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Search results 1 to 69 out of 69 for Ush2a

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Category: Publication
Type Details Score
Publication
First Author: Bhattacharya G
Year: 2004
Journal: J Cell Sci
Title: A domain-specific usherin/collagen IV interaction may be required for stable integration into the basement membrane superstructure.
Volume: 117
Issue: Pt 2
Pages: 233-42
Publication
First Author: Rivolta C
Year: 2000
Journal: Am J Hum Genet
Title: Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing loss.
Volume: 66
Issue: 6
Pages: 1975-8
Publication
First Author: Perrino PA
Year: 2020
Journal: Commun Biol
Title: Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes.
Volume: 3
Issue: 1
Pages: 180
Publication
First Author: Schwaller F
Year: 2021
Journal: Nat Neurosci
Title: USH2A is a Meissner's corpuscle protein necessary for normal vibration sensing in mice and humans.
Volume: 24
Issue: 1
Pages: 74-81
Publication
First Author: Lu B
Year: 2010
Journal: Invest Ophthalmol Vis Sci
Title: Cell transplantation to arrest early changes in an ush2a animal model.
Volume: 51
Issue: 4
Pages: 2269-76
Publication
First Author: van Wijk E
Year: 2006
Journal: Hum Mol Genet
Title: The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1.
Volume: 15
Issue: 5
Pages: 751-65
Publication
First Author: Eudy JD
Year: 1998
Journal: Science
Title: Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Volume: 280
Issue: 5370
Pages: 1753-7
Publication
First Author: Bhattacharya G
Year: 2005
Journal: Biochemistry
Title: Evidence for functional importance of usherin/fibronectin interactions in retinal basement membranes.
Volume: 44
Issue: 34
Pages: 11518-24
Publication
First Author: Huang D
Year: 2002
Journal: Genomics
Title: Identification of the mouse and rat orthologs of the gene mutated in Usher syndrome type IIA and the cellular source of USH2A mRNA in retina, a target tissue of the disease.
Volume: 80
Issue: 2
Pages: 195-203
Publication
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
Publication
First Author: Danciger JS
Year: 1999
Journal: Mamm Genome
Title: Genetic and physical maps of the mouse rd3 locus; exclusion of the ortholog of USH2A.
Volume: 10
Issue: 7
Pages: 657-61
Publication
First Author: Grati M
Year: 2012
Journal: J Neurosci
Title: Localization of PDZD7 to the stereocilia ankle-link associates this scaffolding protein with the Usher syndrome protein network.
Volume: 32
Issue: 41
Pages: 14288-93
Publication
First Author: Chen Q
Year: 2014
Journal: J Biol Chem
Title: Whirlin and PDZ domain-containing 7 (PDZD7) proteins are both required to form the quaternary protein complex associated with Usher syndrome type 2.
Volume: 289
Issue: 52
Pages: 36070-88
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: 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: Zou J
Year: 2011
Journal: Invest Ophthalmol Vis Sci
Title: Whirlin replacement restores the formation of the USH2 protein complex in whirlin knockout photoreceptors.
Volume: 52
Issue: 5
Pages: 2343-51
Publication
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
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: Eudy JD
Year: 2000
Journal: GenBank Submission
Title: Mus musculus putative extracellular matrix protein MUSH2A mRNA, complete cds
Pages: AF151717
Publication
First Author: Mathur PD
Year: 2023
Journal: Sci Rep
Title: Adenylyl cyclase 6 plays a minor role in the mouse inner ear and retina.
Volume: 13
Issue: 1
Pages: 7075
Publication
First Author: Yang J
Year: 2010
Journal: PLoS Genet
Title: Ablation of whirlin long isoform disrupts the USH2 protein complex and causes vision and hearing loss.
Volume: 6
Issue: 5
Pages: e1000955
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: Zou J
Year: 2015
Journal: Hum Mol Genet
Title: Individual USH2 proteins make distinct contributions to the ankle link complex during development of the mouse cochlear stereociliary bundle.
Volume: 24
Issue: 24
Pages: 6944-57
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: 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: Michalski N
Year: 2007
Journal: J Neurosci
Title: Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning.
