Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration. - Wikidata - wikimedia - TriplyDB

Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.

Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.

http://www.wikidata.org/entity/Q33967701

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Stromal Claudin14-heterozygosity, but not deletion, increases tumour blood leakage without affecting tumour growth Cell array-based intracellular localization screening reveals novel functional features of human chromosome 21 proteins Congenital sensorineural deafness in dalmatian dogs associated with quantitative trait loci Claudin-14 regulates renal Ca⁺⁺ transport in response to CaSR signalling via a novel microRNA pathway Tricellulin is a tight-junction protein necessary for hearing.A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice Autosomal recessive nonsyndromic deafness genes: a review Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes.Regulation of electromotility in the cochlear outer hair cell Tricellular Tight Junctions in the Inner Ear Genetics of hearing and deafness Claudins and the kidney The role of claudin in hypercalciuric nephrolithiasis Deletion of Tricellulin Causes Progressive Hearing Loss Associated with Degeneration of Cochlear Hair Cells.Hepatitis C Virus entry: the early steps in the viral replication cycle Physiology and function of the tight junction.Sp1 site is crucial for the mouse claudin-19 gene expression in the kidney cells A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler mice Progressive Hearing Loss in Mice Carrying a Mutation in Usp53.Tricellulin deficiency affects tight junction architecture and cochlear hair cells.A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA Claudin 18 is a novel negative regulator of bone resorption and osteoclast differentiation Deficiency of angulin-2/ILDR1, a tricellular tight junction-associated membrane protein, causes deafness with cochlear hair cell degeneration in mice Characterization of the transcriptome of nascent hair cells and identification of direct targets of the Atoh1 transcription factor Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine.Progression of inner ear pathology in Ames waltzer mice and the role of protocadherin 15 in hair cell development.QTL Mapping of Endocochlear Potential Differences between C57BL/6J and BALB/cJ mice.Potassium ion movement in the inner ear: insights from genetic disease and mouse models ILDR1 deficiency causes degeneration of cochlear outer hair cells and disrupts the structure of the organ of Corti: a mouse model for human DFNB42.ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells.Genetics of auditory mechano-electrical transduction.Supporting cells eliminate dying sensory hair cells to maintain epithelial integrity in the avian inner ear.Inner ear supporting cells: rethinking the silent majority.Changes in the adult vertebrate auditory sensory epithelium after trauma.Cell-cell junctions: a target of acoustic overstimulation in the sensory epithelium of the cochlea.Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51.Cadherins as targets for genetic diseases.Radixin deficiency causes deafness associated with progressive degeneration of cochlear stereocilia.Orphan glutamate receptor delta1 subunit required for high-frequency hearing.A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect.

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Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.

http://www.wikidata.org/entity/Q33967701

description

2003 nî lūn-bûn

@nan

2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի օգոստոսին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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Claudin 14 knockout mice, a mo ...... chlear hair cell degeneration.

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Claudin 14 knockout mice, a mo ...... chlear hair cell degeneration.

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Claudin 14 knockout mice, a mo ...... chlear hair cell degeneration.

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Claudin 14 knockout mice, a mo ...... chlear hair cell degeneration.

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Claudin 14 knockout mice, a mo ...... chlear hair cell degeneration.

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Claudin 14 knockout mice, a mo ...... chlear hair cell degeneration.

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Human Molecular Genetics

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Claudin 14 knockout mice, a mo ...... chlear hair cell degeneration.

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Andrew Forge

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Christina M Van Itallie

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David F Dolan

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Donald J Gardner

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Edward R Wilcox

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Elizabeth D Hughes

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Julia Rasmussen

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Kohei Kawamoto

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2049-2061

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scholarly article

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10.1093/HMG/DDG210

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16

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277431905

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12913076

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