Hearing loss: mechanisms revealed by genetics and cell biology.
about
Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5Mutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing lossPrevalence of various etiologies of hearing loss among cochlear implant recipients: Systematic review and meta-analysisAssembly of hair bundles, an amazing problem for cell biologyMolecular mechanisms of inner ear developmentFunctional development of mechanosensitive hair cells in stem cell-derived organoids parallels native vestibular hair cells.Folic acid deficiency induces premature hearing loss through mechanisms involving cochlear oxidative stress and impairment of homocysteine metabolismEps8 regulates hair bundle length and functional maturation of mammalian auditory hair cells.Stereocilia-staircase spacing is influenced by myosin III motors and their cargos espin-1 and espin-like.CHD7 deficiency in "Looper", a new mouse model of CHARGE syndrome, results in ossicle malformation, otosclerosis and hearing impairmentA Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing ImpairmentChemical screening for hair cell loss and protection in the zebrafish lateral lineA mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIAAlternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia.Parallel evolution of KCNQ4 in echolocating batsDissecting the molecular basis of organ of Corti development: Where are we now?SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss.A short splice form of Xin-actin binding repeat containing 2 (XIRP2) lacking the Xin repeats is required for maintenance of stereocilia morphology and hearing functionNonviral Reprogramming of Human Wharton's Jelly Cells Reveals Differences Between ATOH1 Homologues.Mutation of Npr2 leads to blurred tonotopic organization of central auditory circuits in miceCombined examination of sequence and copy number variations in human deafness genes improves diagnosis for cases of genetic deafness.Cytoplasmic mislocalization of POU3F4 due to novel mutations leads to deafness in humans and mice.Gene therapy for deafness.The zebrafish merovingian mutant reveals a role for pH regulation in hair cell toxicity and function.Virally expressed connexin26 restores gap junction function in the cochlea of conditional Gjb2 knockout mice.Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan® OpenArray™ Genotyping platformOtoprotective effects of erythropoietin on Cdh23erl/erl miceThe challenge of hair cell regeneration.Cochlear implantation in older adults.Rescue of hearing and vestibular function by antisense oligonucleotides in a mouse model of human deafness.Integration of human and mouse genetics reveals pendrin function in hearing and deafnessHearing loss: a common disorder caused by many rare alleles.Inner ear gene transfection in neonatal mice using adeno-associated viral vector: a comparison of two approaches.Genome-wide linkage analyses identify Hfhl1 and Hfhl3 with frequency-specific effects on the hearing spectrum of NIH Swiss miceA multigenerational family study of oral and hand motor sequencing ability provides evidence for a familial speech sound disorder subtype.High-frequency sensorineural hearing loss and its underlying genetics (Hfhl1 and Hfhl2) in NIH Swiss mice.CD44 is a marker for the outer pillar cells in the early postnatal mouse inner ear.Roles of the espin actin-bundling proteins in the morphogenesis and stabilization of hair cell stereocilia revealed in CBA/CaJ congenic jerker mice.Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51.Modifiers of hearing impairment in humans and mice.
P2860
Q24296425-93602991-49E7-4279-9C3A-1052B80E4500Q24300273-F8F21B74-5B26-4FE6-92D9-ED5541EC01C9Q26773933-547CE4A3-551B-4E17-91FF-36D4685BEE26Q26801278-D2381F58-EFFC-456A-AB48-BFF72AB2A58AQ26865155-79CF25C2-C563-4A9F-95D7-35C2ED3BF959Q27317317-A4C12715-BCE2-4360-9C93-EE02AA09711DQ27319467-04054AF8-4229-450B-9A86-DC1B45CC7810Q27321482-88BAAC36-2D9E-4ADD-A3F2-78A1003A48B6Q27329412-40D761D1-73CB-4031-A85D-FF13759EE522Q27332274-620D8BA4-0868-4D06-BD80-F255910D253FQ28115636-ED36D2AE-1360-44A5-926E-E4C2CA795933Q28468560-E5F7F396-6137-4494-8520-33CA1D62936EQ28586478-62C4A2F7-E703-491D-8D00-B236AB6FA5ADQ28587081-837B1F2A-3230-48D3-98A1-2C0F541186CBQ28743501-69560C45-C0C8-4D31-B60D-3D67B30E4DA6Q28744483-D969D1BD-E804-4AF6-9A52-F1AC84CDAC2AQ30274636-9FC3C96E-D172-4015-8119-51E9620A3203Q30300856-80B24B3C-D634-4AB3-9700-1B0C991D1C1FQ30382596-5B3F4BA1-7BD6-4FDF-901A-5F711FEB8411Q30423186-2B4168A6-EDA3-46D9-BEAB-DB4CD6B21018Q30427880-1F90F9F7-C3A8-4CF6-941C-130D38AC1286Q30433617-F6F9BCD1-D7A6-44AF-B6AD-C2892F28464FQ30434063-A2C45DE7-A26E-4E77-A358-B3DC18116039Q30434681-CF145765-80B7-44D3-800F-72E3A8665E40Q30435650-6B9F362D-714C-4BAE-AD46-8D0839B9EF49Q30438646-5FE7AF32-DDB0-4E7B-BDF3-2D23190E5A5AQ30439263-017DA799-0433-4AFE-BB63-60504B17E86FQ30449333-66FA5702-5CE8-4376-B761-0F0462EA5E34Q30450031-6FED5CEF-6DBE-449A-BBF3-FBE4F20F178DQ30450036-CC11A742-C51A-48D4-88C4-711077335923Q30451829-5B7477B5-14BB-4501-BA2F-012E9A369A74Q30453298-520486BA-B4EA-4BAF-83B7-7357C987E6DCQ30464591-71B3F732-2515-4E88-B63A-AAD55A938D13Q30464765-B4738D0C-F1A9-4566-A16F-6E92228BD7ECQ30469175-C2153556-81B8-4A05-BBD9-0A5A33B4A602Q30474049-8210D4AB-7914-4CBD-A4F6-A2A24F92066AQ30474323-5166B162-1F4B-4EB3-8C13-A47250DC3A1EQ30476139-E440539A-87D3-4414-B112-ECD4F7B73CD1Q30477623-D1DC62BF-4A9B-4612-B62A-74DF393F1E48Q30478361-4715BD83-5D03-4399-A720-7B62E38A1C2A
P2860
Hearing loss: mechanisms revealed by genetics and cell biology.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on January 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Hearing loss: mechanisms revealed by genetics and cell biology.
@en
Hearing loss: mechanisms revealed by genetics and cell biology.
@nl
type
label
Hearing loss: mechanisms revealed by genetics and cell biology.
@en
Hearing loss: mechanisms revealed by genetics and cell biology.
@nl
prefLabel
Hearing loss: mechanisms revealed by genetics and cell biology.
@en
Hearing loss: mechanisms revealed by genetics and cell biology.
@nl
P1476
Hearing loss: mechanisms revealed by genetics and cell biology.
@en
P2093
Amiel A Dror
P304
P356
10.1146/ANNUREV-GENET-102108-134135
P577
2009-01-01T00:00:00Z