Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening
about
An Introduction to the Genetics of Normal and Defective HearingESDN, a novel neuropilin-like membrane protein cloned from vascular cells with the longest secretory signal sequence among eukaryotes, is up-regulated after vascular injuryPendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing lossIdentification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues.A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosisThe DFNA15 deafness mutation affects POU4F3 protein stability, localization, and transcriptional activityIsolation from cochlea of a novel human intronless gene with predominant fetal expressionSubcellular localisation, secretion, and post-translational processing of normal cochlin, and of mutants causing the sensorineural deafness and vestibular disorder, DFNA9Nonsyndromic hearing impairment: unparalleled heterogeneityA Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing ImpairmentOtoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22.Cochlin produced by follicular dendritic cells promotes antibacterial innate immunityFdp, a new fibrocyte-derived protein related to MIA/CD-RAP, has an in vitro effect on the early differentiation of the inner ear mesenchymeA novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing.Gene discovery in the auditory system: characterization of additional cochlear-expressed sequences.Gene expression profiles of the rat cochlea, cochlear nucleus, and inferior colliculus.A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunctionExpression studies of osteoglycin/mimecan (OGN) in the cochlea and auditory phenotype of Ogn-deficient miceAge-related changes in cochlear gene expression in normal and shaker 2 miceCochlin and glaucoma: a mini-review.A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness.A subtracted cDNA library from the zebrafish (Danio rerio) embryonic inner ear.Molecular screens for inner ear genes.Selective acquisition of individual cell types in the vestibular periphery for molecular biology studies.Molecular markers for cell types of the inner ear and candidate genes for hearing disordersCharacterization of an abundant COL9A1 transcript in the cochlea with a novel 3' UTR: Expression studies and detection of miRNA target sequence.Predicting candidate genes for human deafness disorders: a bioinformatics approachBeginning of a molecular era in hearing and deafness.A genome-wide association study for age-related hearing impairment in the SaamiThe DMD locus harbours multiple long non-coding RNAs which orchestrate and control transcription of muscle dystrophin mRNA isoforms.Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4.Extralabyrinthine manifestations of DFNA9Cochlin in normal middle ear and abnormal middle ear deposits in DFNA9 and Coch (G88E/G88E) mice.Applications of genomics in the inner ear.A novel mutation in COCH-implications for genotype-phenotype correlations in DFNA9 hearing lossToward a systems biology of mouse inner ear organogenesis: gene expression pathways, patterns and network analysis.Cochlin in the eye: functional implications.Proteomic analysis of the organ of corti using nanoscale liquid chromatography coupled with tandem mass spectrometry.Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan.
P2860
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P2860
Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening
description
1994 nî lūn-bûn
@nan
1994 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Isolation of novel and known g ...... ion and differential screening
@ast
Isolation of novel and known g ...... ion and differential screening
@en
Isolation of novel and known g ...... ion and differential screening
@nl
type
label
Isolation of novel and known g ...... ion and differential screening
@ast
Isolation of novel and known g ...... ion and differential screening
@en
Isolation of novel and known g ...... ion and differential screening
@nl
prefLabel
Isolation of novel and known g ...... ion and differential screening
@ast
Isolation of novel and known g ...... ion and differential screening
@en
Isolation of novel and known g ...... ion and differential screening
@nl
P2093
P356
P1433
P1476
Isolation of novel and known g ...... ion and differential screening
@en
P2093
C C Morton
F R Bieber
G A Gutiérrez-Espeleta
N G Robertson
U Khetarpal
P356
10.1006/GENO.1994.1457
P407
P577
1994-09-01T00:00:00Z