Pages that link to "Q28591690"
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The following pages link to Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice (Q28591690):
Displaying 50 items.
- Myosin VIIA (Q14914032) (← links)
- Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F (Q24291312) (← links)
- The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route (Q24293535) (← links)
- MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes (Q24294793) (← links)
- Functional characterization of the human myosin-7a motor domain (Q24306911) (← links)
- The unconventional myosin-VIIa associates with lysosomes (Q24307214) (← links)
- Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3. (Q24533348) (← links)
- Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex (Q24597349) (← links)
- Usher syndrome: animal models, retinal function of Usher proteins, and prospects for gene therapy (Q24646440) (← links)
- The many different cellular functions of MYO7A in the retina (Q27005972) (← links)
- A comprehensive review of retinal gene therapy (Q27023914) (← links)
- Unconventional myosin VIIA is a novel A-kinase-anchoring protein (Q28140474) (← links)
- Myosin superfamily evolutionary history (Q28207779) (← links)
- Position statement on human aging (Q28216232) (← links)
- Abnormal phagocytosis by retinal pigmented epithelium that lacks myosin VIIa, the Usher syndrome 1B protein (Q28505722) (← links)
- Myosin VIIa participates in opsin transport through the photoreceptor cilium (Q28509436) (← links)
- Cdh23 mutations in the mouse are associated with retinal dysfunction but not retinal degeneration (Q28512195) (← links)
- Retinal degeneration and failure of photoreceptor outer segment formation in mice with targeted deletion of the Joubert syndrome gene, Ahi1 (Q28588396) (← links)
- Role of myosin VIIa and Rab27a in the motility and localization of RPE melanosomes (Q28593151) (← links)
- The Usher 1B protein, MYO7A, is required for normal localization and function of the visual retinoid cycle enzyme, RPE65 (Q28593641) (← links)
- The role of Rab27a in the regulation of melanosome distribution within retinal pigment epithelial cells (Q28594091) (← links)
- Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities (Q30389509) (← links)
- myosin 7aa(-/-) mutant zebrafish show mild photoreceptor degeneration and reduced electroretinographic responses (Q30413024) (← links)
- Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice (Q30455456) (← links)
- Dimerized Drosophila myosin VIIa: a processive motor (Q30477237) (← links)
- The ternary Rab27a-Myrip-Myosin VIIa complex regulates melanosome motility in the retinal pigment epithelium (Q30479761) (← links)
- 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) (← links)
- Function of MYO7A in the human RPE and the validity of shaker1 mice as a model for Usher syndrome 1B (Q30494485) (← links)
- Retinal pigment epithelium defects in humans and mice with mutations in MYO7A: imaging melanosome-specific autofluorescence. (Q30494855) (← links)
- Myosin7a deficiency results in reduced retinal activity which is improved by gene therapy (Q31132177) (← links)
- Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. (Q33618805) (← links)
- Impacts of Usher syndrome type IB mutations on human myosin VIIa motor function (Q33649335) (← links)
- Myosins and deafness. (Q33725399) (← links)
- Molecular motors: sensing a function for myosin-VIIa (Q33780811) (← links)
- Functions of unconventional myosins (Q33840306) (← links)
- Unconventional myosins and the genetics of hearing loss (Q33855126) (← links)
- Myosins: a diverse superfamily (Q33866577) (← links)
- Recent advances in the molecular basis of inherited photoreceptor degeneration (Q33942183) (← links)
- Changes in localization and expression levels of Shroom2 and spectrin contribute to variation in amphibian egg pigmentation patterns (Q33989272) (← links)
- Unconventional myosins: anchors in the membrane traffic relay (Q34156472) (← links)
- The melanosome: membrane dynamics in black and white (Q34389530) (← links)
- Mitochondrial DNA variants mediate energy production and expression levels for CFH, C3 and EFEMP1 genes: implications for age-related macular degeneration (Q34568296) (← links)
- Identification of a rat model for usher syndrome type 1B by N-ethyl-N-nitrosourea mutagenesis-driven forward genetics (Q34573486) (← links)
- Quantitative genetic analysis of retinal degeneration in the blind cavefish Astyanax mexicanus (Q34600359) (← links)
- Lentiviral gene replacement therapy of retinas in a mouse model for Usher syndrome type 1B. (Q34608354) (← links)
- Distinct functional interactions between actin isoforms and nonsarcomeric myosins (Q34907205) (← links)
- Clinical characteristics and current therapies for inherited retinal degenerations (Q35045067) (← links)
- Moderate light-induced degeneration of rod photoreceptors with delayed transducin translocation in shaker1 mice (Q35221217) (← links)
- Pigment Cells: A Model for the Study of Organelle Transport (Q35564835) (← links)
- Gene Therapy for the Retinal Degeneration of Usher Syndrome Caused by Mutations in MYO7A (Q35664199) (← links)