schneider F, Blusch J, Werner T, Hehlmann R, Leib-Mosch C, Proviral structure, chromosomal location, and expression of HERV-K-T47D, a novel human endogenous retrovirus derived from T47D particles. J Virol72(10):8384-91 1998 |
| PubMed ID: 9733890 |
| |
| Shah ZH, Migliosi V, Miller SC, Wang A, Friedman TB, Jacobs HT, Chromosomal locations of three human nuclear genes (RPSM12, TUFM, and AFG3L1) specifying putative components of the mitochondrial gene expression apparatus. Genomics48:384-8 1998 |
| PubMed ID: 9545647 |
| |
| Speel EJ, van der Ven PF, Albrechts JC, Ramaekers FC, Furst DO, Hopman AH, Assignment of the human gene for the sarcomeric M-band protein myomesin (MYOM1) to 18p11.31-p11.32. Genomics54:184-6 1998 |
| PubMed ID: 9806852 |
| |
| Trask BJ, Massa H, Brand-Arpon V, Chan K, Friedman C, Nguyen OT, Eichler E, van den Engh G, Rouquier S, Shizuya H, Giorgi D, Large multi-chromosomal duplications encompass many members of the olfactory receptor gene family in the human genome. Hum Mol Genet7:2007-20 1998 |
| PubMed ID: 9817916 |
| |
| Triepels R, van den Heuvel L, Loeffen J, Smeets R, Trijbels F, Smeitink J, The nuclear-encoded human NADH:ubiquinone oxidoreductase NDUFA8 subunit: cDNA cloning, chromosomal localization, tissue distribution, and mutation detection in complex-I-deficient patients. Hum Genet103:557-63 1998 |
| PubMed ID: 9860297 |
| |
| Van Tine BA, Knops JF, Butler A, Deloukas P, Shaw GM, King PH, Localization of HuC (ELAVL3) to chromosome 19p13.2 by fluorescence in situ hybridization utilizing a novel tyramide labeling technique. Genomics53:296-9 1998 |
| PubMed ID: 9799595 |
| |
| White KE, Econs MJ, Localization of PiUS, a stimulator of cellular phosphate uptake to human chromosome 3p21.3. Somat Cell Mol Genet24:71-4 1998 |
| PubMed ID: 9776982 |
| |
| Winand NJ, Panzer JA, Kolodner RD, Cloning and characterization of the human and Caenorhabditis elegans homologs of the Saccharomyces cerevisiae MSH5 gene. Genomics53:69-80 1998 |
| PubMed ID: 9787078 |
| |
| Xu WF, Andersen H, Whitmore TE, Presnell SR, Yee DP, Ching A, Gilbert T, Davie EW, Foster DC, Cloning and characterization of human protease-activated receptor 4. Proc Natl Acad Sci U S A95(12):6642-6 1998 |
| PubMed ID: 9618465 |
| |
| Yamagoe S, Kameoka Y, Hashimoto K, Mizuno S, Suzuki K, Molecular cloning, structural characterization, and chromosomal mapping of the human LECT2 gene. Genomics48:324-9 1998 |
| PubMed ID: 9545637 |
| |
| Yoshida K, Yoshitomo-Nakagawa K, Seki N, Sasaki M, Sugano S, Cloning, expression analysis, and chromosomal localization of BH- protocadherin (PCDH7), a novel member of the cadherin superfamily. Genomics49:458-61 1998 |
| PubMed ID: 9615233 |
| |
| Albala JS, Thelen MP, Prange C, Fan W, Christensen M, Thompson LH, Lennon GG, Identification of a novel human RAD51 homolog, RAD51B [published erratum appears in Genomics 1998 Aug 1;51(3):480] Genomics46:476-9 1997 |
| PubMed ID: 9441753 |
| |
| Bartuski AJ, Kamachi Y, Schick C, Overhauser J, Silverman GA, Cytoplasmic antiproteinase 2 (PI8) and bomapin (PI10) map to the serpin cluster at 18q21.3. Genomics43:321-8 1997 |
| PubMed ID: 9268635 |
| |
| Bastians H, Krebber H, Hoheisel J, Ohl S, Lichter P, Ponstingl H, Joos S, Assignment of the human serine/threonine protein phosphatase 4 gene (PPP4C) to chromosome 16p11-p12 by fluorescence in situ hybridization. Genomics42:181-2 1997 |
| PubMed ID: 9177794 |
| |
| Bergstein I, Eisenberg LM, Bhalerao J, Jenkins NA, Copeland NG, Osborne MP, Bowcock AM, Brown AM, Isolation of two novel WNT genes, WNT14 and WNT15, one of which (WNT15) is closely linked to WNT3 on human chromosome 17q21. Genomics46:450-8 1997 |
| PubMed ID: 9441749 |
| |
| Budarf M, McDonald T, Sellinger B, Kozak C, Graham C, Wistow G, Localization of the human gene for macrophage migration inhibitory factor (MIF) to chromosome 22q11.2. Genomics39:235-6 1997 |
| PubMed ID: 9027512 |
| |
| Chatterjee TK, Eapen A, Kanis AB, Fisher RA, Genomic organization, 5'-flanking region, and chromosomal localization of the human RGS3 gene. Genomics45:429-33 1997 |
| PubMed ID: 9344672 |
| |
| Davies JP, Cotter PD, Ioannou YA, Cloning and mapping of human Rab7 and Rab9 cDNA sequences and identification of a Rab9 pseudogene. Genomics41:131-4 1997 |
| PubMed ID: 9126495 |
| |
| Eichler EE, Budarf ML, Rocchi M, Deaven LL, Doggett NA, Baldini A, Nelson
DL, Mohrenweiser HW, Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of
pericentromeric plasticity. Hum Mol Genet6(7):991-1002 1997 |
| PubMed ID: 9215666 |
| |
| Ernstsson S, Betz R, Lagercrantz S, Larsson C, Ericksson S, Cederberg A,
Carlsson P, Enerbäck S, Cloning and Characterization of freac-9 (FKHL171), a Novel Kidney-Expressed
Human Forkhead Gene That Maps to Chromosome 1p32-p34. Genomics46(1):78-85 1997 |
| PubMed ID: 9405125 |
| |
| Ernstsson S, Betz R, Lagercrantz S, Larsson C, Ericksson S, Cederberg A, Carlsson P, Enerback S, Cloning and characterization of freac-9 (FKHL17), a novel kidney- expressed human forkhead gene that maps to chromosome 1p32-p34. Genomics46:78-85 1997 |
| PubMed ID: 9403061 |
| |
| Fu GK, Lin D, Zhang MY, Bikle DD, Shackleton CH, Miller WL, Portale AA, Cloning of human 25-hydroxyvitamin D-1 alpha-hydroxylase and mutations causing vitamin D-dependent rickets type 1. Mol Endocrinol11:1961-70 1997 |
| PubMed ID: 9415400 |
| |
| Godiska R, Chantry D, Raport CJ, Sozzani S, Allavena P, Leviten D, Mantovani A, Gray PW, Human macrophage-derived chemokine (MDC), a novel chemoattractant for monocytes, monocyte-derived dendritic cells, and natural killer cells. J Exp Med185(9):1595-604 1997 |
| PubMed ID: 9151897 |
| |
| Haddad LA, Fuzikawa AK, Pena SD, Simultaneous detection of size and sequence polymorphisms in the transcribed trinucleotide repeat D2S196E (EST00493). Hum Genet99:796-800 1997 |
| PubMed ID: 9187676 |
| |
| Harun RB, Smith KK, Leek JP, Markham AF, Norris A, Morrison JF, Characterization of human SHC p66 cDNA and its processed pseudogene mapping to Xq12-q13.1. Genomics42:349-52 1997 |
| PubMed ID: 9192859 |
| |
| Her C, Kaur GP, Athwal RS, Weinshilboum RM, Human sulfotransferase SULT1C1: cDNA cloning, tissue-specific expression, and chromosomal localization. Genomics41:467-70 1997 |
| PubMed ID: 9169148 |
| |
| Hieshima K, Imai T, Opdenakker G, Van Damme J, Kusuda J, Tei H, Sakaki Y, Takatsuki K, Miura R, Yoshie O, Nomiyama H, Molecular cloning of a novel human CC chemokine liver and activation-regulated chemokine (LARC) expressed in liver. Chemotactic activity for lymphocytes and gene localization on chromosome 2. J Biol Chem272(9):5846-53 1997 |
| PubMed ID: 9038201 |
| |
| Howard TD, Paznekas WA, Green ED, Chiang LC, Ma N, Ortiz de Luna RI, Garcia Delgado C, Gonzalez-Ramos M, Kline AD, Jabs EW, Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome [see comments] Nat Genet15:36-41 1997 |
| PubMed ID: 8988166 |
| |
| Huang X, Cheng A, Honkanen RE, Genomic organization of the human PP4 gene encoding a serine/threonine protein phosphatase (PP4) suggests a common ancestry with PP2A. Genomics44:336-43 1997 |
| PubMed ID: 9325055 |
| |
| Ishiai M, Dean FB, Okumura K, Abe M, Moon KY, Amin AA, Kagotani K, Taguchi H, Murakami Y, Hanaoka F, O'Donnell M, Hurwitz J, Eki T, Isolation of human and fission yeast homologues of the budding yeast origin recognition complex subunit ORC5: human homologue (ORC5L) maps to 7q22. Genomics46:294-8 1997 |
| PubMed ID: 9417919 |
| |
| Jones MH, Numata M, Shimane M, Identification and characterization of BRDT: A testis-specific gene related to the bromodomain genes RING3 and Drosophila fsh. Genomics45:529-34 1997 |
| PubMed ID: 9367677 |
| |
| Jones MH, Zhang Y, Tirosvoutis KN, Davey PM, Webster AR, Walsh D, Spurr NK, Affara NA, Chromosomal assignment of 311 sequences transcribed in human adult testis. Genomics40:155-67 1997 |
| PubMed ID: 9070934 |
| |
| Kastury K, Taylor WE, Gutierrez M, Ramirez L, Coucke PJ, Van Hauwe P, Van Camp G, Bhasin S, Chromosomal mapping of two members of the human dynein gene family to chromosome regions 7p15 and 11q13 near the deafness loci DFNA 5 and DFNA 11. Genomics44:362-4 1997 |
| PubMed ID: 9325061 |
| |
| Kehrer-Sawatzki H, Haussler J, Krone W, Bode H, Jenne DE, Mehnert KU, Tummers U, Assum G, The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regions. Hum Genet99:237-47 1997 |
