(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

The Bloom's syndrome gene product is homologous to RecQ helicases

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language of work or name

English

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publication date

September 1997

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100-3

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG0997-100

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

Mutator phenotype of Werner syndrome is characterized by extensive deletions

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

Positional cloning of the Werner's syndrome gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

Human homologues of yeast helicase

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

Escherichia coli RecQ protein is a DNA helicase

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

Human xeroderma pigmentosum group D gene encodes a DNA helicase

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

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.

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

Spontaneous and induced chromosomal instability in Werner syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

Homozygous and compound heterozygous mutations at the Werner syndrome locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

An improved method for the colorimetric determination of phosphate

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-100

7 January 2021