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Search results 1 to 93 out of 93 for Ush1c

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Category: Publication
Type Details Score
Publication
First Author: Johnson KR
Year: 2003
Journal: Hum Mol Genet
Title: Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene.
Volume: 12
Issue: 23
Pages: 3075-86
Publication  
First Author: Tian C
Year: 2010
Journal: Brain Res
Title: Ush1c gene expression levels in the ear and eye suggest different roles for Ush1c in neurosensory organs in a new Ush1c knockout mouse.
Volume: 1328
Pages: 57-70
Publication
First Author: Lentz JJ
Year: 2010
Journal: Dev Neurobiol
Title: Deafness and retinal degeneration in a novel USH1C knock-in mouse model.
Volume: 70
Issue: 4
Pages: 253-67
Publication
First Author: Goldmann T
Year: 2010
Journal: Invest Ophthalmol Vis Sci
Title: Beneficial read-through of a USH1C nonsense mutation by designed aminoglycoside NB30 in the retina.
Volume: 51
Issue: 12
Pages: 6671-80
Publication
First Author: Weil D
Year: 2003
Journal: Hum Mol Genet
Title: Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin.
Volume: 12
Issue: 5
Pages: 463-71
Publication      
First Author: Kane KL
Year: 2009
Journal: MGI Direct Data Submission
Title: A new spontaneous mutation in the Ush1c gene named deaf circler 3 Jackson
Publication      
First Author: Gray SJ
Year: 2019
Journal: MGI Direct Data Submission
Title: The deaf circler 4 Jackson spontaneous mutation
Publication
First Author: Williams DS
Year: 2009
Journal: Invest Ophthalmol Vis Sci
Title: Harmonin in the murine retina and the retinal phenotypes of Ush1c-mutant mice and human USH1C.
Volume: 50
Issue: 8
Pages: 3881-9
Publication
First Author: Johnston AM
Year: 2004
Journal: Genes Cells
Title: Harp (harmonin-interacting, ankyrin repeat-containing protein), a novel protein that interacts with harmonin in epithelial tissues.
Volume: 9
Issue: 10
Pages: 967-82
Publication
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
Publication  
First Author: Donaldson TN
Year: 2018
Journal: Behav Brain Res
Title: Antisense oligonucleotide therapy rescues disruptions in organization of exploratory movements associated with Usher syndrome type 1C in mice.
Volume: 338
Pages: 76-87
Publication
First Author: Lentz JJ
Year: 2013
Journal: Nat Med
Title: Rescue of hearing and vestibular function by antisense oligonucleotides in a mouse model of human deafness.
Volume: 19
Issue: 3
Pages: 345-50
Publication
First Author: Vijayakumar S
Year: 2017
Journal: Hum Mol Genet
Title: Rescue of peripheral vestibular function in Usher syndrome mice using a splice-switching antisense oligonucleotide.
Volume: 26
Issue: 18
Pages: 3482-3494
Publication
First Author: Lentz J
Year: 2007
Journal: Mutat Res
Title: Ush1c216A knock-in mouse survives Katrina.
Volume: 616
Issue: 1-2
Pages: 139-44
Publication
First Author: Grillet N
Year: 2009
Journal: Neuron
Title: Harmonin mutations cause mechanotransduction defects in cochlear hair cells.
Volume: 62
Issue: 3
Pages: 375-87
Publication
First Author: Schneider E
Year: 2009
Journal: Hum Mol Genet
Title: Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment.
Volume: 18
Issue: 4
Pages: 655-66
Publication
First Author: Gregory FD
Year: 2011
Journal: Nat Neurosci
Title: Harmonin inhibits presynaptic Cav1.3 Ca²⁺ channels in mouse inner hair cells.
Volume: 14
Issue: 9
Pages: 1109-11
Publication
First Author: Gregory FD
Year: 2013
Journal: J Physiol
Title: Harmonin enhances voltage-dependent facilitation of Cav1.3 channels and synchronous exocytosis in mouse inner hair cells.
Volume: 591
Issue: 13
Pages: 3253-69
Publication
First Author: Caberlotto E
Year: 2011
Journal: Proc Natl Acad Sci U S A
Title: Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia.
Volume: 108
Issue: 14
Pages: 5825-30
Publication
First Author: Zheng QY
Year: 2012
Journal: Hum Mol Genet
Title: Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes.