| PubMed ID: 9048928 |
| |
| Kim DH, Magoori K, Inoue TR, Mao CC, Kim HJ, Suzuki H, Fujita T, Endo Y, Saeki S, Yamamoto TT, Exon/intron organization, chromosome localization, alternative splicing, and transcription units of the human apolipoprotein E receptor 2 gene. J Biol Chem272(13):8498-504 1997 |
| PubMed ID: 9079678 |
| |
| Kowalski PE, Freeman JD, Nelson DT, Mager DL, Genomic structure and evolution of a novel gene (PLA2L) with duplicated phospholipase A2-like domains. Genomics39:38-46 1997 |
| PubMed ID: 9027484 |
| |
| Kusuda J, Hirai M, Toyoda A, Hashimoto K, Localization of the human transaldolase gene (TALDO) to chromosome 1p33- p34.1 by fluorescence in situ hybridization and PCR analysis of somatic cell hybirds. Genomics40:378-81 1997 |
| PubMed ID: 9119412 |
| |
| Lauer P, Meyer NC, Prass CE, Starnes SM, Wolff RK, Gnirke A, Clone-contig and STS maps of the hereditary hemochromatosis region on human chromosome 6p21.3-p22. Genome Res7(5):457-70 1997 |
| PubMed ID: 9149942 |
| |
| Lench NJ, Macadam R, Markham AF, The human gene encoding FKBP-rapamycin associated protein (FRAP) maps to chromosomal band 1p36.2. Hum Genet99(4):547-9 1997 |
| PubMed ID: 9099849 |
| |
| Li L, Wu Q, Barnoski BL, Cooper MD, High-resolution genetic map of the human glutamyl aminopeptidase gene (ENPEP). Genomics43:380-3 1997 |
| PubMed ID: 9268642 |
| |
| Liang Y, Chen H, Asher JH Jr, Chang CC, Friedman TB, Human inner ear OCP2 cDNA maps to 5q22-5q35.2 with related sequences on chromosomes 4p16.2-4p14, 5p13-5q22, 7pter-q22, 10 and 12p13-12qter. Gene184:163-7 1997 |
| PubMed ID: 9031623 |
| |
| Lutz CM, Richards JE, Scott KL, Sinha S, Yang-Feng TL, Frankel WN, Thompson DA, Neuropeptide Y receptor genes mapped in human and mouse: receptors with high affinity for pancreatic polypeptide are not clustered with receptors specific for neuropeptide Y and peptide YY. Genomics46:287-90 1997 |
| PubMed ID: 9417917 |
| |
| Martinez de Arrieta C, Perez Jurado L, Bernal J, Coloma A, Structure, organization, and chromosomal mapping of the human neurogranin gene (NRGN). Genomics41:243-9 1997 |
| PubMed ID: 9143500 |
| |
| Matthijs G, Schollen E, Pardon E, Veiga-Da-Cunha M, Jaeken J, Cassiman JJ, Van Schaftingen E, Mutations in PMMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome) [published erratum appears in Nat Genet 1997 Jul;16(3):316] Nat Genet16:88-92 1997 |
| PubMed ID: 9140401 |
| |
| Matthijs G, Schollen E, Pirard M, Budarf ML, Van Schaftingen E, Cassiman JJ, PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13. Genomics40:41-7 1997 |
| PubMed ID: 9070917 |
| |
| Melkonyan HS, Chang WC, Shapiro JP, Mahadevappa M, Fitzpatrick PA, Kiefer MC, Tomei LD, Umansky SR, SARPs: a family of secreted apoptosis-related proteins. Proc Natl Acad Sci U S A94:13636-41 1997 |
| PubMed ID: 9391078 |
| |
| Milon L, Rousseau-Merck MF, Munier A, Erent M, Lascu I, Capeau J, Lacombe ML, nm23-H4, a new member of the family of human nm23/nucleoside diphosphate kinase genes localised on chromosome 16p13. Hum Genet99:550-7 1997 |
| PubMed ID: 9099850 |
| |
| Minekura H, Fujino T, Kang MJ, Fujita T, Endo Y, Yamamoto TT, Human acyl-coenzyme A synthetase 3 cDNA and localization of its gene (ACS3) to chromosome band 2q34-q35. Genomics42:180-1 1997 |
| PubMed ID: 9177793 |
| |
| Morton SM, Veile RA, Helms C, Lee M, Kuo WL, Gray J, Donis-Keller H, Subregional localization of 21 chromosome 7-specific expressed sequence tags (ESTs) by FISH using newly identified YACs and P1s. Genomics46:491-4 1997 |
| PubMed ID: 9441757 |
| |
| Nadal M, Moreno S, Pritchard M, Preciado MA, Estivill X, Ramos-Arroyo MA, Down syndrome: characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21) (q26;q22.1) by FISH. J Med Genet34(1):50-4 1997 |
| PubMed ID: 9032650 |
| |
| Nagai M, Sakakibara J, Wakui K, Fukushima Y, Igarashi S, Tsuji S, Arakawa M, Ono T, Localization of the squalene epoxidase gene (SQLE) to human chromosome region 8q24.1. Genomics44:141-3 1997 |
| PubMed ID: 9286711 |
| |
| Nakayama T, Fujiwara T, Miyazawa A, Asakawa S, Shimizu N, Shimizu Y, Mikoshiba K, Akagawa K, Mapping of the human HPC-1/syntaxin 1A gene (STX1A) to chromosome 7 band q11.2. Genomics42:173-6 1997 |
| PubMed ID: 9177791 |
| |
| Odermatt A, Taschner PE, Scherer SW, Beatty B, Khanna VK, Cornblath DR, Chaudhry V, Yee WC, Schrank B, Karpati G, Breuning MH, Knoers N, MacLennan DH, Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody disease. Genomics45:541-53 1997 |
| PubMed ID: 9367679 |
| |
| Pangilinan F, Li Q, Weaver T, Lewis BC, Dang CV, Spencer F, Mammalian BUB1 protein kinases: map positions and in vivo expression. Genomics46:379-88 1997 |
| PubMed ID: 9441741 |
| |
| Pichaud F, Delage-Mourroux R, Pidoux E, Jullienne A, Rousseau-Merck MF, Chromosomal localization of the type-I 15-PGDH gene to 4q34-q35. Hum Genet99(2):279-81 1997 |
| PubMed ID: 9048936 |
| |
| Prinsen CF, de Bruijn DR, Merkx GF, Veerkamp JH, Assignment of the human adipocyte fatty acid-binding protein gene (FABP4) to chromosome 8q21 using somatic cell hybrid and fluorescence in situ hybridization techniques. Genomics40:207-9 1997 |
| PubMed ID: 9070949 |
| |
| Reddy PH, Stockburger E, Gillevet P, Tagle DA, Mapping and characterization of novel (CAG)n repeat cDNAs from adult human brain derived by the oligo capture method. Genomics46:174-82 1997 |
| PubMed ID: 9417904 |
| |
| Reddy UR, Phatak S, Allen C, Nycum LM, Sulman EP, White PS, Biegel JA, Localization of the human Ror1 gene (NTRKR1) to chromosome 1p31-p32 by fluorescence in situ hybridization and somatic cell hybrid analysis. Genomics41:283-5 1997 |
| PubMed ID: 9143508 |
| |
| Seboun E, Barbaux S, Bourgeron T, Nishi S, Agulnik A, Egashira M, Nikkawa N, Bishop C, Fellous M, McElreavey K, Kasahara M, Algonik A$[corrected to Agulnik A], Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene [published erratum appears in Genomics 1997 Oct 15;45(2):477] Genomics41:227-35 1997 |
| PubMed ID: 9143498 |
| |
| Sen S, Zhou H, Ripmaster T, Hittelman WN, Schimmel P, White RA, Expression of a gene encoding a tRNA synthetase-like protein is enhanced in tumorigenic human myeloid leukemia cells and is cell cycle stage- and differentiation-dependent. Proc Natl Acad Sci U S A94:6164-9 1997 |
| PubMed ID: 9177188 |
| |
| Spicer AP, Seldin MF, Olsen AS, Brown N, Wells DE, Doggett NA, Itano N, Kimata K, Inazawa J, McDonald JA, Chromosomal localization of the human and mouse hyaluronan synthase genes. Genomics41:493-7 1997 |
| PubMed ID: 9169154 |
| |
| Sun ZS, Albrecht U, Zhuchenko O, Bailey J, Eichele G, Lee CC, RIGUI, a putative mammalian ortholog of the Drosophila period gene. Cell90:1003-11 1997 |
| PubMed ID: 9323128 |
| |
| Tamimi RM, Steingrimsson E, Montgomery-Dyer K, Copeland NG, Jenkins NA, Tapscott SJ, NEUROD2 and NEUROD3 genes map to human chromosomes 17q12 and 5q23-q31 and mouse chromosomes 11 and 13, respectively. Genomics40:355-7 1997 |
| PubMed ID: 9119405 |
| |
| Tang XX, Pleasure DE, Ikegaki N, cDNA cloning, chromosomal localization, and expression pattern of EPLG8, a new member of the EPLG gene family encoding ligands of EPH- related protein-tyrosine kinase receptors. Genomics41:17-24 1997 |
| PubMed ID: 9126477 |
| |
| Thiagalingam A, Lengauer C, Baylin SB, Nelkin BD, RREB1, a ras responsive element binding protein, maps to human chromosome 6p25. Genomics45:630-2 1997 |
| PubMed ID: 9367691 |
| |
| Thiagalingam A, Lengauer C, Baylin SB, Nelkin BD, RREB1, a ras responsive element binding protein, maps to human chromosome 6p25. Genomics45(3):630-2 1997 |
| PubMed ID: 98035890 |
| |
| Walker RL, Anziano P, Meltzer PS, A PAC containing the human mitochondrial DNA polymerase gamma gene (POLG) maps to chromosome 15q25. Genomics40:376-8 1997 |
| PubMed ID: 9119411 |
| |
| White RA, Adkison LR, Dowler LL, Ray RB, Chromosomal localization of the human gene encoding c-myc promoter- binding protein (MPB1) to chromosome 1p35-pter. Genomics39:406-8 1997 |
| PubMed ID: 9119380 |
| |
| Wickman K, Seldin MF, James MR, Gendler SJ, Clapham DE, Partial structure, chromosome localization, and expression of the mouse Icln gene. Genomics40:402-8 1997 |
| PubMed ID: 9073507 |
| |
| Williams RS, Shohet RV, Stillman B., A human protein related to yeast Cdc6p.
