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Search results 1 to 100 out of 412 for Myo7a

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Category: Publication
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Type Details Score
Publication
15389316 | J:93998
First Author: Rhodes CR
Year: 2004
Journal: Mamm Genome
Title: A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment.
Volume: 15
Issue: 9
Pages: 686-97
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Publication
- | J:91063
     
First Author: Cook SA
Year: 2004
Journal: MGI Direct Data Submission
Title: A new allele, sh1-7J, of the Myo7a gene
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Publication
11753415 | J:73756
First Author: Kros CJ
Year: 2002
Journal: Nat Neurosci
Title: Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations.
Volume: 5
Issue: 1
Pages: 41-7
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Publication
29430167 | J:331966
 
First Author: Lu Y
Year: 2018
Journal: Mol Vis
Title: The genetic dissection of Myo7a gene expression in the retinas of BXD mice.
Volume: 24
Pages: 115-126
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Publication
12966030 | J:86379
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
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Publication
14648237 | J:134369
First Author: Holme RH
Year: 2004
Journal: J Assoc Res Otolaryngol
Title: Progressive hearing loss and increased susceptibility to noise-induced hearing loss in mice carrying a Cdh23 but not a Myo7a mutation.
Volume: 5
Issue: 1
Pages: 66-79
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Publication
31824252 | J:283233
 
First Author: Calabro KR
Year: 2019
Journal: Front Neurosci
Title: A Novel Mouse Model of MYO7A USH1B Reveals Auditory and Visual System Haploinsufficiencies.
Volume: 13
Pages: 1255
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Publication
19463703 | J:289014
First Author: Avni R
Year: 2009
Journal: Behav Brain Res
Title: Mice with vestibular deficiency display hyperactivity, disorientation, and signs of anxiety.
Volume: 202
Issue: 2
Pages: 210-7
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Publication
24983660 | J:216996
 
First Author: Shefer S
Year: 2015
Journal: Behav Brain Res
Title: Balance deficit enhances anxiety and balance training decreases anxiety in vestibular mutant mice.
Volume: 276
Pages: 76-83
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Publication
20043895 | J:158849
 
First Author: Shefer S
Year: 2010
Journal: Brain Res
Title: Progressive vestibular mutation leads to elevated anxiety.
Volume: 1317
Pages: 157-64
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Publication
18160714 | J:132633
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
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Publication
24997346 | J:213636
First Author: Liu Y
Year: 2014
Journal: FEBS Lett
Title: FERM domain-containing unconventional myosin VIIA interacts with integrin β5 subunit and regulates αvβ5-mediated cell adhesion and migration.
Volume: 588
Issue: 17
Pages: 2859-66
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Publication
32350269 | J:292244
First Author: Li S
Year: 2020
Journal: Nat Commun
Title: Myosin-VIIa is expressed in multiple isoforms and essential for tensioning the hair cell mechanotransduction complex.
Volume: 11
Issue: 1
Pages: 2066
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Publication
9435277 | J:46373
First Author: Self T
Year: 1998
Journal: Development
Title: Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells.
Volume: 125
Issue: 4
Pages: 557-66
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Publication
27525485 | J:236403
   
