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Search results 401 to 413 out of 413 for Myo7a

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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

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 413 out of 413 for Myo7a

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