A human protein related to yeast Cdc6p. Proc Natl Acad Sci U S A94(1):142-7 1997 |
| PubMed ID: 8990175 |
| |
| Yamada Y, Nezu J, Shimane M, Hirata Y, Molecular cloning of a novel vascular endothelial growth factor, VEGF-D. Genomics42:483-8 1997 |
| PubMed ID: 9205122 |
| |
| Yoshida R, Imai T, Hieshima K, Kusuda J, Baba M, Kitaura M, Nishimura M, Kakizaki M, Nomiyama H, Yoshie O, Molecular cloning of a novel human CC chemokine EBI1-ligand chemokine that is a specific functional ligand for EBI1, CCR7. J Biol Chem272:13803-9 1997 |
| PubMed ID: 9153236 |
| |
| Young AC, Chavez M, Giambernardi TA, Mattern V, McGill JR, Harris JM, Sarosdy MF, Patel P, Sakaguchi AY, Organization and expression of human telomere repeat binding factor genes. Somat Cell Mol Genet23:275-86 1997 |
| PubMed ID: 9542529 |
| |
| Yu J, Nagarajan S, Knez JJ, Udenfriend S, Chen R, Medof ME, The affected gene underlying the class K glycosylphosphatidylinositol (GPI) surface protein defect codes for the GPI transamidase. Proc Natl Acad Sci U S A94:12580-5 1997 |
| PubMed ID: 9356492 |
| |
| Albertsen HM, Smith SA, Melis R, Williams B, Holik P, Stevens J, White R, Sequence, genomic structure, and chromosomal assignment of human DOC-2. Genomics33:207-13 1996 |
| PubMed ID: 8660969 |
| |
| Aman MJ, Tayebi N, Obiri NI, Puri RK, Modi WS, Leonard WJ, cDNA cloning and characterization of the human interleukin 13 receptor alpha chain. J Biol Chem271(46):29265-70 1996 |
| PubMed ID: 8910586 |
| |
| Amann J, Valentine M, Kidd VJ, Lahti JM, Localization of chi1-related helicase genes to human chromosome regions 12p11 and 12p13: similarity between parts of these genes and conserved human telomeric-associated DNA. Genomics32:260-5 1996 |
| PubMed ID: 8833153 |
| |
| Andersen SE, Lench NJ, Markham AF, YAC clones that extend the human chromosome 12cen-12q15 region contig map. Mamm Genome7(10):780-3 1996 |
| PubMed ID: 8854870 |
| |
| Bergsagel PL, Chesi M, Nardini E, Brents LA, Kirby SL, Kuehl WM, Promiscuous translocations into immunoglobulin heavy chain switch regions in multiple myeloma. Proc Natl Acad Sci U S A93(24):13931-6 1996 |
| PubMed ID: 8943038 |
| |
| Bosio A, Binczek E, Le Beau MM, Fernald AA, Stoffel W, The human gene CGT encoding the UDP-galactose ceramide galactosyl transferase (cerebroside synthase): cloning, characterization, and assignment to human chromosome 4, band q26. Genomics34:69-75 1996 |
| PubMed ID: 8661025 |
| |
| Carrier A, Rosier MF, Guillemot F, Goguel AF, Pulcini F, Bernheim A, Auffray C, Devignes MD, Integrated physical, genetic, and genic map covering 3 Mb around the human NGF gene (NGFB) at 1p13. Genomics31:80-9 1996 |
| PubMed ID: 8808283 |
| |
| Chen H, Gos A, Morris MA, Antonarakis SE, Localization of a human homolog of the mouse pericentrin gene (PCNT) to chromosome 21qter. Genomics35:620-4 1996 |
| PubMed ID: 8812505 |
| |
| Chen H, Rossier C, Lalioti MD, Lynn A, Chakravarti A, Perrin G, Antonarakis SE, Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3. Am J Hum Genet59:66-75 1996 |
| PubMed ID: 8659545 |
| |
| Chiang PW, Fogel E, Jackson CL, Lieuallen K, Lennon G, Qu X, Wang SQ, Kurnit DM, Isolation, sequencing, and mapping of the human homologue of the yeast transcription factor, SPT5. Genomics38:421-4 1996 |
| PubMed ID: 8975720 |
| |
| Chiang PW, Wang SQ, Smithivas P, Song WJ, Crombez E, Akhtar A, Im R, Greenfield J, Ramamoorthy S, Van Keuren M, Blackburn CC, Tsai CH, Kurnit DM, Isolation and characterization of the human and mouse homologues (SUPT4H and Supt4h) of the yeast SPT4 gene. Genomics34:368-75 1996 |
| PubMed ID: 8786137 |
| |
| Coon SL, Mazuruk K, Bernard M, Roseboom PH, Klein DC, Rodriguez IR, The human serotonin N-acetyltransferase (EC 2.3.1.87) gene (AANAT): structure, chromosomal localization, and tissue expression. Genomics34:76-84 1996 |
| PubMed ID: 8661026 |
| |
| DiMarco SP, Glover TW, Miller DE, Reines D, Warren ST, Transcription elongation factor SII (TCEA) maps to human chromosome 3p22 --> p21.3. Genomics36:185-8 1996 |
| PubMed ID: 8812434 |
| |
| Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, Dormishian F, Domingo R Jr, Ellis MC, Fullan A, Hinton LM, Jones NL, Kimmel BE, Kronmal GS, Lauer P, Lee VK, Loeb DB, Mapa FA, McClelland E, Meyer NC, Mintier GA, Moeller N, Moore T, Morikang E, Wolff RK, et al, A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis [see comments] Nat Genet13:399-408 1996 |
| PubMed ID: 8696333 |
| |
| Ferrer J, Aoki M, Behn P, Nestorowicz A, Riggs A, Permutt MA, Mitochondrial glycerol-3-phosphate dehydrogenase. Cloning of an alternatively spliced human islet-cell cDNA, tissue distribution, physical mapping, and identification of a polymorphic genetic marker. Diabetes45(2):262-6 1996 |
| PubMed ID: 8549872 |
| |
| Gastier JM, Brody T, Pulido JC, Businga T, Sunden S, Hu X, Maitra S, Buetow KH, Murray JC, Sheffield VC, Boguski M, Duyk GM, Hudson TJ, Development of a screening set for new (CAG/CTG)n dynamic mutations. Genomics32:75-85 1996 |
| PubMed ID: 8786123 |
| |
| Goldmuntz E, Wang Z, Roe BA, Budarf ML, Cloning, genomic organization, and chromosomal localization of human citrate transport protein to the DiGeorge/velocardiofacial syndrome minimal critical region. Genomics33:271-6 1996 |
| PubMed ID: 8660975 |
| |
| Hahn SA, Hoque AT, Moskaluk CA, da Costa LT, Schutte M, Rozenblum E, Seymour AB, Weinstein CL, Yeo CJ, Hruban RH, Kern SE, Homozygous deletion map at 18q21.1 in pancreatic cancer. Cancer Res56:490-4 1996 |
| PubMed ID: 8564959 |
| |
| Hanai R, Caron PR, Wang JC, Human TOP3: a single-copy gene encoding DNA topoisomerase III. Proc Natl Acad Sci U S A93:3653-7 1996 |
| PubMed ID: 8622991 |
| |
| Hayward BE, Fantes JA, Warner JP, Intody S, Leek JP, Markham AF, Bonthron DT, Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of chromosome 2p23. Mamm Genome7(6):454-8 1996 |
| PubMed ID: 8662230 |
| |
| Her C, Raftogianis R, Weinshilboum RM, Human phenol sulfotransferase STP2 gene: molecular cloning, structural characterization, and chromosomal localization. Genomics33:409-20 1996 |
| PubMed ID: 8661000 |
| |
| Hirai M, Kusuda J, Hashimoto K, Assignment of human ADP ribosylation factor (ARF) genes ARF1 and ARF3 to chromosomes 1q42 and 12q13, respectively. Genomics34(2):263-5 1996 |
| PubMed ID: 8661066 |
| |
| Hu RJ, Lee MP, Johnson LA, Feinberg AP, A novel human homologue of yeast nucleosome assembly protein, 65 kb centromeric
to the p57KIP2 gene, is biallelically expressed in fetal and adult tissues. Hum Mol Genet5(11):1743-8 1996 |
| PubMed ID: 8923002 |
| |
| Ishizuka T, Ahmad I, Kita K, Sonoda T, Ishijima S, Sawa K, Suzuki N, Tatibana M, The human phosphoribosylpyrophosphate synthetase-associated protein 39 gene (PRPSAP1) is located in the chromosome region 17q24-q25. Genomics33:332-4 1996 |
| PubMed ID: 8660991 |
| |
| Jones MH, Furlong RA, Burkin H, Chalmers IJ, Brown GM, Khwaja O, Affara NA, The Drosophila developmental gene fat facets has a human homologue in Xp11.4
which escapes X-inactivation and has related sequences on Yq11.2. Hum Mol Genet5(11):1695-701 1996 |
| PubMed ID: 8922996 |
| |
| Junker S, Brondum-Nielsen K, Newell JW, Matthias P, Tommerup N, Assignment of the human gene for Oct-binding factor-1 (OBF1), a B-cell- specific coactivator of octamer-binding transcription factors 1 and 2, to 11q23.1 by somatic cell hybridization and in situ hybridization. Genomics33:143-5 1996 |
| PubMed ID: 8617501 |
| |
