Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia
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A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family.Molecular mechanisms of fibroblast growth factor signaling in physiology and pathologyTwist1 Is Essential for Tooth Morphogenesis and Odontoblast DifferentiationModulation of Fgf3 dosage in mouse and men mirrors evolution of mammalian dentitionGenetic and familial predisposition to rotator cuff disease: a systematic review.Expression of ERK signaling inhibitors Dusp6, Dusp7, and Dusp9 during mouse ear development.HOXA2 haploinsufficiency in dominant bilateral microtia and hearing loss.Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceansA Network Map of FGF-1/FGFR Signaling System.Controlling destiny through chemistry: small-molecule regulators of cell fate.Identification of differentially expressed genes in early inner ear developmentVariable expressivity of FGF3 mutations associated with deafness and LAMM syndromeIdentification of novel therapeutic targets in the PI3K/AKT/mTOR pathway in hepatocellular carcinoma using targeted next generation sequencing.Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3).The Fibroblast Growth Factor signaling pathwayExploration of molecular genetic etiology for Korean cochlear implantees with severe to profound hearing loss and its implication.Fibroblast growth factors: biology, function, and application for tissue regeneration.Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.Chromodomain proteins in development: lessons from CHARGE syndrome.Fibroblast growth factors: from molecular evolution to roles in development, metabolism and disease.Gestational vitamin A deficiency: a novel cause of sensorineural hearing loss in the developing world?A breath of fresh air on the mesenchyme: impact of impaired mesenchymal development on the pathogenesis of bronchopulmonary dysplasia.The FGF family: biology, pathophysiology and therapyCandidate gene studies in hypodontia suggest role for FGF3Molecular pathology of the fibroblast growth factor family.The best-laid plans go oft awry: synaptogenic growth factor signaling in neuropsychiatric disease.Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentition.Fibroblast growth factor signaling in mammalian tooth development.Fibroblast growth factor (FGF) signaling in development and skeletal diseases.Molecular studies on the roles of Runx2 and Twist1 in regulating FGF signaling.Fgf3 and Fgf16 expression patterns define spatial and temporal domains in the developing chick inner ear.Identification of a second HOXA2 nonsense mutation in a family with autosomal dominant non-syndromic microtia and distinctive ear morphology.Delayed presentation of rickets in a child with labyrinthine aplasia, microtia and microdontia (LAMM) syndrome.Mutational analysis of PACT gene in Chinese patients with microtia.The Role of Fibroblast Growth Factors in Tooth Development and Incisor Renewal.
P2860
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P2860
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia
description
2007 nî lūn-bûn
@nan
2007 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Homozygous mutations in fibrob ...... sis, microtia, and microdontia
@ast
Homozygous mutations in fibrob ...... sis, microtia, and microdontia
@en
Homozygous mutations in fibrob ...... sis, microtia, and microdontia
@nl
type
label
Homozygous mutations in fibrob ...... sis, microtia, and microdontia
@ast
Homozygous mutations in fibrob ...... sis, microtia, and microdontia
@en
Homozygous mutations in fibrob ...... sis, microtia, and microdontia
@nl
prefLabel
Homozygous mutations in fibrob ...... sis, microtia, and microdontia
@ast
Homozygous mutations in fibrob ...... sis, microtia, and microdontia
@en
Homozygous mutations in fibrob ...... sis, microtia, and microdontia
@nl
P2093
P2860
P50
P356
P1476
Homozygous mutations in fibrob ...... sis, microtia, and microdontia
@en
P2093
Asli Sirmaci
Burcu Oztürk Hişmi
E Berrin Yüksel-Konuk
Filiz Başak Cengiz
Idil Aslan
Nejat Akar
Oztan Yasun
Seda Taşir Yilmaz
Suat Fitoz
P2860
P304
P356
10.1086/510920
P407
P577
2006-12-27T00:00:00Z