Volume: 21
Issue: 11
Pages: 2588-98
Publication  
First Author: 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
Publication
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
Publication
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
Publication  
First Author: Cosgrove D
Year: 2014
Journal: Int J Biochem Cell Biol
Title: Usher protein functions in hair cells and photoreceptors.
Volume: 46
Pages: 80-9
Publication
First Author: Crawley SW
Year: 2014
Journal: Cell
Title: Intestinal brush border assembly driven by protocadherin-based intermicrovillar adhesion.
Volume: 157
Issue: 2
Pages: 433-446
Publication
First Author: Yan D
Year: 2006
Journal: J Mol Biol
Title: An isoform of GTPase regulator DOCK4 localizes to the stereocilia in the inner ear and binds to harmonin (USH1C).
Volume: 357
Issue: 3
Pages: 755-64
Publication
First Author: Pompeia C
Year: 2004
Journal: Genomics
Title: Gene expression profile of the mouse organ of Corti at the onset of hearing.
Volume: 83
Issue: 6
Pages: 1000-11
Publication
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
Publication
First Author: Wang L
Year: 2020
Journal: Nucleic Acids Res
Title: Fetal antisense oligonucleotide therapy for congenital deafness and vestibular dysfunction.
Volume: 48
Issue: 9
Pages: 5065-5080
Publication
First Author: Trouillet A
Year: 2018
Journal: Sci Rep
Title: Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments.
Volume: 8
Issue: 1
Pages: 1968
Publication
First Author: Verpy E
Year: 2008
Journal: Nature
Title: Stereocilin-deficient mice reveal the origin of cochlear waveform distortions.
Volume: 456
Issue: 7219
Pages: 255-8
Publication
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
Publication
First Author: Adato A
Year: 2005
Journal: Hum Mol Genet
Title: Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells.
Volume: 14
Issue: 24
Pages: 3921-32
Publication
First Author: Senften M
Year: 2006
Journal: J Neurosci
Title: Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells.
Volume: 26
Issue: 7
Pages: 2060-71
Publication
First Author: 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: 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: 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: 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
Publication
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
Publication
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
Publication
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
Publication
First Author: Maerker T
Year: 2008
Journal: Hum Mol Genet
Title: A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cells.
Volume: 17
Issue: 1
Pages: 71-86
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
First Author: Dunbar LA
Year: 2019
Journal: EMBO Mol Med
Title: Clarin-2 is essential for hearing by maintaining stereocilia integrity and function.
Volume: 11
Issue: 9
Pages: e10288
Publication
First Author: Lefèvre G
Year: 2008
Journal: Development
Title: A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth.
Volume: 135
Issue: 8
Pages: 1427-37
Publication
First Author: Papal S
Year: 2013
Journal: Hum Mol Genet
Title: The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route.
Volume: 22
Issue: 18
Pages: 3773-88
Publication
First Author: Grimsley-Myers CM
Year: 2009
Journal: J Neurosci
Title: The small GTPase Rac1 regulates auditory hair cell morphogenesis.
Volume: 29
Issue: 50
Pages: 15859-69
Publication
First Author: Son EJ
Year: 2012
Journal: PLoS One
Title: Developmental gene expression profiling along the tonotopic axis of the mouse cochlea.
Volume: 7
Issue: 7
Pages: e40735
Publication
First Author: Revenu C
Year: 2012
Journal: Mol Biol Cell
Title: A new role for the architecture of microvillar actin bundles in apical retention of membrane proteins.
Volume: 23
Issue: 2
Pages: 324-36
Publication  
First Author: Liakath-Ali K
Year: 2014
Journal: Nat Commun
Title: Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen.
Volume: 5
Pages: 3540
Publication
First Author: Sanchez-Calderon H
Year: 2010
Journal: PLoS One
Title: RNA microarray analysis in prenatal mouse cochlea reveals novel IGF-I target genes: implication of MEF2 and FOXM1 transcription factors.
Volume: 5
Issue: 1
Pages: e8699
Publication  
First Author: Collin GB
Year: 2020
Journal: Cells
Title: Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss.
Volume: 9
Issue: 4
Publication      
First Author: Mouse Genome Informatics and the Wellcome Trust Sanger Institute Mouse Genetics Project (MGP)
Year: 2011
Journal: Database Release
Title: Obtaining and Loading Phenotype Annotations from the Wellcome Trust Sanger Institute (WTSI) Mouse Resources Portal
Publication
First Author: Hoffman BG
Year: 2008
Journal: Genome Biol
Title: Identification of transcripts with enriched expression in the developing and adult pancreas.