| Kalz-Fuller B, Heidrich-Kaul C, Nothen M, Bause E, Schwanitz G, Localization of the human glucosidase I gene to chromosome 2p12-p13 by fluorescence in situ hybridization and PCR analysis of somatic cell hybrids. Genomics34:442-3 1996 |
| PubMed ID: 8786151 |
| |
| Kekuda R, Prasad PD, Fei YJ, Torres-Zamorano V, Sinha S, Yang-Feng TL, Leibach FH, Ganapathy V, Cloning of the sodium-dependent, broad-scope, neutral amino acid transporter Bo from a human placental choriocarcinoma cell line. J Biol Chem271:18657-61 1996 |
| PubMed ID: 8702519 |
| |
| Kokke FT, Elsawy T, Bengtsson U, Wasmuth JJ, Wang Jabs E, Tse CM, Donowitz M, Brant SR, A NHE3-related pseudogene is on human chromosome 10; the functional gene maps to 5p15.3. Mamm Genome7(3):235-6 1996 |
| PubMed ID: 8833252 |
| |
| Kusuda J, Hidari N, Hirai M, Hashimoto K, Sequence analysis of the cDNA for the human casein kinase I delta (CSNK1D) gene and its chromosomal localization. Genomics32:140-3 1996 |
| PubMed ID: 8786104 |
| |
| Lagercrantz J, Carson E, Larsson C, Nordenskjold M, Weber G, Isolation and characterization of a novel gene close to the human phosphoinositide-specific phospholipase C beta 3 gene on chromosomal region 11q13. Genomics31:380-4 1996 |
| PubMed ID: 8838322 |
| |
| Leenders F, Prescher G, Dolez V, Begue A, de Launoit Y, Adamski J, Assignment of human 17 beta-hydroxysteroid dehydrogenase IV to chromosome 5q2 by fluorescence in situ hybridization. Genomics37:403-4 1996 |
| PubMed ID: 8938456 |
| |
| Lench NJ, Telford EA, Andersen SE, Moynihan TP, Robinson PA, Markham AF, An EST and STS-based YAC contig map of human chromosome 9q22.3. Genomics38:199-205 1996 |
| PubMed ID: 8954802 |
| |
| Li H, Lahti JM, Valentine M, Saito M, Reed SI, Look AT, Kidd VJ, Molecular cloning and chromosomal localization of the human cyclin C (CCNC) and cyclin E (CCNE) genes: deletion of the CCNC gene in human tumors. Genomics32:253-9 1996 |
| PubMed ID: 8833152 |
| |
| Lomako J, Mazuruk K, Lomako WM, Alonso MD, Whelan WJ, Rodriguez IR, The human intron-containing gene for glycogenin maps to chromosome 3, band q24. Genomics33:519-22 1996 |
| PubMed ID: 8661012 |
| |
| Ma T, Yang B, Kuo WL, Verkman AS, cDNA cloning and gene structure of a novel water channel expressed exclusively in human kidney: evidence for a gene cluster of aquaporins at chromosome locus 12q13. Genomics35:543-50 1996 |
| PubMed ID: 8812490 |
| |
| Mao C, Baumgartner AP, Jha PK, Huang TH, Sarkar S, Assignment of the human fast skeletal troponin T gene (TNNT3) to chromosome 11p15.5: evidence for the presence of 11pter in a monochromosome 9 somatic cell hybrid in NIGMS mapping panel 2. Genomics31:385-8 1996 |
| PubMed ID: 8838323 |
| |
| Margolis RL, Stine OC, McInnis MG, Ranen NG, Rubinsztein DC, Leggo J, Brando LV, Kidwai AS, Loev SJ, Breschel TS, Callahan C, Simpson SG, DePaulo JR, McMahon FJ, Jain S, Paykel ES, Walsh C, DeLisi LE, Crow TJ, Torrey EF, Ashworth RG, Macke JP, Nathans J, Ross CA, cDNA cloning of a human homologue of the Caenorhabditis elegans cell fate-determining gene mab-21: expression, chromosomal localization and analysis of a highly polymorphic (CAG)n trinucleotide repeat. Hum Mol Genet5:607-16 1996 |
| PubMed ID: 8733127 |
| |
| Mattei MG, Borg JP, Rosnet O, Marme D, Birnbaum D, Assignment of vascular endothelial growth factor (VEGF) and placenta growth factor (PLGF) genes to human chromosome 6p12-p21 and 14q24-q31 regions, respectively. Genomics32:168-9 1996 |
| PubMed ID: 8786112 |
| |
| Meese E, Gottert E, Zang KD, Sauter M, Schommer S, Mueller-Lantzsch N, Human endogenous retroviral element k10 (HERV-K10): chromosomal localization by somatic hybrid mapping and fluorescence in situ hybridization. Cytogenet Cell Genet72:40-2 1996 |
| PubMed ID: 8565630 |
| |
| Miyagi Y, Yasumitsu H, Eki T, Miyata S, Kkawa N, Hirahara F, Aoki I, Misugi K, Miyazaki K, Assignment of the human PP5/TFPI-2 gene to 7q22 by FISH and PCR-based human/rodent cell hybrid mapping panel analysis. Genomics35:267-8 1996 |
| PubMed ID: 8661135 |
| |
| Mock BA, Liu L, LePaslier D, Huang S, The B-lymphocyte maturation promoting transcription factor BLIMP1/PRDI- BF1 maps to D6S447 on human chromosome 6q21-q22.1 and the syntenic region of mouse chromosome 10. Genomics37:24-8 1996 |
| PubMed ID: 8921366 |
| |
| Neri C, Albanese V, Lebre AS, Holbert S, Saada C, Bougueleret L, Meier-Ewert S, Le Gall I, Millasseau P, Bui H, Giudicelli C, Massart C, Guillou S, Gervy P, Poullier E, Rigault P, Weissenbach J, Lennon G, Chumakov I, Dausset J, Lehrach H, Cohen D, Cann HM, Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disorders. Hum Mol Genet5:1001-9 1996 |
| PubMed ID: 8817338 |
| |
| Nichols RC, Blinder J, Pai SI, Ge Q, Targoff IN, Plotz PH, Liu P, Assignment of two human autoantigen genes-isoleucyl-tRNA synthetase locates to 9q21 and lysyl-tRNA synthetase locates to 16q23-q24. Genomics36:210-3 1996 |
| PubMed ID: 8812440 |
| |
| Riggins GJ, Thiagalingam S, Rozenblum E, Weinstein CL, Kern SE, Hamilton SR, Willson JK, Markowitz SD, Kinzler KW, Vogelstein B, Mad-related genes in the human. Nat Genet13:347-9 1996 |
| PubMed ID: 8673135 |
| |
| Scherer SW, Duvoisin RM, Kuhn R, Heng HH, Belloni E, Tsui LC, Localization of two metabotropic glutamate receptor genes, GRM3 and GRM8, to human chromosome 7q. Genomics31:230-3 1996 |
| PubMed ID: 8824806 |
| |
| Schultz D, Litt M, Smith L, Thayer M, McCormack K, Localization of two potassium channel beta subunit genes, KCNA1B and KCNA2B. Genomics31:389-91 1996 |
| PubMed ID: 8838324 |
| |
| Simon A, Lagercrantz J, Bajalica-Lagercrantz S, Eriksson U, Primary structure of human 11-cis retinol dehydrogenase and organization and chromosomal localization of the corresponding gene. Genomics36:424-30 1996 |
| PubMed ID: 8884265 |
| |
| Stafforini DM, Satoh K, Atkinson DL, Tjoelker LW, Eberhardt C, Yoshida H, Imaizumi T, Takamatsu S, Zimmerman GA, McIntyre TM, Gray PW, Prescott SM, Platelet-activating factor acetylhydrolase deficiency. A missense mutation near the active site of an anti-inflammatory phospholipase. J Clin Invest97(12):2784-91 1996 |
| PubMed ID: 8675689 |
| |
| Stewart AF, Richard CW 3rd, Suzow J, Stephan D, Weremowicz S, Morton CC, Adra CN, Cloning of human RTEF-1, a transcriptional enhancer factor-1-related gene preferentially expressed in skeletal muscle: evidence for an ancient multigene family. Genomics37:68-76 1996 |
| PubMed ID: 8921372 |
| |
| Sunden SL, Businga T, Beck J, McClain A, Gastier JM, Pulido JC, Yandava CN, Brody T, Ghazizadeh J, Weber JL, Duyk GM, Murray JC, Buetow KH, Sheffield VC, Chromosomal assignment of 2900 tri- and tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2. Genomics32:15-20 1996 |
| PubMed ID: 8786107 |
| |
| Sunden SLF, Carr LL, Clements JL, Motto DG, Koretzky GA, Polymorphism in and localization of the gene LCP2 (SLP-76) to chromosome 5q33.1-qter. Genomics35:269-70 1996 |
| PubMed ID: 8661136 |
| |
| Tamimi R, Steingrimsson E, Copeland NG, Dyer-Montgomery K, Lee JE, Hernandez R, Jenkins NA, Tapscott SJ, The NEUROD gene maps to human chromosome 2q32 and mouse chromosome 2. Genomics34:418-21 1996 |
| PubMed ID: 8786144 |
| |
| Thibonnier M, Graves MK, Wagner MS, Auzan C, Clauser E, Willard HF, Structure, sequence, expression, and chromosomal localization of the human V1a vasopressin receptor gene. Genomics31:327-34 1996 |
| PubMed ID: 8838314 |
| |
