scholarly article | Q13442814 |
P50 | author | Gregory I Frolenkov | Q55267329 |
Tomoko Makishima | Q62940124 | ||
Martin Hrabě de Angelis | Q28606776 | ||
P2093 | author name string | Yoshihiro Noguchi | |
Helmut Fuchs | |||
Ken Kitamura | |||
Andrew J Griffith | |||
Kiyoto Kurima | |||
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Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia | Q28593953 | ||
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P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | hearing loss | Q16035842 |
quantitative trait locus | Q853421 | ||
P304 | page(s) | 2111-2119 | |
P577 | publication date | 2006-04-28 | |
P1433 | published in | Genetics | Q3100575 |
P1476 | title | Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (Tmc1Bth) mouse model of progressive hearing loss DFNA36. | |
P478 | volume | 173 |
Q36239574 | A QTL on Chr 5 modifies hearing loss associated with the fascin-2 variant of DBA/2J mice |
Q90240470 | A Tmc1 mutation reduces calcium permeability and expression of mechanoelectrical transduction channels in cochlear hair cells |
Q30482720 | A locus on distal chromosome 11 (ahl8) and its interaction with Cdh23 ahl underlie the early onset, age-related hearing loss of DBA/2J mice |
Q35297950 | A modifier gene alleviates hypothyroidism-induced hearing impairment in Pou1f1dw dwarf mice |
Q28505277 | A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler mice |
Q36200344 | Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairment |
Q49914916 | Co-deficiency of Lysosomal Mucolipins 3 and 1 in Cochlear Hair Cells Diminishes Outer Hair Cell Longevity and Accelerates Age-Related Hearing Loss. |
Q48429300 | Development of distortion product otoacoustic emissions in C57BL/6J mice |
Q46978889 | Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice |
Q28511525 | Disruption of fibroblast growth factor receptor 3 signaling results in defects in cellular differentiation, neuronal patterning, and hearing impairment |
Q30469465 | Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment |
Q30464765 | Genome-wide linkage analyses identify Hfhl1 and Hfhl3 with frequency-specific effects on the hearing spectrum of NIH Swiss mice |
Q30474049 | High-frequency sensorineural hearing loss and its underlying genetics (Hfhl1 and Hfhl2) in NIH Swiss mice |
Q50436365 | Hydrogen in drinking water attenuates noise-induced hearing loss in guinea pigs |
Q37144696 | Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms? |
Q34689630 | Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan |
Q24634356 | Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes |
Q35485037 | Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition |
Q34250259 | Mutations of TMC1 cause deafness by disrupting mechanoelectrical transduction |
Q37087936 | Quiet as a mouse: dissecting the molecular and genetic basis of hearing |
Q37004981 | RNA Interference Prevents Autosomal-Dominant Hearing Loss. |
Q30410497 | Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction |
Q27329412 | Stereocilia-staircase spacing is influenced by myosin III motors and their cargos espin-1 and espin-like |
Q91241233 | Targeted Allele Suppression Prevents Progressive Hearing Loss in the Mature Murine Model of Human TMC1 Deafness |
Q58783095 | Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function |
Q34807434 | Transmembrane channel-like (TMC) genes are required for auditory and vestibular mechanosensation |
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