| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2003PNAS..10013958B |
| P356 | DOI | 10.1073/PNAS.2334417100 |
| P953 | full work available at URL | https://europepmc.org/articles/pmc283528?pdf=render |
| https://doi.org/10.1073/pnas.2334417100 | ||
| https://europepmc.org/articles/PMC283528 | ||
| https://europepmc.org/articles/PMC283528?pdf=render | ||
| https://pnas.org/doi/pdf/10.1073/pnas.2334417100 | ||
| P932 | PMC publication ID | 283528 |
| P698 | PubMed publication ID | 14610277 |
| P5875 | ResearchGate publication ID | 9015796 |
| P50 | author | Thomas B. Friedman | Q90047439 |
| Inna A Belyantseva | Q107693508 | ||
| Erich T Boger | Q114399839 | ||
| P2860 | cites work | Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle | Q24337137 |
| Myosin-I isozymes in neonatal rodent auditory and vestibular epithelia | Q24633897 | ||
| Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2 | Q28115357 | ||
| Molecular basis of mechanosensory transduction | Q28216286 | ||
| Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations | Q28586011 | ||
| Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31 | Q28590107 | ||
| Hair cells in the inner ear of the pirouette and shaker 2 mutant mice | Q28590250 | ||
| An intact SH3 domain is required for myosin I-induced actin polymerization. | Q30168825 | ||
| Sensitivity, polarity, and conductance change in the response of vertebrate hair cells to controlled mechanical stimuli | Q30500976 | ||
| Detection of Ca2+ entry through mechanosensitive channels localizes the site of mechanoelectrical transduction in hair cells | Q33832946 | ||
| Unconventional myosins and the genetics of hearing loss | Q33855126 | ||
| The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cells | Q33911618 | ||
| Myosin-X, a novel myosin with pleckstrin homology domains, associates with regions of dynamic actin. | Q33917620 | ||
| Adaptation in hair cells. | Q33938585 | ||
| Cochlear mechanisms from a phylogenetic viewpoint | Q34069555 | ||
| Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome | Q34104260 | ||
| Myosin-X is an unconventional myosin that undergoes intrafilopodial motility. | Q34115035 | ||
| Mechanical relaxation of the hair bundle mediates adaptation in mechanoelectrical transduction by the bullfrog's saccular hair cell | Q34180933 | ||
| Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. | Q34469642 | ||
| The organization of actin filaments in the stereocilia of cochlear hair cells | Q36201573 | ||
| Actin filaments elongate from their membrane-associated ends | Q36205170 | ||
| Unconventional myosins in inner-ear sensory epithelia | Q36254696 | ||
| Calcium imaging of single stereocilia in hair cells: localization of transduction channels at both ends of tip links | Q36824187 | ||
| Pulling springs to tune transduction: adaptation by hair cells | Q40806697 | ||
| Developmental morphology of the mouse inner ear. A scanning electron microscopic observation | Q41402294 | ||
| Myosin and adaptation by hair cells | Q41656223 | ||
| Unconventional myosins in cell movement, membrane traffic, and signal transduction | Q41687083 | ||
| Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene. | Q42455765 | ||
| Cross-links between stereocilia in the guinea pig organ of Corti, and their possible relation to sensory transduction | Q42457296 | ||
| Postnatal development of the hamster cochlea. II. Growth and differentiation of stereocilia bundles | Q42490085 | ||
| A chemical-genetic strategy implicates myosin-1c in adaptation by hair cells. | Q45712448 | ||
| Compliance of the hair bundle associated with gating of mechanoelectrical transduction channels in the bullfrog's saccular hair cell | Q46565359 | ||
| Myosin VIIa as a common component of cilia and microvilli | Q47788878 | ||
| Myosin Ibeta is located at tip link anchors in vestibular hair bundles. | Q48009530 | ||
| Functional organization of the cytoskeleton. | Q50581273 | ||
| Mechano-electrical transducer currents in hair cells of the cultured neonatal mouse cochlea | Q52415919 | ||
| Actin in the inner ear: the remarkable structure of the stereocilium | Q56937988 | ||
| Rapid renewal of auditory hair bundles | Q59074461 | ||
| Morphological correlates of mechanotransduction in acousticolateral hair cells | Q67895222 | ||
| Localization of myosin-Ibeta near both ends of tip links in frog saccular hair cells | Q77458696 | ||
| P433 | issue | 24 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 13958-13963 | |
| P577 | publication date | 2003-11-10 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle | |
| P478 | volume | 100 |
| Q48255504 | A link between planar polarity and staircase-like bundle architecture in hair cells. |
