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Search results 1 to 100 out of 131 for Pcdh15

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Category: Publication
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Type Details Score
Publication
30057206 | J:328653
First Author: Dionne G
Year: 2018
Journal: Neuron
Title: Mechanotransduction by PCDH15 Relies on a Novel cis-Dimeric Architecture.
Volume: 99
Issue: 3
Pages: 480-492.e5
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Publication
- | J:198553
     
First Author: Beutler B
Year: 2013
Journal: MGI Direct Data Submission
Title: Direct data submission for a Pcdh15 allele
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Publication
16799054 | J:112247
First Author: Haywood-Watson RJ 2nd
Year: 2006
Journal: Invest Ophthalmol Vis Sci
Title: Ames Waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts.
Volume: 47
Issue: 7
Pages: 3074-84
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Publication
19816713 | J:320724
First Author: Huertas-Vazquez A
Year: 2010
Journal: Hum Genet
Title: A nonsynonymous SNP within PCDH15 is associated with lipid traits in familial combined hyperlipidemia.
Volume: 127
Issue: 1
Pages: 83-9
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Publication
- | J:209275
     
First Author: Petit C
Year: 2014
Journal: MGI Direct Data Submission
Title: Direct Data Submission for Pcdh15 floxed allele from Ugds
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Publication
11487575 | J:71203
First Author: Alagramam KN
Year: 2001
Journal: Hum Mol Genet
Title: Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F.
Volume: 10
Issue: 16
Pages: 1709-18
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Publication
11429292 | J:70588
First Author: Murcia CL
Year: 2001
Journal: Mech Dev
Title: Expression of Pcdh15 in the inner ear, nervous system and various epithelia of the developing embryo.
Volume: 105
Issue: 1-2
Pages: 163-6
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Publication
21427143 | J:171627
First Author: Webb SW
Year: 2011
Journal: Development
Title: Regulation of PCDH15 function in mechanosensory hair cells by alternative splicing of the cytoplasmic domain.
Volume: 138
Issue: 8
Pages: 1607-17
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Publication
23035094 | J:190930
First Author: Zallocchi M
Year: 2012
Journal: J Neurosci
Title: Regulated vesicular trafficking of specific PCDH15 and VLGR1 variants in auditory hair cells.
Volume: 32
Issue: 40
Pages: 13841-59
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Publication
- | J:283661
     
First Author: Pepermans E
Year: 2020
Journal: MGI Direct Data Submission
Title: Direct data submission of two Pcdh15 floxed alleles from Unite de Genetique des Deficits Sensoriels
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Publication
14570705 | J:124774
First Author: Ahmed ZM
Year: 2003
Journal: Hum Mol Genet
Title: PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23.
Volume: 12
Issue: 24
Pages: 3215-23
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Publication
10978835 | J:66637
First Author: Alagramam KN
Year: 2000
Journal: Hear Res
Title: Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer.
Volume: 148
Issue: 1-2
Pages: 181-91
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Publication
15952048 | J:148677
First Author: Alagramam KN
Year: 2005
Journal: J Assoc Res Otolaryngol
Title: Characterization of vestibular dysfunction in the mouse model for Usher syndrome 1F.
Volume: 6
Issue: 2
Pages: 106-18
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Publication
12939319 | J:85211
First Author: Ball SL
Year: 2003
Journal: Invest Ophthalmol Vis Sci
Title: Assessment of retinal structure and function in Ames waltzer mice.
Volume: 44
Issue: 9
Pages: 3986-92
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16408167 | J:148675
First Author: Pawlowski KS
Year: 2006
Journal: J Assoc Res Otolaryngol
Title: Progression of inner ear pathology in Ames waltzer mice and the role of protocadherin 15 in hair cell development.
Volume: 7
Issue: 2
Pages: 83-94
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Publication
11138007 | J:66738
First Author: Alagramam KN
Year: 2001
Journal: Nat Genet
Title: The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene.
Volume: 27
Issue: 1
Pages: 99-102
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Publication
23467356 | J:196281
First Author: Geng R
Year: 2013
Journal: J Neurosci
Title: Noddy, a mouse harboring a missense mutation in protocadherin-15, reveals the impact of disrupting a critical interaction site between tip-link cadherins in inner ear hair cells.
Volume: 33
Issue: 10
Pages: 4395-404
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15811708 | J:97048
First Author: Washington JL 3rd
Year: 2005
Journal: Hear Res
Title: Characterization of a new allele of Ames waltzer generated by ENU mutagenesis.
Volume: 202
Issue: 1-2
Pages: 161-9
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Publication
24940003 | J:244761
First Author: Pepermans E
Year: 2014
Journal: EMBO Mol Med
Title: The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells.
Volume: 6
Issue: 7
Pages: 984-92
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Publication
15537665 | J:95655
First Author: Zheng QY
Year: 2005
Journal: Hum Mol Genet
Title: Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans.
Volume: 14
Issue: 1
Pages: 103-11
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25114259 | J:214830
First Author: Maeda R
Year: 2014
Journal: Proc Natl Acad Sci U S A
Title: Tip-link protein protocadherin 15 interacts with transmembrane channel-like proteins TMC1 and TMC2.
Volume: 111
Issue: 35
Pages: 12907-12
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Publication
- | J:28688
 
