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Search results 1 to 100 out of 228 for Cdh23

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Category: Publication
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Type Details Score
Publication
15882574 | J:98268
First Author: Lagziel A
Year: 2005
Journal: Dev Biol
Title: Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development.
Volume: 280
Issue: 2
Pages: 295-306
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Publication
11138009 | J:66740
First Author: Bolz H
Year: 2001
Journal: Nat Genet
Title: Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Volume: 27
Issue: 1
Pages: 108-12
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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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Publication
33595068 | J:303657
     
First Author: Balan S
Year: 2021
Journal: Schizophr Bull
Title: Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia.
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Publication
19487694 | J:152735
First Author: Sengupta S
Year: 2009
Journal: J Biol Chem
Title: EHD4 and CDH23 are interacting partners in cochlear hair cells.
Volume: 284
Issue: 30
Pages: 20121-9
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Publication
11386759 | J:69985
First Author: Wilson SM
Year: 2001
Journal: Genomics
Title: Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice.
Volume: 74
Issue: 2
Pages: 228-33
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Publication
22138310 | J:183757
First Author: Kane KL
Year: 2012
Journal: Hear Res
Title: Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice.
Volume: 283
Issue: 1-2
Pages: 80-8
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Publication
- | J:97759
     
First Author: Harris BS
Year: 2005
Journal: MGI Direct Data Submission
Title: Waltzer 7 Jackson, a remutation of the Cdh23 gene
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Publication
23792079 | J:220660
 
First Author: Watson CJ
Year: 2013
Journal: Hear Res
Title: A new Atp2b2 deafwaddler allele, dfw(i5), interacts strongly with Cdh23 and other auditory modifiers.
Volume: 304
Pages: 41-8
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Publication
22326520 | J:183808
First Author: Liu S
Year: 2012
Journal: Gene
Title: A mutation in the cdh23 gene causes age-related hearing loss in Cdh23(nmf308/nmf308) mice.
Volume: 499
Issue: 2
Pages: 309-17
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Publication
20470874 | J:163035
First Author: Johnson KR
Year: 2010
Journal: Hear Res
Title: Separate and combined effects of Sod1 and Cdh23 mutations on age-related hearing loss and cochlear pathology in C57BL/6J mice.
Volume: 268
Issue: 1-2
Pages: 85-92
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Publication
21689626 | J:174130
First Author: Manji SS
Year: 2011
Journal: Am J Pathol
Title: An ENU-induced mutation of Cdh23 causes congenital hearing loss, but no vestibular dysfunction, in mice.
Volume: 179
Issue: 2
Pages: 903-14
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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
- | J:135835
     
First Author: Kane K
Year: 2008
Journal: MGI Direct Data Submission
Title: Jackson waltzer 11J, a new spontaneous mutation in the Cdh23 gene
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Publication
20644563 | J:174758
First Author: Han F
Year: 2012
Journal: Pharmacogenomics J
Title: A new mouse mutant of the Cdh23 gene with early-onset hearing loss facilitates evaluation of otoprotection drugs.
Volume: 12
Issue: 1
Pages: 30-44
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Publication
18662770 | J:139223
First Author: Johnson KR
Year: 2008
Journal: Genomics
Title: A locus on distal chromosome 11 (ahl8) and its interaction with Cdh23 ahl underlie the early onset, age-related hearing loss of DBA/2J mice.
Volume: 92
Issue: 4
Pages: 219-25
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Publication
18996172 | J:145900
First Author: Rzadzinska AK
Year: 2009
Journal: Neuroscience
Title: Presence of interstereocilial links in waltzer mutants suggests Cdh23 is not essential for tip link formation.
Volume: 158
Issue: 2
Pages: 365-8
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Publication
28287619 | J:241137
 
First Author: Johnson KR
Year: 2017
Journal: Sci Rep
Title: Effects of Cdh23 single nucleotide substitutions on age-related hearing loss in C57BL/6 and 129S1/Sv mice and comparisons with congenic strains.
Volume: 7
Pages: 44450
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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
32774357 | J:320540
 
First Author: Li N
Year: 2020
Journal: Neural Plast
Title: Alternative Splicing of Cdh23 Exon 68 Is Regulated by RBM24, RBM38, and PTBP1.
Volume: 2020
Pages: 8898811
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Publication
32425987 | J:308821
 
