PROK2/PROKR2 Signaling and Kallmann Syndrome.

PROK2/PROKR2 Signaling and Kallmann Syndrome.

Item
http://www.wikidata.org/entity/Q36760693
Central hypogonadotropic hypogonadism: genetic complexity of a complex disease46,XY disorder of sexual development resulting from a novel monoallelic mutation (p.Ser31Phe) in the steroid 5α-reductase type-2 (SRD5A2) gene.Functional rescue of Kallmann syndrome-associated prokineticin receptor 2 (PKR2) mutants deficient in traffickingGnRH, anosmia and hypogonadotropic hypogonadism--where are we?Combined pituitary hormone deficiency with unique pituitary dysplasia and morning glory syndrome related to a heterozygous PROKR2 mutation.Variants in congenital hypogonadotrophic hypogonadism genes identified in an Indonesian cohort of 46,XY under-virilised boys.TSHZ1-dependent gene regulation is essential for olfactory bulb development and olfaction.Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism.Haploinsufficiency of SIX3 Abolishes Male Reproductive Behavior Through Disrupted Olfactory Development, and Impairs Female Fertility Through Disrupted GnRH Neuron Migration.
P2860

PROK2/PROKR2 Signaling and Kallmann Syndrome.

Item
http://www.wikidata.org/entity/Q36760693
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
PROK2/PROKR2 Signaling and Kallmann Syndrome.
@ast
PROK2/PROKR2 Signaling and Kallmann Syndrome.
@en
type
label
PROK2/PROKR2 Signaling and Kallmann Syndrome.
@ast
PROK2/PROKR2 Signaling and Kallmann Syndrome.
@en
prefLabel
PROK2/PROKR2 Signaling and Kallmann Syndrome.
@ast
PROK2/PROKR2 Signaling and Kallmann Syndrome.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P478
P50
P577
P5875
P698
P932
P356
P1433
P1476
PROK2/PROKR2 Signaling and Kallmann Syndrome
@en
P2093
P2860
P304
P31
P356
P478
P50
P577
P5875
P698
P932