First Author: Cook S
Year: 1993
Journal: Mouse Genome
Title: Re-mutation to Ames waltzer
Volume: 91
Pages: 554
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Publication
- | J:140625
     
First Author: Blasius AL
Year: 2008
Journal: MGI Direct Data Submission
Title: Record for "squirm" updated August 12, 2008
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Publication
23135401 | J:192825
First Author: Sotomayor M
Year: 2012
Journal: Nature
Title: Structure of a force-conveying cadherin bond essential for inner-ear mechanotransduction.
Volume: 492
Issue: 7427
Pages: 128-32
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20097680 | J:158344
First Author: Chance MR
Year: 2010
Journal: Hum Mol Genet
Title: Proteomics, bioinformatics and targeted gene expression analysis reveals up-regulation of cochlin and identifies other potential biomarkers in the mouse model for deafness in Usher syndrome type 1F.
Volume: 19
Issue: 8
Pages: 1515-27
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11124469 | J:106625
First Author: Raphael Y
Year: 2001
Journal: Hear Res
Title: Severe vestibular and auditory impairment in three alleles of Ames waltzer (av) mice.
Volume: 151
Issue: 1-2
Pages: 237-249
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10430593 | J:56493
First Author: Alagramam KN
Year: 1999
Journal: Genetics
Title: A new mouse insertional mutation that causes sensorineural deafness and vestibular defects.
Volume: 152
Issue: 4
Pages: 1691-9
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35830793 | J:342094
First Author: Liu L
Year: 2022
Journal: Cell Rep
Title: Template-independent genome editing in the Pcdh15(av-3j) mouse, a model of human DFNB23 nonsyndromic deafness.
Volume: 40
Issue: 2
Pages: 111061
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Publication
12782354 | J:84779
First Author: Hampton LL
Year: 2003
Journal: Hear Res
Title: A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15.
Volume: 180
Issue: 1-2
Pages: 67-75
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34751129 | J:342718
   
First Author: Sethna S
Year: 2021
Journal: Elife
Title: Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndrome.
Volume: 10
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16887306 | J:111661
First Author: Zheng QY
Year: 2006
Journal: Hear Res
Title: A new spontaneous mutation in the mouse protocadherin 15 gene.
Volume: 219
Issue: 1-2
Pages: 110-20
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Publication
24405699 | J:220571
First Author: Ye R
Year: 2014
Journal: Genes Brain Behav
Title: Quantitative trait loci mapping and gene network analysis implicate protocadherin-15 as a determinant of brain serotonin transporter expression.
Volume: 13
Issue: 3
Pages: 261-75
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20498078 | J:245265
First Author: Elledge HM
Year: 2010
Journal: Proc Natl Acad Sci U S A
Title: Structure of the N terminus of cadherin 23 reveals a new adhesion mechanism for a subset of cadherin superfamily members.
Volume: 107
Issue: 23
Pages: 10708-12
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35637313 | J:325092
First Author: Zhen Y
Year: 2022
Journal: Commun Biol
Title: Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways.
Volume: 5
Issue: 1
Pages: 511
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24044941 | J:220658
 
