Literature DB >> 7987395

A radiation hybrid map of 506 STS markers spanning human chromosome 11.

M R James1, C W Richard, J J Schott, C Yousry, K Clark, J Bell, J D Terwilliger, J Hazan, C Dubay, A Vignal.   

Abstract

We present a high resolution radiation hybrid map of human chromosome 11 using 506 sequence tagged sites (STSs) scored on a panel of 86 radiation hybrids. The 506 STSs fall into 299 unique positions (average resolution of about 480 kilobases (kb)) that span the whole chromosome. A subset of 260 STSs (143 positions) form a framework map that has a resolution of approximately 1 megabase between adjacent positions and is ordered with odds of at least 1,000:1. The centromere was clearly defined with pericentric markers unambiguously assigned to the short or long arm. The map contains most genes (125) and expressed sequence tags (26) currently assigned to chromosome 11 and more than half of the STSs are polymorphic microsatellite loci. These markers and the map can be used for high resolution physical and genetic mapping.

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Year:  1994        PMID: 7987395     DOI: 10.1038/ng0994-70

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  28 in total

1.  Disruption of imprinted genes at chromosome region 11p15.5 in paediatric rhabdomyosarcoma.

Authors:  J Anderson; A Gordon; A McManus; J Shipley; K Pritchard-Jones
Journal:  Neoplasia       Date:  1999-10       Impact factor: 5.715

2.  GANESH: software for customized annotation of genome regions.

Authors:  Derek Huntley; Holger Hummerich; Damian Smedley; Sasivimol Kittivoravitkul; Mark McCarthy; Peter Little; Marek Sergot
Journal:  Genome Res       Date:  2003-09       Impact factor: 9.043

3.  Development of a gene-based radiation hybrid map of chicken Chromosome 7 and comparison to human and mouse.

Authors:  Mireille Morisson; Carine Jiguet-Jiglaire; Sophie Leroux; Thomas Faraut; Suzanne Bardes; Katia Feve; Carine Genet; Frédérique Pitel; Denis Milan; Alain Vignal
Journal:  Mamm Genome       Date:  2004-09       Impact factor: 2.957

4.  A high-resolution 15,000(Rad) radiation hybrid panel for the domestic cat.

Authors:  L H Bach; B Gandolfi; J C Grahn; L V Millon; M S Kent; K Narfstrom; S A Cole; J C Mullikin; R A Grahn; L A Lyons
Journal:  Cytogenet Genome Res       Date:  2012-07-06       Impact factor: 1.636

5.  A transcript map for the 2.8-Mb region containing the multiple endocrine neoplasia type 1 locus.

Authors:  S C Guru; S K Agarwal; P Manickam; S E Olufemi; J S Crabtree; J M Weisemann; M B Kester; Y S Kim; Y Wang; M R Emmert-Buck; L A Liotta; A M Spiegel; M S Boguski; B A Roe; F S Collins; S J Marx; L Burns; S C Chandrasekharappa
Journal:  Genome Res       Date:  1997-07       Impact factor: 9.043

6.  Evidence for oligogenic inheritance of type 1 diabetes in a large Bedouin Arab family.

Authors:  C F Verge; P Vardi; S Babu; F Bao; H A Erlich; T Bugawan; D Tiosano; L Yu; G S Eisenbarth; P R Fain
Journal:  J Clin Invest       Date:  1998-10-15       Impact factor: 14.808

7.  Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11.

Authors:  O Bartsch; W Wuyts; W Van Hul; J T Hecht; P Meinecke; D Hogue; W Werner; B Zabel; G K Hinkel; C M Powell; L G Shaffer; P J Willems
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

8.  A radiation hybrid map spanning the entire human X chromosome integrating YACs, genes, and STS markers.

Authors:  J Kumlien; A Grigoriev; H Roest Crollius; M Ross; P N Goodfellow; H Lehrach
Journal:  Mamm Genome       Date:  1996-10       Impact factor: 2.957

9.  Localization of Jacobsen syndrome breakpoints on a 40-Mb physical map of distal chromosome 11q.

Authors:  A Tunnacliffe; C Jones; D Le Paslier; R Todd; D Cherif; M Birdsall; L Devenish; C Yousry; F E Cotter; M R James
Journal:  Genome Res       Date:  1999-01       Impact factor: 9.043

10.  Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 gene.

Authors:  J T Pang; S E Lloyd; C Wooding; B Farren; B Pottinger; B Harding; S E Leigh; M A Pook; F J Benham; G T Gillett; R T Taggart; R V Thakker
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

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