MAP0001
HYBRID MAPPING PANEL
Description:
NIGMS HUMAN/RODENT SOMATIC CELL HYBRID MAPPING PANEL #1 DNA
Aliquot Size:
50 µg each
Brief Description:
50 µg DNA from each hybrid cell line and 100 µg DNA from each of three parental cell lines.
| 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 |
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| 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 |
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| 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 |
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| Onyango P, Koritschoner NP, Patrito LC, Zenke M, Weith A, Assignment of the gene encoding the core promoter element binding protein (COPEB) to human chromosome 10p15 by somatic hybrid analysis and fluorescence in situ hybridization. Genomics48:143-4 1998 |
| PubMed ID: 9503030 |
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| Yu H, Bowden DW, Spray BJ, Rich SS, Freedman BI, Identification of human plasma kallikrein gene polymorphisms and evaluation of their role in end-stage renal disease. Hypertension31(4):906-11 1998 |
| PubMed ID: 9535413 |
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| Freedman R, Coon H, Myles-Worsley M, Orr-Urtreger A, Olincy A, Davis A, Polymeropoulos M, Holik J, Hopkins J, Hoff M, Rosenthal J, Waldo MC, Reimherr F, Wender P, Yaw J, Young DA, Breese CR, Adams C, Patterson D, Adler LE, Kruglyak L, Leonard S, Byerley W, Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus. Proc Natl Acad Sci U S A94:587-92 1997 |
| PubMed ID: 9012828 |
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| 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 |
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| Perelman B, Dafni N, Naiman T, Eli D, Yaakov M, Feng TL, Sinha S, Weber G, Khodaei S, Sancar A, Dotan I, Canaani D, Molecular cloning of a novel human gene encoding a 63-kDa protein and its sublocalization within the 11q13 locus. Genomics41:397-405 1997 |
| PubMed ID: 9169138 |
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| Sjoholt G, Molven A, Lovlie R, Wilcox A, Sikela JM, Steen VM, Genomic structure and chromosomal localization of a human myo-inositol monophosphatase gene (IMPA). Genomics45:113-22 1997 |
| PubMed ID: 9339367 |
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| Skvorak AB, Robertson NG, Yin Y, Weremowicz S, Her H, Bieber FR, Beisel KW, Lynch ED, Beier DR, Morton CC, An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1). Genomics46:191-9 1997 |
| PubMed ID: 9417906 |
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| 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 |
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| 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 |
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| 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 |
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| Ammar DA, Eadie DM, Wong DJ, Ma YY, Kolakowski LF Jr, Yang-Feng TL, Thompson DA, Characterization of the human type 2 neuropeptide Y receptor gene (NPY2R) and localization to the chromosome 4q region containing the type 1 neuropeptide Y receptor gene. Genomics38:392-8 1996 |
| PubMed ID: 8975716 |
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| 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 |
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| 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 |
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| 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 |
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| Howard TD, Akots G, Bowden DW, Physical and genetic mapping of the muscle phosphofructokinase gene (PFKM): reassignment to human chromosome 12q. Genomics34:122-7 1996 |
| PubMed ID: 8661033 |
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| Lechleider RJ, de Caestecker MP, Dehejia A, Polymeropoulos MH, Roberts AB, Serine phosphorylation, chromosomal localization, and transforming growth factor-beta signal transduction by human bsp-1. J Biol Chem271:17617-20 1996 |
| PubMed ID: 8663601 |
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| 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 |
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| Lin X, Swaroop A, Vaccarino FM, Murtha MT, Haas M, Ji X, Ruddle FH, Leckman JF, Characterization and sequence analysis of the human homeobox-containing gene GBX2. Genomics31:335-42 1996 |
| PubMed ID: 8838315 |
