Pages that link to "Q30481050"

The following pages link to A novel allele of myosin VIIa reveals a critical function for the C-terminal FERM domain for melanosome transport in retinal pigment epithelial cells (Q30481050):

Displaying 22 items.

• Structure of MyTH4-FERM domains in myosin VIIa tail bound to cargo (Q27666702) (← links)
• The Usher 1B protein, MYO7A, is required for normal localization and function of the visual retinoid cycle enzyme, RPE65 (Q28593641) (← links)
• Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes (Q30454026) (← links)
• Characterization of Highper, an ENU-induced mouse mutant with abnormal psychostimulant and stress responses (Q30531391) (← links)
• Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness. (Q34208386) (← links)
• Inner ear morphology is perturbed in two novel mouse models of recessive deafness. (Q34516358) (← links)
• Eeyore: a novel mouse model of hereditary deafness (Q35004931) (← links)
• EIAV-based retinal gene therapy in the shaker1 mouse model for usher syndrome type 1B: development of UshStat (Q35140281) (← links)
• Retinal disease course in Usher syndrome 1B due to MYO7A mutations (Q35687907) (← links)
• The Time Course of Deafness and Retinal Degeneration in a Kunming Mouse Model for Usher Syndrome (Q36019717) (← links)
• Retinal gene therapy with a large MYO7A cDNA using adeno-associated virus (Q36808032) (← links)
• Forward genetic approaches to understanding complex behaviors. (Q37980649) (← links)
• New treatment options for hearing loss. (Q38384722) (← links)
• Myosin VIIA is a marker for the cone accessory outer segment in zebrafish. (Q39144674) (← links)
• Identification, modeling, and characterization studies of Tetrahymena thermophila myosin FERM domains suggests a conserved core fold but functional differences. (Q40402355) (← links)
• The Shaker-1 Mouse Myosin VIIa Deafness Mutation Results in a Severely Reduced Rate of the ATP Hydrolysis Step (Q45073728) (← links)
• Analysis of two Arab families reveals additional support for a DFNB2 nonsyndromic phenotype of MYO7A. (Q50356353) (← links)
• TRPV6, TRPM6 and TRPM7 Do Not Contribute to Hair-Cell Mechanotransduction. (Q52363885) (← links)
• Usherin defects lead to early-onset retinal dysfunction in zebrafish (Q54157095) (← links)
• Genetic screening revealed usher syndrome in a paediatric Chinese patient. (Q64950087) (← links)
• Aberrant Splicing Events Associated to CDH23 Noncanonical Splice Site Mutations in a Proband with Atypical Usher Syndrome 1 (Q90224460) (← links)
• FERM domain-containing protein 6 identifies a subpopulation of varicose nerve fibers in different vertebrate species (Q90569856) (← links)