First Author: Zhang L
Year: 2020
Journal: Front Genet
Title: Targeted Next-Generation Sequencing Identified Novel Compound Heterozygous Variants in the CDH23 Gene Causing Usher Syndrome Type ID in a Chinese Patient.
Volume: 11
Pages: 422
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Publication
12910270 | J:86905
First Author: Noben-Trauth K
Year: 2003
Journal: Nat Genet
Title: Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss.
Volume: 35
Issue: 1
Pages: 21-3
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Publication
24172198 | J:250509
First Author: Miyasaka Y
Year: 2013
Journal: Exp Anim
Title: Compound heterozygosity of the functionally null Cdh23(v-ngt) and hypomorphic Cdh23(ahl) alleles leads to early-onset progressive hearing loss in mice.
Volume: 62
Issue: 4
Pages: 333-46
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Publication
- | J:267489
     
First Author: Prince L
Year: 2018
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for hersey.
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31247458 | J:280586
 
First Author: Burghard AL
Year: 2019
Journal: Neurobiol Aging
Title: Mice heterozygous for the Cdh23/Ahl1 mutation show age-related deficits in auditory temporal processing.
Volume: 81
Pages: 47-57
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15820310 | J:97534
First Author: Johnson KR
Year: 2005
Journal: Genomics
Title: The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC.
Volume: 85
Issue: 5
Pages: 582-90
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Publication
11750125 | J:73941
First Author: Di Palma F
Year: 2001
Journal: Gene
Title: Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23).
Volume: 281
Issue: 1-2
Pages: 31-41
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Publication
11090341 | J:87804
First Author: Bork JM
Year: 2001
Journal: Am J Hum Genet
Title: Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.
Volume: 68
Issue: 1
Pages: 26-37
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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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Publication
14759567 | J:87783
First Author: Keithley EM
Year: 2004
Journal: Hear Res
Title: Age-related hearing loss and the ahl locus in mice.
Volume: 188
Issue: 1-2
Pages: 21-8
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11335078 | J:69679
First Author: Davis RR
Year: 2001
Journal: Hear Res
Title: Genetic basis for susceptibility to noise-induced hearing loss in mice.
Volume: 155
Issue: 1-2
Pages: 82-90
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Publication
15276680 | J:117746
First Author: Vázquez AE
Year: 2004
Journal: Hear Res
Title: Evaluating cochlear function and the effects of noise exposure in the B6.CAST+Ahl mouse with distortion product otoacoustic emissions.
Volume: 194
Issue: 1-2
Pages: 87-96
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32327469 | J:289182
 
First Author: Rogalla MM
Year: 2020
Journal: eNeuro
Title: Aging But Not Age-Related Hearing Loss Dominates the Decrease of Parvalbumin Immunoreactivity in the Primary Auditory Cortex of Mice.
Volume: 7
Issue: 3
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10535453 | J:109893
First Author: Mathews CE
Year: 1999
Journal: Diabetes
Title: Resistance of ALR/Lt islets to free radical-mediated diabetogenic stress is inherited as a dominant trait.
Volume: 48
Issue: 11
Pages: 2189-96
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25852546 | J:242536
 
First Author: Murillo-Cuesta S
Year: 2015
Journal: Front Aging Neurosci
Title: Transforming growth factor β1 inhibition protects from noise-induced hearing loss.
Volume: 7
Pages: 32
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11138008 | J:66698
First Author: Di Palma F
Year: 2001
Journal: Nat Genet
Title: Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.
Volume: 27
Issue: 1
Pages: 103-7
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16281288 | J:174759
First Author: Yonezawa S
Year: 2006
Journal: Hum Mutat
Title: Fates of Cdh23/CDH23 with mutations affecting the cytoplasmic region.
Volume: 27
Issue: 1
Pages: 88-97
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26876963 | J:236297
First Author: Mianné J
Year: 2016
Journal: Genome Med
Title: Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair.
Volume: 8
Issue: 1
Pages: 16
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Publication
27255811 | J:234998
 
First Author: Mock BE
Year: 2016
Journal: Neurobiol Aging
Title: Differential effects of Cdh23(753A) on auditory and vestibular functional aging in C57BL/6J mice.
Volume: 43
Pages: 13-22
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35473764 | J:324694
 
