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Search results 101 to 200 out of 413 for Myo7a

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Category: Publication
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Type Details Score
Publication
14978221 | J:91408
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
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Publication
28673385 | J:258210
   
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
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Publication
10414956 | J:56998
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
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Publication
12091321 | J:77122
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
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Publication
1349573 | J:470
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
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Publication
15927964 | J:100821
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
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Publication
34519870 | J:330615
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
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Publication
- | J:97
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
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Publication
- | J:98
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
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Publication
12221080 | J:80040
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
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Publication
15590698 | J:95920
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
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Publication
20554841 | J:171566
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
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Publication
11209059 | J:67045
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
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Publication
14578428 | J:86248
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
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Publication
12717441 | J:83482
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
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Publication
2300582 | J:10283
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
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Publication
- | J:92
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
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Publication
11973280 | J:75944
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
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Publication
11425898 | J:70081
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
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Publication
11023859 | J:64679
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
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Publication
31185200 | J:279271
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
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Publication
1063212 | J:5635
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
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Publication
8422502 | J:3753
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
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Publication
16691564 | J:111604
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
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Publication
28492243 | J:249581
 
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
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Publication
30275467 | J:267223
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
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Publication
21225654 | J:171536
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
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Publication
26988140 | J:251644
 
First Author: Kempfle JS
Year: 2016
Journal: Sci Rep
Title: Sox2 in the differentiation of cochlear progenitor cells.
Volume: 6
Pages: 23293
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Publication
31227770 | J:278634
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
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Publication
12485990 | J:80836
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
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Publication
- | J:13679
 
First Author: Wallace ME
Year: 1975
Journal: Mouse News Lett
Title: Warfarin resistance and a new gene for obesity.
Volume: 53
Pages: 20
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Publication
36689403 | J:332881
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
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Publication
29199954 | J:254987
   
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
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Publication
621381 | J:5918
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
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Publication
8690736 | J:34097
First Author: Hasson T
Year: 1996
Journal: J Biol Chem
Title: Vertebrate unconventional myosins.
Volume: 271
Issue: 28
Pages: 16431-4
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Publication
10320095 | J:54811
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
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Publication
12692478 | J:89965
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
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Publication
15078071 | J:91339
 
First Author: Takebayashi S
Year: 2004
Journal: Acta Otolaryngol Suppl
Title: Expression of beta-catenin in developing auditory epithelia of mice.
Issue: 551
Pages: 18-21
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Publication
16538679 | J:132058
First Author: Bermingham-McDonogh O
Year: 2006
Journal: J Comp Neurol
Title: Expression of Prox1 during mouse cochlear development.
Volume: 496
Issue: 2
Pages: 172-86
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Publication
20639393 | J:163278
First Author: Bahloul A
Year: 2010
Journal: Hum Mol Genet
Title: Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids.
Volume: 19
Issue: 18
Pages: 3557-65
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Publication
30410537 | J:310860
 
First Author: Liu S
Year: 2018
Journal: Neural Plast
Title: The Key Transcription Factor Expression in the Developing Vestibular and Auditory Sensory Organs: A Comprehensive Comparison of Spatial and Temporal Patterns.
Volume: 2018
Pages: 7513258
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Publication
34265170 | J:316158
First Author: Ramzan M
Year: 2021
Journal: Hum Mutat
Title: Variants of human CLDN9 cause mild to profound hearing loss.
Volume: 42
Issue: 10
Pages: 1321-1335
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Publication
27465826 | J:321243
First Author: Chen Y
Year: 2016
Journal: Front Med
Title: Spatiotemporal expression of Ezh2 in the developing mouse cochlear sensory epithelium.
Volume: 10
Issue: 3
Pages: 330-5
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Publication
35975307 | J:329558
First Author: Liu W
Year: 2022
Journal: J Histochem Cytochem
Title: Expression of Calbindin-D28K in the Developing and Adult Mouse Cochlea.
Volume: 70
Issue: 8
Pages: 583-596
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Publication
15905332 | J:98396
First Author: Longo-Guess CM
Year: 2005
Journal: Proc Natl Acad Sci U S A
Title: A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice.
Volume: 102
Issue: 22
Pages: 7894-9
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Publication
27162350 | J:232175
First Author: Diaz-Horta O
Year: 2016
Journal: Proc Natl Acad Sci U S A
Title: ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice.
Volume: 113
Issue: 21
Pages: 5993-8
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Publication
21165971 | J:186025
First Author: Verpy E
Year: 2011
Journal: J Comp Neurol
Title: Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane.
Volume: 519
Issue: 2
Pages: 194-210
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Publication
12833159 | J:86904
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
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Publication
11212352 | J:58855
First Author: Oliver TN
Year: 1999
Journal: Cell Mol Life Sci
Title: Tails of unconventional myosins.
Volume: 56
Issue: 3-4
Pages: 243-57
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Publication
10722873 | J:61347
First Author: Sellers JR
Year: 2000
Journal: Biochim Biophys Acta
Title: Myosins: a diverse superfamily.
Volume: 1496
Issue: 1
Pages: 3-22
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Publication
16219682 | J:102194
First Author: El-Amraoui A
Year: 2005
Journal: J Cell Sci
Title: Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells.
Volume: 118
Issue: Pt 20
Pages: 4593-603
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Publication
13853422 | J:15164
 