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| 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 |
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| Orlicky DJ, Berry R, Sikela JM, Human chromosome 1 localization of the gene for a prostaglandin F2alpha receptor negative regulatory protein. Hum Genet97:655-8 1996 |
| PubMed ID: 8655148 |
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| Pennica D, Swanson TA, Shaw KJ, Kuang WJ, Gray CL, Beatty BG, Wood WI, Human cardiotrophin-1: protein and gene structure, biological and binding activities, and chromosomal localization. Cytokine8:183-9 1996 |
| PubMed ID: 8833032 |
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| 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 |
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| Tominaga S, Inazawa J, Tsuji S, Assignment of the human ST2 gene to chromosome 2 at q11.2. Hum Genet97:561-3 1996 |
| PubMed ID: 8655130 |
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| Wong MH, Rao PN, Pettenati MJ, Dawson PA, Localization of the ileal sodium-bile acid cotransporter gene (SLC10A2) to human chromosome 13q33. Genomics33:538-40 1996 |
| PubMed ID: 8661017 |
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| 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 |
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| Avraham S, London R, Fu Y, Ota S, Hiregowdara D, Li J, Jiang S, Pasztor LM, White RA, Groopman JE, et al, Identification and characterization of a novel related adhesion focal tyrosine kinase (RAFTK) from megakaryocytes and brain. J Biol Chem270:27742-51 1995 |
| PubMed ID: 7499242 |
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| Berry R, Stevens TJ, Walter NA, Wilcox AS, Rubano T, Hopkins JA, Weber J, Goold R, Soares MB, Sikela JM, Gene-based sequence-tagged-sites (STSs) as the basis for a human gene map. Nat Genet10:415-23 1995 |
| PubMed ID: 7670491 |
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| 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 |
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| Borglum AD, Flint T, Madsen P, Celis JE, Kruse TA, Refined mapping of the psoriasin gene S100A7 to chromosome 1cen-q21. Hum Genet96:592-6 1995 |
| PubMed ID: 8530009 |
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| Evans E, Cooley J, Remold-O'Donnell E, Characterization and chromosomal localization of ELANH2, the gene encoding human monocyte/neutrophil elastase inhibitor. Genomics28:235-40 1995 |
| PubMed ID: 8530031 |
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| 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 |
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| 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 |
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| Hejna JA, Saito H, Merkens LS, Tittle TV, Jakobs PM, Whitney MA, Grompe M, Friedberg AS, Moses RE, Cloning and characterization of a human cDNA (INPPL1) sharing homology with inositol polyphosphate phosphatases. Genomics29:285-7 1995 |
| PubMed ID: 8530088 |
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| Hellevuo K, Berry R, Sikela JM, Tabakoff B, Localization of the gene for a novel human adenylyl cyclase (ADCY7) to chromosome 16. Hum Genet95:197-200 1995 |
| PubMed ID: 7860067 |
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| Hess JF, Casselman JT, FitzGerald PG, Chromosomal locations of the genes for the beaded filament proteins CP 115 and CP 47. Curr Eye Res14:11-8 1995 |
| PubMed ID: 7720401 |
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| 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 |
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| 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 |
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| Liang R, Fei YJ, Prasad PD, Ramamoorthy S, Han H, Yang-Feng TL, Hediger MA, Ganapathy V, Leibach FH, Human intestinal H+/peptide cotransporter. Cloning, functional expression, and chromosomal localization. J Biol Chem270(12):6456-63 1995 |
| PubMed ID: 7896779 |
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| McDonnell, Localization of the human stress responsive MAP kinase-like CSAIDs binding protein (CSBP) gene to chromosome 6p21.3/21 .2. Genomics28:301 (1995):6456-63 1995 |
| PubMed ID: 7896779 |
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| 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 |
