Literature DB >> 6280496

Assignment of first random restriction fragment length polymorphism (RFLP) locus ((D14S1) to a region of human chromosome 14.

B de Martinville, A R Wyman, R White, U Francke.   

Abstract

A locus responsible for a restriction fragment length polymorphism (RFLP) has been identified by hybridization of Eco RI fragments to the random human DNA sequence in recombinant plasmid pAW101. We have examined DNA extracted from 20 human X Chinese hamster somatic cell hybrids for the presence of sequences homologous to the human insert in pAW101. The hybrids were derived from six different human donors, five of whom were heterozygous, producing two bands on Southern transfers. The presence of homologous sequences in the hybrids correlated exclusively with the presence of human chromosome 14. Three hybrids contained chromosome 14 in a frequency of greater than one per cell and were positive for two alleles. Two hybrids contained only the distal half of the long arm of 14 as part of a translocation and were still positive. These results assign the first highly polymorphic random RFPL locus (D14S1) to region q21 leads to qter of chromosome 14.

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Year:  1982        PMID: 6280496      PMCID: PMC1685300     

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


  19 in total

1.  Regional localization of the human genes for malate dehydrogenase-1 and isocitrate dehydrogenase-1 on chromosome 2 by interspecific hybridization using human cells with the balanced reciprocal translocation t(1;2) (q32;q13).

Authors:  U Francke
Journal:  Cytogenet Cell Genet       Date:  1975

2.  Enzyme electrophoresis on cellulose acetate gel: zymogram patterns in mgh-mouse and man--Chinese hamster somatic cell hybrids.

Authors:  P Meera Khan
Journal:  Arch Biochem Biophys       Date:  1971-08       Impact factor: 4.013

3.  Enzyme electrophoresis on cellulose acetate gel. II. Zymogram patterns in man-Chinese hamster somatic cell hybrids.

Authors:  H van Someren; H Beijersbergen van Henegouwen; W Los; E Wurzer-Figurelli; B Doppert; M Vervloet; P Meera Khan
Journal:  Humangenetik       Date:  1974

4.  Inherited variants of human nucleoside phosphorylase.

Authors:  Y H Edwards; D A Hopkinson; H Harris
Journal:  Ann Hum Genet       Date:  1971-05       Impact factor: 1.670

5.  Regional assignment of genes for mannose phosphate isomerase, pyruvate kinase-3, and beta 2-microglobulin expression on human chromosome 15 by hybridization of cells from a t(15;22) (q14;q13.3) translocation carrier.

Authors:  N Oliver; U Francke; M A Pellegrino
Journal:  Cytogenet Cell Genet       Date:  1978

6.  Isolation of high-molecular-weight DNA from mammalian cells.

Authors:  M Gross-Bellard; P Oudet; P Chambon
Journal:  Eur J Biochem       Date:  1973-07-02

7.  Quantitative analysis of high-resolution trypsin-giemsa bands on human prometaphase chromosomes.

Authors:  U Francke; N Oliver
Journal:  Hum Genet       Date:  1978-12-18       Impact factor: 4.132

8.  Intrachromosomal gene mapping in man: assignment of nucleoside phosphorylase to region 14cen leads to 14q21 by interspecific hybridization of cells with a t(X;14) (p22;q21) translocation.

Authors:  U Francke; N Busby; D Shaw; S Hansen; M G Brown
Journal:  Somatic Cell Genet       Date:  1976-01

9.  Intrachromosomal gene mapping in man: the gene for tryptophyl-tRNA synthetase maps in region q21 leads to qter of chromosome 14.

Authors:  U Francke; R M Denney; F H Ruddle
Journal:  Somatic Cell Genet       Date:  1977-07

10.  Assignment of the major histocompatibility complex to a region of the short arm of human chromosome 6.

Authors:  U Francke; M A Pellegrino
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

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  29 in total

1.  Human tissue-type plasminogen activator gene located near chromosomal breakpoint in myeloproliferative disorder.

Authors:  T L Yang-Feng; G Opdenakker; G Volckaert; U Francke
Journal:  Am J Hum Genet       Date:  1986-07       Impact factor: 11.025

2.  Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes.

Authors:  T L Yang-Feng; L J DeGennaro; U Francke
Journal:  Proc Natl Acad Sci U S A       Date:  1986-11       Impact factor: 11.205

3.  Inverted duplication of JH associated with chromosome 14 translocation and T-cell leukemia in ataxia-telangiectasia.

Authors:  J P Johnson; R A Gatti; T S Sears; R L White
Journal:  Am J Hum Genet       Date:  1986-12       Impact factor: 11.025

4.  2012 William Allan Award: Adventures in cytogenetics.

Authors:  Uta Francke
Journal:  Am J Hum Genet       Date:  2013-03-07       Impact factor: 11.025

5.  The pronatriodilatin gene is located on the distal short arm of human chromosome 1 and on mouse chromosome 4.

Authors:  T L Yang-Feng; G Floyd-Smith; M Nemer; J Drouin; U Francke
Journal:  Am J Hum Genet       Date:  1985-11       Impact factor: 11.025

6.  Localization of the restriction fragment length polymorphism D14S1 (pAW-101) to chromosome 14q32.1 leads to 32.2 by in situ hybridization.

Authors:  T A Donlon; M Litt; S R Newcom; R E Magenis
Journal:  Am J Hum Genet       Date:  1983-11       Impact factor: 11.025

7.  DNA analysis of first-trimester chorionic villous biopsies: test for maternal contamination.

Authors:  B de Martinville; K J Blakemore; M J Mahoney; U Francke
Journal:  Am J Hum Genet       Date:  1984-11       Impact factor: 11.025

8.  Analysis of a break in chromosome 14 mapping to the region of the immunoglobulin heavy chain locus.

Authors:  P S Linsley; N T Bech-Hansen; L Siminovitch; D W Cox
Journal:  Proc Natl Acad Sci U S A       Date:  1983-04       Impact factor: 11.205

9.  Molecular characterization of ataxia telangiectasia T cell clones. III. Mapping the 14q32.1 distal breakpoint.

Authors:  M H Stern; F R Zhang; G Thomas; C Griscelli; A Aurias
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

10.  Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions.

Authors:  U Francke; J F Harper; B T Darras; J M Cowan; E R McCabe; A Kohlschütter; W K Seltzer; F Saito; J Goto; J P Harpey
Journal:  Am J Hum Genet       Date:  1987-03       Impact factor: 11.025

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