| P50 | author | Hamish S. Scott | Q53110183 |
| | Robert K. Shepherd | Q53396446 |
| P2093 | author name string | Qingyu Wu | |
| | Justin Tan | |
| | Michel Guipponi | |
| | Maria Clarke | |
| | Ping Z F Cannon | |
| | Pauline Crewther | |
| | Lauren Donley | |
| P2860 | cites work | Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness | Q24290692 |
| | From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30 | Q24298272 |
| | Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss | Q24301501 |
| | Mutations of MYO6 are associated with recessive deafness, DFNB37 | Q24532041 |
| | Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4) | Q24533372 |
| | Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9 | Q24534496 |
| | MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss | Q24535864 |
| | Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness | Q24680175 |
| | Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness | Q28207545 |
| | Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients | Q28208859 |
| | Mutations in the myosin VIIA gene cause non-syndromic recessive deafness | Q28239749 |
| | The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene | Q28239757 |
| | A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein | Q28261878 |
| | Control of peripheral nerve myelination by the beta-secretase BACE1 | Q28264800 |
| | Thyroid hormone receptor beta-dependent expression of a potassium conductance in inner hair cells at the onset of hearing | Q28292052 |
| | Polypeptide composition of the mammalian tectorial membrane | Q28300248 |
| | Thyroid hormone receptor beta is essential for development of auditory function | Q28510090 |
| | Expression of Ca2+-activated BK channel mRNA and its splice variants in the rat cochlea | Q28580648 |
| | Distortion product otoacoustic emissions and outer hair cell defects in the hyt/hyt mutant mouse | Q28590657 |
| | Deletion of the Ca2+-activated potassium (BK) alpha-subunit but not the BKbeta1-subunit leads to progressive hearing loss | Q28595088 |
| | Chronic depolarization enhances the trophic effects of brain-derived neurotrophic factor in rescuing auditory neurons following a sensorineural hearing loss. | Q30499424 |
| | Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. | Q34469642 |
| | Molecular mechanisms of age-related hearing loss | Q34688008 |
| | Thyroid functions of mouse cathepsins B, K, and L. | Q35019251 |
| | Age-related hearing loss: current research | Q35539902 |
| | Hearing loss and retarded cochlear development in mice lacking type 2 iodothyronine deiodinase | Q37073731 |
| | Generation and characterization of mice deficient in hepsin, a hepatic transmembrane serine protease | Q37377341 |
| | Genetic epidemiology of hearing impairment | Q37519270 |
| | Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing | Q40373249 |
| | Hearing loss in athyroid pax8 knockout mice and effects of thyroxine substitution | Q42457578 |
| | Retardation of cochlear maturation and impaired hair cell function caused by deletion of all known thyroid hormone receptors. | Q48692469 |
| | Thyroid hormone deficiency affects postnatal spiking activity and expression of Ca2+ and K+ channels in rodent inner hair cells. | Q50458423 |
| | Contribution of BK Ca2+-activated K+ channels to auditory neurotransmission in the Guinea pig cochlea. | Q50484630 |
| | Thyroid hormone deficiency before the onset of hearing causes irreversible damage to peripheral and central auditory systems. | Q50496402 |
| | Thyroid hormone affects Schwann cell and oligodendrocyte gene expression at the glial transition zone of the VIIIth nerve prior to cochlea function. | Q50504448 |
| | Hearing loss and cochlear abnormalities in the congenital hypothyroid (hyt/hyt) mouse. | Q50518773 |
| | Effects of hypothyroidism on the structural development of the organ of Corti in the rat. | Q50599195 |
| | Periods of sensitivity to thyroid hormone during the development of the organ of Corti. | Q52263776 |
| | Type II transmembrane serine proteases | Q73273646 |
| P4510 | describes a project that uses | ImageQuant | Q112270642 |
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | transmembrane protein | Q424204 |
| | hearing loss | Q16035842 |
| | Hepsin | Q21981170 |
| P304 | page(s) | 608-616 | |
| P577 | publication date | 2007-07-09 | |
| P1433 | published in | The American Journal of Pathology | Q4744259 |
| P1476 | title | Mice deficient for the type II transmembrane serine protease, TMPRSS1/hepsin, exhibit profound hearing loss | |
| P478 | volume | 171 | |