Characterization of RPE65 and RDH12, two enzymes associated with retinal dystrophy and retinoid processing
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- Type
- dissertation
- Published
- 2010-01-01
- Cited by
- 0
- References
- 237
- Access
- Open access
- OpenAlex
- https://openalex.org/W101580168
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:81724019
Keywords
RPE65, Retinoid, Enzyme, Retinal, Biochemistry
References
- Downregulation of cone-specific gene expression and degeneration of cone photoreceptors in the Rpe65-/- mouse at early ages.
- Retinol esterification in bovine retinal pigment epithelium: reversibility of lecithin:retinol acyltransferase.
- Membrane receptors for retinol-binding protein in cultured human retinal pigment epithelium.
- Growth characteristics and ultrastructure of human retinal pigment epithelium in vitro.
- Isomerization and oxidation of vitamin a in cone-dominant retinas: a novel pathway for visual-pigment regeneration in daylight.
- Photoreceptor cells in the vitiligo mouse die by apoptosis. TRPM-2/clusterin expression is increased in the neural retina and in the retinal pigment epithelium.
- Genetic analysis of RPE65: from human disease to mouse model.
- Isolation and provisional identification of plasma membrane populations from cultured human retinal pigment epithelium.
- Specific binding of peanut lectin to a class of retinal photoreceptor cells. A species comparison.
- An opsin homologue in the retina and pigment epithelium.
- Retinoic acid produces rod photoreceptor selective apoptosis in developing mammalian retina.
- RDH12 Expression Relative to Other Short Chain Dehydrogenase/Reductase Isoforms Present in the Retina
- Regulation of Retinol Dehydrogenase RDH12 by Light and 4-Hydroxynonenal-Induced Stress
- Constitutive Activation and Photoreceptor Degeneration in RPE65 Knockout Mice
- Polarity and the development of the outer blood-retinal barrier.
- High-performance liquid chromatography of retinoid isomers.
- Biochemistry of visual pigment regeneration: the Friedenwald lecture.
- Human retinol dehydrogenase 13 (RDH13) is a mitochondrial short‐chain dehydrogenase/reductase with a retinaldehyde reductase activity
- Genetic defects in vitamin A metabolism of the retinal pigment epithelium.
- High-performance liquid chromatography analysis of visual cycle retinoids.
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