Elucidation of the Fanconi Anemia Protein Network in Meiosis and Its Function in the Regulation of Histone Modifications-Reference-Cited by-同舟云学术

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Elucidation of the Fanconi Anemia Protein Network in Meiosis and Its Function in the Regulation of Histone Modifications

Published:2016-10 Issue:4 Volume:17 Page:1141-1157
ISSN:2211-1247
Container-title:Cell Reports
language:en
Short-container-title:Cell Reports

Author:

Alavattam Kris G.,Kato Yasuko,Sin Ho-Su,Maezawa So,Kowalski Ian J.,Zhang Fan,Pang Qishen,Andreassen Paul R.,Namekawa Satoshi H.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference85 articles.

1. UBR2 of the N-end rule pathway is required for chromosome stability via histone ubiquitylation in spermatocytes and somatic cells;An;PLoS ONE,2012

2. Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M;Bakker;Hum. Mol. Genet.,2009

3. Surveillance of different recombination defects in mouse spermatocytes yields distinct responses despite elimination at an identical developmental stage;Barchi;Mol. Cell. Biol.,2005

4. Chromosome synapsis defects and sexually dimorphic meiotic progression in mice lacking Spo11;Baudat;Mol. Cell,2000

5. SPO11 is required for sex-body formation, and Spo11 heterozygosity rescues the prophase arrest of Atm-/- spermatocytes;Bellani;J. Cell Sci.,2005

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1. Fance deficiency impaired DNA damage repair of prospermatogonia and altered the repair dynamics of spermatocytes;Reproductive Biology and Endocrinology;2024-08-29

2. Protein disulfide isomerase is essential for spermatogenesis in mice;JCI Insight;2024-06-24

3. Research progress on the fanconi anemia signaling pathway in non-obstructive azoospermia;Frontiers in Endocrinology;2024-05-23

4. Novel compound heterozygous variants in FANCI cause premature ovarian insufficiency;Human Genetics;2024-03

5. The DNA helicase FANCJ (BRIP1) functions in double strand break repair processing, but not crossover formation during prophase I of meiosis in male mice;PLOS Genetics;2024-02-20

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