proline has been researched along with Retinal Degeneration in 25 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 9 (36.00) | 18.7374 |
| 1990's | 6 (24.00) | 18.2507 |
| 2000's | 7 (28.00) | 29.6817 |
| 2010's | 3 (12.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chao, JR; Dinterman, M; Du, J; Engel, AL; Hauer, A; Huang, J; Lohner, D; Wang, Y; Yam, M; Zhang, R; Zhao, C; Zhu, S | 1 |
| Acosta, ML; Fletcher, EL; Kalloniatis, M; Misra, S; Mistra, S; Nivison-Smith, L; Zhu, Y | 1 |
| Chichilnisky, EJ; Dabrowski, W; Hottowy, P; Hulse, C; Jepson, LH; Litke, AM; Sekirnjak, C; Sher, A | 1 |
| Ferrell, WD; Jones, BW; Lee, DC; Marc, RE; Moritz, OL; Tam, BM; Vazquez-Chona, FR | 1 |
| Findlay, JB; Nevett, CL; Wrigley, JD | 1 |
| Geller, S; LaVail, M; Lee, D; Matthes, M; Stone, J; Valter, K; Walsh, N; Yasumura, D | 1 |
| ACHER, R; FROMAGEOT, C; JUTISZ, M | 1 |
| Allen, D; Hao, Y; Kraft, TW; Peng, YW; Petters, RM; Wong, F | 1 |
| Allocca, M; Auricchio, A; Bozzoni, I; Denti, MA; Di Vicino, U; Domenici, L; Parisi, F; Tessitore, A | 1 |
| Hiraiwa, N; Inagaki, E; Ishiguro, I; Iwasaki, K; Matsuzawa, T | 1 |
| Hayasaka, S; Mizuno, K; Omura, K; Saito, T; Tada, K | 1 |
| Matsuzawa, T | 1 |
| Feist, RM; Skalka, H; Stone, EM; White, MF | 1 |
| Creel, DJ; Richards, SC | 1 |
| Ferrell, RE; Gass, JD; Gorin, MB; Jackson, KE; Jacobson, SG; Mitchell, E; Sheffield, VC; Stone, EM | 1 |
| Dryja, TP; Li, T; Olsson, JE; Snyder, WK | 1 |
| Bush, RA; Kononen, L; Machida, S; Sieving, PA | 1 |
| Birch, DG; Bowne, SJ; Daiger, SP; Heckenlively, JR; Lewis, RA; Mintz-Hittner, H; Northrup, H; Rodriquez, JA; Ruiz, RS; Saperstein, DA; Sohocki, MM; Sullivan, LS | 1 |
| Fishman, GA; Khadivi, P; Kimura, AE; Nichols, BE; Sheffield, VC; Stone, EM | 1 |
| Chan, KH; Li, WW; Yew, DT | 1 |
| Brody, LC; Engelhardt, JF; Kaiser-Kupfer, M; Looney, JE; Mitchell, GA; Obie, C; Patel, AS; Sipila, I; Steel, G; Wong, C | 1 |
| Jones, ME | 1 |
| Grafstein, B; Ingoglia, NA; Murray, M | 1 |
| Grafstein, B; Specht, S | 1 |
| Albert, J; Collombel, C; David, M; Guerrier, G; Guibaud, P; Jeune, M; Michel, M | 1 |
25 other study(ies) available for proline and Retinal Degeneration
| Article | Year |
|---|---|
Proline mediates metabolic communication between retinal pigment epithelial cells and the retina.
Topics: Animals; Carbon Radioisotopes; Cell Differentiation; Energy Metabolism; Humans; Male; Mice; Mice, Inbred C57BL; Mitochondria; Oxidation-Reduction; Proline; Retina; Retinal Degeneration; Retinal Pigment Epithelium | 2019 |
Mapping cation entry in photoreceptors and inner retinal neurons during early degeneration in the P23H-3 rat retina.
Topics: Age Factors; Agmatine; Animals; Apoptosis; Gene Expression Regulation, Developmental; Histidine; Humans; Mutation; Nerve Tissue Proteins; Neurons; Photoreceptor Cells; Proline; Rats; Rats, Sprague-Dawley; Rats, Transgenic; Retina; Retinal Degeneration; Rhodopsin; Silver Staining | 2013 |
Loss of responses to visual but not electrical stimulation in ganglion cells of rats with severe photoreceptor degeneration.
Topics: Action Potentials; Animals; Animals, Genetically Modified; Animals, Newborn; Disease Models, Animal; Electric Stimulation; Histidine; Light; Membrane Proteins; Mutation; Perilipin-2; Photoreceptor Cells; Proline; Rats; Rats, Sprague-Dawley; Reaction Time; Retinal Degeneration; Retinal Ganglion Cells | 2009 |
Dysmorphic photoreceptors in a P23H mutant rhodopsin model of retinitis pigmentosa are metabolically active and capable of regenerating to reverse retinal degeneration.
