(Q34088393)

30 July 2017

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title

Lessons from human progeroid syndromes (English)

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30 July 2017

Martin GM

1

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30 July 2017

Oshima J

series ordinal

2

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30 July 2017

language of work or name

English

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publication date

1 November 2000

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30 July 2017

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30 July 2017

volume

408

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30 July 2017

issue

6809

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30 July 2017

page(s)

263-266

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Spontaneous mutation in man.

30 July 2017

cites work

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Positional cloning of the Werner's syndrome gene

21 January 2018

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Mutator phenotype of Werner syndrome is characterized by extensive deletions

21 January 2018

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A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging Process

21 January 2018

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An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants

21 January 2018

1 reference

The premature ageing syndrome protein, WRN, is a 3'-->5' exonuclease

21 January 2018

1 reference

Werner syndrome protein. I. DNA helicase and dna exonuclease reside on the same polypeptide.

21 January 2018

1 reference

Werner syndrome helicase contains a 5'-->3' exonuclease activity that digests DNA and RNA strands in DNA/DNA and RNA/DNA duplexes dependent on unwinding

21 January 2018

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Impaired S-phase transit of Werner syndrome cells expressed in lymphoblastoid cell lines

21 January 2018

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Replication focus-forming activity 1 and the Werner syndrome gene product

21 January 2018

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The Werner syndrome gene product co-purifies with the DNA replication complex and interacts with PCNA and topoisomerase I.

21 January 2018

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The Werner syndrome protein is a DNA helicase

21 January 2018

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Functional interaction between Ku and the werner syndrome protein in DNA end processing

21 January 2018

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The Werner syndrome protein is involved in RNA polymerase II transcription

21 January 2018

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Physical and functional interaction between p53 and the Werner's syndrome protein

21 January 2018

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RecQ DNA helicase is a suppressor of illegitimate recombination in Escherichia coli

21 January 2018

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Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases

21 January 2018

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An unstable triplet repeat in a gene related to myotonic muscular dystrophy

21 January 2018

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Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy

21 January 2018

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Role of glycation in aging

21 January 2018

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Severe islet amyloidosis in congenital generalized lipodystrophy.

21 January 2018

1 reference

Mutation of the mouse klotho gene leads to a syndrome resembling ageing

21 January 2018

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A Gene for Congenital Generalized Lipodystrophy Maps to Human Chromosome 9q34

21 January 2018

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Mitotic misregulation and human aging

21 January 2018

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Telomere length predicts replicative capacity of human fibroblasts

21 January 2018

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Reduced DNA repair in progeria cells and effects of gamma-ray irradiation on UV-induced unscheduled DNA synthesis in normal and progeria cells

21 January 2018

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Oxidative stress, caloric restriction, and aging

21 January 2018

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Genetic analysis of ageing: role of oxidative damage and environmental stresses.

21 January 2018

1 reference

The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH

21 January 2018

1 reference

ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes

21 January 2018

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Cockayne syndrome: Review of 140 cases

21 January 2018

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A single ataxia telangiectasia gene with a product similar to PI-3 kinase

21 January 2018

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Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome

21 January 2018

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Nijmegen breakage syndrome

21 January 2018

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New mice for old questions

21 January 2018

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In vivo human somatic mutation: frequency and spectrum with age

21 January 2018

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7 January 2021

Somatic mutations are frequent and increase with age in human kidney epithelial cells

1 reference

7 January 2021

Polymorphisms at the Werner locus: I. Newly identified polymorphisms, ethnic variability of 1367Cys/Arg, and its stability in a population of Finnish centenarians

1 reference

7 January 2021

Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population

1 reference

7 January 2021

Myotonic dystrophy: the role of the CUG triplet repeats in splicing of a novel DMPK exon and altered cytoplasmic DMPK mRNA isoform ratios

1 reference

7 January 2021

Radiological features in generalized lipodystrophy

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7 January 2021

Progeria: a human-disease model of accelerated aging

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7 January 2021

No detectable mutations at Werner helicase locus in progeria

1 reference

7 January 2021

Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

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7 January 2021

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Identifiers

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30 July 2022

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1012583155

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Fatcat ID

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30 July 2022

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https://api.fatcat.wiki/v0/release/csdein3pazcixpgouo7w36cypm

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30 July 2022