Literature DB >> 8786091

Integration of four genes, a pseudogene, thirty-one STSs, and a highly polymorphic STRP into the 7-10 Mb YAC contig of 5q34-q35.

M Kostrzewa1, D L Grady, R K Moyzis, L Flöter, U Müller.   

Abstract

Thirty-one sequence tagged sites and a highly polymorphic short tandem repeat polymorphism have been isolated from 5q34-q35 and integrated into the yeast artificial chromosome (YAC) contig of 5q34-q35. In addition, four genes (MSX2, CSX, DRD1, and CL100) and a pseudogene (GLUT6) were localized on this map. The high density of new markers in the region allowed further refinement of the YAC contig of distal 5q. This is a prerequisite for the conversion of this YAC into a cosmid contig.

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Year:  1996        PMID： 8786091     DOI： 10.1007/bf02185781

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  16 in total

1.  A second-generation linkage map of the human genome.

Authors:  J Weissenbach; G Gyapay; C Dib; A Vignal; J Morissette; P Millasseau; G Vaysseix; M Lathrop
Journal:  Nature       Date:  1992-10-29       Impact factor: 49.962

Review 2.  The structure and function of the homeodomain.

Authors:  M P Scott; J W Tamkun; G W Hartzell
Journal:  Biochim Biophys Acta       Date:  1989-07-28

3.  A procedure for in vitro amplification of DNA segments that lie outside the boundaries of known sequences.

Authors:  T Triglia; M G Peterson; D J Kemp
Journal:  Nucleic Acids Res       Date:  1988-08-25       Impact factor: 16.971

4.  Construction of a YAC contig and a STS map spanning at least seven megabasepairs in chromosome 5q34-35.

Authors:  J M Lu-Kuo; D Le Paslier; J Weissenbach; I Chumakov; D Cohen; D C Ward
Journal:  Hum Mol Genet       Date:  1994-01       Impact factor: 6.150

5.  Assignment of cardiac homeobox gene CSX to human chromosome 5q34.

Authors:  I Shiojima; I Komuro; J Inazawa; Y Nakahori; I Matsushita; T Abe; R Nagai; Y Yazaki
Journal:  Genomics       Date:  1995-05-01       Impact factor: 5.736

6.  A YAC contig encompassing the Treacher Collins syndrome critical region at 5q31.3-32.

Authors:  J Dixon; A J Gladwin; S K Loftus; J H Riley; R Perveen; J J Wasmuth; R Anand; M J Dixon
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

7.  Assignment of a gene locus involved in craniosynostosis to chromosome 5qter.

Authors:  U Müller; M L Warman; J B Mulliken; J L Weber
Journal:  Hum Mol Genet       Date:  1993-02       Impact factor: 6.150

8.  Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1).

Authors:  S Cichon; M M Nöthen; J Erdmann; P Propping
Journal:  Hum Mol Genet       Date:  1994-01       Impact factor: 6.150

9.  The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping.

Authors:  J Hästbacka; A de la Chapelle; M M Mahtani; G Clines; M P Reeve-Daly; M Daly; B A Hamilton; K Kusumi; B Trivedi; A Weaver
Journal:  Cell       Date:  1994-09-23       Impact factor: 41.582

10.  The CL100 gene, which encodes a dual specificity (Tyr/Thr) MAP kinase phosphatase, is highly conserved and maps to human chromosome 5q34.

Authors:  E A Emslie; T A Jones; D Sheer; S M Keyse
Journal:  Hum Genet       Date:  1994-05       Impact factor: 4.132
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