Hearing loss: a common disorder caused by many rare alleles.
about
Early development of the vertebrate inner earA point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus).A phylomedicine approach to understanding the evolution of auditory sensory perception and disease in mammalsA short splice form of Xin-actin binding repeat containing 2 (XIRP2) lacking the Xin repeats is required for maintenance of stereocilia morphology and hearing functionThe expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy.Functional and structural changes throughout the auditory system following congenital and early-onset deafness: implications for hearing restoration.Probing the Xenopus laevis inner ear transcriptome for biological function.Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL.Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing lossCell type-specific transcriptome analysis reveals a major role for Zeb1 and miR-200b in mouse inner ear morphogenesis.Subcellular localization of the transmembrane inner ear (Tmie) protein in a stable Tmie-expressing cell line.A 5.8 Mb interstitial deletion on chromosome Xq21.1 in a boy with intellectual disability, cleft palate, hearing impairment and combined growth hormone deficiency.Proteomic analysis of the organ of corti using nanoscale liquid chromatography coupled with tandem mass spectrometry.Protein-engineered hydrogel encapsulation for 3-D culture of murine cochlea.Clinical applications and implications of common and founder mutations in Indian subpopulations.New treatment options for hearing loss.The genetics of hair-cell function in zebrafish.Activity-dependent formation of a vesicular inhibitory amino acid transporter gradient in the superior olivary complex of NMRI mice.ESRP1 Mutations Cause Hearing Loss due to Defects in Alternative Splicing that Disrupt Cochlear Development.
P2860
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P2860
Hearing loss: a common disorder caused by many rare alleles.
description
2010 nî lūn-bûn
@nan
2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
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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
Hearing loss: a common disorder caused by many rare alleles.
@ast
Hearing loss: a common disorder caused by many rare alleles.
@en
type
label
Hearing loss: a common disorder caused by many rare alleles.
@ast
Hearing loss: a common disorder caused by many rare alleles.
@en
prefLabel
Hearing loss: a common disorder caused by many rare alleles.
@ast
Hearing loss: a common disorder caused by many rare alleles.
@en
P2860
P1476
Hearing loss: a common disorder caused by many rare alleles.
@en
P2093
Amiel A Dror
Dorith Raviv
P2860
P304
P356
10.1111/J.1749-6632.2010.05868.X
P407
P577
2010-12-01T00:00:00Z