First Author: KOCHER W
Year: 1960
Journal: Z Vererbungsl
Title: [Studies on the genetics and pathology of the development of 8 labyrinth mutants (deaf-waltzer-shaker mutants) in the mouse (Mus musculus)].
Volume: 91
Pages: 114-40
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Publication
10224267 | J:54592
First Author: Rinchik EM
Year: 1999
Journal: Genetics
Title: N-ethyl-N-nitrosourea mutagenesis of a 6- to 11-cM subregion of the Fah-Hbb interval of mouse chromosome 7: Completed testing of 4557 gametes and deletion mapping and complementation analysis of 31 mutations.
Volume: 152
Issue: 1
Pages: 373-83
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Publication
28031293 | J:241430
First Author: Zou J
Year: 2017
Journal: Hum Mol Genet
Title: The roles of USH1 proteins and PDZ domain-containing USH proteins in USH2 complex integrity in cochlear hair cells.
Volume: 26
Issue: 3
Pages: 624-636
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Publication
18039969 | J:129203
First Author: Raft S
Year: 2007
Journal: Development
Title: Cross-regulation of Ngn1 and Math1 coordinates the production of neurons and sensory hair cells during inner ear development.
Volume: 134
Issue: 24
Pages: 4405-15
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Publication
21360794 | J:169673
First Author: Weston MD
Year: 2011
Journal: Dev Dyn
Title: MicroRNA-183 family expression in hair cell development and requirement of microRNAs for hair cell maintenance and survival.
Volume: 240
Issue: 4
Pages: 808-19
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Publication
26620972 | J:229323
First Author: Jansen F
Year: 2016
Journal: Hum Mol Genet
Title: Impact of the Usher syndrome on olfaction.
Volume: 25
Issue: 3
Pages: 524-33
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Publication
17663432 | J:132913
First Author: Cabraja M
Year: 2007
Journal: J Comp Neurol
Title: Vestibular ganglion neurons survive hair cell defects in jerker, shaker, and Varitint-waddler mutants and downregulate calretinin expression.
Volume: 504
Issue: 4
Pages: 418-26
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Publication
15702992 | J:105404
First Author: Bossi G
Year: 2005
Journal: Traffic
Title: Normal lytic granule secretion by cytotoxic T lymphocytes deficient in BLOC-1, -2 and -3 and myosins Va, VIIa and XV.
Volume: 6
Issue: 3
Pages: 243-51
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Publication
31085606 | J:277160
First Author: Sherrill HE
Year: 2019
Journal: J Neurosci
Title: Pou4f1 Defines a Subgroup of Type I Spiral Ganglion Neurons and Is Necessary for Normal Inner Hair Cell Presynaptic Ca2+ Signaling.
Volume: 39
Issue: 27
Pages: 5284-5298
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Publication
- | J:13533
 
First Author: Eicher EM
Year: 1972
Journal: Mouse News Lett
Title: Hypophosphatemia (Hyp); Chr 7 linkage.
Volume: 47
Pages: 36
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Publication
25149275 | J:316552
First Author: Radojevic V
Year: 2014
Journal: Cell Tissue Res
Title: Expression and localization of somatostatin receptor types 3, 4 and 5 in the wild-type, SSTR1 and SSTR1/SSTR2 knockout mouse cochlea.
Volume: 358
Issue: 3
Pages: 717-27
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Publication
34004180 | J:310063
 
First Author: Balendran V
Year: 2021
Journal: Dev Biol
Title: Chromatin remodeler CHD7 is critical for cochlear morphogenesis and neurosensory patterning.
Volume: 477
Pages: 11-21
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Publication
32665247 | J:294163
 
First Author: Ono K
Year: 2020
Journal: Development
Title: Retinoic acid synthesis and autoregulation mediate zonal patterning of vestibular organs and inner ear morphogenesis.
Volume: 147
Issue: 15
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Publication
22340499 | J:181471
First Author: Ahmed M
Year: 2012
Journal: Dev Cell
Title: Eya1-Six1 interaction is sufficient to induce hair cell fate in the cochlea by activating Atoh1 expression in cooperation with Sox2.
Volume: 22
Issue: 2
Pages: 377-90
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Publication
33015071 | J:299026
 
First Author: Kannan-Sundhari A
Year: 2020
Journal: Front Cell Dev Biol
Title: Bromodomain Protein BRD4 Is Essential for Hair Cell Function and Survival.
Volume: 8
Pages: 576654
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Publication
33046506 | J:301046
 