First Author: Morgan CP
Year: 2016
Journal: Elife
Title: PDZD7-MYO7A complex identified in enriched stereocilia membranes.
Volume: 5
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Publication
23251483 | J:195666
First Author: Miller KA
Year: 2012
Journal: PLoS One
Title: Inner ear morphology is perturbed in two novel mouse models of recessive deafness.
Volume: 7
Issue: 12
Pages: e51284
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Publication
18463160 | J:137661
First Author: Jacobson SG
Year: 2008
Journal: Hum Mol Genet
Title: Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.
Volume: 17
Issue: 15
Pages: 2405-15
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Publication
23991031 | J:204919
First Author: Colella P
Year: 2013
Journal: PLoS One
Title: Myosin7a deficiency results in reduced retinal activity which is improved by gene therapy.
Volume: 8
Issue: 8
Pages: e72027
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Publication
12743369 | J:83622
First Author: Gibbs D
Year: 2003
Journal: Proc Natl Acad Sci U S A
Title: Abnormal phagocytosis by retinal pigmented epithelium that lacks myosin VIIa, the Usher syndrome 1B protein.
Volume: 100
Issue: 11
Pages: 6481-6
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Publication
24705452 | J:215022
First Author: Zallocchi M
Year: 2014
Journal: PLoS One
Title: EIAV-based retinal gene therapy in the shaker1 mouse model for usher syndrome type 1B: development of UshStat.
Volume: 9
Issue: 4
Pages: e94272
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Publication
20016096 | J:157102
First Author: Schwander M
Year: 2009
Journal: J Neurosci
Title: A novel allele of myosin VIIa reveals a critical function for the C-terminal FERM domain for melanosome transport in retinal pigment epithelial cells.
Volume: 29
Issue: 50
Pages: 15810-8
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Publication
11468276 | J:70842
First Author: Boëda B
Year: 2001
Journal: Hum Mol Genet
Title: A specific promoter of the sensory cells of the inner ear defined by transgenesis.
Volume: 10
Issue: 15
Pages: 1581-9
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Publication
9171832 | J:46924
First Author: Liu XZ
Year: 1997
Journal: Nat Genet
Title: Mutations in the myosin VIIA gene cause non-syndromic recessive deafness.
Volume: 16
Issue: 2
Pages: 188-90
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Publication
16481439 | J:105750
First Author: Senften M
Year: 2006
Journal: J Neurosci
Title: Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells.
Volume: 26
Issue: 7
Pages: 2060-71
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Publication
11222540 | J:67802
First Author: Libby RT
Year: 2001
Journal: Invest Ophthalmol Vis Sci
Title: Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B.
Volume: 42
Issue: 3
Pages: 770-8
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Publication
21436032 | J:171218
First Author: Caberlotto E
Year: 2011
Journal: Proc Natl Acad Sci U S A
Title: Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia.
Volume: 108
Issue: 14
Pages: 5825-30
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21493626 | J:173770
First Author: Lopes VS
Year: 2011
Journal: Hum Mol Genet
Title: The Usher 1B protein, MYO7A, is required for normal localization and function of the visual retinoid cycle enzyme, RPE65.
Volume: 20
Issue: 13
Pages: 2560-70
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Publication
19324852 | J:154563
First Author: Gibbs D
Year: 2009
Journal: Invest Ophthalmol Vis Sci
Title: Retinal pigment epithelium defects in humans and mice with mutations in MYO7A: imaging melanosome-specific autofluorescence.
Volume: 50
Issue: 9
Pages: 4386-93
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Publication
14609561 | J:109546
First Author: Libby RT
Year: 2003
Journal: Exp Eye Res
Title: Cdh23 mutations in the mouse are associated with retinal dysfunction but not retinal degeneration.
Volume: 77
Issue: 6
Pages: 731-9
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Publication
12121736 | J:108877
First Author: Holme RH
Year: 2002
Journal: Hear Res
Title: Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice.
Volume: 169
Issue: 1-2
Pages: 13-23
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Publication
22279587 | J:220929
First Author: Pan N
Year: 2012
Journal: PLoS One
Title: A novel Atoh1 "self-terminating" mouse model reveals the necessity of proper Atoh1 level and duration for hair cell differentiation and viability.
Volume: 7
Issue: 1
Pages: e30358
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Publication
22381527 | J:183898
First Author: Zheng QY
Year: 2012
Journal: Hum Mol Genet
Title: Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes.
Volume: 21
Issue: 11
Pages: 2588-98
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9927480 | J:52799
First Author: Keats BJ
Year: 1999
Journal: Genome Res
Title: Genomics and hearing impairment.
Volume: 9
Issue: 1
Pages: 7-16
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19363478 | J:151354
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
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Publication
21146598 | J:169044
First Author: Pan N
Year: 2011
Journal: Hear Res
Title: Conditional deletion of Atoh1 using Pax2-Cre results in viable mice without differentiated cochlear hair cells that have lost most of the organ of Corti.
Volume: 275
Issue: 1-2
Pages: 66-80
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Publication
- | J:81149
     
