The Werner syndrome protein is a DNA helicase (Q24310486)

GOA release 2020-03-11

human ageing

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GOA release 2020-03-11

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M D Gray

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J C Shen

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A S Kamath-Loeb

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A Blank

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B L Sopher

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G M Martin

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J Oshima

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L A Loeb

https://scigraph.springernature.com/pub.10.1038/ng0997-100

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language of work or name

English

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publication date

September 1997

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published in

Nature Genetics

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volume

17

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issue

1

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page(s)

100-3

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exact match

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cites work

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

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Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism

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Mutator phenotype of Werner syndrome is characterized by extensive deletions

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Positional cloning of the Werner's syndrome gene

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Structure and function of transcription-repair coupling factor. I. Structural domains and binding properties.

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Expression of simian virus 40 T antigen in insect cells using a baculovirus expression vector

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A dominant negative allele of the Escherichia coli uvrD gene encoding DNA helicase II. A biochemical and genetic characterization.

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Human homologues of yeast helicase

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Escherichia coli RecQ protein is a DNA helicase

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Human xeroderma pigmentosum group D gene encodes a DNA helicase

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RecQ DNA helicase of Escherichia coli. Characterization of the helix-unwinding activity with emphasis on the effect of single-stranded DNA-binding protein.

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Isolation and genetic characterization of a thymineless death-resistant mutant of Escherichia coli K12: identification of a new mutation (recQ1) that blocks the RecF recombination pathway.

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Sgs1: a eukaryotic homolog of E. coli RecQ that interacts with topoisomerase II in vivo and is required for faithful chromosome segregation

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Spontaneous and induced chromosomal instability in Werner syndrome

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Homozygous and compound heterozygous mutations at the Werner syndrome locus

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recF and recR are required for the resumption of replication at DNA replication forks in Escherichia coli

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

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An improved method for the colorimetric determination of phosphate

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Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process

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