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Not Found

Description:

CEPH/UTAH PEDIGREE 1345

Affected:

No Data

Gender

No Data

Age:

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Culture Protocols

Overview

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Repository No Data
Subcollection CEPH
Repository Linkage Families
License Required No Data
Sample Source No Data
Subject Type No Data
Family Type No Data
Ethnicity No Data
Family Member No Data
Genetic Data No Data

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase Isoenzyme Electrophoresis
 

Phenotypic Data

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No data is available

Publications

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Tynan JA, Mahboubi P, Cagasan LL, van den Boom D, Ehrich M, Oeth P, Restriction enzyme-mediated enhanced detection of circulating cell-free fetal DNA in maternal plasma The Journal of molecular diagnostics : JMD13:382-9 2010
PubMed ID: 21704271
 
Liu X, Campbell MR, Pittman GS, Faulkner EC, Watson MA, Bell DA, Expression-based discovery of variation in the human glutathione S-transferase M3 promoter and functional analysis in a glioma cell line using allele-specific chromatin immunoprecipitation. Cancer Res65(1):99-104 2005
PubMed ID: 15665284
 
Miretti MM, Walsh EC, Ke X, Delgado M, Griffiths M, Hunt S, Morrison J, Whittaker P, Lander ES, Cardon LR, Bentley DR, Rioux JD, Beck S, Deloukas P, A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms. Am J Hum Genet76(4):634-46 2005
PubMed ID: 15747258
 
Norman PJ, Cook MA, Carey BS, Carrington CV, Verity DH, Hameed K, Ramdath DD, Chandanayingyong D, Leppert M, Stephens HA, Vaughan RW, SNP haplotypes and allele frequencies show evidence for disruptive and balancing selection in the human leukocyte receptor complex Immunogenetics56:225-37 2004
PubMed ID: 15185041
 
Hall MA, Norman PJ, Thiel B, Tiwari H, Peiffer A, Vaughan RW, Prescott S, Leppert M, Schork NJ, Lanchbury JS, Quantitative trait loci on chromosomes 1, 2, 3, 4, 8, 9, 11, 12, and 18 control variation in levels of T and B lymphocyte subpopulations. Am J Hum Genet70(5):1172-82 2002
PubMed ID: 11951176
 
Bowman ED, Bromeke B, Lensing W, Shields PG, Apolipoprotein E allelic frequency in elderly smokers. Am J Med Genet76(1):32-6 1998
PubMed ID: 9508061
 
Brown CJ, Baldry SE, Evidence that heteronuclear proteins interact with XIST RNA in vitro. Somat Cell Mol Genet22:403-17 1996
PubMed ID: 9039849
 
Rupert JL, Brown CJ, Willard HF, Direct detection of non-random X chromosome inactivation by use of a transcribed polymorphism in the XIST gene. Eur J Hum Genet3:333-43 1995
PubMed ID: 8825575
 
Haaf T, Willard HF, Organization, polymorphism, and molecular cytogenetics of chromosome- specific alpha-satellite DNA from the centromere of chromosome 2. Genomics13:122-8 1992
PubMed ID: 1577477
 
Goldman D, O'Brien SJ, Lucas-Derse S, Dean M, Linkage mapping of human polymorphic proteins identified by two-dimensional electrophoresis. Genomics11:875-84 1991
PubMed ID: 1686020
 
Nicholls RD, Knoll JH, Glatt K, Hersh JH, Brewster TD, Graham JM Jr, Wurster-Hill D, Wharton R, Latt SA, Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome. Am J Med Genet33:66-77 1989
PubMed ID: 2568752
 
Simon M, Phillips M, Green H, Stroh H, Glatt K, Burns G, Latt SA, Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP. Am J Hum Genet45:910-6 1989
PubMed ID: 2574003
 
Board PG, Chapple R, Coggan M, Haplotypes of the coagulation factor XIII A subunit locus in normal and deficient subjects. Am J Hum Genet42:712-7 1988
PubMed ID: 2895980
 
Bufton L, Bruns GA, Magenis RE, Tomar D, Shaw D, Brook D, Litt M, Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19. Am J Hum Genet38:447-60 1986
PubMed ID: 3010711
 
Buroker NE, Magenis RE, Weliky K, Bruns G, Litt M, Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to human chromosome 12q. Hum Genet72:86-94 1986
PubMed ID: 3002956

External Links

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dbSNP dbSNP ID: 204
GEO GEO Accession No: GSM25419
GEO Accession No: GSM420575
PharmGKB Pharmgkb ID (requires login): PA126710398

Culture Protocols

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Split Ratio 1:3
Temperature 37 C
Percent CO2 5%
Medium Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not Inactivated
Substrate None specified
Subcultivation Method dilution - add fresh medium
Supplement -
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