First Author: Si Y
Year: 2022
Journal: eNeuro
Title: High-Frequency Hearing Is Required to Compute a Topographic Map of Auditory Space in the Mouse Superior Colliculus.
Volume: 9
Issue: 3
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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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16579977 | J:110459
First Author: Johnson KR
Year: 2006
Journal: Brain Res
Title: Strain background effects and genetic modifiers of hearing in mice.
Volume: 1091
Issue: 1
Pages: 79-88
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33318051 | J:303596
     
First Author: Lewis MA
Year: 2020
Journal: Dis Model Mech
Title: Hearing impairment due to Mir183/96/182 mutations suggests both loss and gain of function effects.
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20628639 | J:163117
First Author: Noben-Trauth K
Year: 2010
Journal: PLoS One
Title: Phenotype and genetics of progressive sensorineural hearing loss (Snhl1) in the LXS set of recombinant inbred strains of mice.
Volume: 5
Issue: 7
Pages: e11459
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33222382 | J:299272
First Author: Bermúdez-Muñoz JM
Year: 2020
Journal: Aging Cell
Title: G6PD overexpression protects from oxidative stress and age-related hearing loss.
Volume: 19
Issue: 12
Pages: e13275
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11175788 | J:67312
First Author: Johnson KR
Year: 2001
Journal: Nat Genet
Title: A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice.
Volume: 27
Issue: 2
Pages: 191-4
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Publication
18280008 | J:139222
First Author: Zheng QY
Year: 2009
Journal: Neurobiol Aging
Title: A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice.
Volume: 30
Issue: 10
Pages: 1693-705
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Publication
18971469 | J:143256
First Author: Xu Z
Year: 2008
Journal: J Neurosci
Title: MAGI-1, a candidate stereociliary scaffolding protein, associates with the tip-link component cadherin 23.
Volume: 28
Issue: 44
Pages: 11269-76
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33997712 | J:310082
First Author: Liu O
Year: 2021
Journal: iScience
Title: Adipose-mesenchymal stromal cells suppress experimental Sjögren syndrome by IL-33-driven expansion of ST2+ regulatory T cells.
Volume: 24
Issue: 5
Pages: 102446
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Publication
28818524 | J:249779
 
First Author: Zhang C
Year: 2017
Journal: Neuroscience
Title: Loss of sestrin 2 potentiates the early onset of age-related sensory cell degeneration in the cochlea.
Volume: 361
Pages: 179-191
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22238076 | J:179911
First Author: Zilberstein Y
Year: 2012
Journal: J Neurosci
Title: Inner hair cells are not required for survival of spiral ganglion neurons in the adult cochlea.
Volume: 32
Issue: 2
Pages: 405-10
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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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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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26936824 | J:235883
First Author: Miyasaka Y
Year: 2016
Journal: Hum Mol Genet
Title: Heterozygous mutation of Ush1g/Sans in mice causes early-onset progressive hearing loss, which is recovered by reconstituting the strain-specific mutation in Cdh23.
Volume: 25
Issue: 10
Pages: 2045-2059
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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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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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17050716 | J:113401
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
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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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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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17360538 | J:118927
First Author: Liu X
Year: 2007
Journal: Proc Natl Acad Sci U S A
Title: Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells.
Volume: 104
Issue: 11
Pages: 4413-8
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9325047 | J:38429
First Author: Noben-Trauth K
Year: 1997
Journal: Genomics
Title: mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw).
Volume: 44
Issue: 3
Pages: 266-72
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11423214 | J:70964
First Author: Zheng QY
Year: 2001
Journal: Hear Res
Title: Hearing loss associated with the modifier of deaf waddler (mdfw) locus corresponds with age-related hearing loss in 12 inbred strains of mice.
Volume: 154
Issue: 1-2
Pages: 45-53
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21875659 | J:220430
First Author: Hurd EA
Year: 2011
Journal: Hear Res
Title: Mature middle and inner ears express Chd7 and exhibit distinctive pathologies in a mouse model of CHARGE syndrome.
Volume: 282
Issue: 1-2
Pages: 184-95
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Publication
21423608 | J:171701
First Author: Manji SS
Year: 2011
Journal: PLoS One
Title: A mutation in synaptojanin 2 causes progressive hearing loss in the ENU-mutagenised mouse strain Mozart.
Volume: 6
Issue: 3
Pages: e17607
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Publication
28345280 | J:267808
First Author: Wang Q
Year: 2017
Journal: J Neurosci Res
Title: Otoprotective effects of mouse nerve growth factor in DBA/2J mice with early-onset progressive hearing loss.
Volume: 95
Issue: 10
Pages: 1937-1950
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24221507 | J:285863
First Author: Tanimoto N
Year: 2014
Journal: Doc Ophthalmol
Title: Auditory event-related signals in mouse ERG recordings.
Volume: 128
Issue: 1
Pages: 25-32
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25762674 | J:219993
First Author: Nagtegaal AP
Year: 2015
Journal: J Neurosci
Title: Cockayne syndrome group B (Csb) and group a (Csa) deficiencies predispose to hearing loss and cochlear hair cell degeneration in mice.
Volume: 35
Issue: 10
Pages: 4280-6
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23658152 | J:197137
First Author: Perrin BJ
Year: 2013
Journal: J Neurosci
Title: β-Actin and fascin-2 cooperate to maintain stereocilia length.
Volume: 33
Issue: 19
Pages: 8114-21
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21211561 | J:186964
First Author: Fetoni AR
Year: 2011
Journal: Exp Gerontol
Title: Pathogenesis of presbycusis in animal models: a review.
Volume: 46
Issue: 6
Pages: 413-25
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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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20505086 | J:160824
First Author: Zheng L
Year: 2010
Journal: J Neurosci
Title: Targeting of the hair cell proteins cadherin 23, harmonin, myosin XVa, espin, and prestin in an epithelial cell model.
Volume: 30
Issue: 21
Pages: 7187-201
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19756182 | J:263485
 
