Literature DB >> 8188264

Twenty-one polymorphic markers from human chromosome 12 for integration of genetic and physical maps.

J M LeBlanc-Straceski1, K T Montgomery, H Kissel, L Murtaugh, P Tsai, D C Ward, K S Krauter, R Kucherlapati.   

Abstract

Twenty-one physically mapped, polymorphic markers have been developed from a chromosome 12-specific cosmid library. The markers consist of CA repeat-containing sequence-tagged sites (STSs) derived from cosmid clones mapped by fluorescence in situ hybridization (FISH). Three methods for determining the sequence flanking CA microsatellites were used, including one using degenerate primer sets for direct sequence analysis. Oligonucleotide primer pairs suitable for use in polymerase chain reaction (PCR) were selected from the sequences flanking the CA microsatellite and were tested for their ability to generate unique PCR products. The informativeness of these STSs as genetic markers was determined by typing 10 unrelated individuals who are part of the Centre d'Etude du Polymorphisme Humaine (EPH) pedigrees. Eleven of the 21 FISH-mapped, polymorphic STSs are heterozygous in 7 or more of the individuals tested. Since these markers are derived from physically mapped cosmids, genetic linkage analysis with them will facilitate the integration of the developing physical and genetic maps of chromosome 12.

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Year:  1994        PMID: 8188264     DOI: 10.1006/geno.1994.1067

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  6 in total

1.  Localization of the Darier disease gene to a 2-cM portion of 12q23-24.1.

Authors:  P Wakem; S Ikeda; A Haake; R Polakowska; N Ewing; Y Sarret; M Duvic; D Berg; A Bassett; J L Kennedy; A Tuskis; E H Epstein; L A Goldsmith
Journal:  J Invest Dermatol       Date:  1996-02       Impact factor: 8.551

2.  A 3-Mb high-resolution BAC/PAC contig of 12q22 encompassing the 830-kb consensus minimal deletion in male germ cell tumors.

Authors:  V V Murty; K Montgomery; S Dutta; S Bala; B Renault; G J Bosl; R Kucherlapati; R S Chaganti
Journal:  Genome Res       Date:  1999-07       Impact factor: 9.043

3.  Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome.

Authors:  B Morrow; R Goldberg; C Carlson; R Das Gupta; H Sirotkin; J Collins; I Dunham; H O'Donnell; P Scambler; R Shprintzen
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

4.  An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex.

Authors:  S M Mulders; D G Bichet; J P Rijss; E J Kamsteeg; M F Arthus; M Lonergan; M Fujiwara; K Morgan; R Leijendekker; P van der Sluijs; C H van Os; P M Deen
Journal:  J Clin Invest       Date:  1998-07-01       Impact factor: 14.808

5.  Congenital fibrosis of the extraocular muscles (autosomal dominant congenital external ophthalmoplegia): genetic homogeneity, linkage refinement, and physical mapping on chromosome 12.

Authors:  E C Engle; I Marondel; W A Houtman; B de Vries; A Loewenstein; M Lazar; D C Ward; R Kucherlapati; A H Beggs
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025

6.  Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus.

Authors:  Erik-Jan Kamsteeg; Daniel G Bichet; Irene B M Konings; Hubert Nivet; Michelle Lonergan; Marie-Françoise Arthus; Carel H van Os; Peter M T Deen
Journal:  J Cell Biol       Date:  2003-12-08       Impact factor: 10.539

  6 in total

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