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| Pappas GJ, Polymeropoulos MH, Boyle JM, Trent JM, Regional assignment by hybrid mapping of 36 expressed sequence tags (ESTs) on human chromosome 6. Genomics25:124-9 1995 |
| PubMed ID: 7774909 |
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| 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 |
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| Polymeropoulos MH, Torres R, Yanovski JA, Chandrasekharappa SC, Ledbetter DH, The human corticotropin-releasing factor receptor (CRHR) gene maps to chromosome 17q12-q22. Genomics28:123-4 1995 |
| PubMed ID: 7590738 |
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| Stapleton P, Kozmik Z, Weith A, Busslinger M, The gene coding for the B cell surface protein CD19 is localized on human chromosome 16p11. Hum Genet95:223-5 1995 |
| PubMed ID: 7532151 |
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| 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 |
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| 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 |
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| Ali G, Wasco W, Cai X, Szabo P, Sheu KF, Cooper AJ, Gaston SM, Gusella JF, Tanzi RE, Blass JP, Isolation, characterization, and mapping of gene encoding dihydrolipoyl succinyltransferase (E2k) of human alpha-ketoglutarate dehydrogenase complex. Somat Cell Mol Genet20:99-105 1994 |
| PubMed ID: 8009371 |
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| 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 |
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| Durkin AS, Nierman WC, Zoghbi H, Jones C, Kozak CA, Maglott DR, Chromosome assignment of human brain expressed sequence tags (ESTs) by analyzing fluorescently labeled PCR products from hybrid cell panels. Cytogenet Cell Genet65:86-91 1994 |
| PubMed ID: 8404072 |
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| George AL Jr, Knops JF, Han J, Finley WH, Knittle TJ, Tamkun MM, Brown GB, Assignment of a human voltage-dependent sodium channel alpha-subunit gene (SCN6A) to 2q21-q23. Genomics19:395-7 1994 |
| PubMed ID: 8188276 |
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| Gu JJ, Kaiser-Rogers K, Rao K, Mitchell BS, Assignment of the human type I IMP dehydrogenase gene (IMPDH1) to chromosome 7q31.3-q32). Genomics24:179-81 1994 |
| PubMed ID: 7896275 |
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| Makita, Voltage-gated Na+ channel B1 subunit mRNA expressed in adult human skeletal muscle, heart, and brain is encoded by a single gene. J Cell Biol269:7571 (1994):179-81 1994 |
| PubMed ID: 7896275 |
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| 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 |
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| 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 |
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| Smith CP, Weremowicz S, Kanai Y, Stelzner M, Morton CC, Hediger MA, Assignment of the gene coding for the human high-affinity glutamate transporter EAAC1 to 9p24: potential role in dicarboxylic aminoaciduria and neurodegenerative disorders. Genomics20:335-6 1994 |
| PubMed ID: 8020993 |
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| Szabo P, Cai X, Ali G, Blass JP, Localization of the gene (OGDH) coding for the E1k component of the alpha-ketoglutarate dehydrogenase complex to chromosome 7p13-p11.2. Genomics20:324-6 1994 |
| PubMed ID: 8020988 |
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| 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 |
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| 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 |
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| 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 |
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| Yang-Feng TL, Han H, Lomasney JW, Caron MG, Localization of the cDNA for an alpha 1-adrenergic receptor subtype (ADRA1D) to chromosome band 20p13. Cytogenet Cell Genet66:170-1 1994 |
| PubMed ID: 8125015 |
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| Bahou WF, Nierman WC, Durkin AS, Potter CL, Demetrick DJ, Chromosomal assignment of the human thrombin receptor gene: localization to region q13 of chromosome 5. Blood82:1532-7 1993 |
| PubMed ID: 8395910 |
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| Brant SR, Bernstein M, Wasmuth JJ, Taylor EW, McPherson JD, Li X, Walker S, Pouyssegur J, Donowitz M, Tse CM, et al, Physical and genetic mapping of a human apical epithelial Na+/H+ exchanger (NHE3) isoform to chromosome 5p15.3. Genomics15:668-72 1993 |