| Q58805948 | A novel nonsense mutation in MYO15A is associated with non-syndromic hearing loss: a case report |
| Q44927419 | Accelerated mortality from hydrocephalus and pneumonia in mice with a combined deficiency of SPAG6 and SPAG16L reveals a functional interrelationship between the two central apparatus proteins |
| Q30454015 | Actin in hair cells and hearing loss |
| Q30492549 | Age-related changes in cochlear gene expression in normal and shaker 2 mice |
| Q42137234 | Asymmetric distribution of cadherin 23 and protocadherin 15 in the kinocilial links of avian sensory hair cells |
| Q37903075 | Auditory and vestibular hair cell stereocilia: relationship between functionality and inner ear disease |
| Q48420858 | Auditory mechanotransduction in the absence of functional myosin-XVa. |
| Q47894540 | Beyond Cell-Cell Adhesion: Sensational Cadherins for Hearing and Balance. |
| Q30465350 | Calcium signaling in the cochlea - Molecular mechanisms and physiopathological implications. |
| Q24648345 | Cargos and genes: insights into vesicular transport from inherited human disease |
| Q34120199 | Chaperone-enhanced purification of unconventional myosin 15, a molecular motor specialized for stereocilia protein trafficking |
| Q89571583 | Cochlear Implantation From the Perspective of Genetic Background |
| Q36965061 | Competition and compensation: dissecting the biophysical and functional differences between the class 3 myosin paralogs, myosins 3a and 3b. |
| Q24596426 | Development and regeneration of sensory transduction in auditory hair cells requires functional interaction between cadherin-23 and protocadherin-15. |
| Q28584195 | Differential localization and dynamics of class I myosins in the enterocyte microvillus |
| Q41091624 | Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing |
| Q34148005 | Double gene deletion reveals lack of cooperation between claudin 11 and claudin 14 tight junction proteins. |
| Q36320487 | Drosophila melanogaster Cad99C, the orthologue of human Usher cadherin PCDH15, regulates the length of microvilli |
| Q39968477 | Effects of genetic correction on the differentiation of hair cell-like cells from iPSCs with MYO15A mutation |
| Q27321482 | Eps8 regulates hair bundle length and functional maturation of mammalian auditory hair cells |
| Q50300924 | Expansion of phenotypic spectrum of MYO15A pathogenic variants to include postlingual onset of progressive partial deafness |
| Q37346464 | Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1D |
| Q30009918 | FCHSD1 and FCHSD2 are expressed in hair cell stereocilia and cuticular plate and regulate actin polymerization in vitro |
| Q30488481 | Fast adaptation and Ca2+ sensitivity of the mechanotransducer require myosin-XVa in inner but not outer cochlear hair cells |
| Q30484207 | Fate of mammalian cochlear hair cells and stereocilia after loss of the stereocilia |
| Q35998873 | Fifty years of contractility research post sliding filament hypothesis |
| Q30482629 | Function and expression pattern of nonsyndromic deafness genes |
| Q37770479 | Fundamental role of microvilli in the main functions of differentiated cells: Outline of an universal regulating and signaling system at the cell periphery |
| Q92085492 | GPSM2-GNAI Specifies the Tallest Stereocilia and Defines Hair Bundle Row Identity |
| Q30480367 | Gelsolin plays a role in the actin polymerization complex of hair cell stereocilia |
| Q38393019 | Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness |
| Q38022141 | Gene transfer in inner ear cells: a challenging race |
| Q51067426 | Generic Transport Mechanisms for Molecular Traffic in Cellular Protrusions. |
| Q35813847 | Genetic insights into the morphogenesis of inner ear hair cells. |
| Q33783963 | Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families. |
| Q38235746 | Hearing molecules, mechanism and transportation: modeled in Drosophila melanogaster |
| Q48695635 | Helios(®) Gene Gun-Mediated Transfection of the Inner Ear Sensory Epithelium: Recent Updates |
| Q33346003 | Human hereditary hearing impairment: mouse models can help to solve the puzzle |
| Q36107256 | Identification and Clinical Implications of Novel MYO15A Mutations in a Non-consanguineous Korean Family by Targeted Exome Sequencing |
| Q30404099 | Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss |
| Q34822265 | Identification of genes concordantly expressed with Atoh1 during inner ear development. |
| Q34437737 | Improved biolistic transfection of hair cells |
| Q36119730 | It takes two. |
| Q30448353 | Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS. |
