Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
about
Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79Autosomal recessive nonsyndromic deafness genes: a reviewConditional gene expression in the mouse inner ear using Cre-loxP.Family Wide Molecular Adaptations to Underground Life in African Mole-Rats Revealed by Phylogenomic Analysis.Secreted Factors from Human Vestibular Schwannomas Can Cause Cochlear Damage.The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani PopulationsPla2g12b and Hpn are genes identified by mouse ENU mutagenesis that affect HDL cholesterolFinding new genes for non-syndromic hearing loss through an in silico prioritization studyMutations in KARS, encoding lysyl-tRNA synthetase, cause autosomal-recessive nonsyndromic hearing impairment DFNB89Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing lossGenetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families.Genetic associations for keratoconus: a systematic review and meta-analysis.Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42Novel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3.A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.Challenges and solutions for gene identification in the presence of familial locus heterogeneity.Novel TMPRSS3 variants in Pakistani families with autosomal recessive non-syndromic hearing impairment.Appl1 and Appl2 are Expendable for Mouse Development But Are Essential for HGF-Induced Akt Activation and Migration in Mouse Embryonic Fibroblasts.Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population.Prenatal expression of MET receptor tyrosine kinase in the fetal mouse dorsal raphe nuclei and the visceral motor/sensory brainstemHepatocyte Growth Factor-c-MET Signaling Mediates the Development of Nonsensory Structures of the Mammalian Cochlea and Hearing.Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86.Gene of the month: HGF.The Promoter and Multiple Enhancers of the pou4f3 Gene Regulate Expression in Inner Ear Hair Cells.Genetic causes of moderate to severe hearing loss point to modifiers.A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing ImpairmentThe role of hepatocyte growth factor in corneal wound healing.Genetic Testing of Non-familial Deaf Patients for CIB2 and GJB2 Mutations: Phenotype and Genetic Counselling.Modifier variant of METTL13 suppresses human GAB1-associated profound deafness.Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss.Targeting the cMET pathway augments radiation response without adverse effect on hearing in NF2 schwannoma models.HGF-Met Pathway in Regeneration and Drug Discovery.
P2860
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P2860
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
description
2009 nî lūn-bûn
@nan
2009 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
@ast
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
@en
type
label
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
@ast
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
@en
prefLabel
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
@ast
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
@en
P2093
P2860
P1476
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
@en
P2093
Ali M Waryah
Barbara Ploplis
David Velásquez
Dhananjay Chhatre
Edward R Wilcox
Ghazanfar Ali
Glenn Merlino
Julie M Schultz
Madhulika Kabra
Manju Ghosh
P2860
P356
10.1016/J.AJHG.2009.06.003
P407
P577
2009-07-02T00:00:00Z