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Search results 1201 to 1300 out of 1619 for Myo7a

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Type Details Score
GXD Expression
Probe: MGI:2446090
Assay Type: Immunohistochemistry
Annotation Date: 2012-01-31
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729522
Pattern: Regionally restricted
Stage: TS22
Assay Id: MGI:5304363
Age: embryonic day 14.5
Image: 3D
Note: Expression is present in the hair cells. They are have abnormal morphology and layering in the mutant.
Specimen Label: 3D
Detected: true
Specimen Num: 4
GXD Expression
Probe: MGI:6762180
Assay Type: Immunohistochemistry
Annotation Date: 2021-09-28
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729526
Pattern: Regionally restricted
Stage: TS26
Assay Id: MGI:6763027
Age: embryonic day 18.5
Image: 6G
Note: Expressed in the hair cells.
Specimen Label: 6G
Detected: true
Specimen Num: 7
GXD Expression
Probe: MGI:6762180
Assay Type: Immunohistochemistry
Annotation Date: 2021-09-28
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729526
Pattern: Regionally restricted
Stage: TS26
Assay Id: MGI:6763027
Age: embryonic day 18.5
Image: 6H
Note: The utricular macula is extremely small with very few positive hair cells.
Specimen Label: 6H
Detected: true
Specimen Num: 8
GXD Expression  
Probe: MGI:7287403
Assay Type: Immunohistochemistry
Annotation Date: 2022-06-21
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729523
Pattern: Not Specified
Stage: TS23
Assay Id: MGI:7287435
Age: embryonic day 15.5
Image: 3A2
Specimen Label: 3A2
Detected: true
Specimen Num: 5
GXD Expression  
Probe: MGI:7287403
Assay Type: Immunohistochemistry
Annotation Date: 2022-06-21
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729526
Pattern: Not Specified
Stage: TS26
Assay Id: MGI:7287437
Age: embryonic day 18.5
Image: 3C2
Specimen Label: 3C2
Detected: true
Specimen Num: 5
GXD Expression  
Probe: MGI:7287403
Assay Type: Immunohistochemistry
Annotation Date: 2022-06-21
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729523
Pattern: Regionally restricted
Stage: TS23
Assay Id: MGI:7287435
Age: embryonic day 15.5
Image: 5A
Specimen Label: 5A
Detected: true
Specimen Num: 13
GXD Expression  
Probe: MGI:7287403
Assay Type: Immunohistochemistry
Annotation Date: 2022-06-21
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729524
Pattern: Not Specified
Stage: TS24
Assay Id: MGI:7287435
Age: embryonic day 16.5
Image: 5B
Specimen Label: 5B
Detected: true
Specimen Num: 14
GXD Expression  
Probe: MGI:7287403
Assay Type: Immunohistochemistry
Annotation Date: 2022-06-21
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729528
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:7287435
Age: postnatal day 7
Image: 6C2
Specimen Label: 6C2
Detected: true
Specimen Num: 17
GXD Expression    
Probe: MGI:7526514
Assay Type: Immunohistochemistry
Annotation Date: 2023-09-18
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729526
Pattern: Not Specified
Stage: TS26
Assay Id: MGI:7526712
Age: embryonic day 18.5
Specimen Label: 2H
Detected: true
Specimen Num: 1
GXD Expression  
Probe: MGI:7526514
Assay Type: Immunohistochemistry
Annotation Date: 2023-09-18
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729526
Pattern: Not Specified
Stage: TS26
Assay Id: MGI:7526712
Age: embryonic day 18.5
Note: A clear reduction of sensory epithelium and hair cells compared with controls.
Specimen Label: 2I
Detected: true
Specimen Num: 2
GXD Expression  
Probe: MGI:7526514
Assay Type: Immunohistochemistry
Annotation Date: 2023-09-18
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729526
Pattern: Not Specified
Stage: TS26
Assay Id: MGI:7526712
Age: embryonic day 18.5
Note: Structure could be identifiable by its thickened appearance but was largely reduced in size when compared with normal animals.
