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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2014 | 1 |
2016 | 2 |
2020 | 1 |
2022 | 2 |
2024 | 1 |
PubMed (GeneRIF) for id: 55063
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A loss-of-function variant in ZCWPW1 causes human male infertility with sperm head defect and high DNA fragmentation.
Reprod Health. 2024 Feb 3;21(1):18. doi: 10.1186/s12978-024-01746-9.
Reprod Health. 2024.
PMID: 38310235
Free PMC article.
The histone modification reader ZCWPW1 promotes double-strand break repair by regulating cross-talk of histone modifications and chromatin accessibility at meiotic hotspots.
Yuan S, Huang T, Bao Z, Wang S, Wu X, Liu J, Liu H, Chen ZJ.
Yuan S, et al.
Genome Biol. 2022 Sep 6;23(1):187. doi: 10.1186/s13059-022-02758-z.
Genome Biol. 2022.
PMID: 36068616
Free PMC article.
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PRDM9 losses in vertebrates are coupled to those of paralogs ZCWPW1 and ZCWPW2.
Cavassim MIA, Baker Z, Hoge C, Schierup MH, Schumer M, Przeworski M.
Cavassim MIA, et al.
Proc Natl Acad Sci U S A. 2022 Mar 1;119(9):e2114401119. doi: 10.1073/pnas.2114401119.
Proc Natl Acad Sci U S A. 2022.
PMID: 35217607
Free PMC article.
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ZCWPW1 is recruited to recombination hotspots by PRDM9 and is essential for meiotic double strand break repair.
Wells D, Bitoun E, Moralli D, Zhang G, Hinch A, Jankowska J, Donnelly P, Green C, Myers SR.
Wells D, et al.
Elife. 2020 Aug 3;9:e53392. doi: 10.7554/eLife.53392.
Elife. 2020.
PMID: 32744506
Free PMC article.
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ZCWPW1 is associated with late-onset Alzheimer's disease in Han Chinese: a replication study and meta-analyses.
Gao Y, Tan MS, Wang HF, Zhang W, Wang ZX, Jiang T, Yu JT, Tan L.
Gao Y, et al.
Oncotarget. 2016 Apr 12;7(15):20305-11. doi: 10.18632/oncotarget.7945.
Oncotarget. 2016.
PMID: 26958812
Free PMC article.
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Alzheimer's Disease Risk Polymorphisms Regulate Gene Expression in the ZCWPW1 and the CELF1 Loci.
Karch CM, Ezerskiy LA, Bertelsen S; Alzheimer’s Disease Genetics Consortium (ADGC); Goate AM.
Karch CM, et al.
PLoS One. 2016 Feb 26;11(2):e0148717. doi: 10.1371/journal.pone.0148717. eCollection 2016.
PLoS One. 2016.
PMID: 26919393
Free PMC article.
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Connecting the dots: potential of data integration to identify regulatory SNPs in late-onset Alzheimer's disease GWAS findings.
Rosenthal SL, Barmada MM, Wang X, Demirci FY, Kamboh MI.
Rosenthal SL, et al.
PLoS One. 2014 Apr 17;9(4):e95152. doi: 10.1371/journal.pone.0095152. eCollection 2014.
PLoS One. 2014.
PMID: 24743338
Free PMC article.
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