|  Help  |  About  |  Contact Us

Search our database by keyword

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 100 out of 852 for Myo7a

<< First    < Previous  |  Next >    Last >>
0.049s
Type Details Score
Gene
Type: gene
Organism: Homo sapiens
Gene
Type: gene
Organism: Rattus norvegicus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Publication
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
Publication      
First Author: Cook SA
Year: 2004
Journal: MGI Direct Data Submission
Title: A new allele, sh1-7J, of the Myo7a gene
Publication
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
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: 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
Publication  
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
Publication
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
Publication  
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
Publication  
First Author: Shefer S
Year: 2010
Journal: Brain Res
Title: Progressive vestibular mutation leads to elevated anxiety.
Volume: 1317
Pages: 157-64
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: 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
Publication
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
Publication
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
Publication    
First Author: Morgan CP
Year: 2016
Journal: Elife
Title: PDZD7-MYO7A complex identified in enriched stereocilia membranes.
Volume: 5
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
First Author: Keats BJ
Year: 1999
Journal: Genome Res
Title: Genomics and hearing impairment.
Volume: 9
Issue: 1
Pages: 7-16
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: 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
Publication      
First Author: The Tennessee Mouse Genome Consortium
Year: 2003
Journal: MGI Direct Data Submission
Title: Targeted mutagenesis of the mouse genome and neural phenotypes
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus caroli
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus pahari
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus spretus
Publication
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
Publication
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
Publication
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
Publication      
First Author: Samples RM
Year: 2002
Journal: MGI Direct Data Submission
Title: A new shaker 1 mutation of the Myo7 gene in the mouse
Publication      
First Author: SoRelle J
Year: 2014
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for coward
Publication      
First Author: Karst SY
Year: 2014
Journal: MGI Direct Data Submission
Title: A new spontaneous mutation in myosin VIIa
Publication
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
Publication
First Author: Letts VA
Year: 1994
Journal: Mouse Genome
Title: Remutation at the shaker-1 locus
Volume: 92
Issue: 1
Pages: 116
Publication  
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
Publication  
First Author: Kikuchi K
Year: 1965
Journal: Acta Otolaryngol (Stockh)
Title: The defective organ of Corti in Shaker-1 mice.
Volume: 60
Pages: 287-303
Publication
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
Publication  
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication  
First Author: Brown SD
Year: 1994
Journal: Hum Mol Genet
Title: Genetic deafness--progress with mouse models.
Volume: 3 Spec No
Pages: 1453-6
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication  
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
GXD Expression      
Probe: MGI:6514433
Assay Type: RT-PCR
Annotation Date: 2021-04-01
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1619324
Stage: TS24
Assay Id: MGI:6514438
Age: embryonic day 16.0
Detected: true
Specimen Num: 1
GXD Expression      
Probe: MGI:6514433
Assay Type: RT-PCR
Annotation Date: 2021-04-01
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1619324
Stage: TS24
Assay Id: MGI:6514438
Age: embryonic day 16.0
Detected: true
Specimen Num: 2
GXD Expression      
Probe: MGI:6514433
Assay Type: RT-PCR
Annotation Date: 2021-04-01
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1619326
Stage: TS26
Assay Id: MGI:6514438
Age: embryonic day 18.5
Detected: true
Specimen Num: 3
GXD Expression      
Probe: MGI:6514433
Assay Type: RT-PCR
Annotation Date: 2021-04-01
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1619326
Stage: TS26
Assay Id: MGI:6514438
Age: embryonic day 18.5
Detected: true
Specimen Num: 4
GXD Expression    
Probe: MGI:6414644
Assay Type: RT-PCR
Annotation Date: 2020-05-05
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1619427
Stage: TS27
Assay Id: MGI:6414804
Age: postnatal day 1
Image: 1
Detected: true
Specimen Num: 1
GXD Expression    
Probe: MGI:6414644
Assay Type: RT-PCR
Annotation Date: 2020-05-05
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1619427
Stage: TS27
Assay Id: MGI:6414804
Age: postnatal day 1
Image: 1
Detected: true
Specimen Num: 2
GXD Expression      
Probe: MGI:4867242
Assay Type: RT-PCR
Annotation Date: 2011-01-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759725
Stage: TS25
Assay Id: MGI:4867258
Age: embryonic day 17.0
Detected: true
Specimen Num: 1
GXD Expression      
Probe: MGI:4867242
Assay Type: RT-PCR
Annotation Date: 2011-01-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759726
Stage: TS26
Assay Id: MGI:4867258
Age: embryonic day 18.0
Detected: true
Specimen Num: 2
GXD Expression      
Probe: MGI:4867242
Assay Type: RT-PCR
Annotation Date: 2011-01-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759727
Stage: TS27
Assay Id: MGI:4867258
Age: postnatal day 0
Detected: true
Specimen Num: 3
GXD Expression      
Probe: MGI:4867242
Assay Type: RT-PCR
Annotation Date: 2011-01-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759727
Stage: TS27
Assay Id: MGI:4867258
Age: postnatal day 2
Detected: true
Specimen Num: 4
GXD Expression      
Probe: MGI:4867242
Assay Type: RT-PCR
Annotation Date: 2011-01-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759728
Stage: TS28
Assay Id: MGI:4867258
Age: postnatal day 4
Detected: true
Specimen Num: 5
GXD Expression      
Probe: MGI:4867242
Assay Type: RT-PCR
Annotation Date: 2011-01-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759728
Stage: TS28
Assay Id: MGI:4867258
Age: postnatal day 6
Detected: true
Specimen Num: 6
GXD Expression      
Probe: MGI:4867242
Assay Type: RT-PCR
Annotation Date: 2011-01-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759728
Stage: TS28
Assay Id: MGI:4867258
Age: postnatal day 8
Detected: true
Specimen Num: 7
GXD Expression  
Probe: MGI:26008
Assay Type: RNA in situ
Annotation Date: 2002-04-26
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729022
Pattern: Regionally restricted
Stage: TS22
Assay Id: MGI:2178213
Age: embryonic day 14.5
Note: Expression in the sensory epithelia of the vestibular system (the saccular and utricular maculae and the three cristae).
Detected: true
Specimen Num: 2
GXD Expression    
Probe: MGI:5556119
Assay Type: Immunohistochemistry
Annotation Date: 2017-01-20
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729028
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:5818546
Age: postnatal day 18
Detected: true
Specimen Num: 2
GXD Expression  
Probe: MGI:5308606
Assay Type: Immunohistochemistry
Annotation Date: 2018-02-22
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729025
Pattern: Not Specified
Stage: TS25
Assay Id: MGI:6117315
Age: embryonic day 17.5
Image: 7C'
Detected: true
Specimen Num: 1
GXD Expression  
Probe: MGI:6273645
Assay Type: Immunohistochemistry
Annotation Date: 2019-01-16
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729022
Pattern: Not Specified
Stage: TS22
Assay Id: MGI:6273651
Age: embryonic day 14.5
Image: 6B
Detected: true
Specimen Num: 8