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Human Molecular Genetics, ISSN 0964-6906, 12/2010, Volume 19, Issue 24, pp. 4799 - 4812
Cysteine 150 of retinal degeneration slow protein (RDS) mediates the intermolecular disulfide bonding necessary for large RDS complex assembly and... 
RETINAL DEGENERATION | PHOTORECEPTOR PERIPHERIN/RDS | MUTANT MICE | NUCLEOTIDE-GATED CHANNEL | BIOCHEMISTRY & MOLECULAR BIOLOGY | DEGENERATION SLOW GENE | GENETICS & HEREDITY | OUTER SEGMENT MORPHOGENESIS | DISK MEMBRANES | MEMBRANE-PROTEINS | DOMINANT RETINITIS-PIGMENTOSA | TRANSGENIC MICE | Retinal Rod Photoreceptor Cells - ultrastructure | Membrane Glycoproteins - metabolism | Membrane Glycoproteins - chemistry | Retinal Rod Photoreceptor Cells - metabolism | Retinal Degeneration - metabolism | Nerve Tissue Proteins - chemistry | Light Signal Transduction | Rod Cell Outer Segment - ultrastructure | Retinal Cone Photoreceptor Cells - pathology | Intermediate Filament Proteins - genetics | Rod Cell Outer Segment - pathology | Membrane Proteins - metabolism | Peripherins | Transgenes - genetics | Mutant Proteins - genetics | Mice, Transgenic | Mutant Proteins - metabolism | Nerve Tissue Proteins - genetics | Membrane Glycoproteins - genetics | Protein Transport | Nerve Tissue Proteins - metabolism | Animals | Eye Proteins - metabolism | Opsins - metabolism | Amino Acid Substitution - genetics | Mice | Retinal Degeneration - pathology | Genes, Dominant - genetics | Intermediate Filament Proteins - metabolism | Retinal Cone Photoreceptor Cells - metabolism | Retinal Rod Photoreceptor Cells - pathology | Intermediate Filament Proteins - chemistry
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Biochemical Journal, ISSN 0264-6021, 06/2005, Volume 388, Issue 2, pp. 605 - 613
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