| P50 | author | Sally A. Camper | Q40082925 |
| P2093 | author name string | David F Dolan | |
| | Qing Fang | |
| | Mirna Mustapha | |
| | Alicia M Giordimaina | |
| P2860 | cites work | KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness | Q22008780 |
| | Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger | Q24290545 |
| | Thyroid hormone is a critical determinant for the regulation of the cochlear motor protein prestin | Q24531197 |
| | Microtubule-associated protein 1A is a modifier of tubby hearing (moth1). | Q24630241 |
| | Prestin is the motor protein of cochlear outer hair cells | Q28144919 |
| | Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier | Q28202651 |
| | Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse | Q28269823 |
| | Thyroid hormone receptor beta-dependent expression of a potassium conductance in inner hair cells at the onset of hearing | Q28292052 |
| | Distortion product otoacoustic emissions and outer hair cell defects in the hyt/hyt mutant mouse | Q28590657 |
| | Calcium- and otoferlin-dependent exocytosis by immature outer hair cells | Q28592125 |
| | Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness | Q28594332 |
| | Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants. | Q30445850 |
| | Genetic modification of hearing in tubby mice: evidence for the existence of a major gene (moth1) which protects tubby mice from hearing loss | Q30471657 |
| | Consequences of hypothyroidism on auditory system function in Tshr mutant (hyt) mice | Q30473511 |
| | Hearing loss and cochlear abnormalities in the congenital hypothyroid (hyt/hyt) mouse. | Q50518773 |
| | Hearing in congenital hypothyroidism. | Q50594336 |
| | Developmental expression of the potassium current IK,n contributes to maturation of mouse outer hair cells. | Q52173467 |
| | Expression of prestin, a membrane motor protein, in the mammalian auditory and vestibular periphery. | Q54749499 |
| | Congenital deafness and hypothyroidism | Q69998365 |
| | Cochlear synaptogenesis in the hypothyroid rat | Q71732639 |
| | The effect of maternal and fetal thyroidectomy on fetal brain development in the sheep | Q71805032 |
| | Prevention of auditory dysfunction in hypothyroid Tshr mutant mice by thyroxin treatment during development. | Q30473513 |
| | A major effect QTL on chromosome 18 for noise injury to the mouse cochlear lateral wall | Q30477247 |
| | Limiting frequency of the cochlear amplifier based on electromotility of outer hair cells | Q30503528 |
| | Thyroid hormone action in the absence of thyroid hormone receptor DNA-binding in vivo | Q30532205 |
| | Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (Tmc1Bth) mouse model of progressive hearing loss DFNA36. | Q30540894 |
| | Identification of members of the Wnt signaling pathway in the embryonic pituitary gland | Q30812593 |
| | The impact of maternal uterine genotype on postnatal growth and adult body size in mice | Q33955324 |
| | Mapping quantitative trait loci for hearing loss in Black Swiss mice | Q34486560 |
| | KCNQ4: a gene for age-related hearing impairment? | Q34558530 |
| | Uterine and postnatal maternal effects in mice selected for differential rate of early development | Q34607805 |
| | Maturation of ribbon synapses in hair cells is driven by thyroid hormone | Q34611014 |
| | A modifier gene alleviates hypothyroidism-induced hearing impairment in Pou1f1dw dwarf mice | Q35297950 |
| | KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway. | Q35682356 |
| | Consequences of disrupting the dystrophin-sarcoglycan complex in cardiac and skeletal myopathy | Q36732999 |
| | What are maternal effects (and what are they not)? | Q37153030 |
| | The role of the placenta in thyroid hormone delivery to the fetus. | Q37349803 |
| | Molecular aspects of thyroid hormone transporters, including MCT8, MCT10, and OATPs, and the effects of genetic variation in these transporters | Q37525771 |
| | Anterior pituitary cells defective in the cell-autonomous factor, df, undergo cell lineage specification but not expansion. | Q38287452 |
| | Myosin VI is required for the proper maturation and function of inner hair cell ribbon synapses | Q39801019 |
| | Endemic cretinism: toward a unifying hypothesis | Q40910165 |
| | Hearing loss in athyroid pax8 knockout mice and effects of thyroxine substitution | Q42457578 |
| | Prestin is expressed on the whole outer hair cell basolateral surface | Q42495588 |
| | KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential | Q42515610 |
| | Thyroid hormone-deficient period prior to the onset of hearing is associated with reduced levels of beta-tectorin protein in the tectorial membrane: implication for hearing loss | Q43698986 |
| | Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell. | Q43779285 |
| | Donor and recipient genotype and heterosis effects on survival and prenatal growth of transferred mouse embryos | Q44860374 |
| | Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice | Q46978889 |
| | Olivocochlear efferent innervation of the organ of corti in hypothyroid rats | Q48340377 |
| | Development of distortion product otoacoustic emissions in C57BL/6J mice | Q48429300 |
| | Corrective effects of thyroxine on cochlear abnormalities induced by congenital hypothyroidism in the rat. II. Electrophysiological study | Q48511606 |
| | Corrective effects of thyroxine on cochlear abnormalities induced by congenital hypothyroidism in the rat. I. Morphological study. | Q48511617 |
| | Maternal thyroid autoantibodies during the third trimester and hearing deficits in children: an epidemiologic assessment | Q50453967 |
| | Thyroid hormone deficiency affects postnatal spiking activity and expression of Ca2+ and K+ channels in rodent inner hair cells. | Q50458423 |
| | Two quantitative trait loci affecting progressive hearing loss in 101/H mice | Q50462699 |
| | Thyroid hormone receptors TRalpha1 and TRbeta differentially regulate gene expression of Kcnq4 and prestin during final differentiation of outer hair cells | Q50463760 |
| | Thyroid hormone deficiency before the onset of hearing causes irreversible damage to peripheral and central auditory systems. | Q50496402 |
| | Study of the olivocochlear neurons using two different tracers, fast blue and cholera toxin, in hypothyroid rats. | Q50512310 |
| | Long-term sequelae of hearing impairment in congenital hypothyroidism. | Q50514717 |
| P433 | issue | 2 | |
| P921 | main subject | hearing loss | Q16035842 |
| P304 | page(s) | 173-184 | |
| P577 | publication date | 2011-12-06 | |
| P1433 | published in | J A R O | Q15752405 |
| P1476 | title | Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment | |
| P478 | volume | 13 | |