Volume: 9
Issue: 6
Pages: R99
Publication
First Author: Ingham NJ
Year: 2019
Journal: PLoS Biol
Title: Mouse screen reveals multiple new genes underlying mouse and human hearing loss.
Volume: 17
Issue: 4
Pages: e3000194
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2001
Title: RIKEN Data Curation in Mouse Genome Informatics
Publication      
First Author: Wellcome Trust Sanger Institute
Year: 2009
Journal: MGI Direct Data Submission
Title: Alleles produced for the KOMP project by the Wellcome Trust Sanger Institute
Publication      
First Author: Mouse Genome Informatics and the International Mouse Phenotyping Consortium (IMPC)
Year: 2014
Journal: Database Release
Title: Obtaining and Loading Phenotype Annotations from the International Mouse Phenotyping Consortium (IMPC) Database
Publication        
First Author: The Gene Ontology Consortium
Year: 2014
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-rat orthologs
Publication        
First Author: UniProt-GOA
Year: 2012
Title: Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Chromosome assignment of mouse genes using the Mouse Genome Sequencing Consortium (MGSC) assembly and the ENSEMBL Database
Publication
First Author: Kawai J
Year: 2001
Journal: Nature
Title: Functional annotation of a full-length mouse cDNA collection.
Volume: 409
Issue: 6821
Pages: 685-90
Publication
First Author: Adams DJ
Year: 2024
Journal: Nature
Title: Genetic determinants of micronucleus formation in vivo.
Volume: 627
Issue: 8002
Pages: 130-136
Publication        
First Author: MGD Nomenclature Committee
Year: 1995
Title: Nomenclature Committee Use
Publication        
First Author: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
Publication
First Author: Skarnes WC
Year: 2011
Journal: Nature
Title: A conditional knockout resource for the genome-wide study of mouse gene function.
Volume: 474
Issue: 7351
Pages: 337-42
Publication
First Author: Okazaki Y
Year: 2002
Journal: Nature
Title: Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.
Volume: 420
Issue: 6915
Pages: 563-73
Publication        
First Author: The Gene Ontology Consortium
Year: 2010
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-human orthologs
Publication
First Author: Diez-Roux G
Year: 2011
Journal: PLoS Biol
Title: A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Volume: 9
Issue: 1
Pages: e1000582
Publication        
First Author: Marc Feuermann, Huaiyu Mi, Pascale Gaudet, Dustin Ebert, Anushya Muruganujan, Paul Thomas
Year: 2010
Title: Annotation inferences using phylogenetic trees
Publication      
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
Publication      
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Gene 1.0 ST Array Platform
Publication      
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
Publication      
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
Publication      
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
Publication      
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
Publication
First Author: Crawley SW
Year: 2016
Journal: Dev Cell
Title: ANKS4B Is Essential for Intermicrovillar Adhesion Complex Formation.
Volume: 36
Issue: 2
Pages: 190-200
Publication
First Author: Yan J
Year: 2010
Journal: Proc Natl Acad Sci U S A
Title: The structure of the harmonin/sans complex reveals an unexpected interaction mode of the two Usher syndrome proteins.
Volume: 107
Issue: 9
Pages: 4040-5
Publication
First Author: Bauß K
Year: 2014
Journal: Hum Mol Genet
Title: Phosphorylation of the Usher syndrome 1G protein SANS controls Magi2-mediated endocytosis.
Volume: 23
Issue: 15
Pages: 3923-42
Publication    
First Author: Morgan CP
Year: 2016
Journal: Elife
Title: PDZD7-MYO7A complex identified in enriched stereocilia membranes.
Volume: 5
Publication  
First Author: Morgan CP
Year: 2018
Journal: Front Cell Neurosci
Title: TRPV6, TRPM6 and TRPM7 Do Not Contribute to Hair-Cell Mechanotransduction.
Volume: 12
Pages: 41
Publication      
First Author: Harris BS
Year: 2016
Journal: MGI Direct Data Submission
Title: Whirlpool, a new circling mutation on Chromosome 11
Publication
First Author: Zou J
Year: 2014
Journal: Hum Mol Genet
Title: Deletion of PDZD7 disrupts the Usher syndrome type 2 protein complex in cochlear hair cells and causes hearing loss in mice.
Volume: 23
Issue: 9
Pages: 2374-90
Publication
First Author: Wu L
Year: 2011
Journal: Science
Title: Structure of MyTH4-FERM domains in myosin VIIa tail bound to cargo.
Volume: 331
Issue: 6018
Pages: 757-60