(Q27935480)

1 December 2016

title

SGS1, the Saccharomyces cerevisiae homologue of BLM and WRN, suppresses genome instability and homeologous recombination (English)

1 reference

PubMed

PubMed publication ID

11138010

ATP-dependent DNA helicase SGS1 YMR190C

1 December 2016

main subject

Saccharomyces cerevisiae

0 references

1 reference

GOA release 2020-03-11

1 reference

K Myung

1

0 references

A Datta

series ordinal

2

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C Chen

series ordinal

3

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R D Kolodner

series ordinal

4

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language of work or name

English

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publication date

January 2001

0 references

1 reference

PubMed publication ID

11138010

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 December 2016

volume

27

0 references

issue

1

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page(s)

113-6

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cites work

1 reference

7 January 2021

The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase

1 reference

7 January 2021

Purification and characterization of the Sgs1 DNA helicase activity of Saccharomyces cerevisiae.

1 reference

7 January 2021

WRN mutations in Werner syndrome

1 reference

7 January 2021

Chromosomal rearrangements occur in S. cerevisiae rfa1 mutator mutants due to mutagenic lesions processed by double-strand-break repair

1 reference

7 January 2021

Gross chromosomal rearrangements in Saccharomyces cerevisiae replication and recombination defective mutants

1 reference

7 January 2021

A new human topoisomerase III that interacts with SGS1 protein

1 reference

7 January 2021

Mitotic crossovers between diverged sequences are regulated by mismatch repair proteins in Saccaromyces cerevisiae

1 reference

7 January 2021

Interspecies gene exchange in bacteria: the role of SOS and mismatch repair systems in evolution of species.

1 reference

7 January 2021

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

1 reference

7 January 2021

RecQ helicase, in concert with RecA and SSB proteins, initiates and disrupts DNA recombination

1 reference

7 January 2021

Homologous recombination is responsible for cell death in the absence of the Sgs1 and Srs2 helicases

1 reference

7 January 2021

Fission yeast rad12+ regulates cell cycle checkpoint control and is homologous to the Bloom's syndrome disease gene

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

The saccharomyces PIF1 DNA helicase inhibits telomere elongation and de novo telomere formation

1 reference

7 January 2021

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

1 reference

7 January 2021

Positional cloning of the Werner's syndrome gene

1 reference

7 January 2021

Establishment of B-lymphoid cell lines retaining cytogenetic characteristics of Bloom syndrome

1 reference

7 January 2021

Cytogenetic aspects of Werner syndrome

1 reference

7 January 2021

Increased frequency of 6-thioguanine-resistant peripheral blood lymphocytes in Werner syndrome patients.

1 reference

7 January 2021

Nucleotide sequence analysis of human hypoxanthine phosphoribosyltransferase (HPRT) gene deletions

1 reference

7 January 2021

Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome

1 reference

7 January 2021

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

1 reference

7 January 2021