| Vocero-Akbani A, Helms C, Wang JC, Sanjurjo FJ, Korte-Sarfaty J, Veile RA, Liu L, Jauch A, Burgess AK, Hing AV, Holt MS, Ramachandra S, Whelan AJ, Anker R, Ahrent L, Chen M, Gavin MR, Iannantuoni K, Morton SM, Pandit SD, Read CM, Steinbrueck T, Warlick C, Smoller DA, Donis-Keller H, Mapping human telomere regions with YAC and P1 clones: chromosome- specific markers for 27 telomeres including 149 STSs and 24 polymorphisms for 14 proterminal regions. Genomics36:492-506 1996 |
| PubMed ID: 8884273 |
| |
| Watson B Jr, Bergman SM, Myracle A, Callen DF, Acton RT, Warnock DG, Genetic association of 11 beta-hydroxysteroid dehydrogenase type 2 (HSD11B2) flanking microsatellites with essential hypertension in blacks. Hypertension28(3):478-82 1996 |
| PubMed ID: 8794836 |
| |
| White RA, Hughes RT, Adkison LR, Bruns G, Zon LI, The gene encoding protein kinase SEK1 maps to mouse chromosome 11 and human chromosome 17. Genomics34:430-2 1996 |
| PubMed ID: 8786147 |
| |
| Yasuda J, Navarro JM, Malkhosyan S, Velazquez A, Arribas R, Sekiya T, Perucho M, Chromosomal assignment of human DNA fingerprint sequences by simultaneous hybridization to arbitrarily primed PCR products from human/rodent monochromosome cell hybrids. Genomics34:1-8 1996 |
| PubMed ID: 8661018 |
| |
| Yu F, Warburton D, Wellington S, Danziger RS, Assignment of GUCIA2, the gene coding for the alpha 2 subunit of soluble guanylyl cyclase, to position 11q21-q22 on human chromosome 11. Genomics33:334-6 1996 |
| PubMed ID: 8660992 |
| |
| Angrist M, Wells DE, Chakravarti A, Pandey A, Chromosomal localization of the mouse Src-like adapter protein (Slap) gene and its putative human homolog SLA. Genomics30:623-5 1995 |
| PubMed ID: 8825655 |
| |
| Avraham S, Jiang S, Ota S, Fu Y, Deng B, Dowler LL, White RA, Avraham H, Structural and functional studies of the intracellular tyrosine kinase MATK gene and its translated product. J Biol Chem270:1833-42 1995 |
| PubMed ID: 7530249 |
| |
| Bailey A, Norris AL, Leek JP, Clissold PM, Carr IM, Ogilvie DJ, Morrison JF, Meredith DM, Markham AF, Yeast artificial chromosome cloning of the beta-catenin locus on human chromosome 3p21-22. Chromosome Res3:201-3 1995 |
| PubMed ID: 7780664 |
| |
| Bloch KD, Wolfram JR, Brown DM, Roberts JD Jr, Zapol DG, Lepore JJ, Filippov G, Thomas JE, Jacob HJ, Bloch DB, Three members of the nitric oxide synthase II gene family (NOS2A, NOS2B, and NOS2C) colocalize to human chromosome 17. Genomics27:526-30 1995 |
| PubMed ID: 7558036 |
| |
| Campion D, Martin C, Heilig R, Charbonnier F, Moreau V, Flaman JM, Petit JL, Hannequin D, Brice A, Frebourg T, The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease. Genomics26:254-7 1995 |
| PubMed ID: 7601450 |
| |
| Chakravarti S, Stallings RL, SundarRaj N, Cornuet PK, Hassell JR, Primary structure of human lumican (keratan sulfate proteoglycan) and localization of the gene (LUM) to chromosome 12q21.3-q22. Genomics27:481-8 1995 |
| PubMed ID: 7558030 |
| |
| Chen H, Leipprandt JR, Traviss CE, Sopher BL, Jones MZ, Cavanagh KT, Friderici KH, Molecular cloning and characterization of bovine beta-mannosidase. J Biol Chem270(8):3841-8 1995 |
| PubMed ID: 7876128 |
| |
| Chiang PW, Dzida G, Grumet J, Cheng JF, Song WJ, Crombez E, Van Keuren ML, Kurnit DM, Expressed sequence tags from the long arm of human chromosome 21. Genomics29:383-9 1995 |
| PubMed ID: 8666385 |
| |
| Chu W, Burns DK, Swerlick RA, Presky DH, Identification and characterization of a novel cytokine-inducible nuclear protein from human endothelial cells. J Biol Chem270(17):10236-45 1995 |
| PubMed ID: 7730328 |
| |
| el-Maghrabi MR, Lange AJ, Jiang W, Yamagata K, Stoffel M, Takeda J, Fernald AA, Le Beau MM, Bell GI, Baker L, et al, Human fructose-1,6-bisphosphatase gene (FBP1): exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiency. Genomics27:520-5 1995 |
| PubMed ID: 7558035 |
| |
| Gastier JM, Pulido JC, Sunden S, Brody T, Buetow KH, Murray JC, Weber JL, Hudson TJ, Sheffield VC, Duyk GM, Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markers. Hum Mol Genet4:1829-36 1995 |
| PubMed ID: 8595403 |
| |
| Gelernter J, Rao PA, Pauls DL, Hamblin MW, Sibley DR, Kidd KK, Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with Tourette syndrome. Genomics26:207-9 1995 |
| PubMed ID: 7601444 |
| |
| Gimbel W, Klein V, Brass N, Fischer U, Piontek K, Overmyer K, Gottert E, Zang KD, Meese E, Isolation and localization of transcribed sequences on human chromosome 22. Cytogenet Cell Genet71:81-5 1995 |
| PubMed ID: 7606934 |
| |
| Henning KA, Li L, Iyer N, McDaniel LD, Reagan MS, Legerski R, Schultz RA, Stefanini M, Lehmann AR, Mayne LV, et al, The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH. Cell82:555-64 1995 |
| PubMed ID: 7664335 |
| |
| Heppell-Parton A, Cahn A, Bench A, Lowe N, Lehrach H, Zehetner G, Rabbitts P, Thioredoxin, a mediator of growth inhibition, maps to 9q31. Genomics26:379-81 1995 |
| PubMed ID: 7601465 |
| |
| Hunt CC, Eyre HJ, Akkari PA, Meredith C, Dorosz SM, Wilton SD, Callen DF, Laing NG, Baker E, Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation. Cytogenet Cell Genet71:94-5 1995 |
| PubMed ID: 7606936 |
| |
| Johnson DW, Qumsiyeh M, Benkhalifa M, Marchuk DA, Assignment of human transforming growth factor-beta type I and type III receptor genes (TGFBR1 and TGFBR3) to 9q33-q34 and 1p32-p33, respectively. Genomics28:356-7 1995 |
| PubMed ID: 8530052 |
| |
| Khanna M, Qin KN, Klisak I, Belkin S, Sparkes RS, Cheng KC, Localization of multiple human dihydrodiol dehydrogenase (DDH1 and DDH2) and chlordecone reductase (CHDR) genes in chromosome 10 by the polymerase chain reaction and fluorescence in situ hybridization. Genomics25:588-90 1995 |
| PubMed ID: 7789999 |
| |
| Kiefer MC, Brauer MJ, Powers VC, Wu JJ, Umansky SR, Tomei LD, Barr PJ, Modulation of apoptosis by the widely distributed Bcl-2 homologue Bak. Nature374:736-9 1995 |
| PubMed ID: 7715731 |
| |
| Klanke CA, Su YR, Callen DF, Wang Z, Meneton P, Baird N, Kandasamy RA, Orlowski J, Otterud BE, Leppert M, et al, Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1. Genomics25:615-22 1995 |
| PubMed ID: 7759094 |
| |
| Koehler MR, Bosserhoff A, von Beust G, Bauer A, Blesch A, Buettner R, Schlegel J, Bogdahn U, Schmid M, Assignment of the human melanoma inhibitory activity gene (MIA) to 19q13.32-q13.33 by fluorescence in situ hybridization (FISH). Genomics35:265-7 1995 |
| PubMed ID: 8661134 |
| |
| Kuo WL, Stafford DW, Cruces J, Gray J, Solera J, Chromosomal localization of the gamma-glutamyl carboxylase gene at 2p12. Genomics25:746-8 1995 |
| PubMed ID: 7759116 |
| |
| Kusuda J, Tanuma R, Gotoh E, Toyoda A, Hashimoto K, Assignment of a human autoimmune antigen, p80-coilin gene to chromosome 17q21-q23 and of its possible pseudogene to chromosome 14. Hum Genet95:233-4 1995 |
| PubMed ID: 7860074 |
| |
| Larsson C, Hellqvist M, Pierrou S, White I, Enerback S, Carlsson P, Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), - 3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHL12). Genomics30:464-9 1995 |
| PubMed ID: 8825632 |
| |
| Larsson C, Lardelli M, White I, Lendahl U, The human NOTCH1, 2, and 3 genes are located at chromosome positions 9q34, 1p13-p11, and 19p13.2-p13.1 in regions of neoplasia-associated translocation. Genomics24:253-8 1995 |
| PubMed ID: 7698746 |
| |
| Larsson C, White I, Johansson C, Stark A, Meijer J, Localization of the human soluble epoxide hydrolase gene (EPHX2) to chromosomal region 8p21-p12. Hum Genet95:356-8 1995 |
| PubMed ID: 7868134 |
| |
