Literature DB >> 6320640

Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.

W Cavenee, R Leach, T Mohandas, P Pearson, R White.   

Abstract

A recombinant DNA library enriched for portions of human chromosome 13 has been constructed from a hamster-human somatic cell hybrid that contained human chromosomes 13, 12, and 6p. A total of 733 phages were identified that contain human DNA inserts, and 46 single-copy subfragments have been derived and used as probes on Southern transfers of genomic DNA isolated from unrelated individuals. From this set, nine fragments revealing polymorphic loci (RFLP) in Msp I- or Taq I-digested DNA have been identified, of which three are polymorphic with both enzymes. Six of these probes have been shown to segregate concordantly with human chromosome 13 in a somatic cell hybrid mapping panel, and the RFLPs at these loci have been shown to behave as codominant Mendelian alleles. Additionally, hybridization to DNA isolated from cells containing various deletions of chromosome 13 has allowed regional localization. This recombinant DNA library will be useful in the study of retinoblastoma as well as in the study of the mechanisms responsible for abnormalities of this autosome.

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Year:  1984        PMID: 6320640      PMCID: PMC1684373     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  18 in total

1.  In vitro packaging of lambda and cosmid DNA.

Authors:  B Hohn
Journal:  Methods Enzymol       Date:  1979       Impact factor: 1.600

2.  Assignment of PGM3 to the long arm of human chromosome 6. Studies using Chinese hamster X human cell hybrids containing a human 6/15 translocation.

Authors:  T Mohandas; R S Sparkes; J D Shulkin; M C Sparkes; S Moedjono
Journal:  Cytogenet Cell Genet       Date:  1980

3.  Retinoblastoma: a prototypic hereditary neoplasm.

Authors:  A G Knudson
Journal:  Semin Oncol       Date:  1978-03       Impact factor: 4.929

4.  A highly polymorphic locus in human DNA.

Authors:  A R Wyman; R White
Journal:  Proc Natl Acad Sci U S A       Date:  1980-11       Impact factor: 11.205

5.  Isolation and localization of DNA segments from specific human chromosomes.

Authors:  J F Gusella; C Keys; A VarsanyiBreiner; F T Kao; C Jones; T T Puck; D Housman
Journal:  Proc Natl Acad Sci U S A       Date:  1980-05       Impact factor: 11.205

6.  Retinoblastoma and subband deletion of chromosome 13.

Authors:  J J Yunis; N Ramsay
Journal:  Am J Dis Child       Date:  1978-02

7.  Regional assignment of the steroid sulfatase-X-linked ichthyosis locus: implications for a noninactivated region on the short arm of human X chromosome.

Authors:  T Mohandas; L J Shapiro; R S Sparkes; M C Sparkes
Journal:  Proc Natl Acad Sci U S A       Date:  1979-11       Impact factor: 11.205

Review 8.  Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

Authors:  D Botstein; R L White; M Skolnick; R W Davis
Journal:  Am J Hum Genet       Date:  1980-05       Impact factor: 11.025

9.  A general theory of carcinogenesis.

Authors:  D E Comings
Journal:  Proc Natl Acad Sci U S A       Date:  1973-12       Impact factor: 11.205

10.  Patient with 13 chromosome deletion: evidence that the retinoblastoma gene is a recessive cancer gene.

Authors:  W F Benedict; A L Murphree; A Banerjee; C A Spina; M C Sparkes; R S Sparkes
Journal:  Science       Date:  1983-02-25       Impact factor: 47.728

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  60 in total

1.  Ethnic variations of a retinoblastoma susceptibility gene (RB1) polymorphism in eight Asian populations.

Authors:  Priya Kadam-Pai; Xin-Yi Su; Jasmin Jiji Miranda; Agustinus Soemantri; Nilmani Saha; Chew-Kiat Heng; Poh-San Lai
Journal:  J Genet       Date:  2003 Apr-Aug       Impact factor: 1.166

2.  A novel POU homeodomain gene specifically expressed in cells of the developing mammalian nervous system.

Authors:  R G Collum; P E Fisher; M Datta; S Mellis; C Thiele; K Huebner; C M Croce; M A Israel; T Theil; T Moroy
Journal:  Nucleic Acids Res       Date:  1992-09-25       Impact factor: 16.971

3.  Genomic imprinting of the human serotonin-receptor (HTR2) gene involved in development of retinoblastoma.

Authors:  M V Kato; T Shimizu; M Nagayoshi; A Kaneko; M S Sasaki; Y Ikawa
Journal:  Am J Hum Genet       Date:  1996-11       Impact factor: 11.025

4.  Application of intragenic DNA probes in prenatal screening for retinoblastoma gene carriers in the United Kingdom.

Authors:  Z O Onadim; C D Mitchell; P C Rutland; B G Buckle; M Jay; J L Hungerford; K Harper; J K Cowell
Journal:  Arch Dis Child       Date:  1990-07       Impact factor: 3.791

5.  Construction of the physical map for three loci in chromosome band 13q14: comparison to the genetic map.

Authors:  M J Higgins; C Turmel; J Noolandi; P E Neumann; M Lalande
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

6.  Restriction fragment length polymorphism studies show consistent loss of chromosome 3p alleles in small cell lung cancer patients' tumors.

Authors:  B E Johnson; A Y Sakaguchi; A F Gazdar; J D Minna; D Burch; A Marshall; S L Naylor
Journal:  J Clin Invest       Date:  1988-08       Impact factor: 14.808

7.  Mapping of seven polymorphic loci on human chromosome 13 by in situ hybridization.

Authors:  T P Dryja; C C Morton
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

8.  Alteration in the retinoblastoma gene associated with immortalization of human fibroblasts treated with 60Co gamma rays.

Authors:  A Endo; Y Kano; K Mihara; K Orita; M Namba
Journal:  J Cancer Res Clin Oncol       Date:  1993       Impact factor: 4.553

9.  Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies.

Authors:  I Aksentijevich; E Pras; L Gruberg; Y Shen; K Holman; S Helling; L Prosen; G R Sutherland; R I Richards; M Ramsburg
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

10.  Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndrome.

Authors:  R A Spritz; D Mager; R M Pauli; R Laxova
Journal:  Am J Hum Genet       Date:  1986-08       Impact factor: 11.025

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