The phenotype of FancB-mutant mouse embryonic stem cells.
about
RAD51 mutants cause replication defects and chromosomal instabilityRECQL5 and BLM exhibit divergent functions in cells defective for the Fanconi anemia pathwayFANCB is essential in the male germline and regulates H3K9 methylation on the sex chromosomes during meiosis.Defining a genotoxic profile with mouse embryonic stem cellsModelling Fanconi anemia pathogenesis and therapeutics using integration-free patient-derived iPSCsTrex2 enables spontaneous sister chromatid exchanges without facilitating DNA double-strand break repair.A mechanism for 1,4-Benzoquinone-induced genotoxicity.Parallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia.
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P2860
The phenotype of FancB-mutant mouse embryonic stem cells.
description
2011 nî lūn-bûn
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2011 թուականի Մարտին հրատարակուած գիտական յօդուած
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2011 թվականի մարտին հրատարակված գիտական հոդված
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2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
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name
The phenotype of FancB-mutant mouse embryonic stem cells.
@ast
The phenotype of FancB-mutant mouse embryonic stem cells.
@en
type
label
The phenotype of FancB-mutant mouse embryonic stem cells.
@ast
The phenotype of FancB-mutant mouse embryonic stem cells.
@en
prefLabel
The phenotype of FancB-mutant mouse embryonic stem cells.
@ast
The phenotype of FancB-mutant mouse embryonic stem cells.
@en
P2093
P2860
P1433
P1476
The phenotype of FancB-mutant mouse embryonic stem cells.
@en
P2093
Lingchuan Hu
Paul Hasty
Tae Moon Kim
Yong Jun Choi
P2860
P356
10.1016/J.MRFMMM.2011.03.010
P407
P577
2011-03-30T00:00:00Z