Volume: 27
Issue: 24
Pages: 6478-88
Publication      
First Author: MouseBookTM
Year: 2005
Journal: Unpublished
Title: Information obtained from MouseBookTM, Medical Research Council Mammalian Genetics Unit, Harwell, UK.
Publication      
First Author: Shanghai Model Organisms Center
Year: 2017
Journal: MGI Direct Data Submission
Title: Information obtained from the Shanghai Model Organisms Center (SMOC), Shanghai, China
Publication      
First Author: European Mouse Mutant Archive
Year: 2003
Journal: Unpublished
Title: Information obtained from the European Mouse Mutant Archive (EMMA)
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: Bailey PJ
Year: 2006
Journal: Exp Cell Res
Title: A global genomic transcriptional code associated with CNS-expressed genes.
Volume: 312
Issue: 16
Pages: 3108-19
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2001
Title: RIKEN Data Curation in Mouse Genome Informatics
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2001
Title: Gene Ontology Annotation by the MGI Curatorial Staff
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Mouse Synonym Curation
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2003
Journal: Database Download
Title: Integrating Computational Gene Models into the Mouse Genome Informatics (MGI) Database
Publication      
First Author: Wellcome Trust Sanger Institute
Year: 2010
Journal: MGI Direct Data Submission
Title: Alleles produced for the EUCOMM and EUCOMMTools projects by the Wellcome Trust Sanger Institute
Publication        
First Author: Cyagen Biosciences Inc.
Year: 2022
Title: Cyagen Biosciences Website.
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Title: Rat to Mouse ISO GO annotation transfer
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2003
Title: MGI Sequence Curation Reference
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: Zambrowicz BP
Year: 2003
Journal: Proc Natl Acad Sci U S A
Title: Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention.
Volume: 100
Issue: 24
Pages: 14109-14
Publication        
First Author: MGD Nomenclature Committee
Year: 1995
Title: Nomenclature Committee Use
Publication      
First Author: Mouse Genome Informatics (MGI) and National Center for Biotechnology Information (NCBI)
Year: 2008
Journal: Database Download
Title: Mouse Gene Trap Data Load from dbGSS
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: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
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: Mouse Genome Informatics Scientific Curators
Year: 2000
Title: Gene Ontology Annotation by electronic association of SwissProt Keywords with GO terms
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Title: Human to Mouse ISO GO annotation transfer
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: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Mouse Genome Informatics Computational Sequence to Gene Associations
Publication
First Author: Gaudet P
Year: 2011
Journal: Brief Bioinform
Title: Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium.
Volume: 12
Issue: 5
Pages: 449-62
Publication      
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
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: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
Publication      
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
Publication      
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
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 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: 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
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
Publication
First Author: Jacobson SG
Year: 2008
Journal: Hum Mol Genet
Title: Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.
Volume: 17
Issue: 15
Pages: 2405-15
Publication
First Author: Guan Y
Year: 2023
Journal: Adv Sci (Weinh)
Title: Deafness-Associated ADGRV1 Mutation Impairs USH2A Stability through Improper Phosphorylation of WHRN and WDSUB1 Recruitment.
Volume: 10
Issue: 16
Pages: e2205993
Publication
First Author: Kersten FF
Year: 2012
Journal: Cilia
Title: The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitotically.
Volume: 1
Issue: 1
Pages: 2
Publication
First Author: Pieke-Dahl S
Year: 1997
Journal: Hear Res
Title: Hearing loss in the RBF/DnJ mouse, a proposed animal model of Usher syndrome type IIa.
Volume: 112
Issue: 1-2
Pages: 1-12
Publication
First Author: Sorusch N
Year: 2017
Journal: Hum Mol Genet
Title: Characterization of the ternary Usher syndrome SANS/ush2a/whirlin protein complex.
Volume: 26
Issue: 6
Pages: 1157-1172
Publication
First Author: Yao L
Year: 2016
Journal: PLoS One
Title: The Time Course of Deafness and Retinal Degeneration in a Kunming Mouse Model for Usher Syndrome.
Volume: 11
Issue: 5
Pages: e0155619
Publication
First Author: Noordmans GA
Year: 2014
Journal: PLoS One
Title: Genetic analysis of intracapillary glomerular lipoprotein deposits in aging mice.
Volume: 9
Issue: 10
Pages: e111308