Homozygosity mapping and Werner's syndrome

scientific article published on April 18, 1992

Homozygosity mapping and Werner's syndrome is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/0140-6736(92)91590-5
P698PubMed publication ID1348795

P2093author name stringT. Miki
T. Ogihara
G. D. Schellenberg
G. M. Martin
E. M. Wijsman
J. Nakura
P433issue8799
P407language of work or nameEnglishQ1860
P921main subjecthomozygosityQ114049690
homozygoteQ49985
P304page(s)1002
P577publication date1992-04-01
1992-04-18
P1433published inThe LancetQ939416
P1476titleHomozygosity mapping and Werner's syndrome
P478volume339

Reverse relations

cites work (P2860)
Q41051557A comparative analysis of the proteins between the fibroblasts from Werner's syndrome patients and age-matched normal individuals using two-dimensional gel electrophoresis
Q28589633A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity
Q24312979A unique human gene that spans over 230 kb in the human chromosome 8p11-12 and codes multiple family proteins sharing RNA-binding motifs
Q57250868Accelerated loss of telomeric repeats may not explain accelerated replicative decline of Werner syndrome cells
Q24561538Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1
Q34594343Contemporary human genetic strategies in aging research
Q24311934Evidence against DNA polymerase beta as a candidate gene for Werner syndrome
Q35211822Genetics and the pathobiology of ageing
Q24673323Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct
Q36750456Isolation and mapping of microsatellites from a library microdissected from the Werner syndrome region, 8p11.2-p22.
Q42038284Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome.
Q37363234Linkage of combined factors V and VIII deficiency to chromosome 18q by homozygosity mapping
Q34345703Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping
Q40970128Potential for pharmacological intervention in Werner syndrome
Q39724600Structure and function of the human Werner syndrome gene promoter: evidence for transcriptional modulation
Q35882781Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers
Q78022550Transcriptional activation by the Werner syndrome gene product in yeast
Q40519651V(D)J recombination and double-strand break repair