Specimen Label: 2J
Detected: true
Specimen Num: 3
GXD Expression  
Probe: MGI:5556119
Assay Type: Immunohistochemistry
Annotation Date: 2024-02-20
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729528
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:7595663
Age: postnatal day 6
Image: 8B Utricle
Specimen Label: 8B Utricle
Detected: true
Specimen Num: 2
GXD Expression  
Probe: MGI:5308606
Assay Type: Immunohistochemistry
Annotation Date: 2024-02-20
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729528
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:7595664
Age: postnatal day 6
Image: 8C Utricle
Specimen Label: 8C Utricle
Detected: true
Specimen Num: 2
GXD Expression
Probe: MGI:5308606
Assay Type: Immunohistochemistry
Annotation Date: 2017-06-08
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3686828
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:5902116
Age: postnatal day 30
Image: 1E
Note: Expressed in hair cells.
Specimen Label: 1E
Detected: true
Specimen Num: 1
GXD Expression
Probe: MGI:5308606
Assay Type: Immunohistochemistry
Annotation Date: 2017-06-08
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3686828
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:5902116
Age: postnatal day 30
Image: 1F
Note: Expressed in hair cells.
Specimen Label: 1F
Detected: true
Specimen Num: 2
GXD Expression
Probe: MGI:5308606
Assay Type: Immunohistochemistry
Annotation Date: 2017-06-08
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3686828
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:5902116
Age: postnatal day 30
Image: 1G
Note: Expressed in hair cells.
Specimen Label: 1G
Detected: true
Specimen Num: 3
GXD Expression
Probe: MGI:5308606
Assay Type: Immunohistochemistry
Annotation Date: 2017-06-08
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3686828
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:5902116
Age: postnatal day 30
Image: 1H
Note: Expressed in hair cells.
Specimen Label: 1H
Detected: true
Specimen Num: 4
GXD Expression
Probe: MGI:5308606
Assay Type: Immunohistochemistry
Annotation Date: 2018-10-30
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3696024
Pattern: Regionally restricted
Stage: TS24
Assay Id: MGI:6209738
Age: embryonic day 16.5
Image: 7G
Note: Expression in anterior crista.
Specimen Label: 7G
Detected: true
Specimen Num: 4
GXD Expression
Probe: MGI:5308606
Assay Type: Immunohistochemistry
Annotation Date: 2018-10-30
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3696024
Pattern: Regionally restricted
Stage: TS24
Assay Id: MGI:6209738
Age: embryonic day 16.5
Image: 7I
Note: Authors report normal lateral crista.
Specimen Label: 7I
Detected: true
Specimen Num: 6
GXD Expression
Probe: MGI:5308606
Assay Type: Immunohistochemistry
Annotation Date: 2018-10-30
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3696024
Pattern: Regionally restricted
Stage: TS24
Assay Id: MGI:6209738
Age: embryonic day 16.5
Image: 7K
Note: Expression in posterior crista.
Specimen Label: 7K
Detected: true
Specimen Num: 8
GXD Expression  
Probe: MGI:5308606
Assay Type: Immunohistochemistry
Annotation Date: 2018-10-30
Strength: Ambiguous
Sex: Not Specified
Emaps: EMAPS:3696024
Pattern: Regionally restricted
Stage: TS24
Assay Id: MGI:6209738
Age: embryonic day 16.5
Image: 7H
Note: Authors report no expression in cristae.
Specimen Label: 7H
Specimen Num: 5
GXD Expression  
Probe: MGI:5308606
Assay Type: Immunohistochemistry
Annotation Date: 2018-10-30
Strength: Ambiguous
Sex: Not Specified
Emaps: EMAPS:3696024
Pattern: Regionally restricted
Stage: TS24
Assay Id: MGI:6209738
Age: embryonic day 16.5
Image: 7J
Note: Authors report normal lateral crista.
Specimen Label: 7J
Specimen Num: 7
GXD Expression  
Probe: MGI:5308606
Assay Type: Immunohistochemistry
Annotation Date: 2018-10-30
Strength: Ambiguous
Sex: Not Specified
Emaps: EMAPS:3696024
Pattern: Regionally restricted
Stage: TS24
Assay Id: MGI:6209738
Age: embryonic day 16.5
Image: 7L
Note: Authors state embryo lacks posterior crista.