| Lee D, Szumlanski C, Houtman J, Honchel R, Rojas K, Overhauser J, Wieben ED, Weinshilboum RM, Thiopurine methyltransferase pharmacogenetics. Cloning of human liver cDNA and a processed pseudogene on human chromosome 18q21.1. Drug Metab Dispos23:398-405 1995 |
| PubMed ID: 7628307 |
| |
| Li J, Ma J, Potter H, Identification and expression analysis of a potential familial Alzheimer disease gene on chromosome 1 related to AD3. Proc Natl Acad Sci U S A92:12180-4 1995 |
| PubMed ID: 8618867 |
| |
| Liu J, Fujiwara TM, Buu NT, Sanchez FO, Cellier M, Paradis AJ, Frappier D, Skamene E, Gros P, Morgan K, et al, Identification of polymorphisms and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein gene. Am J Hum Genet56:845-53 1995 |
| PubMed ID: 7717395 |
| |
| Marigo V, Roberts DJ, Lee SM, Tsukurov O, Levi T, Gastier JM, Epstein DJ, Gilbert DJ, Copeland NG, Seidman CE, et al, Cloning, expression, and chromosomal location of SHH and IHH: two human homologues of the Drosophila segment polarity gene hedgehog. Genomics28:44-51 1995 |
| PubMed ID: 7590746 |
| |
| Moghrabi NN, Dawson DB, Bennett MJ, Assignment of the human peroxisomal palmitoyl-CoA oxidase gene to chromosome 17q23-qter by PCR technique. J Inherit Metab Dis18:705-9 1995 |
| PubMed ID: 8750608 |
| |
| Monitto CL, Levitt RC, DiSilvestre D, Holroyd KJ, Localization of the A3 adenosine receptor gene (ADORA3) to human chromosome 1p. Genomics26:637-8 1995 |
| PubMed ID: 7607699 |
| |
| Nichols RC, Pai SI, Ge Q, Targoff IN, Plotz PH, Liu P, Localization of two human autoantigen genes by PCR screening and in situ hybridization--glycyl-tRNA synthetase locates to 7p15 and alanyl- tRNA synthetase locates to 16q22. Genomics30:131-2 1995 |
| PubMed ID: 8595897 |
| |
| Otterness DM, Mohrenweiser HW, Brandriff BF, Weinshilboum RM, Dehydroepiandrosterone sulfotransferase gene (STD): localization to human chromosome band 19q13.3. Cytogenet Cell Genet70:45-7 1995 |
| PubMed ID: 7736787 |
| |
| Piontek K, Muller HW, Fischer U, Gottert E, Batzer MA, Meltzer PS, Trent JM, Meese E, Generation and characterization of a human chromosome 6-specific hncDNA library from a somatic cell hybrid. Cytogenet Cell Genet69:273-8 1995 |
| PubMed ID: 7698027 |
| |
| Purandare SM, Huntsman Breidenbach H, Li Y, Zhu XL, Sawada S, Neil SM, Brothman A, White R, Cawthon R, Viskochil D, Identification of neurofibromatosis 1 (NF1) homologous loci by direct sequencing, fluorescence in situ hybridization, and PCR amplification of somatic cell hybrids. Genomics30:476-85 1995 |
| PubMed ID: 8825634 |
| |
| Robinson PA, Leek JP, Thompson J, Carr IM, Bailey A, Moynihan TP, Coletta PL, Lench NJ, Markham AF, A human ubiquitin conjugating enzyme, L-UBC, maps in the Alzheimer's disease locus on chromosome 14q24.3. Mamm Genome6:725-31 1995 |
| PubMed ID: 8563171 |
| |
| Sheffield VC, Weber JL, Buetow KH, Murray JC, Even DA, Wiles K, Gastier JM, Pulido JC, Yandava C, Sunden SL, et al, A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. Hum Mol Genet4:1837-44 1995 |
| PubMed ID: 8595404 |
| |
| Simmons CF Jr, Clancy TE, Quan R, Knoll JH, The oxytocin receptor gene (OXTR) localizes to human chromosome 3p25 by fluorescence in situ hybridization and PCR analysis of somatic cell hybrids. Genomics26:623-5 1995 |
| PubMed ID: 7607693 |
| |
| Slaugenhaupt SA, Roca AL, Liebert CB, Altherr MR, Gusella JF, Reppert SM, Mapping of the gene for the Mel1a-melatonin receptor to human chromosome 4 (MTNR1A) and mouse chromosome 8 (Mtnr1a). Genomics27:355-7 1995 |
| PubMed ID: 7558006 |
| |
| Starborg M, Brundell E, Gell K, Larsson C, White I, Daneholt B, Hoog C, A murine replication protein accumulates temporarily in the heterochromatic regions of nuclei prior to initiation of DNA replication. J Cell Sci108 ( Pt 3):927-34 1995 |
| PubMed ID: 7622621 |
| |
| Steinkasserer A, Jones T, Sheer D, Koettnitz K, Hauber J, Bevec D, The eukaryotic cofactor for the human immunodeficiency virus type 1 (HIV-1) rev protein, eIF-5A, maps to chromosome 17p12-p13: three eIF-5A pseudogenes map to 10q23.3, 17q25, and 19q13.2. Genomics25:749-52 1995 |
| PubMed ID: 7759117 |
| |
| Stirling B, Cox NJ, Bell GI, Hanis CL, Spielman RS, Concannon P, Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs. Diabetes44(8):999-1001 1995 |
| PubMed ID: 7622007 |
| |
| Stoffel M, Stein R, Wright CV, Espinosa R 3rd, Le Beau MM, Bell GI, Localization of human homeodomain transcription factor insulin promoter factor 1 (IPF1) to chromosome band 13q12.1. Genomics28:125-6 1995 |
| PubMed ID: 7590740 |
| |
| Takeda J, Espinosa R 3rd, Eng S, Le Beau MM, Bell GI, Chromosomal assignment and tissue distribution of novel expressed sequence tags from a human pancreatic islet cDNA library. Genomics29:276-81 1995 |
| PubMed ID: 8530086 |
| |
| Tan KL, Webb GC, Baker RT, Board PG, Molecular cloning of a cDNA and chromosomal localization of a human theta-class glutathione S-transferase gene (GSTT2) to chromosome 22. Genomics25:381-7 1995 |
| PubMed ID: 7789971 |
| |
| Tirosvoutis KN, Divane A, Jones M, Affara NA, Characterization of a novel zinc finger gene (ZNF165) mapping to 6p21 that is expressed specifically in testis. Genomics28:485-90 1995 |
| PubMed ID: 7490084 |
| |
| Tsaur ML, Menzel S, Lai FP, Espinosa R 3rd, Concannon P, Spielman RS, Hanis CL, Cox NJ, Le Beau MM, German MS, et al, Isolation of a cDNA clone encoding a KATP channel-like protein expressed in insulin-secreting cells, localization of the human gene to chromosome band 21q22.1, and linkage studies with NIDDM. Diabetes44(5):592-6 1995 |
| PubMed ID: 7729621 |
| |
| Tucker SJ, James MR, Adelman JP, Assignment of KATP-1, the cardiac ATP-sensitive potassium channel gene (KCNJ5), to human chromosome 11q24. Genomics28:127-8 1995 |
| PubMed ID: 7590741 |
| |
| Warner JP, Leek JP, Intody S, Markham AF, Bonthron DT, Human glucokinase regulatory protein (GCKR): cDNA and genomic cloning, complete primary structure, and chromosomal localization. Mamm Genome6:532-6 1995 |
| PubMed ID: 8589523 |
| |
| Webb GC, Vaska VL, Gali RR, Ford JH, Board PG, The gene encoding human glutathione synthetase (GSS) maps to the long arm of chromosome 20 at band 11.2. Genomics30:617-9 1995 |
| PubMed ID: 8825653 |
| |
| White RA, Angeloni SV, Pasztor LM, Chromosomal localization of the beta-adducin gene to mouse chromosome 6 and human chromosome 2. Mamm Genome6:741-3 1995 |
| PubMed ID: 8563174 |
| |
| White RA, Dowler LL, Angeloni SV, Pasztor LM, MacArthur CA, Assignment of FGF8 to human chromosome 10q25-q26: mutations in FGF8 may be responsible for some types of acrocephalosyndactyly linked to this region. Genomics30:109-11 1995 |
| PubMed ID: 8595889 |
| |
| White RA, Dowler LL, Pasztor LM, Gatson LL, Adkison LR, Angeloni SV, Wilson DB, Assignment of the transcription factor GATA4 gene to human chromosome 8 and mouse chromosome 14: Gata4 is a candidate gene for Ds (disorganization). Genomics27:20-6 1995 |
| PubMed ID: 7665171 |
| |
| Whitmore TE, Day JR, Albers JJ, Localization of the human phospholipid transfer protein gene to chromosome 20q12-q13.1. Genomics28:599-600 1995 |
| PubMed ID: 7490104 |
| |
| Willenbrink W, Halaschek J, Schuffenhauer S, Kunz J, Steinkasserer A, Cyclophilin A, the major intracellular receptor for the immunosuppressant cyclosporin A, maps to chromosome 7p11.2-p13: four pseudogenes map to chromosomes 3, 10, 14, and 18. Genomics28:101-4 1995 |
| PubMed ID: 7590732 |
| |
| Yang B, Ma T, Verkman AS, cDNA cloning, gene organization, and chromosomal localization of a human mercurial insensitive water channel. Evidence for distinct transcriptional units. J Biol Chem270:22907-13 1995 |
