Literature DB >> 2878609

A fine structure physical map of the short arm of chromosome 5.

J Overhauser, A L Beaudet, J J Wasmuth.   

Abstract

A series of somatic cell hybrids that retain abnormal chromosomes 5 from 11 different persons with deletions or translocations involving 5p have been isolated. One hundred twenty DNA fragments isolated from a genomic library enriched for sequences from 5p were regionally localized by Southern blot analysis of the hybrid cell deletion mapping panel, including five DNA fragments that reveal restriction fragment length polymorphisms. The fine structure physical map of 5p together with the identification of additional polymorphic loci will facilitate the construction of a complete linkage map of this region. In addition, DNA fragments localized to a region near the 5p15.2-5p15.3 border, which appears to be the segment of 5p that is critical in producing the phenotype associated with the cri du chat syndrome when it is rendered hemizygous by deletion, will be useful in a molecular and DNA level analysis of this deletion syndrome.

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Year:  1986        PMID: 2878609      PMCID: PMC1684052     

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


  11 in total

1.  Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype.

Authors:  J Overhauser; M S Golbus; S A Schonberg; J J Wasmuth
Journal:  Am J Hum Genet       Date:  1986-07       Impact factor: 11.025

2.  "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1984-02       Impact factor: 3.365

3.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1983-07-01       Impact factor: 3.365

4.  Removal of repeated sequences from hybridisation probes.

Authors:  P G Sealey; P A Whittaker; E M Southern
Journal:  Nucleic Acids Res       Date:  1985-03-25       Impact factor: 16.971

5.  Cytologic observations in 35 individuals with a 5p- karyotype.

Authors:  E Niebuhr
Journal:  Hum Genet       Date:  1978-06-09       Impact factor: 4.132

6.  Linkage of the leuS, emtB, and chr genes on chromosome 5 in humans and expression of human genes encoding protein synthetic components in human--Chinese hamster hybrids.

Authors:  S Dana; J J Wasmuth
Journal:  Somatic Cell Genet       Date:  1982-03

7.  Molecular approach to analyzing the human 5p deletion syndrome, cri du chat.

Authors:  L R Carlock; J J Wasmuth
Journal:  Somat Cell Mol Genet       Date:  1985-05

Review 8.  The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features.

Authors:  E Niebuhr
Journal:  Hum Genet       Date:  1978-11-16       Impact factor: 4.132

9.  Interstitial deletion of the short arm of chromosome 5 in a mother and three children.

Authors:  J L Walker; C E Blank; B A Smith
Journal:  J Med Genet       Date:  1984-12       Impact factor: 6.318

10.  A cell hybrid and recombinant DNA library that facilitate identification of polymorphic loci in the vicinity of the Huntington disease gene.

Authors:  J J Wasmuth; L R Carlock; B Smith; L L Immken
Journal:  Am J Hum Genet       Date:  1986-09       Impact factor: 11.025

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  8 in total

1.  Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5.

Authors:  J Overhauser; U Bengtsson; J McMahon; J Ulm; M G Butler; L Santiago; J J Wasmuth
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

2.  Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation.

Authors:  Acácia Fernandes Lacerda de Carvalho; Fernanda Teixeira da Silva Bellucco; Leslie Domenici Kulikowski; Maria Betânia Pereira Toralles; Maria Isabel Melaragno
Journal:  Hum Genet       Date:  2008-09-07       Impact factor: 4.132

3.  Isolation of a cDNA clone for human threonyl-tRNA synthetase: amplification of the structural gene in borrelidin-resistant cell lines.

Authors:  K J Kontis; S M Arfin
Journal:  Mol Cell Biol       Date:  1989-05       Impact factor: 4.272

4.  Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus.

Authors:  B Smith; D Skarecky; U Bengtsson; R E Magenis; N Carpenter; J J Wasmuth
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

5.  Identification of 28 DNA fragments that detect RFLPs in 13 distinct physical regions of the short arm of chromosome 5.

Authors:  J Overhauser; J McMahan; J J Wasmuth
Journal:  Nucleic Acids Res       Date:  1987-06-11       Impact factor: 16.971

Review 6.  Molecular analysis of the 18q- syndrome--and correlation with phenotype.

Authors:  A D Kline; M E White; R Wapner; K Rojas; L G Biesecker; J Kamholz; E H Zackai; M Muenke; C I Scott; J Overhauser
Journal:  Am J Hum Genet       Date:  1993-05       Impact factor: 11.025

7.  De novo 15.5-Mb Interstitial Deletion in 5p in a Male Ascertained by Oligospermia.

Authors:  I Papoulidis; A Vetro; K Kefalas; S Orru; L Thomaidis; Z Iliodromiti; O Zuffardi; E Manolakos
Journal:  Mol Syndromol       Date:  2013-06-12

8.  Evidence for a distinct region causing a cat-like cry in patients with 5p deletions.

Authors:  M Gersh; S A Goodart; L M Pasztor; D J Harris; L Weiss; J Overhauser
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

  8 in total

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