Pages that link to "Q34139587"
Jump to navigation
Jump to search
The following pages link to A genetic approach to understanding auditory function (Q34139587):
Displaying 50 items.
- Sequence similarity between stereocilin and otoancorin points to a unified mechanism for mechanotransduction in the mammalian inner ear. (Q21093634) (← links)
- Congenital sensorineural deafness in dalmatian dogs associated with quantitative trait loci (Q21559534) (← links)
- Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues (Q24324566) (← links)
- CRYM mutations cause deafness through thyroid hormone binding properties in the fibrocytes of the cochlea (Q24338496) (← links)
- Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3. (Q24533348) (← links)
- The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions (Q24538474) (← links)
- Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice (Q24538566) (← links)
- A duplicated motif controls assembly of zona pellucida domain proteins (Q24568053) (← links)
- An actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewal (Q24676711) (← links)
- Focusing on the genetics of hearing: you ain't heard nothin' yet. (Q24791942) (← links)
- Molecular epidemiology of DFNB1 deafness in France (Q24803748) (← links)
- The Genetics of Deafness in Domestic Animals (Q26776085) (← links)
- Functional analysis and regulation of purified connexin hemichannels (Q26829380) (← links)
- Molecular mechanisms and potentials for differentiating inner ear stem cells into sensory hair cells (Q27008795) (← links)
- Decreased temporal precision of neuronal signaling as a candidate mechanism of auditory processing disorder (Q28081905) (← links)
- Structure and innervation of the cochlea (Q28176775) (← links)
- Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure (Q28203023) (← links)
- Neurodevelopmental control by thyroid hormone receptors (Q28203265) (← links)
- Molecular basis of mechanosensory transduction (Q28216286) (← links)
- The ZP domain is a conserved module for polymerization of extracellular proteins (Q28218444) (← links)
- Ca(2 )-activated K channels: molecular determinants and function of the SK family (Q28283065) (← links)
- Gap junctions in the inner ear: comparison of distribution patterns in different vertebrates and assessement of connexin composition in mammals (Q28508885) (← links)
- Jxc1/Sobp, encoding a nuclear zinc finger protein, is critical for cochlear growth, cell fate, and patterning of the organ of corti (Q28510448) (← links)
- Blindness and auditory impairment caused by loss of the sodium bicarbonate cotransporter NBC3 (Q28511021) (← links)
- Transient expression of the t-isoform of plastins/fimbrin in the stereocilia of developing auditory hair cells (Q28580200) (← links)
- Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media (Q28586559) (← links)
- Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells (Q28592402) (← links)
- Static material properties of the tectorial membrane: a summary (Q29038611) (← links)
- A short splice form of Xin-actin binding repeat containing 2 (XIRP2) lacking the Xin repeats is required for maintenance of stereocilia morphology and hearing function (Q30300856) (← links)
- Genetic Correction of Induced Pluripotent Stem Cells From a Deaf Patient With MYO7A Mutation Results in Morphologic and Functional Recovery of the Derived Hair Cell-Like Cells. (Q30357879) (← links)
- Basilar membrane and tectorial membrane stiffness in the CBA/CaJ mouse (Q30401941) (← links)
- Cochlear implantation in the very young child: issues unique to the under-1 population (Q30424907) (← links)
- Time-dependent gene expression analysis of the developing superior olivary complex (Q30431285) (← links)
- 3D model of frequency representation in the cochlear nucleus of the CBA/J mouse (Q30439170) (← links)
- Conditional and inducible gene recombineering in the mouse inner ear (Q30444031) (← links)
- Studying inner ear protein-protein interactions using FRET and FLIM. (Q30444410) (← links)
- Hearing loss in children with very low birth weight: current review of epidemiology and pathophysiology (Q30457383) (← links)
- Filling the silent void: genetic therapies for hearing impairment (Q30459235) (← links)
- An epidemiological study on children with syndromic hearing loss (Q30461641) (← links)
- Organ of Corti kinematics (Q30473443) (← links)
- Gene discovery in the auditory system: characterization of additional cochlear-expressed sequences (Q30473494) (← links)
- Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss. Genetic Evaluation of Congenital Hearing Loss Expert Panel. ACMG statement (Q30474292) (← links)
- ENU induced single mutation locus on chr 16 leads to high-frequency hearing loss in mice (Q30474524) (← links)
- Progressive hearing loss and increased susceptibility to noise-induced hearing loss in mice carrying a Cdh23 but not a Myo7a mutation (Q30492669) (← links)
- Radixin deficiency causes deafness associated with progressive degeneration of cochlear stereocilia (Q30496716) (← links)
- Gene expression associated with the onset of hearing detected by differential display in rat organ of Corti (Q30497660) (← links)
- Inner ear drug delivery via a reciprocating perfusion system in the guinea pig. (Q30500338) (← links)
- At the speed of sound: gene discovery in the auditory system (Q30502974) (← links)
- Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes (Q30716734) (← links)
- Detection of mitochondrial DNA from human inner ear using real-time polymerase chain reaction and laser microdissection (Q33218787) (← links)