| PubMed ID: 7559426 |
| |
| Aksoy IA, Callen DF, Apostolou S, Her C, Weinshilboum RM, Thermolabile phenol sulfotransferase gene (STM): localization to human chromosome 16p11.2. Genomics23:275-7 1994 |
| PubMed ID: 7829089 |
| |
| Allander SV, Larsson C, Ehrenborg E, Suwanichkul A, Weber G, Morris SL, Bajalica S, Kiefer MC, Luthman H, Powell DR, Characterization of the chromosomal gene and promoter for human insulin- like growth factor binding protein-5. J Biol Chem269:10891-8 1994 |
| PubMed ID: 7511611 |
| |
| Blachly-Dyson E, Baldini A, Litt M, McCabe ER, Forte M, Human genes encoding the voltage-dependent anion channel (VDAC) of the outer mitochondrial membrane: mapping and identification of two new isoforms. Genomics20:62-7 1994 |
| PubMed ID: 7517385 |
| |
| Bronner CE, Baker SM, Morrison PT, Warren G, Smith LG, Lescoe MK, Kane M, Earabino C, Lipford J, Lindblom A, et al, Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer. Nature368:258-61 1994 |
| PubMed ID: 8145827 |
| |
| Brown A, Lemieux N, Rossant J, Kothary R, Human homolog of a mouse sequence from the dystonia musculorum locus is on chromosome 6p12. Mamm Genome5:434-7 1994 |
| PubMed ID: 7919656 |
| |
| Chang MS, McNinch J, Basu R, Simonet S, Cloning and characterization of the human neutrophil-activating peptide (ENA-78) gene. J Biol Chem269:25277-82 1994 |
| PubMed ID: 7929219 |
| |
| Day JR, Albers JJ, Gilbert TL, Whitmore TE, McConathy WJ, Wolfbauer G, Purification and molecular cloning of human apolipoprotein F. Biochem Biophys Res Commun203:1146-51 1994 |
| PubMed ID: 8093033 |
| |
| Day JR, Albers JJ, Lofton-Day CE, Gilbert TL, Ching AF, Grant FJ, O'Hara PJ, Marcovina SM, Adolphson JL, Complete cDNA encoding human phospholipid transfer protein from human endothelial cells. J Biol Chem269:9388-91 1994 |
| PubMed ID: 8132678 |
| |
| Engle LJ, Kennett RH, Cloning, analysis, and chromosomal localization of myoxin (MYH12), the human homologue to the mouse dilute gene. Genomics19:407-16 1994 |
| PubMed ID: 8188282 |
| |
| Hanes J, von der Kammer H, Klaudiny J, Scheit KH, Characterization by cDNA cloning of two new human protein kinases. Evidence by sequence comparison of a new family of mammalian protein kinases. J Mol Biol244:665-72 1994 |
| PubMed ID: 7990150 |
| |
| Hough MR, Rosten PM, Sexton TL, Kay R, Humphries RK, Mapping of CD24 and homologous sequences to multiple chromosomal loci. Genomics22:154-61 1994 |
| PubMed ID: 7959762 |
| |
| Koppel DA, Wolfe SA, Fogelfeld LA, Merchant PS, Prouty L, Grimes SR, Primate testicular histone H1t genes are highly conserved and the human H1t gene is located on chromosome 6. J Cell Biochem54:219-30 1994 |
| PubMed ID: 8175896 |
| |
| Kos CH, Tihy F, Econs MJ, Murer H, Lemieux N, Tenenhouse HS, Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35. Genomics19:176-7 1994 |
| PubMed ID: 8188224 |
| |
| Kuestner RE, Elrod RD, Grant FJ, Hagen FS, Kuijper JL, Matthewes SL, O'Hara PJ, Sheppard PO, Stroop SD, Thompson DL, et al, Cloning and characterization of an abundant subtype of the human calcitonin receptor. Mol Pharmacol46:246-55 1994 |
| PubMed ID: 8078488 |
| |
| Kutty RK, Kutty G, Rodriguez IR, Chader GJ, Wiggert B, Chromosomal localization of the human heme oxygenase genes: heme oxygenase-1 (HMOX1) maps to chromosome 22q12 and heme oxygenase-2 (HMOX2) maps to chromosome 16p13.3. Genomics20:513-6 1994 |
| PubMed ID: 8034330 |
| |
| Laliberte J, Momparler RL, Human cytidine deaminase: purification of enzyme, cloning, and expression of its complementary DNA. Cancer Res54:5401-7 1994 |
| PubMed ID: 7923172 |
| |
| Leach RJ, Reus BE, Hundley JE, Johnson-Pais TL, Windle JJ, Confirmation of the assignment of the human tartrate-resistant acid phosphatase gene (ACP5) to chromosome 19. Genomics19:180-1 1994 |
| PubMed ID: 8188227 |
| |
| MacCollin M, Peterfreund R, MacDonald M, Fink JS, Gusella J, Mapping of a human A2a adenosine receptor (ADORA2) to chromosome 22. Genomics20:332-3 1994 |
| PubMed ID: 8020991 |
| |
| Macina RA, Negorev DG, Spais C, Ruthig LA, Hu XL, Riethman HC, Sequence organization of the human chromosome 2q telomere. Hum Mol Genet3:1847-53 1994 |
| PubMed ID: 7545974 |
| |
| Malo MS, Srivastava K, Andresen JM, Chen XN, Korenberg JR, Ingram VM, Targeted gene walking by low stringency polymerase chain reaction: assignment of a putative human brain sodium channel gene (SCN3A) to chromosome 2q24-31. Proc Natl Acad Sci U S A91:2975-9 1994 |
| PubMed ID: 8159690 |
| |
| McGregor LM, Baylin SB, Griffin CA, Hawkins AL, Nelkin BD, Molecular cloning of the cDNA for human TrkC (NTRK3), chromosomal assignment, and evidence for a splice variant. Genomics22:267-72 1994 |
| PubMed ID: 7806211 |
| |
| McPherson JD, Morton RA, Ewing CM, Wasmuth JJ, Overhauser J, Nagafuchi A, Tsukita S, Isaacs WB, Assignment of the human alpha-catenin gene (CTNNA1) to chromosome 5q21- q22. Genomics19:188-90 1994 |
| PubMed ID: 8188230 |
| |
| Negorev DG, Macina RA, Spais C, Ruthig LA, Hu XL, Riethman HC, Physical analysis of the terminal 270 kb of DNA from human chromosome 1q. Genomics22:569-78 1994 |
| PubMed ID: 8001968 |
| |
| Nomura N, Miyajima N, Sazuka T, Tanaka A, Kawarabayasi Y, Sato S, Nagase T, Seki N, Ishikawa K, Tabata S, Prediction of the coding sequences of unidentified human genes. I. The coding sequences of 40 new genes (KIAA0001-KIAA0040) deduced by analysis of randomly sampled cDNA clones from human immature myeloid cell line KG-1 [published erratum appears in DNA Res 1995 Aug 31;2(4):211] DNA Res1:27-35 1994 |
| PubMed ID: 7584026 |
| |
| Paschen W, Blackstone CD, Huganir RL, Ross CA, Human GluR6 kainate receptor (GRIK2): molecular cloning, expression, polymorphism, and chromosomal assignment. Genomics20:435-40 1994 |
| PubMed ID: 8034316 |
| |
| Perfetti R, Hawkins AL, Griffin CA, Egan JM, Zenilman ME, Shuldiner AR, Assignment of the human pancreatic regenerating (REG) gene to chromosome 2p12. Genomics20:305-7 1994 |
| PubMed ID: 8020983 |
| |
| Sakai J, Hoshino A, Takahashi S, Miura Y, Ishii H, Suzuki H, Kawarabayasi Y, Yamamoto T, Structure, chromosome location, and expression of the human very low density lipoprotein receptor gene. J Biol Chem269:2173-82 1994 |
| PubMed ID: 8294473 |
| |
| Seki M, Miyazawa H, Tada S, Yanagisawa J, Yamaoka T, Hoshino S, Ozawa K, Eki T, Nogami M, Okumura K, et al, Molecular cloning of cDNA encoding human DNA helicase Q1 which has homology to Escherichia coli Rec Q helicase and localization of the gene at chromosome 12p12. Nucleic Acids Res22:4566-73 1994 |
| PubMed ID: 7527136 |
| |
| Stoffel M, Espinosa R 3rd, Powell KL, Philipson LH, Le Beau MM, Bell GI, Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): localization to chromosome 2 and identification of a simple tandem repeat polymorphism. Genomics21:254-6 1994 |
| PubMed ID: 8088798 |
| |
| Su YR, Klanke CA, Houseal TW, Linn SC, Burk SE, Varvil TS, Otterud BE, Shull GE, Leppert MF, Menon AG, Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36. Genomics22:605-9 1994 |
| PubMed ID: 8001971 |
| |
| Tombran-Tink J, Pawar H, Swaroop A, Rodriguez I, Chader GJ, Localization of the gene for pigment epithelium-derived factor (PEDF) to chromosome 17p13.1 and expression in cultured human retinoblastoma cells. Genomics19:266-72 1994 |
| PubMed ID: 8188257 |
| |
| Tomlinson IM, Cook GP, Carter NP, Elaswarapu R, Smith S, Walter G, Buluwela L, Rabbitts TH, Winter G, Human immunoglobulin VH and D segments on chromosomes 15q11.2 and 16p11.2. Hum Mol Genet3:853-60 1994 |