Specimen Label: 7L
Specimen Num: 9
Publication  
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication  
First Author: Wallace ME
Year: 1963
Journal: Mouse News Lett
Title: bh (brain hernia)
Volume: 29
Pages: 22
Publication  
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)
Publication      
First Author: Cook S
Year: 1998
Journal: MGI Direct Data Submission
Title: The Jackson Laboratory Mouse Mutant Resource 1998 Mutation Reports
Publication
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
Publication
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
Publication
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
Publication  
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
Publication
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
Publication  
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
Publication
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
Publication  
First Author: Steel K
Year: 1989
Journal: Hered Deaf News
Title: Molecular mapping of the mouse shaker-1 locus.
Volume: 2
Pages: 18-19
Publication  
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.)
Publication  
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)
Publication
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
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: 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
Publication
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
Publication
First Author: Sirmaci A
Year: 2010
Journal: Am J Hum Genet
Title: A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss.
Volume: 86
Issue: 5
Pages: 797-804
Publication
First Author: El-Amraoui A
Year: 2002
Journal: EMBO Rep
Title: MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes.
Volume: 3
Issue: 5
Pages: 463-70
Publication
First Author: DEOL MS
Year: 1956
Journal: Proc R Soc Lond B Biol Sci
Title: The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse.
Volume: 145
Issue: 919
Pages: 206-13
Publication
First Author: Rinchik EM
Year: 1993
Journal: Genetics
Title: Deletion mapping of four loci defined by N-ethyl-N-nitrosourea-induced postimplantation-lethal mutations within the pid-Hbb region of mouse chromosome 7.
Volume: 135
Issue: 4
Pages: 1117-23
Publication
First Author: Futter CE
Year: 2004
Journal: Mol Biol Cell
Title: The role of Rab27a in the regulation of melanosome distribution within retinal pigment epithelial cells.
Volume: 15
Issue: 5
Pages: 2264-75
Publication
First Author: Liu X
Year: 1999
Journal: J Neurosci
Title: Myosin VIIa participates in opsin transport through the photoreceptor cilium.
Volume: 19
Issue: 15
Pages: 6267-74
Publication
First Author: Chen P
Year: 1999
Journal: Development
Title: p27(Kip1) links cell proliferation to morphogenesis in the developing organ of Corti.
Volume: 126
Issue: 8
Pages: 1581-90
Publication  
First Author: Rinchik EM
Year: 1991
Journal: Ann N Y Acad Sci
Title: Reverse genetics in the mouse and its application to the study of deafness.
Volume: 630
Pages: 80-92
Publication
First Author: Johnson DK
Year: 1989
Journal: Proc Natl Acad Sci U S A
Title: Molecular mapping within the mouse albino-deletion complex.
Volume: 86
Issue: 22
Pages: 8862-6
Publication
First Author: Phillips KR
Year: 2006
Journal: J Neurosci
Title: Stereociliary myosin-1c receptors are sensitive to calcium chelation and absent from cadherin 23 mutant mice.
Volume: 26
Issue: 42
Pages: 10777-88
Publication
First Author: Li S
Year: 2002
Journal: Development
Title: Hearing loss caused by progressive degeneration of cochlear hair cells in mice deficient for the Barhl1 homeobox gene.
Volume: 129
Issue: 14
Pages: 3523-32
Publication  
First Author: Zhang Y
Year: 2015
Journal: Front Cell Neurosci
Title: Dynamic expression of Lgr6 in the developing and mature mouse cochlea.
Volume: 9
Pages: 165
Publication
First Author: Freeman SD
Year: 2015
Journal: Dev Dyn
Title: Expression of the heparan sulfate 6-O-endosulfatases, Sulf1 and Sulf2, in the avian and mammalian inner ear suggests a role for sulfation during inner ear development.
Volume: 244
Issue: 2
Pages: 168-80
Publication    
First Author: Fan F
Year: 2017
Journal: Elife
Title: Exophilin-8 assembles secretory granules for exocytosis in the actin cortex via interaction with RIM-BP2 and myosin-VIIa.
