Pages that link to "Q64672038"
Jump to navigation
Jump to search
The following pages link to Mhamed Grati (Q64672038):
Displaying 50 items.
- A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness (Q22009151) (← links)
- FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing. (Q24299788) (← links)
- Mutation of the ATP-gated P2X(2) receptor leads to progressive hearing loss and increased susceptibility to noise. (Q24310646) (← links)
- Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family (Q24314717) (← links)
- A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation (Q24315139) (← links)
- OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9. (Q24538784) (← links)
- Characterization of ATPase Activity of P2RX2 Cation Channel (Q27307804) (← links)
- In vitro interaction of Pseudomonas aeruginosa with human middle ear epithelial cells (Q27315407) (← links)
- Stereocilia-staircase spacing is influenced by myosin III motors and their cargos espin-1 and espin-like (Q27329412) (← links)
- Association of PRPS1 Mutations with Disease Phenotypes (Q28080625) (← links)
- The application of genome editing in studying hearing loss (Q28081706) (← links)
- Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse (Q28269823) (← links)
- Whirlin, a cytoskeletal scaffolding protein, stabilizes the paranodal region and axonal cytoskeleton in myelinated axons (Q28506822) (← links)
- Myosin VIIa and sans localization at stereocilia upper tip-link density implicates these Usher syndrome proteins in mechanotransduction (Q28569812) (← links)
- Rapid turnover of stereocilia membrane proteins: evidence from the trafficking and mobility of plasma membrane Ca(2 )-ATPase 2. (Q28572115) (← links)
- Molecular determinants for differential membrane trafficking of PMCA1 and PMCA2 in mammalian hair cells (Q28578197) (← links)
- A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60 (Q30357625) (← links)
- ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice. (Q30764277) (← links)
- DFNB9 and DFNB12. (Q33950947) (← links)
- Intermolecular autophosphorylation regulates myosin IIIa activity and localization in parallel actin bundles. (Q34285278) (← links)
- Role of innate immunity in the pathogenesis of otitis media (Q35027403) (← links)
- CLIC5 stabilizes membrane-actin filament linkages at the base of hair cell stereocilia in a molecular complex with radixin, taperin, and myosin VI. (Q35795161) (← links)
- Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice (Q35840689) (← links)
- Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53 (Q36449240) (← links)
- Pseudomonas aeruginosa Activates PKC-Alpha to Invade Middle Ear Epithelial Cells (Q36650036) (← links)
- Tectorins crosslink type II collagen fibrils and connect the tectorial membrane to the spiral limbus (Q36723345) (← links)
- MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform (Q36803634) (← links)
- Current concepts in the pathogenesis and treatment of chronic suppurative otitis media. (Q36810844) (← links)
- Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis (Q37108023) (← links)
- PDZD7-MYO7A complex identified in enriched stereocilia membranes. (Q37217653) (← links)
- Otopathogenic Pseudomonas aeruginosa Enters and Survives Inside Macrophages (Q37421175) (← links)
- Otopathogenic Pseudomonas aeruginosa induces MyD88-dependent auditory hair cell damage (Q37476046) (← links)
- Immunity genes and susceptibility to otitis media: a comprehensive review (Q38272793) (← links)
- Molecular Structure and Regulation of P2X Receptors With a Special Emphasis on the Role of P2X2 in the Auditory System. (Q38655779) (← links)
- Intricate Functions of Matrix Metalloproteinases in Physiological and Pathological Conditions. (Q38836225) (← links)
- Neurotransmitters: The Critical Modulators Regulating Gut-Brain Axis. (Q38924615) (← links)
- Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene (Q38970459) (← links)
- Indispensable Role of Ion Channels and Transporters in the Auditory System. (Q38972580) (← links)
- Signaling in the Auditory System: Implications in Hair Cell Regeneration and Hearing Function (Q39015106) (← links)
- CRISPR: a versatile tool for both forward and reverse genetics research. (Q39627059) (← links)
- Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents. (Q40681828) (← links)
- Corrigendum: Stereocilia-staircase spacing is influenced by myosin III motors and their cargos espin-1 and espin-like. (Q42346921) (← links)
- Rescue from early-onset hearing loss in a mouse model lacking the cyclin-dependent kinase inhibitor p19Ink4d (Q42912945) (← links)
- A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E (Q57554998) (← links)
- Methylation Status and Presbycusis Risk in Elderly Women (Q58797359) (← links)
- (Q87150470) (redirect page) (← links)
- A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss (Q88962073) (← links)
- Zebrafish Model for Nonsyndromic X-Linked Sensorineural Deafness, DFNX1 (Q92383090) (← links)
- Refining surgical techniques for efficient posterior semicircular canal gene delivery in the adult mammalian inner ear with minimal hearing loss (Q112716449) (← links)
- Transcription co-factor LBH is necessary for the survival of cochlear hair cells (Q112723323) (← links)