Dearth and Delayed Maturation of Testicular Germ Cells in Fanconi Anemia E Mutant Male Mice

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Dearth and Delayed Maturation of Testicular Germ Cells in Fanconi Anemia E Mutant Male Mice

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2016 nî lūn-bûn

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2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

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2016年论文

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2016年论文

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Dearth and Delayed Maturation ...... coni Anemia E Mutant Male Mice

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Dearth and Delayed Maturation ...... coni Anemia E Mutant Male Mice

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Dearth and Delayed Maturation ...... coni Anemia E Mutant Male Mice

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Dearth and Delayed Maturation ...... coni Anemia E Mutant Male Mice

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Dearth and Delayed Maturation ...... coni Anemia E Mutant Male Mice

@ast

Dearth and Delayed Maturation ...... coni Anemia E Mutant Male Mice

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P1476

Dearth and Delayed Maturation ...... coni Anemia E Mutant Male Mice

@en

P2093

Chun Fu

http://www.w3.org/2001/XMLSchema#string

Yan He

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P2860

The Fanconi anemia group E gene, FANCE, maps to chromosome 6p

Learning from a paradox: recent insights into Fanconi anaemia through studying mouse models

Meiosis-specific cohesin component, Stag3 is essential for maintaining centromere chromatid cohesion, and required for DNA repair and synapsis between homologous chromosomes

Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice

Targeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell hypoplasia

Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway

The Chinese hamster FANCG/XRCC9 mutant NM3 fails to express the monoubiquitinated form of the FANCD2 protein, is hypersensitive to a range of DNA damaging agents and exhibits a normal level of spontaneous sister chromatid exchange

Reduced fertility and hypersensitivity to mitomycin C characterize Fancg/Xrcc9 null mice

Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia

Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia

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e0159800

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scholarly article

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10.1371/JOURNAL.PONE.0159800

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English

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http://www.w3.org/2001/XMLSchema#string

P478

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Paul A Overbeek

Philip W. Jordan

Khurshida Begum

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2016-08-03T00:00:00Z

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27486799

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P932

4972424

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