Volume: 6
Publication
First Author: Brown KA
Year: 1992
Journal: Genomics
Title: Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1.
Volume: 13
Issue: 1
Pages: 189-93
Publication
First Author: Kuroda TS
Year: 2005
Journal: J Biol Chem
Title: Functional analysis of Slac2-c/MyRIP as a linker protein between melanosomes and myosin VIIa.
Volume: 280
Issue: 30
Pages: 28015-22
Publication
First Author: Rim JH
Year: 2022
Journal: Hum Genet
Title: Differential genetic diagnoses of adult post-lingual hearing loss according to the audiogram pattern and novel candidate gene evaluation.
Volume: 141
Issue: 3-4
Pages: 915-927
Publication
First Author: Gruneberg H
Year: 1935
Journal: J Genet
Title: A three-factor linkage experiment in the mouse.
Volume: 31
Issue: 2
Pages: 157-62
Publication
First Author: Gruneberg H
Year: 1936
Journal: J Genet
Title: Further linkage data on the albino chromosome of the house-mouse.
Volume: 33
Issue: 2
Pages: 255-265
Publication
First Author: Fukuda M
Year: 2002
Journal: J Biol Chem
Title: Slac2-c (synaptotagmin-like protein homologue lacking C2 domains-c), a novel linker protein that interacts with Rab27, myosin Va/VIIa, and actin.
Volume: 277
Issue: 45
Pages: 43096-103
Publication
First Author: Delprat B
Year: 2005
Journal: Hum Mol Genet
Title: Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly.
Volume: 14
Issue: 3
Pages: 401-10
Publication
First Author: Kim E
Year: 2010
Journal: J Neurophysiol
Title: Regulation of cellular calcium in vestibular supporting cells by otopetrin 1.
Volume: 104
Issue: 6
Pages: 3439-50
Publication
First Author: Aponte JL
Year: 2001
Journal: Proc Natl Acad Sci U S A
Title: Point mutations in the murine fumarylacetoacetate hydrolase gene: Animal models for the human genetic disorder hereditary tyrosinemia type 1.
Volume: 98
Issue: 2
Pages: 641-5
Publication
First Author: Etournay R
Year: 2005
Journal: J Cell Sci
Title: PHR1, an integral membrane protein of the inner ear sensory cells, directly interacts with myosin 1c and myosin VIIa.
Volume: 118
Issue: Pt 13
Pages: 2891-9
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: Reiners J
Year: 2003
Journal: Invest Ophthalmol Vis Sci
Title: Differential distribution of harmonin isoforms and their possible role in Usher-1 protein complexes in mammalian photoreceptor cells.
Volume: 44
Issue: 11
Pages: 5006-15
Publication
First Author: Potter MD
Year: 1993
Journal: Mamm Genome
Title: Deletion mapping of the chocolate (cht) locus within the Fes-Hbb region of mouse chromosome 7.
Volume: 4
Issue: 1
Pages: 46-8
Publication
First Author: Corns LF
Year: 2018
Journal: Nat Commun
Title: Mechanotransduction is required for establishing and maintaining mature inner hair cells and regulating efferent innervation.
Volume: 9
Issue: 1
Pages: 4015
Publication
First Author: Falconer DS
Year: 1952
Journal: J Hered
Title: Two new hair mutants, rough and frizzy in the house mouse.
Volume: 43
Issue: 1
Pages: 53-57
Publication  
First Author: Wallace ME
Year: 1975
Journal: Mouse News Lett
Title: Warfarin resistance and a new gene for obesity.
Volume: 53
Pages: 20
Publication
First Author: Chen P
Year: 2003
Journal: Nat Cell Biol
Title: Progressive hearing loss in mice lacking the cyclin-dependent kinase inhibitor Ink4d.
Volume: 5
Issue: 5
Pages: 422-6
Publication
First Author: Pauley S
Year: 2006
Journal: Dev Dyn
Title: Foxg1 is required for morphogenesis and histogenesis of the mammalian inner ear.
Volume: 235
Issue: 9
Pages: 2470-82
Publication
First Author: Rinchik EM
Year: 1990
Journal: Proc Natl Acad Sci U S A
Title: A strategy for fine-structure functional analysis of a 6- to 11-centimorgan region of mouse chromosome 7 by high-efficiency mutagenesis.