| PubMed ID: 8096830 |
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| Chang-Yeh A, Jabs EW, Li X, Dracopoli NC, Huang RC, The IPP gene is assigned to human chromosome 1p32-1p22. Genomics15:239-41 1993 |
| PubMed ID: 8432546 |
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| 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 |
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| 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 |
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| Figlewicz DA, Delattre O, Guellaen G, Krizus A, Thomas G, Zucman J, Rouleau GA, Mapping of human gamma-glutamyl transpeptidase genes on chromosome 22 and other human autosomes. Genomics17:299-305 1993 |
| PubMed ID: 8104871 |
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| Gaynor RB, Shieh BH, Klisak I, Sparkes RS, Lusis AJ, Localization of the transcription factor SP1 gene to human chromosome 12q12-->q13.2. Cytogenet Cell Genet64:210-2 1993 |
| PubMed ID: 8404040 |
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| 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 |
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| Griffin CA, Ding CL, Jabs EW, Hawkins AL, Li X, Levine MA, Human rod cGMP-gated cation channel gene maps to 4p12-->centromere by chromosomal in situ hybridization. Genomics16:302-3 1993 |
| PubMed ID: 7683629 |
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| Jeanpierre C, Whitmore SA, Austruy E, Cohen-Salmon M, Callen DF, Junien C, Chromosomal assignment of the uromodulin gene (UMOD) to 16p13.11. Cytogenet Cell Genet62:185-7 1993 |
| PubMed ID: 8382593 |
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| Johnson B, Brooks BA, Heinzmann C, Diep A, Mohandas T, Sparkes RS, Reyes H, Hoffman E, Lange E, Gatti RA, et al, The Ah receptor nuclear translocator gene (ARNT) is located on q21 of human chromosome 1 and on mouse chromosome 3 near Cf-3. Genomics17:592-8 1993 |
| PubMed ID: 8244375 |
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| Kolble K, Lu J, Mole SE, Kaluz S, Reid KB, Assignment of the human pulmonary surfactant protein D gene (SFTP4) to 10q22-q23 close to the surfactant protein A gene cluster. Genomics17:294-8 1993 |
| PubMed ID: 8406480 |
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| Lees JA, Saito M, Vidal M, Valentine M, Look T, Harlow E, Dyson N, Helin K, The retinoblastoma protein binds to a family of E2F transcription factors. Mol Cell Biol13:7813-25 1993 |
| PubMed ID: 8246996 |
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| Martinsson T, Vujic M, Tomkinson B, Localization of the human tripeptidyl peptidase II gene (TPP2) to 13q32- q33 by nonradioactive in situ hybridization and somatic cell hybrids. Genomics17:493-5 1993 |
| PubMed ID: 8406500 |
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| Nishimura DY, Purchio AF, Murray JC, Linkage localization of TGFB2 and the human homeobox gene HLX1 to chromosome 1q. Genomics15:357-64 1993 |
| PubMed ID: 8095486 |
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| 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 |
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| Schiebel K, Weiss B, Wohrle D, Rappold G, A human pseudoautosomal gene, ADP/ATP translocase, escapes X- inactivation whereas a homologue on Xq is subject to X-inactivation. Nat Genet3:82-7 1993 |
| PubMed ID: 8490661 |
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| Stapleton P, Weith A, Urbanek P, Kozmik Z, Busslinger M, Chromosomal localization of seven PAX genes and cloning of a novel family member, PAX-9. Nat Genet3:292-8 1993 |
| PubMed ID: 7981748 |
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| Szabo P, Panneerselvam C, Clinton M, Frangou-Lazaridis M, Weksler D, Whittington E, Macera MJ, Grzeschik KH, Selvakumar A, Horecker BL, Prothymosin alpha gene in humans: organization of its promoter region and localization to chromosome 2 [published erratum appears in Hum Genet 1993 Aug;92(1):104] Hum Genet90:629-34 1993 |
| PubMed ID: 7916742 |
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| Umbricht CB, Erdile LF, Jabs EW, Kelly TJ, Cloning, overexpression, and genomic mapping of the 14-kDa subunit of human replication protein A. J Biol Chem268:6131-8 1993 |
| PubMed ID: 8454588 |