First Author: Torres AA
Year: 2013
Journal: Mutat Res
Title: The circling mutant Pcdh15roda is a new mouse model for hearing loss.
Volume: 751-752
Pages: 29-35
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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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29069081 | J:248825
First Author: Mahendrasingam S
Year: 2017
Journal: PLoS One
Title: Spatiotemporal changes in the distribution of LHFPL5 in mice cochlear hair bundles during development and in the absence of PCDH15.
Volume: 12
Issue: 10
Pages: e0185285
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23217710 | J:193334
First Author: Xiong W
Year: 2012
Journal: Cell
Title: TMHS is an integral component of the mechanotransduction machinery of cochlear hair cells.
Volume: 151
Issue: 6
Pages: 1283-95
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17805295 | J:125331
First Author: Kazmierczak P
Year: 2007
Journal: Nature
Title: Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells.
Volume: 449
Issue: 7158
Pages: 87-91
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21532990 | J:172400
First Author: Alagramam KN
Year: 2011
Journal: PLoS One
Title: Mutations in protocadherin 15 and cadherin 23 affect tip links and mechanotransduction in mammalian sensory hair cells.
Volume: 6
Issue: 4
Pages: e19183
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22363448 | J:219988
First Author: Zallocchi M
Year: 2012
Journal: PLoS One
Title: Role for a novel Usher protein complex in hair cell synaptic maturation.
Volume: 7
Issue: 2
Pages: e30573
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38806495 | J:348850
First Author: Mori D
Year: 2024
Journal: Transl Psychiatry
Title: Mice with deficiency in Pcdh15, a gene associated with bipolar disorders, exhibit significantly elevated diurnal amplitudes of locomotion and body temperature.
Volume: 14
Issue: 1
Pages: 216
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33009420 | J:299425
First Author: Michel V
Year: 2020
Journal: Sci Rep
Title: Interaction of protocadherin-15 with the scaffold protein whirlin supports its anchoring of hair-bundle lateral links in cochlear hair cells.
Volume: 10
Issue: 1
Pages: 16430
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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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30061390 | J:266273
First Author: Honda A
Year: 2018
Journal: Proc Natl Acad Sci U S A
Title: FGFR1-mediated protocadherin-15 loading mediates cargo specificity during intraflagellar transport in inner ear hair-cell kinocilia.
Volume: 115
Issue: 33
Pages: 8388-8393
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15928608 | J:99757
 
First Author: Reiners J
Year: 2005
Journal: Mol Vis
Title: Photoreceptor expression of the Usher syndrome type 1 protein protocadherin 15 (USH1F) and its interaction with the scaffold protein harmonin (USH1C).
Volume: 11
Pages: 347-55
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23144817 | J:195357
First Author: Roeseler DA
Year: 2012
Journal: PLoS One
Title: Elongation factor 1 alpha1 and genes associated with Usher syndromes are downstream targets of GBX2.
Volume: 7
Issue: 11
Pages: e47366
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22318628 | J:182748
First Author: Chacon-Heszele MF
Year: 2012
Journal: Development
Title: Regulation of cochlear convergent extension by the vertebrate planar cell polarity pathway is dependent on p120-catenin.
Volume: 139
Issue: 5
Pages: 968-78
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37011103 | J:346281
First Author: Krey JF
Year: 2023
Journal: PLoS Biol
Title: Control of stereocilia length during development of hair bundles.
Volume: 21
Issue: 4
Pages: e3001964
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5093631 | J:5225
First Author: Osako S
Year: 1971
Journal: Acta Otolaryngol
Title: Electron microscopic studies of capillary permeability in normal and ames waltzer deaf mice.
Volume: 71
Issue: 5
Pages: 365-76
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Publication
- | J:14990
 