| PubMed ID: 7951227 |
| |
| Uetz P, Abdelatty F, Villarroel A, Rappold G, Weiss B, Koenen M, Organisation of the murine 5-HT3 receptor gene and assignment to human chromosome 11. FEBS Lett339:302-6 1994 |
| PubMed ID: 8112471 |
| |
| Vamvakopoulos NC, Kunz J, Olberding U, Scherer SW, Sioutopoulou TO, Schneider V, Durkin AS, Nierman WC, Mapping the human growth hormone-releasing hormone receptor (GHRHR) gene to the short arm of chromosome 7 (7p13-p21) near the epidermal growth factor receptor (EGFR) gene. Genomics20:338-40 1994 |
| PubMed ID: 8020995 |
| |
| von der Kammer, The gene for the amyloid precursor-like protein APLP2 is assigned to human chromosome 11q23-q25. Genomics10:308 (1994):338-40 1994 |
| PubMed ID: 8020995 |
| |
| Webb GC, Baker RT, Coggan M, Board PG, Localization of the human UBA52 ubiquitin fusion gene to chromosome band 19p13.1-p12. Genomics19:567-9 1994 |
| PubMed ID: 8188300 |
| |
| Weber G, Friedman E, Grimmond S, Hayward NK, Phelan C, Skogseid B, Gobl A, Zedenius J, Sandelin K, Teh BT, et al, The phospholipase C beta 3 gene located in the MEN1 region shows loss of expression in endocrine tumours. Hum Mol Genet3:1775-81 1994 |
| PubMed ID: 7849701 |
| |
| Yandava CN, Meyers V, Watkins H, Duyk G, A trinucleotide repeat polymorphism in XT00444 (D13S635E). Hum Mol Genet3:1209 1994 |
| PubMed ID: 7981706 |
| |
| Yasuda K, Espinosa R 3rd, Takeda J, Le Beau MM, Bell GI, Localization of the kappa opioid receptor gene to human chromosome band 8q11.2. Genomics19:596-7 1994 |
| PubMed ID: 8188308 |
| |
| Chen H, Kalaitsidaki M, Warren AC, Avramopoulos D, Antonarakis SE, A novel zinc finger cDNA with a polymorphic pentanucleotide repeat (ATTTT)n maps on human chromosome 19p. Genomics15:621-5 1993 |
| PubMed ID: 8468057 |
| |
| Dixon B, Mansour M, Pohajdak B, Assignment of human B2-1 gene (D17S811E) to chromosome 17qter by PCR analysis of somatic cell hybrids and fluorescence in situ hybridization. Cytogenet Cell Genet63:42-4 1993 |
| PubMed ID: 8449036 |
| |
| Drwinga HL, Toji LH, Kim CH, Greene AE, Mulivor RA, NIGMS human/rodent somatic cell hybrid mapping panels 1 and 2. Genomics16:311-4 1993 |
| PubMed ID: 8314568 |
| |
| Dubois BL, Naylor SL, Characterization of NIGMS human/rodent somatic cell hybrid mapping panel 2 by PCR. Genomics16:315-9 1993 |
| PubMed ID: 8314569 |
| |
| Durkin AS, Maglott DR, Vamvakopoulos NC, Zoghbi HY, Nierman WC, Assignment of an intron-containing human heat-shock protein gene (hsp90 beta, HSPCB) to chromosome 6 near TCTE1 (6p21) and two intronless pseudogenes to chromosomes 4 and 15 by polymerase chain reaction amplification from a panel of hybrid cell lines. Genomics18:452-4 1993 |
| PubMed ID: 8288256 |
| |
| Fishel R, Lescoe MK, Rao MR, Copeland NG, Jenkins NA, Garber J, Kane M, Kolodner R, The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer [published erratum appears in Cell 1994 Apr 8;77(1):167] Cell75:1027-38 1993 |
| PubMed ID: 8252616 |
| |
| Gregor P, Reeves RH, Jabs EW, Yang X, Dackowski W, Rochelle JM, Brown RH Jr, Haines JL, O'Hara BF, Uhl GR, et al, Chromosomal localization of glutamate receptor genes: relationship to familial amyotrophic lateral sclerosis and other neurological disorders of mice and humans. Proc Natl Acad Sci U S A90:3053-7 1993 |
| PubMed ID: 8464923 |
| |
| Jabs EW, Muller U, Li X, Ma L, Luo W, Haworth IS, Klisak I, Sparkes R, Warman ML, Mulliken JB, et al, A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell75:443-50 1993 |
| PubMed ID: 8106171 |
| |
| Lane SA, Baker E, Sutherland GR, Tonks I, Hayward N, Ellem K, The human cell cycle gene CDC25B is located at 20p13. Genomics15:693-4 1993 |
| PubMed ID: 8468065 |
| |
| Li SH, McInnis MG, Margolis RL, Antonarakis SE, Ross CA, Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms. Genomics16:572-9 1993 |
| PubMed ID: 8325628 |
| |
| McClatchey AI, Cannon SC, Slaugenhaupt SA, Gusella JF, The cloning and expression of a sodium channel beta 1-subunit cDNA from human brain. Hum Mol Genet2:745-9 1993 |
| PubMed ID: 8394762 |
| |
| Myers JC, Sun MJ, D'Ippolito JA, Jabs EW, Neilson EG, Dion AS, Human cDNA clones transcribed from an unusually high-molecular-weight RNA encode a new collagen chain. Gene123:211-7 1993 |
| PubMed ID: 7916703 |
| |
| Nagao Y, Platero JS, Waheed A, Sly WS, Human mitochondrial carbonic anhydrase: cDNA cloning, expression, subcellular localization, and mapping to chromosome 16. Proc Natl Acad Sci U S A90:7623-7 1993 |
| PubMed ID: 8356065 |
| |
| Okuyama T, Batanian JR, Sly WS, Genomic organization and localization of gene for human carbonic anhydrase IV to chromosome 17q. Genomics16:678-84 1993 |
| PubMed ID: 8325641 |
| |
| Puranam RS, Eubanks JH, Heinemann SF, McNamara JO, Chromosomal localization of gene for human glutamate receptor subunit-7. Somat Cell Mol Genet19:581-8 1993 |
| PubMed ID: 8128318 |
| |
| Ramesh N, Ramesh V, Gusella JF, Geha R, Chromosomal localization of the gene for human B-cell antigen CD40. Somat Cell Mol Genet19:295-8 1993 |
| PubMed ID: 7687385 |
| |
| Riethman HC, Spais C, Buckingham J, Grady D, Moyzis RK, Physical analysis of the terminal 240 kb of DNA from human chromosome 7q. Genomics17:25-32 1993 |
| PubMed ID: 8406463 |
| |
| Shipley JM, Klinkenberg M, Wu BM, Bachinsky DR, Grubb JH, Sly WS, Mutational analysis of a patient with mucopolysaccharidosis type VII, and identification of pseudogenes. Am J Hum Genet52:517-26 1993 |
| PubMed ID: 7680524 |
| |
| Surratt CK, Persico AM, Yang XD, Edgar SR, Bird GS, Hawkins AL, Griffin CA, Li X, Jabs EW, Uhl GR, A human synaptic vesicle monoamine transporter cDNA predicts posttranslational modifications, reveals chromosome 10 gene localization and identifies TaqI RFLPs. FEBS Lett318:325-30 1993 |
| PubMed ID: 8095030 |
| |
| Talbot CC Jr, Warren AC, Avramopoulos D, Antonarakis SE, Polymorphic dinucleotide repeats at the D3S1417, D3S1418 and D12S271 loci. Hum Mol Genet2:1325 1993 |
| PubMed ID: 8401519 |
| |
| Virtaneva KI, Angelisova P, Baumruker T, Horejsi V, Nevanlinna H, Schroder J, The genes for CD37, CD53, and R2, all members of a novel gene family, are located on different chromosomes. Immunogenetics37:461-5 1993 |
| PubMed ID: 8436422 |
| |
| Westberg JA, Entler B, Prohaska R, Schroder JP, The gene coding for erythrocyte protein band 7.2b (EPB72) is located in band q34.1 of human chromosome 9. Cytogenet Cell Genet63:241-3 1993 |
| PubMed ID: 8500356 |
| |
| Chen H, Phillips HA, Callen DF, Kim RY, Wistow GJ, Antonarakis SE, Localization of the human gene for mu-crystallin to chromosome 16p. Genomics14:1115-6 1992 |
| PubMed ID: 1478656 |
| |
| Hudson TJ, Engelstein M, Lee MK, Ho EC, Rubenfield MJ, Adams CP, Housman DE, Dracopoli NC, Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms. Genomics13:622-9 1992 |
| PubMed ID: 1639389 |
| |
| Peinado MA, Malkhosyan S, Velazquez A, Perucho M, Isolation and characterization of allelic losses and gains in colorectal tumors by arbitrarily primed polymerase chain reaction. Proc Natl Acad Sci U S A89:10065-9 1992 |
| PubMed ID: 1359533 |
| |
| Tsai SP, Drayna D, The gene encoding human plasma carboxypeptidase B (CPB2) resides on chromosome 13. Genomics14:549-50 1992 |
| PubMed ID: 1427879 |
| |
| Vandenbergh DJ, Persico AM, Hawkins AL, Griffin CA, Li X, Jabs EW, Uhl GR, Human dopamine transporter gene (DAT1) maps to chromosome 5p15.3 and displays a VNTR. Genomics14:1104-6 1992 |
| PubMed ID: 1478653 |
|