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| Vamvakopoulos NC, Griffin CA, Hawkins AL, Lee C, Chrousos GP, Jabs EW, Mapping the intron-containing human hsp90 alpha (HSPCAL4) gene to chromosome band 14q32. Cytogenet Cell Genet64:224-6 1993 |
| PubMed ID: 8404044 |
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| Vamvakopoulos NC, Rojas K, Overhauser J, Durkin AS, Nierman WC, Chrousos GP, Mapping the human melanocortin 2 receptor (adrenocorticotropic hormone receptor; ACTHR) gene (MC2R) to the small arm of chromosome 18 (18p11.21-pter). Genomics18:454-5 1993 |
| PubMed ID: 8288257 |
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| 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 |
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| Adams BS, Leung K, Meltzer PS, Lewis KA, Wagner-McPherson C, Evans GA, Nabel GJ, Localization of the gene encoding R kappa B (NFRKB), a tissue-specific DNA binding protein, to chromosome 11q24-q25. Genomics14:270-4 1992 |
| PubMed ID: 1427843 |
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| Aplan PD, Raimondi SC, Kirsch IR, Disruption of the SCL gene by a t(1;3) translocation in a patient with T cell acute lymphoblastic leukemia. J Exp Med176:1303-10 1992 |
| PubMed ID: 1402676 |
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| Corcos IA, Lafreniere RG, Begy CR, Loch-Caruso R, Willard HF, Glover TW, Refined localization of human connexin32 gene locus, GJB1, to Xq13.1. Genomics13:479-80 1992 |
| PubMed ID: 1319395 |
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| Dietzsch E, Murphy BF, Kirszbaum L, Walker ID, Garson OM, Regional localization of the gene for clusterin (SP-40,40; gene symbol CLI) to human chromosome 8p12-->p21. Cytogenet Cell Genet61:178-9 1992 |
| PubMed ID: 1424805 |
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| Durkin AS, Maglott DR, Nierman WC, Chromosomal assignment of 38 human brain expressed sequence tags (ESTs) by analyzing fluorescently labeled PCR products from hybrid cell panels. Genomics14:808-10 1992 |
| PubMed ID: 1427913 |
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| Hahn GV, Cohen RB, Wozney JM, Levitz CL, Shore EM, Zasloff MA, Kaplan FS, A bone morphogenetic protein subfamily: chromosomal localization of human genes for BMP5, BMP6, and BMP7. Genomics14:759-62 1992 |
| PubMed ID: 1427904 |
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| 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 |
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| Inaba T, Matsushime H, Valentine M, Roussel MF, Sherr CJ, Look AT, Genomic organization, chromosomal localization, and independent expression of human cyclin D genes. Genomics13:565-74 1992 |
| PubMed ID: 1386335 |
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| Kaneko K, Kobayashi H, Onodera O, Miyatake T, Tsuji S, Genomic organization of a cDNA (QM) demonstrating an altered mRNA level in nontumorigenic Wilms' microcell hybrid cells and its localization to Xq28. Hum Mol Genet1:529-33 1992 |
| PubMed ID: 1339145 |
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| Lidberg U, Nilsson J, Stromberg K, Stenman G, Sahlin P, Enerback S, Bjursell G, Genomic organization, sequence analysis, and chromosomal localization of the human carboxyl ester lipase (CEL) gene and a CEL-like (CELL) gene. Genomics13:630-40 1992 |
| PubMed ID: 1639390 |
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| Lipkowitz S, Gobel V, Varterasian ML, Nakahara K, Tchorz K, Kirsch IR, A comparative structural characterization of the human NSCL-1 and NSCL- 2 genes. Two basic helix-loop-helix genes expressed in the developing nervous system. J Biol Chem267:21065-71 1992 |
| PubMed ID: 1328219 |
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| Macera MJ, Szabo P, Wadgaonkar R, Siddiqui MA, Verma RS, Localization of the gene coding for ventricular myosin regulatory light chain (MYL2) to human chromosome 12q23-q24.3. Genomics13:829-31 1992 |
| PubMed ID: 1386340 |
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| Mariyama M, Zheng K, Yang-Feng TL, Reeders ST, Colocalization of the genes for the alpha 3(IV) and alpha 4(IV) chains of type IV collagen to chromosome 2 bands q35-q37. Genomics13:809-13 1992 |
| PubMed ID: 1639407 |
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| Polymeropoulos MH, Xiao H, Glodek A, Gorski M, Adams MD, Moreno RF, Fitzgerald MG, Venter JC, Merril CR, Chromosomal assignment of 46 brain cDNAs. Genomics12:492-6 1992 |
| PubMed ID: 1559700 |
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