First Author: The Tennessee Mouse Genome Consortium
Year: 2003
Journal: MGI Direct Data Submission
Title: Targeted mutagenesis of the mouse genome and neural phenotypes
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9680294 | J:49926
First Author: Mburu P
Year: 1997
Journal: Genes Funct
Title: Mutation analysis of the mouse myosin VIIA deafness gene.
Volume: 1
Issue: 3
Pages: 191-203
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10574757 | J:58526
First Author: Hasson T
Year: 1999
Journal: Curr Biol
Title: Molecular motors: sensing a function for myosin-VIIa.
Volume: 9
Issue: 22
Pages: R838-41
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33046691 | J:303536
First Author: Cohen R
Year: 2020
Journal: Nat Commun
Title: Mechanical forces drive ordered patterning of hair cells in the mammalian inner ear.
Volume: 11
Issue: 1
Pages: 5137
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Publication
9186010 | J:42644
First Author: Hasson T
Year: 1997
Journal: Cell Motil Cytoskeleton
Title: Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression.
Volume: 37
Issue: 2
Pages: 127-38
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Publication
21447681 | J:181430
First Author: Peng YW
Year: 2011
Journal: Invest Ophthalmol Vis Sci
Title: Moderate light-induced degeneration of rod photoreceptors with delayed transducin translocation in shaker1 mice.
Volume: 52
Issue: 9
Pages: 6421-7
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Publication
- | J:209272
     
First Author: Karst SY
Year: 2014
Journal: MGI Direct Data Submission
Title: A new spontaneous mutation in myosin VIIa
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Publication
- | J:15554
 
First Author: Lord EM
Year: 1929
Journal: Am Naturalist
Title: Shaker, a new mutation of the house mouse (Mus musculus).
Volume: 63
Pages: 435-42
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Publication
9620764 | J:48237
First Author: Liu X
Year: 1998
Journal: Nat Genet
Title: Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice.
Volume: 19
Issue: 2
Pages: 117-8
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Publication
11162241 | J:110706
First Author: Sun JC
Year: 2001
Journal: Neurobiol Dis
Title: Origin of vestibular dysfunction in Usher syndrome type 1B.
Volume: 8
Issue: 1
Pages: 69-77
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6627025 | J:28477
First Author: Shnerson A
Year: 1983
Journal: Brain Res
Title: The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: ultrastructural observations.
Volume: 285
Issue: 3
Pages: 305-15
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5795329 | J:5118
First Author: Deol MS
Year: 1969
Journal: J Exp Zool
Title: Cattanach's translocation as a tool for studying the action of the shaker-1 gene in the mouse.
Volume: 170
Issue: 3
Pages: 301-9
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Publication
- | J:14846
 
First Author: Kikuchi K
Year: 1965
Journal: Acta Otolaryngol
Title: The defective organ of Corti in Shaker-1 mice.
Volume: 60
Pages: 287-303
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14198707 | J:14858
 
First Author: MIKAELIAN DO
Year: 1964
Journal: Arch Otolaryngol
Title: HEARING DEGENERATION IN SHAKER-1 MOUSE. CORRELATION OF PHYSIOLOGICAL OBSERVATIONS WITH BEHAVIORAL RESPONSES AND WITH COCHLEAR ANATOMY.
Volume: 80
Pages: 418-30
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Publication
- | J:17340
First Author: Letts VA
Year: 1994
Journal: Mouse Genome
Title: Remutation at the shaker-1 locus
Volume: 92
Issue: 1
Pages: 116
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Publication
- | J:77937
     
First Author: Samples RM
Year: 2002
Journal: MGI Direct Data Submission
Title: A new shaker 1 mutation of the Myo7 gene in the mouse
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Publication
- | J:213050
     
First Author: SoRelle J
Year: 2014
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for coward
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7568224 | J:29409
First Author: Hasson T
Year: 1995
Journal: Proc Natl Acad Sci U S A
Title: Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B.
Volume: 92
Issue: 21
Pages: 9815-9
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Publication
8842737 | J:34515
First Author: el-Amraoui A
Year: 1996
Journal: Hum Mol Genet
Title: Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells.
Volume: 5
Issue: 8
Pages: 1171-8
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Publication
7870171 | J:23239
First Author: Weil D
Year: 1995
Journal: Nature
Title: Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Volume: 374
Issue: 6517
Pages: 60-1
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7849737 | J:20702
 