First Author: Lagziel A
Year: 2009
Journal: Mol Vis
Title: Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1D.
Volume: 15
Pages: 1843-57
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9447922 | J:44966
First Author: Johnson KR
Year: 1997
Journal: Hear Res
Title: A major gene affecting age-related hearing loss in C57BL/6J mice.
Volume: 114
Issue: 1-2
Pages: 83-92
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32694816 | J:269980
First Author: Enríquez JA
Year: 2019
Journal: Nat Metab
Title: Mind your mouse strain.
Volume: 1
Issue: 1
Pages: 5-7
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Publication
22952717 | J:191663
First Author: Bosco A
Year: 2012
Journal: PLoS One
Title: Early reduction of microglia activation by irradiation in a model of chronic glaucoma.
Volume: 7
Issue: 8
Pages: e43602
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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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20976199 | J:167543
First Author: Perrin BJ
Year: 2010
Journal: PLoS Genet
Title: β-actin and γ-actin are each dispensable for auditory hair cell development but required for Stereocilia maintenance.
Volume: 6
Issue: 10
Pages: e1001158
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35100259 | J:326721
First Author: Newton S
Year: 2022
Journal: PLoS Genet
Title: Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing.
Volume: 18
Issue: 1
Pages: e1009937
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- | J:29159
First Author: Lutz CM
Year: 1995
Journal: Mouse Genome
Title: Remutation at the waltzer locus
Volume: 93
Issue: 3
Pages: 862
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23384607 | J:201372
 
First Author: Han F
Year: 2013
Journal: Neuroscience
Title: Otoprotective effects of erythropoietin on Cdh23erl/erl mice.
Volume: 237
Pages: 1-6
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Publication
27882946 | J:250092
First Author: Hu J
Year: 2016
Journal: Cell Death Dis
Title: ER stress inhibitor attenuates hearing loss and hair cell death in Cdh23erl/erl mutant mice.
Volume: 7
Issue: 11
Pages: e2485
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Publication
26748055 | J:231160
 
First Author: Hu J
Year: 2016
Journal: Neuroscience
Title: Tauroursodeoxycholic acid prevents hearing loss and hair cell death in Cdh23(erl/erl) mice.
Volume: 316
Pages: 311-20
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Publication
23359017 | J:195927
First Author: Vu AA
Year: 2013
Journal: PLoS One
Title: Integrity and regeneration of mechanotransduction machinery regulate aminoglycoside entry and sensory cell death.
Volume: 8
Issue: 1
Pages: e54794
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Publication
- | J:30784
       
First Author: Keeler CE
Year: 1931
Title: The Laboratory Mouse Its Origin, Heredity, and Culture
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11322776 | J:69028
First Author: Wada T
Year: 2001
Journal: Biochem Biophys Res Commun
Title: A point mutation in a cadherin gene, Cdh23, causes deafness in a novel mutant, Waltzer mouse niigata.
Volume: 283
Issue: 1
Pages: 113-7
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Publication
- | J:49035
     
First Author: Pelletier KM
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