Literature DB >> 1741060

Genetic linkage of Werner's syndrome to five markers on chromosome 8.

M Goto1, M Rubenstein, J Weber, K Woods, D Drayna.   

Abstract

Werner's syndrome (WS) is a rare autosomal recessive disease in which the affected individuals display symptoms of premature ageing. The substantial phenotypic overlap between WS and normal ageing indicates that these two conditions may have pathogenetic mechanisms in common. The WS mutation has pleiotropic effects, and patients and their cells show many differences compared with normals. Despite extensive study of the clinical and biochemical features of this disorder, the primary genetic defect remains unknown. We have undertaken a genetic linkage study in an effort to identify the locus of the primary defect. Here we report close genetic linkage of the WS mutation to a group of markers on chromosome 8.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1741060     DOI: 10.1038/355735a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  27 in total

1.  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

2.  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

Review 3.  Progeroid syndromes: probing the molecular basis of aging?

Authors:  D Kipling; R G Faragher
Journal:  Mol Pathol       Date:  1997-10

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

Authors:  K Nagano; J Nakura; K Kihara; L Ye; K Kamino; N Mitsuda; T Ohta; Y Jinno; N Niikawa; T Miki
Journal:  Jpn J Hum Genet       Date:  1993-12

7.  Deletion mapping of chromosome 8p in colorectal carcinoma and dysplasia arising in ulcerative colitis, prostatic carcinoma, and malignant fibrous histiocytomas.

Authors:  M Chang; K Tsuchiya; R H Batchelor; P S Rabinovitch; B G Kulander; R C Haggitt; G C Burmer
Journal:  Am J Pathol       Date:  1994-01       Impact factor: 4.307

8.  Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies.

Authors:  I Aksentijevich; E Pras; L Gruberg; Y Shen; K Holman; S Helling; L Prosen; G R Sutherland; R I Richards; M Ramsburg
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

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

Authors:  M Chang; G C Burmer; J Sweasy; L A Loeb; S Edelhoff; C M Disteche; C E Yu; L Anderson; J Oshima; J Nakura
Journal:  Hum Genet       Date:  1994-05       Impact factor: 4.132

10.  Neural expression and chromosomal mapping of Neu differentiation factor to 8p12-p21.

Authors:  A Orr-Urtreger; L Trakhtenbrot; R Ben-Levy; D Wen; G Rechavi; P Lonai; Y Yarden
Journal:  Proc Natl Acad Sci U S A       Date:  1993-03-01       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.