First Author: Brown SD
Year: 1994
Journal: Hum Mol Genet
Title: Genetic deafness--progress with mouse models.
Volume: 3 Spec No
Pages: 1453-6
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8622919 | J:35133
First Author: Weil D
Year: 1996
Journal: Proc Natl Acad Sci U S A
Title: Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia.
Volume: 93
Issue: 8
Pages: 3232-7
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Publication
9027465 | J:40118
First Author: Saw D Jr
Year: 1997
Journal: Exp Anim
Title: Shaker mice and a peek into the House of Usher.
Volume: 46
Issue: 1
Pages: 1-9
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Publication
9382088 | J:43134
First Author: Hasson T
Year: 1997
Journal: Am J Hum Genet
Title: Unconventional myosins, the basis for deafness in mouse and man.
Volume: 61
Issue: 4
Pages: 801-5
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9278160 | J:76464
First Author: Sahly I
Year: 1997
Journal: Anat Embryol (Berl)
Title: Expression of myosin VIIA during mouse embryogenesis.
Volume: 196
Issue: 2
Pages: 159-70
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Publication
21212272 | J:170528
First Author: Haithcock J
Year: 2011
Journal: J Biol Chem
Title: The kinetic mechanism of mouse myosin VIIA.
Volume: 286
Issue: 11
Pages: 8819-28
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Publication
25957791 | J:223776
 
First Author: Yang XY
Year: 2015
Journal: Brain Res
Title: Role of the planar cell polarity pathway in regulating ectopic hair cell-like cells induced by Math1 and testosterone treatment.
Volume: 1615
Pages: 22-30
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Publication
- | J:48658
 
First Author: Steel KP
Year: 1998
Journal: Hered Deaf News
Title: Stereocilia defects in a mouse mutant with defective myosin VI, Snell's waltzer.
Volume: 15
Pages: 37
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8111122 | J:16407
First Author: Brown KA
Year: 1994
Journal: Mamm Genome
Title: Sequencing of the olfactory marker protein gene in normal and shaker-1 mutant mice.
Volume: 5
Issue: 1
Pages: 11-4
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11506947 | J:74163
First Author: El-Amraoui A
Year: 2001
Journal: Hear Res
Title: Spatiotemporal expression of otogelin in the developing and adult mouse inner ear.
Volume: 158
Issue: 1-2
Pages: 151-9
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Publication
7870172 | J:23257
First Author: Gibson F
Year: 1995
Journal: Nature
Title: A type VII myosin encoded by the mouse deafness gene shaker-1.
Volume: 374
Issue: 6517
Pages: 62-4
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Publication
34903829 | J:332716
First Author: Pacentine IV
Year: 2021
Journal: Sci Rep
Title: Cy3-ATP labeling of unfixed, permeabilized mouse hair cells.
Volume: 11
Issue: 1
Pages: 23855
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Publication
21986210 | J:181053
First Author: Beyer LA
Year: 2011
Journal: Hear Res
Title: Age-related changes in expression of CTL2/SLC44A2 and its isoforms in the mouse inner ear.
Volume: 282
Issue: 1-2
Pages: 63-8
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Publication
14534255 | J:85926
First Author: Goodyear RJ
Year: 2003
Journal: J Neurosci
Title: A receptor-like inositol lipid phosphatase is required for the maturation of developing cochlear hair bundles.
Volume: 23
Issue: 27
Pages: 9208-19
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Publication
8307326 | J:15677
First Author: Rinchik EM
Year: 1993
Journal: Genetics
Title: Molecular analysis of radiation-induced albino (c)-locus mutations that cause death at preimplantation stages of development.
Volume: 135
Issue: 4
Pages: 1107-16
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Publication
- | J:49039
     