First Author: Ratzan EM
Year: 2020
Journal: Development
Title: Fgf8 genetic labeling reveals the early specification of vestibular hair cell type in mouse utricle.
Volume: 147
Issue: 22
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Publication
21798896 | J:175242
First Author: Togashi H
Year: 2011
Journal: Science
Title: Nectins establish a checkerboard-like cellular pattern in the auditory epithelium.
Volume: 333
Issue: 6046
Pages: 1144-7
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Publication
30850599 | J:273293
First Author: Du TT
Year: 2019
Journal: Nat Commun
Title: LMO7 deficiency reveals the significance of the cuticular plate for hearing function.
Volume: 10
Issue: 1
Pages: 1117
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Publication
35038200 | J:326361
First Author: Li S
Year: 2022
Journal: Dev Dyn
Title: Fate-mapping analysis of cochlear cells expressing Atoh1 mRNA via a new Atoh13*HA-P2A-Cre knockin mouse strain.
Volume: 251
Issue: 7
Pages: 1156-1174
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Publication
20332152 | J:158897
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
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Publication
32152201 | J:289982
First Author: Morell RJ
Year: 2020
Journal: J Neurosci
Title: Noncoding Microdeletion in Mouse Hgf Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyndromic Deafness DFNB39.
Volume: 40
Issue: 15
Pages: 2976-2992
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Publication
9735355 | J:43752
First Author: Xiang M
Year: 1998
Journal: Development
Title: Requirement for Brn-3c in maturation and survival, but not in fate determination of inner ear hair cells.
Volume: 125
Issue: 20
Pages: 3935-46
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Publication
20727948 | J:166789
First Author: Dong Y
Year: 2010
Journal: Neuroscience
Title: Phosphatase and tensin homolog deleted on chromosome 10 regulates sensory cell proliferation and differentiation of hair bundles in the mammalian cochlea.
Volume: 170
Issue: 4
Pages: 1304-13
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Publication
24481416 | J:206951
First Author: Sun C
Year: 2014
Journal: Neuroreport
Title: PTEN regulation of the proliferation and differentiation of auditory progenitors through the PTEN/PI3K/Akt-signaling pathway in mice.
Volume: 25
Issue: 3
Pages: 177-83
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Publication
15657400 | J:95877
First Author: Osterweil E
Year: 2005
Journal: J Cell Biol
Title: A role for myosin VI in postsynaptic structure and glutamate receptor endocytosis.
Volume: 168
Issue: 2
Pages: 329-38
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Publication
20503364 | J:160591
First Author: Liu Z
Year: 2010
Journal: Dev Dyn
Title: Dynamic expression pattern of Sonic hedgehog in developing cochlear spiral ganglion neurons.
Volume: 239
Issue: 6
Pages: 1674-83
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Publication
24191262 | J:206322
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
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Publication
31678344 | J:285587
 
First Author: Lu J
Year: 2019
Journal: Neuroscience
Title: Increased Type I and Decreased Type II Hair Cells after Deletion of Sox2 in the Developing Mouse Utricle.
Volume: 422
Pages: 146-160
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Publication
26092122 | J:225514
First Author: Ahmed M
Year: 2015
Journal: Dis Model Mech
Title: Auditory hair cell defects as potential cause for sensorineural deafness in Wolf-Hirschhorn syndrome.
Volume: 8
Issue: 9
Pages: 1027-35
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Publication
23684581 | J:200791
 
First Author: Wakaoka T
Year: 2013
Journal: Hear Res
Title: Tracing Sox10-expressing cells elucidates the dynamic development of the mouse inner ear.
Volume: 302
Pages: 17-25
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Publication
24718611 | J:215095
First Author: Mao Y
Year: 2014
Journal: PLoS One
Title: Targeted deletion of Sox10 by Wnt1-cre defects neuronal migration and projection in the mouse inner ear.
Volume: 9
Issue: 4
Pages: e94580
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Publication
21448975 | J:171621
First Author: Kopecky B
Year: 2011
Journal: Dev Dyn
Title: Conditional deletion of N-Myc disrupts neurosensory and non-sensory development of the ear.
Volume: 240
Issue: 6
Pages: 1373-90
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Publication
16410827 | J:115783
First Author: Kiernan AE
Year: 2006
Journal: PLoS Genet
Title: The Notch ligand JAG1 is required for sensory progenitor development in the mammalian inner ear.
Volume: 2
Issue: 1
Pages: e4
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Publication
34395423 | J:311142
 
First Author: Sun H
Year: 2021
Journal: Front Cell Dev Biol
Title: Gpr125 Marks Distinct Cochlear Cell Types and Is Dispensable for Cochlear Development and Hearing.
Volume: 9
Pages: 690955
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Publication
23172918 | J:189954
First Author: Bank LM
Year: 2012
Journal: Development
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