Direct and indirect requirements of Shh/Gli signaling in early pituitary development.
about
Fox tales: regulation of gonadotropin gene expression by forkhead transcription factorsPituitary gland development and disease: from stem cell to hormone productionCeramide is involved in alcohol-induced neural proliferation.Pituitary androgen receptor signalling regulates prolactin but not gonadotrophins in the male mouse.Prenatal ethanol exposure in mice phenocopies Cdon mutation by impeding Shh function in the etiology of optic nerve hypoplasiaDisruption of SoxB1-dependent Sonic hedgehog expression in the hypothalamus causes septo-optic dysplasia.Genetic regulation of murine pituitary development.Identification of novel pathways involved in the pathogenesis of human adamantinomatous craniopharyngioma.Functional characterization of a heterozygous GLI2 missense mutation in patients with multiple pituitary hormone deficiency.Sonic Hedgehog Signaling and VACTERL Association.Deletion of OTX2 in neural ectoderm delays anterior pituitary developmentInhibition of Sox2-dependent activation of Shh in the ventral diencephalon by Tbx3 is required for formation of the neurohypophysis.PROP1 triggers epithelial-mesenchymal transition-like process in pituitary stem cellsSOX2 is sequentially required for progenitor proliferation and lineage specification in the developing pituitaryFoxo1 Is Required for Normal Somatotrope DifferentiationNotch signaling in postnatal pituitary expansion: proliferation, progenitors, and cell specification.Pathology and pathogenesis of craniopharyngiomas.Hedgehog: Multiple Paths for Multiple Roles in Shaping the Brain and Spinal Cord.Hypothalamic sonic hedgehog is required for cell specification and proliferation of LHX3/LHX4 pituitary embryonic precursors.Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.The role of the sonic hedgehog signalling pathway in patients with midline defects and congenital hypopituitarism.Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly.Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly.The origins of the circumventricular organs.
P2860
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P2860
Direct and indirect requirements of Shh/Gli signaling in early pituitary development.
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Direct and indirect requirements of Shh/Gli signaling in early pituitary development.
@ast
Direct and indirect requirements of Shh/Gli signaling in early pituitary development.
@en
type
label
Direct and indirect requirements of Shh/Gli signaling in early pituitary development.
@ast
Direct and indirect requirements of Shh/Gli signaling in early pituitary development.
@en
prefLabel
Direct and indirect requirements of Shh/Gli signaling in early pituitary development.
@ast
Direct and indirect requirements of Shh/Gli signaling in early pituitary development.
@en
P2093
P2860
P1476
Direct and indirect requirements of Shh/Gli signaling in early pituitary development.
@en
P2093
C Brian Bai
James F Martin
Yiwei Wang
P2860
P304
P356
10.1016/J.YDBIO.2010.09.024
P407
P577
2010-10-08T00:00:00Z