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Literature DB >> 1348795

Homozygosity mapping and Werner's syndrome.

G D Schellenberg, G M Martin, E M Wijsman, J Nakura, T Miki, T Ogihara.

Abstract

Entities: Disease

Mesh：

Year: 1992 PMID： 1348795 DOI： 10.1016/0140-6736(92)91590-5

Source DB: PubMed Journal: Lancet ISSN： 0140-6736 Impact factor: 79.321

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Cited

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14 in total

1. Linkage of combined factors V and VIII deficiency to chromosome 18q by homozygosity mapping.

Authors: W C Nichols; U Seligsohn; A Zivelin; V H Terry; N D Arnold; D R Siemieniak; R J Kaufman; D Ginsburg
Journal: J Clin Invest Date: 1997-02-15 Impact factor: 14.808

2. Accelerated loss of telomeric repeats may not explain accelerated replicative decline of Werner syndrome cells.

Authors: V P Schulz; V A Zakian; C E Ogburn; J McKay; A A Jarzebowicz; S D Edland; G M Martin
Journal: Hum Genet Date: 1996-06 Impact factor: 4.132

3. A unique human gene that spans over 230 kb in the human chromosome 8p11-12 and codes multiple family proteins sharing RNA-binding motifs.

Authors: A Shimamoto; S Kitao; K Ichikawa; N Suzuki; Y Yamabe; O Imamura; Y Tokutake; M Satoh; T Matsumoto; J Kuromitsu; H Kataoka; K Sugawara; M Sugawara; M Sugimoto; M Goto; Y Furuichi
Journal: Proc Natl Acad Sci U S A Date: 1996-10-01 Impact factor: 11.205

4. Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.

Authors: K A Goddard; C E Yu; J Oshima; T Miki; J Nakura; C Piussan; G M Martin; G D Schellenberg; E M Wijsman
Journal: Am J Hum Genet Date: 1996-06 Impact factor: 11.025

Review 5. Genetics and the pathobiology of ageing.

Authors: G M Martin
Journal: Philos Trans R Soc Lond B Biol Sci Date: 1997-12-29 Impact factor: 6.237

6. Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct.

Authors: M Callaghan; C K Hand; S M Kennedy; J S FitzSimon; L M Collum; N A Parfrey
Journal: Br J Ophthalmol Date: 1999-01 Impact factor: 4.638

Homozygosity mapping and Werner's syndrome.

1. Linkage of combined factors V and VIII deficiency to chromosome 18q by homozygosity mapping.

2. Accelerated loss of telomeric repeats may not explain accelerated replicative decline of Werner syndrome cells.

3. A unique human gene that spans over 230 kb in the human chromosome 8p11-12 and codes multiple family proteins sharing RNA-binding motifs.

4. Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.

Review 5. Genetics and the pathobiology of ageing.

6. Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct.

7. Isolation and mapping of microsatellites from a library microdissected from the Werner syndrome region, 8p11.2-p22.

Review 8. Potential for pharmacological intervention in Werner syndrome.

9. Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome.

10. Evidence against DNA polymerase beta as a candidate gene for Werner syndrome.