First Author: Schaible RH
Year: 1956
Journal: Mouse News Lett
Title: av
Volume: 15
Pages: 29
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- | J:81272
     
First Author: Gagnon LH
Year: 2003
Journal: MGI Direct Data Submission
Title: A new allele of protocadherin 15 (Pcdh15) named Ames waltzer 4 Jackson. Mouse Mutant Resources Web Site, The Jackson Laboratory, Bar Harbor, Maine
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- | J:203622
     
First Author: Daniel C
Year: 2014
Journal: MGI Direct Data Submission
Title: Direct data submission for mcduck
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Publication
- | J:236676
     
First Author: Ludwig S
Year: 2016
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for sphere
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Publication
- | J:255213
     
First Author: Prince L
Year: 2018
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for tortilla
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35962067 | J:345076
First Author: Ballesteros A
Year: 2022
Journal: Sci Rep
Title: Selective binding and transport of protocadherin 15 isoforms by stereocilia unconventional myosins in a heterologous expression system.
Volume: 12
Issue: 1
Pages: 13764
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Publication
- | J:193
 
First Author: Schaible RH
Year: 1961
Journal: Mouse News Lett
Title: Ames waltzer, av
Volume: 24
Pages: 38
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Publication
16235133 | J:116914
First Author: Jones SM
Year: 2005
Journal: J Assoc Res Otolaryngol
Title: A quantitative survey of gravity receptor function in mutant mouse strains.
Volume: 6
Issue: 4
Pages: 297-310
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19057657 | J:142695
 
First Author: Ahmed ZM
Year: 2008
Journal: Mol Vis
Title: Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration.
Volume: 14
Pages: 2227-36
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11532347 | J:111611
First Author: Benito AI
Year: 2001
Journal: Exp Hematol
Title: Absence of major histocompatibility class II expression does not impair hematopoiesis in mice.
Volume: 29
Issue: 9
Pages: 1070-5
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19270079 | J:147149
First Author: Schwander M
Year: 2009
Journal: Proc Natl Acad Sci U S A
Title: A mouse model for nonsyndromic deafness (DFNB12) links hearing loss to defects in tip links of mechanosensory hair cells.
Volume: 106
Issue: 13
Pages: 5252-7
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- | J:13458
 
First Author: Russell ES
Year: 1966
Journal: Mouse News Lett
Title: Linkage tests, dy and av.
Volume: 35
Pages: 32
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30078710 | J:272676
First Author: Sun S
Year: 2018
Journal: Cell
Title: Hair Cell Mechanotransduction Regulates Spontaneous Activity and Spiral Ganglion Subtype Specification in the Auditory System.
Volume: 174
Issue: 5
Pages: 1247-1263.e15
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16426780 | J:105889
First Author: Drayton M
Year: 2006
Journal: Hear Res
Title: Mapping quantitative trait loci for hearing loss in Black Swiss mice.
Volume: 212
Issue: 1-2
Pages: 128-39
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Publication
16301216 | J:106804
First Author: Reiners J
Year: 2005
Journal: Hum Mol Genet
Title: Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2.
Volume: 14
Issue: 24
Pages: 3933-43
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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
- | J:78134
     
First Author: JAX Neuroscience Mutagenesis Facility
Year: 2002
Journal: MGI Direct Data Submission
Title: Heritable mouse mutants from JAX NMF ENU Mutagenesis Program
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Publication
16972005 | J:227974
First Author: Massironi SM
Year: 2006
Journal: Braz J Med Biol Res
Title: Inducing mutations in the mouse genome with the chemical mutagen ethylnitrosourea.
Volume: 39
Issue: 9
Pages: 1217-26
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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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28504928 | J:249939
   