Volume: 87
Issue: 3
Pages: 896-900
Publication
First Author: Wallace ME
Year: 1976
Journal: J Hyg (Lond)
Title: A major gene controlling warfarin-resistance in the house mouse.
Volume: 76
Issue: 2
Pages: 173-81
Publication
First Author: Kersigo J
Year: 2011
Journal: Genesis
Title: The role of sensory organs and the forebrain for the development of the craniofacial shape as revealed by Foxg1-cre-mediated microRNA loss.
Volume: 49
Issue: 4
Pages: 326-41
Publication
First Author: Zheng JL
Year: 2000
Journal: Development
Title: Hes1 is a negative regulator of inner ear hair cell differentiation.
Volume: 127
Issue: 21
Pages: 4551-60
Publication
First Author: Zine A
Year: 2001
Journal: J Neurosci
Title: Hes1 and Hes5 activities are required for the normal development of the hair cells in the mammalian inner ear.
Volume: 21
Issue: 13
Pages: 4712-20
Publication
First Author: Boëda B
Year: 2002
Journal: EMBO J
Title: Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle.
Volume: 21
Issue: 24
Pages: 6689-99
Publication
First Author: Chen P
Year: 2002
Journal: Development
Title: The role of Math1 in inner ear development: Uncoupling the establishment of the sensory primordium from hair cell fate determination.
Volume: 129
Issue: 10
Pages: 2495-505
Publication  
First Author: Xu J
Year: 2017
Journal: Nat Commun
Title: Identification of mouse cochlear progenitors that develop hair and supporting cells in the organ of Corti.
Volume: 8
Pages: 15046
Publication
First Author: Ellis K
Year: 2019
Journal: Dev Biol
Title: GSK3 regulates hair cell fate in the developing mammalian cochlea.
Volume: 453
Issue: 2
Pages: 191-205
Publication  
First Author: O'Connor AP
Year: 2024
Journal: JCI Insight
Title: In vivo AAV9-Myo7a gene rescue restores hearing and cholinergic efferent innervation in inner hair cells.
Volume: 9
Issue: 23
Publication  
First Author: Kempfle JS
Year: 2016
Journal: Sci Rep
Title: Sox2 in the differentiation of cochlear progenitor cells.
Volume: 6
Pages: 23293
Publication    
First Author: Mann ZF
Year: 2017
Journal: Elife
Title: Shaping of inner ear sensory organs through antagonistic interactions between Notch signalling and Lmx1a.
Volume: 6
Publication
First Author: Wilkerson BA
Year: 2019
Journal: Sci Rep
Title: Open chromatin dynamics in prosensory cells of the embryonic mouse cochlea.
Volume: 9
Issue: 1
Pages: 9060
Publication
First Author: Kwon TJ
Year: 2014
Journal: Hum Mol Genet
Title: Methionine sulfoxide reductase B3 deficiency causes hearing loss due to stereocilia degeneration and apoptotic cell death in cochlear hair cells.
Volume: 23
Issue: 6
Pages: 1591-601
Publication
First Author: Chiereghin C
Year: 2023
Journal: PLoS One
Title: In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear.
Volume: 18
Issue: 1
Pages: e0273586
Publication
First Author: MacSwiney FJ
Year: 1978
Journal: J Hyg (Lond)
Title: Genetics of warfarin-resistance in house mice of three separate localities.
Volume: 80
Issue: 1
Pages: 69-75
Publication
First Author: Hasson T
Year: 1996
Journal: J Biol Chem
Title: Vertebrate unconventional myosins.
Volume: 271
Issue: 28
Pages: 16431-4
Publication
First Author: Probst FJ
Year: 1999
Journal: Hear Res
Title: The role of mouse mutants in the identification of human hereditary hearing loss genes.
Volume: 130
Issue: 1-2
Pages: 1-6
Publication
First Author: Dong Y
Year: 2003
Journal: Neuroreport
Title: Role of the F-box protein Skp2 in cell proliferation in the developing auditory system in mice.
Volume: 14
Issue: 5
Pages: 759-61