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Quo vadis, hair cell regeneration?Genetic insights into the mechanisms of Fgf signalingPax2 contributes to inner ear patterning and optic nerve trajectoryMAP3K1 function is essential for cytoarchitecture of the mouse organ of Corti and survival of auditory hair cells.Genetic rescue of Muenke syndrome model hearing loss reveals prolonged FGF-dependent plasticity in cochlear supporting cell fates.Fgf signaling regulates development and transdifferentiation of hair cells and supporting cells in the basilar papillaPolygenic inheritance of sensorineural hearing loss (Snhl2, -3, and -4) and organ of Corti patterning defect in the ALR/LtJ mouse strainCD44 is a marker for the outer pillar cells in the early postnatal mouse inner ear.Auditory hair cell defects as potential cause for sensorineural deafness in Wolf-Hirschhorn syndromeRegulation of cell fate and patterning in the developing mammalian cochlea.Hearing loss in syndromic craniosynostoses: introduction and consideration of mechanismsPhenotype profile of a genetic mouse model for Muenke syndrome.Expression patterns of FGF receptors in the developing mammalian cochlea.The Fibroblast Growth Factor signaling pathwayThyroid hormone increases fibroblast growth factor receptor expression and disrupts cell mechanics in the developing organ of cortiExpanding the mutation spectrum in 182 Spanish probands with craniosynostosis: identification and characterization of novel TCF12 variants.Fibroblast growth factor receptor 3 regulates microtubule formation and cell surface mechanical properties in the developing organ of CortiA familial case of Muenke syndrome. Diverse expressivity of the FGFR3 Pro252Arg mutation--case report and review of the literature.Achondroplasia: Development, pathogenesis, and therapy.Editorial: Sensory Hair Cell Death and Regeneration.FGF signaling: diverse roles during cochlear development.Muenke syndrome: An international multicenter natural history study.A second family with CATSHL syndrome: Confirmatory report of another unique FGFR3 syndrome.CraniosynostosisFGFR3 mutation causes abnormal membranous ossification in achondroplasia
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Hearing loss in a mouse model of Muenke syndrome
@ast
Hearing loss in a mouse model of Muenke syndrome
@en
type
label
Hearing loss in a mouse model of Muenke syndrome
@ast
Hearing loss in a mouse model of Muenke syndrome
@en
prefLabel
Hearing loss in a mouse model of Muenke syndrome
@ast
Hearing loss in a mouse model of Muenke syndrome
@en
P2093
P2860
P50
P356
P1476
Hearing loss in a mouse model of Muenke syndrome
@en
P2093
Chaoying Li
Rowena M Freeland
Steven A Wall
P2860
P356
10.1093/HMG/DDN311
P577
2008-09-25T00:00:00Z