First Author: Cook S
Year: 1998
Journal: MGI Direct Data Submission
Title: The Jackson Laboratory Mouse Mutant Resource 1998 Mutation Reports
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Publication
15316067 | J:92181
First Author: Libby RT
Year: 2004
Journal: J Cell Sci
Title: Myosin Va is required for normal photoreceptor synaptic activity.
Volume: 117
Issue: Pt 19
Pages: 4509-15
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Publication
- | J:14891
 
First Author: Tan Creti DM
Year: 1969
Journal: J Neuropathol Exp Neurol
Title: Neuropathology of mutant mice with auditory and/or vestibular deficiencies
Volume: 28
Pages: 159 (Abstr)
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Publication
- | J:203
 
First Author: Wallace ME
Year: 1963
Journal: Mouse News Lett
Title: bh (brain hernia)
Volume: 29
Pages: 22
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Publication
11374883 | J:69809
First Author: Morishita H
Year: 2001
Journal: Biochem Biophys Res Commun
Title: Deafness due to degeneration of cochlear neurons in caspase-3-deficient mice.
Volume: 284
Issue: 1
Pages: 142-9
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Publication
863237 | J:5809
First Author: Eicher EM
Year: 1977
Journal: Genetics
Title: Influence of gene duplication and X-inactivation on mouse mitochondrial malic enzyme activity and electrophoretic patterns.
Volume: 85
Issue: 4
Pages: 647-58
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Publication
16790479 | J:119034
First Author: Lee YS
Year: 2006
Journal: Development
Title: A morphogenetic wave of p27Kip1 transcription directs cell cycle exit during organ of Corti development.
Volume: 133
Issue: 15
Pages: 2817-26
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Publication
14487977 | J:107
 
First Author: POPP RA
Year: 1962
Journal: J Hered
Title: Studies on the mouse hemoglobin loci. II. Position of the hemoglobin locus with respect to albinism and shaker-1 loci.
Volume: 53
Pages: 73-80
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Publication
21722859 | J:186803
First Author: Cheng J
Year: 2011
Journal: Am J Hum Genet
Title: Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64.
Volume: 89
Issue: 1
Pages: 56-66
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Publication
- | J:257
 
First Author: Gates WH
Year: 1931
Journal: Z Indukt Abstamm Vererbungsl
Title: Linkage of the factor shaker with albinism and pink-eye in the house mouse
Volume: 59
Pages: 220-6
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Publication
16207888 | J:342400
First Author: Beisel KW
Year: 2005
Journal: J Neurosci
Title: Differential expression of KCNQ4 in inner hair cells and sensory neurons is the basis of progressive high-frequency hearing loss.
Volume: 25
Issue: 40
Pages: 9285-93
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Publication
- | J:95
 
First Author: Gates WH
Year: 1929
Journal: Anat Rec
Title: Linkage of the characters albinism and shaker in the house mouse
Volume: 41
Pages: 104 (S28 Abstr.)
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Publication
- | J:96
 
First Author: Gates WH
Year: 1929
Journal: Anat Rec
Title: Linkage of shaker with albinism and pink-eye in the house mouse
Volume: 44
Pages: 287 (Abstr. 22)
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Publication
- | J:12980
 
First Author: Steel K
Year: 1989
Journal: Hered Deaf News
Title: Molecular mapping of the mouse shaker-1 locus.
Volume: 2
Pages: 18-19
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Publication
30610177 | J:273017
First Author: Li C
Year: 2019
Journal: Proc Natl Acad Sci U S A
Title: Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss.
Volume: 116
Issue: 4
Pages: 1347-1352
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Publication
15654330 | J:102099
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
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Publication
23122586 | J:203658
First Author: Yariz KO
Year: 2012
Journal: Am J Hum Genet
Title: Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss.
Volume: 91
Issue: 5
Pages: 872-82
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Publication
12768423 | J:84152
First Author: Meunier D
Year: 2003
Journal: Anat Embryol (Berl)
Title: Preferential expression of the G90 gene in post-mitotic cells during mouse embryonic development.
Volume: 207
Issue: 2
Pages: 109-17
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Publication
20451170 | J:164931
First Author: Sirmaci A
Year: 2010
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