Comprehensive pathway-based analysis identifies associations of BCL2, GNAO1 and CHD2 with non-obstructive azoospermia risk.
about
Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.Architects of the genome: CHD dysfunction in cancer, developmental disorders and neurological syndromesClinically relevant known and candidate genes for obesity and their overlap with human infertility and reproduction.Genetic polymorphism at BCL2 as a predictor for rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone efficacy in patients with diffuse large B-cell lymphoma.
P2860
Comprehensive pathway-based analysis identifies associations of BCL2, GNAO1 and CHD2 with non-obstructive azoospermia risk.
description
2014 nî lūn-bûn
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name
Comprehensive pathway-based an ...... -obstructive azoospermia risk.
@en
Comprehensive pathway-based an ...... -obstructive azoospermia risk.
@nl
type
label
Comprehensive pathway-based an ...... -obstructive azoospermia risk.
@en
Comprehensive pathway-based an ...... -obstructive azoospermia risk.
@nl
prefLabel
Comprehensive pathway-based an ...... -obstructive azoospermia risk.
@en
Comprehensive pathway-based an ...... -obstructive azoospermia risk.
@nl
P2093
P2860
P356
P1433
P1476
Comprehensive pathway-based an ...... -obstructive azoospermia risk.
@en
P2093
Chuncheng Lu
Guizhen Du
Jiahao Sha
Juncheng Dai
Xinru Wang
Yankai Xia
Yufeng Qin
P2860
P304
P356
10.1093/HUMREP/DEU013
P407
P50
P577
2014-02-18T00:00:00Z