about
Sequence similarity between stereocilin and otoancorin points to a unified mechanism for mechanotransduction in the mammalian inner ear.Congenital sensorineural deafness in dalmatian dogs associated with quantitative trait lociFrom flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%Mutations of MYO6 are associated with recessive deafness, DFNB37Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafnessLarge genomic rearrangements within the PCDH15 gene are a significant cause of USH1F syndromePrevalence of various etiologies of hearing loss among cochlear implant recipients: Systematic review and meta-analysisMice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness.Genetic frequencies related to severe or profound sensorineural hearing loss in Inner Mongolia Autonomous RegionNoise exposure modulates cochlear inner hair cell ribbon volumes, correlating with changes in auditory measures in the FVB/nJ mouse.Evidence for genotype-phenotype correlation for OTOF mutations.Genetics of peripheral vestibular dysfunction: lessons from mutant mouse strains.Hearing loss: a common disorder caused by many rare alleles.A mutation in the cdh23 gene causes age-related hearing loss in Cdh23(nmf308/nmf308) miceThe LINC complex is essential for hearing.Viral vector tropism for supporting cells in the developing murine cochlea.Linking genes underlying deafness to hair-bundle development and function.Functional consequences of novel connexin 26 mutations associated with hereditary hearing lossAbnormal cochlear potentials from deaf patients with mutations in the otoferlin geneAssociation of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing lossNoncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.The transmembrane inner ear (Tmie) protein is essential for normal hearing and balance in the zebrafish.DEX-1 and DYF-7 establish sensory dendrite length by anchoring dendritic tips during cell migration.Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss.Gap-junction channels dysfunction in deafness and hearing loss.Radixin deficiency causes deafness associated with progressive degeneration of cochlear stereocilia.Gene expression associated with the onset of hearing detected by differential display in rat organ of CortiMaternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese familyA nonsense mutation in the gene encoding a zebrafish myosin VI isoform causes defects in hair-cell mechanotransduction.Analysis and functional evaluation of the hair-cell transcriptome.Molecular dynamics simulations highlight structural and functional alterations in deafness-related M34T mutation of connexin 26.Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell deathGenetic analysis through OtoSeq of Pakistani families segregating prelingual hearing lossPathogenetic role of the deafness-related M34T mutation of Cx26.A comparison of vestibular and auditory phenotypes in inbred mouse strains.[Etiologic profile of severe and profound sensorineural hearing loss in children in the region of north-central Morocco].Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study.Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).Estimation of carrier frequencies of six autosomal-recessive Mendelian disorders in the Korean population.
P2860
Q21093634-191264E2-59F4-48C1-ACEE-F530FFE0644BQ21559534-0322DB65-88F6-4B6E-AF44-CCF6FE9CFD87Q24298272-C8CD11E2-59B1-45A1-8424-F9C97FF4A8A5Q24336023-236E782B-14BC-460A-834E-4DA6A0196A10Q24532041-ABB77308-F063-4CFF-BA18-04D7CF142FC8Q24540491-2FF21D05-84B8-448C-9AB8-AEFCD2CA66BBQ24652829-305F7962-B6F4-4CED-9FA8-C57BCA212D75Q26773933-A6F40BE7-3A17-4BB0-8359-384E3F27EC44Q28594332-6FAEBE9C-D8EE-42F6-8ABB-C9FE56344944Q30368252-548A541F-EB2D-4F69-9BB6-41BC910103FFQ30383419-A7CA8632-FEFB-4E72-AE04-5C8E0CBD5C82Q30410274-1F32B659-91C6-438C-BF35-77EF6C161D0FQ30420179-FE9F5140-E037-432B-B004-B1B3F218CA19Q30453298-249D05F3-B1E9-4D4E-A5FC-B8DA6EC4C124Q30454595-015F4430-D2AF-4359-AA94-A668E57E95EAQ30458666-14C81359-01B2-409D-9640-4DB9EAB3FFDBQ30466103-D7A21086-52C3-41DD-BEB1-FEC5733F5FFDQ30468355-EDD2FA58-D208-4B9F-AFA2-5D31BF74DBBFQ30478094-AFAF5DA0-0B4E-4DE8-B0CF-716763D644DEQ30478414-A67B2CB7-0AA4-4B25-A27B-38B6E9579AA2Q30481606-5E8FA965-0E85-452C-B6C3-10AA8632F478Q30484106-A5417DAD-5BDF-4173-A144-16DC930143B9Q30485178-7B25125C-BCEE-490B-A95E-D58BCA897923Q30487217-07C6C8F9-219B-472D-9AAA-0C3A5E8E8160Q30487513-80BA4CAE-78C6-4888-929E-EA7D44B8FA77Q30490087-FA794CC3-5DA9-49B9-9802-1CAB96B467D0Q30496716-563B1210-8C7E-4661-B9C7-1B4435531BECQ30497660-7F596B9C-BC26-468A-912F-7E52E7B65A6BQ30499211-9B9DD62E-78EB-4DD4-8D57-33DB9456871EQ30500251-FF5E503E-FCE7-40F7-9E60-1EE987581E53Q30502563-6AE76F8D-EAE9-4125-8247-02CEBD604556Q30573245-06008B6A-FDE8-4906-A388-51E71324B16AQ30578611-D0ECE575-AC43-4DAE-BCEE-798202955688Q33647400-3179E86A-4CD3-486E-9A82-E50B4DC93EF6Q33691804-FE44F6FF-3093-430E-85D7-0AE6DF8F9393Q33808646-C449F94F-79B7-4826-95ED-73D3670B495CQ33843349-D08D6C6B-0CE2-437C-8ECD-F66C246ED438Q33905363-AA930548-CD0D-403B-926C-596995DBED5AQ33905602-C6A21632-2CDB-404B-BDE4-7AC4D4588CE8Q34101472-E132EEE4-8E43-461C-ADB7-C679004B0DFA
P2860
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Molecular genetics of hearing loss.
@ast
Molecular genetics of hearing loss.
@en
Molecular genetics of hearing loss.
@nl
type
label
Molecular genetics of hearing loss.
@ast
Molecular genetics of hearing loss.
@en
Molecular genetics of hearing loss.
@nl
prefLabel
Molecular genetics of hearing loss.
@ast
Molecular genetics of hearing loss.
@en
Molecular genetics of hearing loss.
@nl
P1476
Molecular genetics of hearing loss.
@en
P2093
J Levilliers
J P Hardelin
P304
P356
10.1146/ANNUREV.GENET.35.102401.091224
P577
2001-01-01T00:00:00Z