Topics: Amino Acid Substitution; Animals; Animals, Genetically Modified; Disease Models, Animal; Histidine; Mutation; Nerve Regeneration; Proline; Retinal Degeneration; Retinal Rod Photoreceptor Cells; Retinitis Pigmentosa; Rhodopsin; Xenopus laevis | 2012 |
Topological analysis of peripherin/rds and abnormal glycosylation of the pathogenic Pro216-->Leu mutation.
Topics: Amino Acid Sequence; Animals; Asparagine; Glycosylation; Intermediate Filament Proteins; Leucine; Membrane Glycoproteins; Molecular Sequence Data; Mutagenesis; Nerve Tissue Proteins; Peripherins; Point Mutation; Proline; Recombinant Proteins; Retinal Degeneration | 2002 |
Photoreceptor degeneration in Pro23His and S334ter transgenic rats.
Topics: Animals; Animals, Genetically Modified; Animals, Newborn; Apoptosis; Histidine; In Situ Nick-End Labeling; Mutation; Peptide Fragments; Photoreceptor Cells, Vertebrate; Proline; Rats; Retinal Degeneration; Rhodopsin; Serine | 2003 |
[Chromatographic separation of amino acids and peptides; the individual amino acids of insulin with a note on the determination of proline].
Topics: Amino Acids; Antifibrinolytic Agents; Chromatography; Insulin; Peptides; Proline; Retinal Degeneration | 1950 |
Altered light responses of single rod photoreceptors in transgenic pigs expressing P347L or P347S rhodopsin.
Topics: Amino Acid Substitution; Animals; Animals, Genetically Modified; Electrophysiology; Immunohistochemistry; Kinetics; Leucine; Light; Mutation; Proline; Retinal Degeneration; Retinal Rod Photoreceptor Cells; Rhodopsin; Swine; Vision, Ocular | 2005 |
Preferential silencing of a common dominant rhodopsin mutation does not inhibit retinal degeneration in a transgenic model.
Topics: Alleles; Animals; Animals, Genetically Modified; Base Sequence; Dependovirus; Gene Silencing; Genetic Vectors; Mice; Models, Animal; Molecular Sequence Data; Mutation; Proline; Rats; Retinal Degeneration; Rhodopsin; RNA, Small Interfering | 2006 |
Disease of ornithine-proline pathway: a delta 1-pyrroline-5-carboxylate reductase deficiency in the retina or retinal degeneration mice.
Topics: Animals; Arginase; Cattle; Cornea; Female; Glutamates; Glutamic Acid; Male; Mice; Mice, Inbred C3H; Ornithine; Ornithine Carbamoyltransferase; Ornithine-Oxo-Acid Transaminase; Oxidoreductases Acting on CH-NH Group Donors; Proline; Pyrroline Carboxylate Reductases; Retina; Retinal Degeneration | 1982 |
Hyperornithinaemia associated with gyrate atrophy of the choroid and retina: in vivo and in vitro response to vitamin B6.
Topics: Adolescent; Child; Child, Preschool; Choroid; Fibroblasts; Humans; Lymphocytes; Male; Ornithine; Ornithine-Oxo-Acid Transaminase; Proline; Pyridoxine; Retinal Degeneration; Transaminases; Uveal Diseases | 1981 |
Disease of the ornithine-proline pathway: delta 1-pyrroline-5-carboxylate reductase deficiency in the retina of retinal degeneration mice.
Topics: Animals; Cattle; Eye; Liver; Mice; Mice, Inbred Strains; Ornithine; Ornithine Carbamoyltransferase; Ornithine-Oxo-Acid Transaminase; Proline; Pyrroles; Retinal Degeneration; Weaning | 1982 |
Choroidal neovascularization in a patient with adult foveomacular dystrophy and a mutation in the retinal degeneration slow gene (Pro 210 Arg)
Topics: Arginine; Choroid; Eye Proteins; Fovea Centralis; Humans; Intermediate Filament Proteins; Macular Degeneration; Male; Membrane Glycoproteins; Middle Aged; Mutation; Neovascularization, Pathologic; Nerve Tissue Proteins; Peripherins; Proline; Retinal Degeneration | 1994 |
Pattern dystrophy and retinitis pigmentosa caused by a peripherin/RDS mutation.
Topics: Adult; Aged; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 6; Eye Proteins; Humans; Intermediate Filament Proteins; Male; Membrane Glycoproteins; Middle Aged; Mutation; Nerve Tissue Proteins; Neuropeptides; Pedigree; Peripherins; Proline; Retina; Retinal Degeneration; Retinitis Pigmentosa; Serine | 1995 |
A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration.
