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Search results 401 to 426 out of 426 for Myo7a

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Publication

- | J:144086

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

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Publication

- | J:155721

First Author:	Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year:	2010
Journal:	Database Download
Title:	Consensus CDS project

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Publication

- | J:85324

First Author:	Mouse Genome Informatics Group
Year:	2003
Journal:	Database Procedure
Title:	Automatic Encodes (AutoE) Reference

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Publication

- | J:53168

First Author:	Bairoch A
Year:	1999
Journal:	Database Release
Title:	SWISS-PROT Annotated protein sequence database

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Publication

- | J:91388

First Author:	Mouse Genome Informatics Scientific Curators
Year:	2005

Title:	Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations

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Publication

- | J:155221

First Author:	Mouse Genome Informatics
Year:	2010
Journal:	Database Release
Title:	Protein Ontology Association Load.

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Publication

- | J:90438

First Author:	Mouse Genome Informatics Scientific Curators
Year:	2005

Title:	Obtaining and loading genome assembly coordinates from NCBI annotations

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Publication

- | J:144087

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

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Publication

19643958 | J:160432

First Author:	Gibbs D
Year:	2010
Journal:	Invest Ophthalmol Vis Sci
Title:	Function of MYO7A in the human RPE and the validity of shaker1 mice as a model for Usher syndrome 1B.
Volume:	51
Issue:	2
Pages:	1130-5

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Publication

21936790 | -

First Author:	Williams DS
Year:	2011
Journal:	Biochem Soc Trans
Title:	The many different cellular functions of MYO7A in the retina.
Volume:	39
Issue:	5
Pages:	1207-10

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Publication

12588794 | J:82023

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

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Publication

20142502 | -

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

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Publication

24608321 | J:210992

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

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Publication

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

21709241 | J:174394

First Author:	Grati M
Year:	2011
Journal:	Proc Natl Acad Sci U S A
Title:	Myosin VIIa and sans localization at stereocilia upper tip-link density implicates these Usher syndrome proteins in mechanotransduction.
Volume:	108
Issue:	28
Pages:	11476-81

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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

19457086 | J:150858

First Author:	Fernández-Medarde A
Year:	2009
Journal:	J Neurochem
Title:	RasGRF1 disruption causes retinal photoreception defects and associated transcriptomic alterations.
Volume:	110
Issue:	2
Pages:	641-52

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Publication

24259566 | J:204163

First Author:	Gilels F
Year:	2013
Journal:	J Neurosci
Title:	Mutation of Foxo3 causes adult onset auditory neuropathy and alters cochlear synapse architecture in mice.
Volume:	33
Issue:	47
Pages:	18409-24

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Publication

9070921 | J:38566

First Author:	Kelley PM
Year:	1997
Journal:	Genomics
Title:	The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A).
Volume:	40
Issue:	1
Pages:	73-9

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Publication

29167268 | J:256072

First Author:	Xiong A
Year:	2018
Journal:	J Biol Chem
Title:	The shaker-1 mouse myosin VIIa deafness mutation results in a severely reduced rate of the ATP hydrolysis step.
Volume:	293
Issue:	3
Pages:	819-829

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Publication

29361540 | J:257650

First Author:	Liu Y
Year:	2018
Journal:	J Cell Sci
Title:	Unconventional myosin VIIA promotes melanoma progression.
Volume:	131
Issue:	4

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Publication

33400922 | J:315709

First Author:	McGrath J
Year:	2021
Journal:	Curr Biol
Title:	Actin at stereocilia tips is regulated by mechanotransduction and ADF/cofilin.
Volume:	31
Issue:	6
Pages:	1141-1153.e7

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Publication

21311020 | -

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

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Publication

23457544 | J:197180

First Author:	Buniello A
Year:	2013
Journal:	PLoS One
Title:	Headbobber: a combined morphogenetic and cochleosaccular mouse model to study 10qter deletions in human deafness.
Volume:	8
Issue:	2
Pages:	e56274

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Publication

- | J:350897

First Author:	Chang B
Year:	2024
Journal:	MGI Direct Data Submission
Title:	The retinal cone dysfunction mutation.

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Publication

9171833 | J:40770

First Author:	Weil D
Year:	1997
Journal:	Nat Genet
Title:	The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene.
Volume:	16
Issue:	2
Pages:	191-3

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Search results 401 to 426 out of 426 for Myo7a

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