| Q40459823 | Mechanism of action of myosin X, a membrane-associated molecular motor. |
| Q37608717 | Mechanotransduction by hair cells: models, molecules, and mechanisms |
| Q36382019 | Molecular genetics of non-syndromic deafness |
| Q30481360 | Mosaic complementation demonstrates a regulatory role for myosin VIIa in actin dynamics of stereocilia |
| Q28510668 | Mutant analysis reveals whirlin as a dynamic organizer in the growing hair cell stereocilium |
| Q38885154 | Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness |
| Q34634062 | Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing. |
| Q28505655 | Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse |
| Q33911494 | Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss. |
| Q30467882 | Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia |
| Q39005661 | MyTH4-FERM myosins in the assembly and maintenance of actin-based protrusions |
| Q30497077 | Myosin VI and VIIa distribution among inner ear epithelia in diverse fishes |
| Q28590821 | Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly |
| Q30468706 | Myosin light-chain kinase is necessary for membrane homeostasis in cochlear inner hair cells |
| Q34985570 | Myosin motor function: the ins and outs of actin-based membrane protrusions. |
| Q30480441 | Myosin-1a powers the sliding of apical membrane along microvillar actin bundles. |
| Q42365129 | Myosin-7b Promotes Distal Tip Localization of the Intermicrovillar Adhesion Complex |
| Q24299253 | Myosin-X is a molecular motor that functions in filopodia formation |
| Q47139973 | Myosin-X knockout is semi-lethal and demonstrates that myosin-X functions in neural tube closure, pigmentation, hyaloid vasculature regression, and filopodia formation. |
| Q90172876 | Myosin-XVa Controls Both Staircase Architecture and Diameter Gradation of Stereocilia Rows in the Auditory Hair Cell Bundles |
| Q28593953 | Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia |
| Q33506085 | MyosinVIIa interacts with Twinfilin-2 at the tips of mechanosensory stereocilia in the inner ear. |
| Q27004163 | Myosins in cell junctions |
| Q51377017 | Myosins: Domain Organisation, Motor Properties, Physiological Roles and Cellular Functions. |
| Q37309871 | Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing |
| Q61444640 | Phenotypic analysis of Myo10 knockout (Myo10) mice lacking full-length (motorized) but not brain-specific headless myosin X |
| Q37087936 | Quiet as a mouse: dissecting the molecular and genetic basis of hearing |
| Q41047666 | ROS induced distribution of mitochondria to filopodia by Myo19 depends on a class specific tryptophan in the motor domain. |
| Q37231122 | Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family |
| Q30479228 | Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner ear. |
| Q28509348 | Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development |
| Q36389545 | Splice-site A choice targets plasma-membrane Ca2+-ATPase isoform 2 to hair bundles |
| Q37255247 | Submembraneous microtubule cytoskeleton: biochemical and functional interplay of TRP channels with the cytoskeleton |
| Q92884372 | TRIOBP-5 sculpts stereocilia rootlets and stiffens supporting cells enabling hearing |
| Q40090620 | TRPV1 expression-dependent initiation and regulation of filopodia. |
| Q24300298 | Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79 |
| Q28594919 | Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutation |
| Q34340843 | Targeting of the hair cell proteins cadherin 23, harmonin, myosin XVa, espin, and prestin in an epithelial cell model. |
| Q36119739 | The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing |
| Q27320134 | The Stereociliary Paracrystal Is a Dynamic Cytoskeletal Scaffold In Vivo |
| Q42145176 | The acquisition of mechano-electrical transducer current adaptation in auditory hair cells requires myosin VI |
| Q35887294 | The co-workers of actin filaments: from cell structures to signals |
| Q30422890 | The mechanosensory structure of the hair cell requires clarin-1, a protein encoded by Usher syndrome III causative gene |
| Q27011868 | The myosin superfamily at a glance. |
| Q55003816 | Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss. |
| Q30435999 | Tonotopic gradient in the developmental acquisition of sensory transduction in outer hair cells of the mouse cochlea |
| Q24324361 | Twinfilin 2 regulates actin filament lengths in cochlear stereocilia |
| Q55670476 | Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness |
| Q34833228 | Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families |
| Q41456507 | Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation |
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