A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway.
about
Whole-exome sequencing identified a homozygous BRDT mutation in a patient with acephalic spermatozoaInfluence of gonadotropins on ovarian follicle growth and development in vivo and in vitro.Sequence variants of KHDRBS1 as high penetrance susceptibility risks for primary ovarian insufficiency by mis-regulating mRNA alternative splicing.A familial study of twins with severe asthenozoospermia identified a homozygous SPAG17 mutation by whole-exome sequencing.A homozygous NOBOX truncating variant causes defective transcriptional activation and leads to primary ovarian insufficiency.
P2860
A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
A dominant negative mutation a ...... ian hormone signaling pathway.
@en
A dominant negative mutation a ...... ian hormone signaling pathway.
@nl
type
label
A dominant negative mutation a ...... ian hormone signaling pathway.
@en
A dominant negative mutation a ...... ian hormone signaling pathway.
@nl
prefLabel
A dominant negative mutation a ...... ian hormone signaling pathway.
@en
A dominant negative mutation a ...... ian hormone signaling pathway.
@nl
P2093
P2860
P50
P356
P1476
A dominant negative mutation a ...... rian hormone signaling pathway
@en
P2093
P2860
P304
P356
10.1093/MOLEHR/GAW040
P577
2016-07-18T00:00:00Z