The checkpoint kinases Chk1 and Chk2 regulate the functional associations between hBRCA2 and Rad51 in response to DNA damage (Q24320698)

GOA release 2020-03-11

author name string

E M Bahassi

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J L Ovesen

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A L Riesenberg

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W Z Bernstein

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P E Hasty

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P J Stambrook

The breast cancer susceptibility allele CHEK2*1100delC promotes genomic instability in a knock-in mouse model.

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language of work or name

English

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publication date

26 June 2008

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published in

Oncogene

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volume

27

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page(s)

3977-85

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issue

28

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cites work

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Human Rad51 protein promotes ATP-dependent homologous pairing and strand transfer reactions in vitro

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Internal repeats in the BRCA2 protein sequence

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Role of BRCA2 in control of the RAD51 recombination and DNA repair protein.

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Deletion of Brca2 exon 27 causes hypersensitivity to DNA crosslinks, chromosomal instability, and reduced life span in mice.

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CDK-dependent phosphorylation of BRCA2 as a regulatory mechanism for recombinational repair

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RAB22 and RAB163/mouse BRCA2: proteins that specifically interact with the RAD51 protein

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BRCA2 is required for homology-directed repair of chromosomal breaks

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Insights into DNA recombination from the structure of a RAD51-BRCA2 complex

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Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases. Anglian Breast Cancer Study Group

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Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2

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A region of human BRCA2 containing multiple BRC repeats promotes RAD51-mediated strand exchange

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The cell-cycle checkpoint kinase Chk1 is required for mammalian homologous recombination repair

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The breast cancer susceptibility gene, BRCA2: at the crossroads between DNA replication and recombination?

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Cancer susceptibility and the functions of BRCA1 and BRCA2

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BRCA1 and BRCA2 and the genetics of breast and ovarian cancer

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RAD51 interacts with the evolutionarily conserved BRC motifs in the human breast cancer susceptibility gene brca2

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Deficiency of human BRCA2 leads to impaired homologous recombination but maintains normal nonhomologous end joining

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