|  Help  |  About  |  Contact Us

Search our database by keyword

- or -

Examples

  • Search this entire website. Enter identifiers, names or keywords for genes, diseases, strains, ontology terms, etc. (e.g. Pax6, Parkinson, ataxia)
  • Use OR to search for either of two terms (e.g. OR mus) or quotation marks to search for phrases (e.g. "dna binding").
  • Boolean search syntax is supported: e.g. Balb* for partial matches or mus AND NOT embryo to exclude a term

Search results 1 to 41 out of 41 for Myo15

Category restricted to Publication (x)

0.023s

Categories

Category: Publication
Type Details Score
Publication
First Author: Wang A
Year: 1998
Journal: Science
Title: Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.
Volume: 280
Issue: 5368
Pages: 1447-51
Publication
First Author: Karolyi IJ
Year: 2003
Journal: Hum Mol Genet
Title: Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia.
Volume: 12
Issue: 21
Pages: 2797-805
Publication
First Author: Held N
Year: 2011
Journal: PLoS One
Title: A mutation in Myo15 leads to Usher-like symptoms in LEW/Ztm-ci2 rats.
Volume: 6
Issue: 3
Pages: e15669
Publication
First Author: Grati M
Year: 2012
Journal: J Neurosci
Title: Localization of PDZD7 to the stereocilia ankle-link associates this scaffolding protein with the Usher syndrome protein network.
Volume: 32
Issue: 41
Pages: 14288-93
Publication
First Author: Holme RH
Year: 2002
Journal: J Comp Neurol
Title: Elongation of hair cell stereocilia is defective in the mouse mutant whirler.
Volume: 450
Issue: 1
Pages: 94-102
Publication
First Author: Mburu P
Year: 2003
Journal: Nat Genet
Title: Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.
Volume: 34
Issue: 4
Pages: 421-8
Publication
First Author: Mogensen MM
Year: 2007
Journal: Cell Motil Cytoskeleton
Title: The deaf mouse mutant whirler suggests a role for whirlin in actin filament dynamics and stereocilia development.
Volume: 64
Issue: 7
Pages: 496-508
Publication
First Author: de Nooij JC
Year: 2015
Journal: J Neurosci
Title: The PDZ-domain protein Whirlin facilitates mechanosensory signaling in mammalian proprioceptors.
Volume: 35
Issue: 7
Pages: 3073-84
Publication
First Author: Mathur PD
Year: 2015
Journal: Hum Mol Genet
Title: A study of whirlin isoforms in the mouse vestibular system suggests potential vestibular dysfunction in DFNB31-deficient patients.
Volume: 24
Issue: 24
Pages: 7017-30
Publication
First Author: Wang L
Year: 2012
Journal: Hum Mol Genet
Title: Whirlin interacts with espin and modulates its actin-regulatory function: an insight into the mechanism of Usher syndrome type II.
Volume: 21
Issue: 3
Pages: 692-710
Publication
First Author: Mathur PD
Year: 2015
Journal: Hum Mol Genet
Title: Distinct expression and function of whirlin isoforms in the inner ear and retina: an insight into pathogenesis of USH2D and DFNB31.
Volume: 24
Issue: 21
Pages: 6213-28
Publication  
First Author: LANE PW
Year: 1963
Journal: J Hered
Title: WHIRLER MICE: A RECESSIVE BEHAVIOR MUTATION IN LINKAGE GROUP VIII.
Volume: 54
Pages: 263-6
Publication
First Author: Ebrahim S
Year: 2016
Journal: Cell Rep
Title: Alternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia.
Volume: 15
Issue: 5
Pages: 935-943
Publication
First Author: Ciardo MG
Year: 2016
Journal: Biochim Biophys Acta
Title: Whirlin increases TRPV1 channel expression and cellular stability.
Volume: 1863
Issue: 1
Pages: 115-27
Publication  
First Author: Kiernan BW
Year: 1998
Journal: Hered Deaf News
Title: Abnormalities of the inner ear in a deaf mouse mutant whirler (wi).
Volume: 15
Pages: 36-7
Publication  
First Author: Tian M
Year: 2014
Journal: Exp Eye Res
Title: Photoreceptors in whirler mice show defective transducin translocation and are susceptible to short-term light/dark changes-induced degeneration.
Volume: 118
Pages: 145-53
Publication
First Author: Paige AJ
Year: 2000
Journal: Mamm Genome
Title: A deletion on chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidate.
Volume: 11
Issue: 1
Pages: 51-7
Publication  
First Author: Kim EJ
Year: 2019
Journal: Front Cell Neurosci
Title: Impact of Auditory Experience on the Structural Plasticity of the AIS in the Mouse Brainstem Throughout the Lifespan.
Volume: 13
Pages: 456
Publication
First Author: Lewis MA
Year: 2009
Journal: Nat Genet