Topics: Adolescent; Adult; Aged; Amino Acid Sequence; Arginine; Base Sequence; Chromosome Deletion; DNA Mutational Analysis; Electrophoresis, Polyacrylamide Gel; Eye Proteins; Female; Fluorescein Angiography; Fundus Oculi; Humans; Intermediate Filament Proteins; Macular Degeneration; Male; Membrane Glycoproteins; Middle Aged; Molecular Sequence Data; Nerve Tissue Proteins; Pedigree; Peripherins; Phenotype; Point Mutation; Polymerase Chain Reaction; Proline; Retinal Degeneration; Visual Fields | 1995 |
Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segments.
Topics: Animals; Electroretinography; Genes, Dominant; Humans; Mice; Mice, Transgenic; Microscopy, Confocal; Microscopy, Electron; Microscopy, Electron, Scanning; Point Mutation; Proline; Retinal Degeneration; Rhodopsin; Rod Cell Outer Segment; Serine | 1996 |
The effect of calcium channel blocker diltiazem on photoreceptor degeneration in the rhodopsin Pro213His rat.
Topics: Animals; Calcium Channel Blockers; Cell Count; Cell Survival; Diltiazem; Electroretinography; Female; Histidine; Injections, Intraperitoneal; Male; Point Mutation; Proline; Rats; Rats, Mutant Strains; Rats, Sprague-Dawley; Retinal Degeneration; Rhodopsin; Rod Cell Outer Segment | 2000 |
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies.
Topics: Amino Acid Substitution; Animals; Arginine; Cysteine; Genetic Variation; Glutamine; Homeodomain Proteins; Humans; Intermediate Filament Proteins; Leucine; Membrane Glycoproteins; Mutation; Nerve Tissue Proteins; Optic Atrophies, Hereditary; Peripherins; Prevalence; Proline; Retinal Degeneration; Retinal Diseases; Retinitis Pigmentosa; Rhodopsin; Trans-Activators; Tyrosine | 2001 |
Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin gene.
Topics: Adolescent; Adult; Aged; Amino Acid Sequence; Base Sequence; Codon; DNA; Female; Histidine; Humans; Male; Middle Aged; Molecular Sequence Data; Mutation; Pedigree; Polymerase Chain Reaction; Proline; Retinal Degeneration; Retinitis Pigmentosa; Rhodopsin; Visual Fields | 1991 |
Uptake of labelled proline in the degenerating retina of goldfish.
Topics: Animals; Disease Models, Animal; Goldfish; Neurons; Photoreceptor Cells; Proline; Retina; Retinal Degeneration | 1990 |
At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.
Topics: Alleles; Arginine; Atrophy; Choroid; DNA; Female; Finland; Genes; Humans; Leucine; Male; Mutation; Ornithine-Oxo-Acid Transaminase; Pedigree; Proline; Retina; Retinal Degeneration; Threonine; Transaminases; Uveal Diseases | 1989 |
Conversion of glutamate to ornithine and proline: pyrroline-5-carboxylate, a possible modulator of arginine requirements.
Topics: Amino Acids; Animals; Arginine; Biotransformation; Glutamates; Glutamic Acid; Humans; Intestinal Mucosa; Kidney; Liver; Ornithine; Ornithine-Oxo-Acid Transaminase; Proline; Proline Oxidase; Pyrroles; Retinal Degeneration; Spleen | 1985 |
Protein synthesis and axonal transport in retinal ganglion cells of mice lacking visual receptors.
Topics: Animals; Axonal Transport; Ganglia; Leucine; Mice; Mutation; Nerve Degeneration; Nerve Tissue Proteins; Optic Nerve; Proline; Retina; Retinal Degeneration; Sensory Receptor Cells | 1972 |
Accumulation of radioactive protein in mouse cerebral cortex after injection of 3H-fucose into the eye.
Topics: Animals; Autoradiography; Cerebral Cortex; Cycloheximide; Eye; Fucose; Geniculate Bodies; Hippocampus; Injections; Mice; Optic Nerve; Proline; Retina; Retinal Degeneration; Superior Colliculi; Tritium; Visual Cortex | 1973 |
[Hyperleucinisoleucinemia due to partial transamination defect associated with type 2 hyperprolinemia. Familial case of double aminoacidopathy].
Topics: Amino Acid Metabolism, Inborn Errors; Auditory Cortex; Child, Preschool; Deafness; Electroencephalography; Evoked Potentials; Female; Humans; Infant; Isoleucine; Leucine; Leukocytes; Male; Proline; Retinal Degeneration; Transaminases | 1970 |