Molecular Cloning and Characterization of Mammalian Homologues of theDrosophila retinal degeneration BGene
- 1 July 1997
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 236 (3) , 559-564
- https://doi.org/10.1006/bbrc.1997.7009
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- The vibrator Mutation Causes Neurodegeneration via Reduced Expression of PITPα: Positional Complementation Cloning and Extragenic SuppressionNeuron, 1997
- Calcium channel blockers inhibit retinal degeneration in the retinal-degeneration-B mutant of Drosophila.Proceedings of the National Academy of Sciences, 1992
- Retinal degeneration in the rd mouse is caused by a defect in the β subunit of rod cGMP-phosphodiesteraseNature, 1990
- The identification and suppression of inherited neurodegeneration in Caenorhabditis elegansNature, 1990
- A point mutation of the rhodopsin gene in one form of retinitis pigmentosaNature, 1990
- Developmental patterns in rat brain of phosphatidylinositol synthetic enzymes and phosphatidylinositol transfer proteinBiochimica et Biophysica Acta (BBA) - Biomembranes, 1989
- The scanning model for translation: an update.The Journal of cell biology, 1989
- Phosphatidylinositol transfer activity in rat cerebral hemispheres during developmentJournal of Neurochemistry, 1979
- Hereditary retinal degeneration in Drosophila melanogaster. A mutant defect associated with the phototransduction process.The Journal of general physiology, 1977
- 3′ Non-coding region sequences in eukaryotic messenger RNANature, 1976