A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice
about
Polycomb protein SCML2 associates with USP7 and counteracts histone H2A ubiquitination in the XY chromatin during male meiosisRespiratory failure, cleft palate and epilepsy in the mouse model of human Xq22.1 deletion syndrome.Non-synonymous mutations mapped to chromosome X associated with andrological and growth traits in beef cattle.Regulation of X-linked gene expression during early mouse development by RlimCopy number gain of VCX, X-linked multi-copy gene, leads to cell proliferation and apoptosis during spermatogenesis.
P2860
A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice
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2013 nî lūn-bûn
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2013 թուականի Յունիսին հրատարակուած գիտական յօդուած
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2013 թվականի հունիսին հրատարակված գիտական հոդված
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2013年の論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年论文
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A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice
@ast
A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice
@en
type
label
A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice
@ast
A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice
@en
prefLabel
A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice
@ast
A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice
@en
P2860
P1476
A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice
@en
P2093
John R McCarrey
P Jeremy Wang
P2860
P356
10.1095/BIOLREPROD.112.106963
P407
P50
P577
2013-06-27T00:00:00Z