First Author: Cunningham CL
Year: 2017
Journal: Elife
Title: The murine catecholamine methyltransferase mTOMT is essential for mechanotransduction by cochlear hair cells.
Volume: 6
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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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16962269 | J:113021
First Author: Calderon A
Year: 2006
Journal: Hear Res
Title: Cochlear developmental defect and background-dependent hearing thresholds in the Jackson circler (jc) mutant mouse.
Volume: 221
Issue: 1-2
Pages: 44-58
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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
35044843 | J:334959
First Author: Halford J
Year: 2022
Journal: Mol Biol Cell
Title: Ca2+ entry through mechanotransduction channels localizes BAIAP2L2 to stereocilia tips.
Volume: 33
Issue: 4
Pages: br6
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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
38228630 | J:349395
First Author: Lee JH
Year: 2024
Journal: Nat Commun
Title: The Piezo channel is a mechano-sensitive complex component in the mammalian inner ear hair cell.
Volume: 15
Issue: 1
Pages: 526
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Publication
15590703 | J:95929
First Author: Adato A
Year: 2005
Journal: Hum Mol Genet
Title: Interactions in the network of Usher syndrome type 1 proteins.
Volume: 14
Issue: 3
Pages: 347-56
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Publication
31776257 | J:282794
First Author: Avan P
Year: 2019
Journal: Proc Natl Acad Sci U S A
Title: Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane.
Volume: 116
Issue: 51
Pages: 25948-25957
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15572405 | J:94444
First Author: Gibbs D
Year: 2004
Journal: J Cell Sci
Title: Role of myosin VIIa and Rab27a in the motility and localization of RPE melanosomes.
Volume: 117
Issue: Pt 26
Pages: 6473-83
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Publication
16545802 | J:116295
First Author: Reiners J
Year: 2006
Journal: Exp Eye Res
Title: Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease.
Volume: 83
Issue: 1
Pages: 97-119
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Publication
9653653 | J:45743
First Author: Zobeley E
Year: 1998
Journal: Genomics
Title: Fine genetic and comparative mapping of the deafness mutation Ames waltzer on mouse chromosome 10.
Volume: 50
Issue: 2
Pages: 260-6
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Publication
28705869 | J:244775
First Author: Libé-Philippot B
Year: 2017
Journal: Proc Natl Acad Sci U S A
Title: Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction.
Volume: 114
Issue: 30
Pages: 7765-7774
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Publication
35296311 | J:327181
First Author: Lewis MA
Year: 2022
Journal: BMC Biol
Title: Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme.
Volume: 20
Issue: 1
Pages: 67
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Publication
16897347 | J:111682
First Author: Mashimo T
Year: 2006
Journal: Mamm Genome
Title: Two quantitative trait loci affecting progressive hearing loss in 101/H mice.
Volume: 17
Issue: 8
Pages: 841-50
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Publication
19339464 | J:151359
First Author: Lelli A
Year: 2009
Journal: J Neurophysiol
Title: Tonotopic gradient in the developmental acquisition of sensory transduction in outer hair cells of the mouse cochlea.
Volume: 101
Issue: 6
Pages: 2961-73
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Publication
20058854 | J:219989
First Author: Zallocchi M
Year: 2010
Journal: Biochemistry
Title: Biochemical characterization of native Usher protein complexes from a vesicular subfraction of tracheal epithelial cells.
Volume: 49
Issue: 6
Pages: 1236-47
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Publication
26754646 | J:230827
First Author: Lelli A
Year: 2016
Journal: J Cell Biol
Title: Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth.
Volume: 212
Issue: 2
Pages: 231-44
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Title: CIB2 interacts with TMC1 and TMC2 and is essential for mechanotransduction in auditory hair cells.
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First Author: Mouse Genome Informatics Scientific Curators
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Title: Gene Ontology Annotation by the MGI Curatorial Staff
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First Author: Mouse Genome Informatics and the International Mouse Phenotyping Consortium (IMPC)
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Title: Obtaining and Loading Phenotype Annotations from the International Mouse Phenotyping Consortium (IMPC) Database
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First Author: The Gene Ontology Consortium
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Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-rat orthologs
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First Author: UniProt-GOA
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Title: Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
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