Title: An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice.
Volume: 41
Issue: 5
Pages: 614-8
Publication
First Author: Rogers MJ
Year: 1999
Journal: Mamm Genome
Title: Genetic mapping of the whirler mutation.
Volume: 10
Issue: 5
Pages: 513-9
Publication
First Author: Weltman AS
Year: 1970
Journal: Physiol Behav
Title: Metabolism rate, biochemical and endocrine alterations in male whirler mice.
Volume: 5
Issue: 1
Pages: 17-22
Publication
First Author: Sackler AM
Year: 1967
Journal: J Exp Zool
Title: Metabolic and endocrine differences between the mutation whirler and normal female mice.
Volume: 164
Issue: 2
Pages: 133-40
Publication
First Author: British Society of Audiology short papers meeting on experimental studies of hearing and deafness. Cambridge, United Kingdom, 22-23 September 1996. Kiernan BW
Year: 1997
Journal: Br J Audiol
Title: Analysis of the deaf mouse mutant, whirler.
Volume: 31
Issue: 2
Pages: 73-132 (84-5 Abstr.)
Publication
First Author: Anderson DW
Year: 2000
Journal: Hum Mol Genet
Title: The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cells.
Volume: 9
Issue: 12
Pages: 1729-38
Publication
First Author: Zou J
Year: 2014
Journal: Hum Mol Genet
Title: Deletion of PDZD7 disrupts the Usher syndrome type 2 protein complex in cochlear hair cells and causes hearing loss in mice.
Volume: 23
Issue: 9
Pages: 2374-90
Publication
First Author: Belyantseva IA
Year: 2005
Journal: Nat Cell Biol
Title: Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia.
Volume: 7
Issue: 2
Pages: 148-56
Publication
First Author: Mburu P
Year: 2006
Journal: Proc Natl Acad Sci U S A
Title: Whirlin complexes with p55 at the stereocilia tip during hair cell development.
Volume: 103
Issue: 29
Pages: 10973-8
Publication
First Author: Kikkawa Y
Year: 2005
Journal: Hum Mol Genet
Title: Mutant analysis reveals whirlin as a dynamic organizer in the growing hair cell stereocilium.
Volume: 14
Issue: 3
Pages: 391-400
Publication
First Author: Etournay R
Year: 2010
Journal: Development
Title: Cochlear outer hair cells undergo an apical circumference remodeling constrained by the hair bundle shape.
Volume: 137
Issue: 8
Pages: 1373-83
Publication
First Author: Prosser HM
Year: 2008
Journal: Mol Cell Biol
Title: Mosaic complementation demonstrates a regulatory role for myosin VIIa in actin dynamics of stereocilia.
Volume: 28
Issue: 5
Pages: 1702-12
Publication
First Author: Probst FJ
Year: 1998
Journal: Science
Title: Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.
Volume: 280
Issue: 5368
Pages: 1444-7
Publication
First Author: Manor U
Year: 2011
Journal: Curr Biol
Title: Regulation of stereocilia length by myosin XVa and whirlin depends on the actin-regulatory protein Eps8.
Volume: 21
Issue: 2
Pages: 167-72
Publication  
First Author: Cook SA
Year: 1993
Journal: Mouse Genome
Title: Re-mutation to shaker-2 (sh-2)
Volume: 91
Pages: 312
Publication    
First Author: Fang Q
Year: 2015
Journal: Elife
Title: The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing.
Volume: 4
Publication
First Author: Tadenev ALD
Year: 2019
Journal: Curr Biol
Title: GPSM2-GNAI Specifies the Tallest Stereocilia and Defines Hair Bundle Row Identity.
Volume: 29
Issue: 6
Pages: 921-934.e4
Publication
First Author: Liu R
Year: 2008
Journal: Development
Title: Sisyphus, the Drosophila myosin XV homolog, traffics within filopodia transporting key sensory and adhesion cargos.
Volume: 135
Issue: 1
Pages: 53-63
Publication
First Author: Rehman AU
Year: 2016
Journal: Hum Mutat
Title: Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness.
Volume: 37
Issue: 10
Pages: 991-1003
Publication
First Author: McGrath J
Year: 2021
Journal: Curr Biol
Title: Actin at stereocilia tips is regulated by mechanotransduction and ADF/cofilin.
Volume: 31
Issue: 6
Pages: 1141-1153.e7
Publication  
First Author: Cosgrove D
Year: 2014
Journal: Int J Biochem Cell Biol
Title: Usher protein functions in hair cells and photoreceptors.
Volume: 46
Pages: 80-9
Publication
First Author: Tepass U
Year: 2009
Journal: Curr Opin Genet Dev
Title: FERM proteins in animal morphogenesis.
Volume: 19
Issue: 4
Pages: 357-67
Publication      
First Author: Shanghai Model Organisms Center
Year: 2017
Journal: MGI Direct Data Submission
Title: Information obtained from the Shanghai Model Organisms Center (SMOC), Shanghai, China