Nonsyndromic hearing impairment is associated with a mutation in DFNA5
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Congenital sensorineural deafness in dalmatian dogs associated with quantitative trait lociThe DFNA5 gene, responsible for hearing loss and involved in cancer, encodes a novel apoptosis-inducing proteinAberrant promoter methylation and tumor suppressive activity of the DFNA5 gene in colorectal carcinomaMutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathyFinding new genes for non-syndromic hearing loss through an in silico prioritization studySudden bilateral hearing loss in gastric cancer as the only symptom of disease.Apoptosis in acquired and genetic hearing impairment: the programmed death of the hair cellIn CEM cells the autosomal deafness gene dfna5 is regulated by glucocorticoids and forskolinA gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.At the speed of sound: gene discovery in the auditory systemCleavage of DFNA5 by caspase-3 during apoptosis mediates progression to secondary necrotic/pyroptotic cell death.Beginning of a molecular era in hearing and deafness.DFNA5 promoter methylation a marker for breast tumorigenesisNovel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss.Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes.Progress and prospects in human genetic research into age-related hearing impairment.TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data.Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74Is DFNA5 a susceptibility gene for age-related hearing impairment?Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles.DFNA5, a gene involved in hearing loss and cancer: a review.Non-syndromic autosomal-dominant deafness.Methylation of the DFNA5 increases risk of lymph node metastasis in human breast cancerNovel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3.Inherited deafness in childhood--the genetic revolution unmasks the clinical challenge.The genetic bases for non-syndromic hearing loss among ChineseAn Integrated Bioinformatics and Computational Biology Approach Identifies New BH3-Only Protein CandidatesAssociations of genetic variations in EYA4, GRHL2 and DFNA5 with noise-induced hearing loss in Chinese population: a case- control studyEvidence for a founder mutation causing DFNA5 hearing loss in East AsiansGenetics of deafness: recent advances and clinical implications.IVS8+1 DelG, a Novel Splice Site Mutation Causing DFNA5 Deafness in a Chinese Family.Distinct Expression Patterns Of Causative Genes Responsible For Hereditary Progressive Hearing Loss In Non-Human Primate Cochlea.Identification of Two Disease-causing Genes TJP2 and GJB2 in a Chinese Family with Unconditional Autosomal Dominant Nonsyndromic Hereditary Hearing Impairment.Expression of GSDML Associates with Tumor Progression in Uterine Cervix CancerFunctional conservation of Gsdma cluster genes specifically duplicated in the mouse genome.Differential gene expression in human cerebrovascular malformations.Therapeutic regulation of gene expression in the inner ear using RNA interference.Gasdermin B expression predicts poor clinical outcome in HER2-positive breast cancer'Hints' in the killer protein gasdermin D: unveiling the secrets of gasdermins driving cell death.
P2860
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P2860
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
description
1998 nî lūn-bûn
@nan
1998 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
@ast
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
@en
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
@en-gb
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
@nl
type
label
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
@ast
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
@en
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
@en-gb
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
@nl
prefLabel
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
@ast
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
@en
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
@en-gb
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
@nl
P2093
P2860
P3181
P356
P1433
P1476
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
@en
P2093
D van Zuijlen
E H Huizing
G P Richardson
G Van Camp
J G Wauters
L Van Laer
M Verstreken
P J Bossuyt
P J Willems
P2860
P2888
P304
P3181
P356
10.1038/2503
P407
P577
1998-10-01T00:00:00Z
P5875
P6179
1004705456