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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2012 | 1 |
2013 | 1 |
2014 | 1 |
2015 | 1 |
2024 | 0 |
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4 results
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MNS1 is essential for spermiogenesis and motile ciliary functions in mice.
PLoS Genet. 2012;8(3):e1002516. doi: 10.1371/journal.pgen.1002516. Epub 2012 Mar 1.
PLoS Genet. 2012.
PMID: 22396656
Free PMC article.
A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice.
Zhou J, McCarrey JR, Wang PJ.
Zhou J, et al.
Biol Reprod. 2013 Jun 27;88(6):159. doi: 10.1095/biolreprod.112.106963. Print 2013 Jun.
Biol Reprod. 2013.
PMID: 23677977
Free PMC article.
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Respiratory failure, cleft palate and epilepsy in the mouse model of human Xq22.1 deletion syndrome.
Zhou J, Goldberg EM, Leu NA, Zhou L, Coulter DA, Wang PJ.
Zhou J, et al.
Hum Mol Genet. 2014 Jul 15;23(14):3823-9. doi: 10.1093/hmg/ddu095. Epub 2014 Feb 25.
Hum Mol Genet. 2014.
PMID: 24569167
Free PMC article.
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Polycomb protein SCML2 associates with USP7 and counteracts histone H2A ubiquitination in the XY chromatin during male meiosis.
Luo M, Zhou J, Leu NA, Abreu CM, Wang J, Anguera MC, de Rooij DG, Jasin M, Wang PJ.
Luo M, et al.
PLoS Genet. 2015 Jan 29;11(1):e1004954. doi: 10.1371/journal.pgen.1004954. eCollection 2015 Jan.
PLoS Genet. 2015.
PMID: 25634095
Free PMC article.
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