The molecular basis of impaired follicle-stimulating hormone action: evidence from human mutations and mouse models
about
Role of the Extracellular and Intracellular Loops of Follicle-Stimulating Hormone Receptor in Its FunctionThe genetic basis of female reproductive disorders: etiology and clinical testingEndocrine control of spermatogenesis: Role of FSH and LH/ testosteroneAKAP9 is essential for spermatogenesis and sertoli cell maturation in miceSignaling through FSH receptors on human umbilical vein endothelial cells promotes angiogenesis.Gonadotropin Signaling in Zebrafish Ovary and Testis Development: Insights From Gene Knockout Study.Targeting testis-specific proteins to inhibit spermatogenesis: lesson from endocrine disrupting chemicals.Reproductive physiology in young men is cumulatively affected by FSH-action modulating genetic variants: FSHR -29G/A and c.2039 A/G, FSHB -211G/T.Hypoglycosylated hFSH Has Greater Bioactivity Than Fully Glycosylated Recombinant hFSH in Human Granulosa CellsModifiers of ovarian function in girls and women with classic galactosemia.Follicle stimulating hormone modulates ovarian stem cells through alternately spliced receptor variant FSH-R3.In Vitro Effects of the Endocrine Disruptor p,p'-DDT on Human Follitropin Receptor.Diagnosis and treatment of infertility-related male hormonal dysfunction.First mutation in the FSHR cytoplasmic tail identified in a non-pregnant woman with spontaneous ovarian hyperstimulation syndrome.A Case of MECP2 Duplication Syndrome with Gonadotropin-Dependent Precocious Puberty.ING5 activity in self-renewal of glioblastoma stem cells via calcium and follicle stimulating hormone pathways.Further characterization of adult sheep ovarian stem cells and their involvement in neo-oogenesis and follicle assembly.Fshb Knockout Mouse Model, Two Decades Later and Into the Future.Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports
P2860
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P2860
The molecular basis of impaired follicle-stimulating hormone action: evidence from human mutations and mouse models
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2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
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2012年學術文章
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2012年學術文章
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name
The molecular basis of impaire ...... man mutations and mouse models
@en
The molecular basis of impaire ...... an mutations and mouse models.
@nl
type
label
The molecular basis of impaire ...... man mutations and mouse models
@en
The molecular basis of impaire ...... an mutations and mouse models.
@nl
prefLabel
The molecular basis of impaire ...... man mutations and mouse models
@en
The molecular basis of impaire ...... an mutations and mouse models.
@nl
P2093
P2860
P356
P1476
The molecular basis of impaire ...... man mutations and mouse models
@en
P2093
Eric T Siegel
Hiromi Koso Nishimoto
Hyung-Goo Kim
Lawrence C Layman
P2860
P304
P356
10.1177/1933719112461184
P577
2012-11-26T00:00:00Z