lysine has been researched along with Retinal Degeneration in 15 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (46.67) | 18.7374 |
| 1990's | 1 (6.67) | 18.2507 |
| 2000's | 4 (26.67) | 29.6817 |
| 2010's | 3 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, D; Cheng, L; Liu, Y; Wang, Y; Xiao, L; Yan, N; Zhang, J; Zheng, S | 1 |
| Alsarraf, O; Chou, CJ; Crosson, CE; Dahrouj, M; Fan, J; Menick, DR | 1 |
| Conley, SM; Naash, MI; Stricker, HM | 1 |
| PIEZ, KA | 1 |
| Baumert, U; Koenekoop, RK; Loyer, M; Piña, AL | 1 |
| Fiona, WJ; Santos, L; Walter, JH | 1 |
| Dinculescu, A; Orisme, W; Peterson, JJ; Smith, WC | 1 |
| Heckenlively, J | 1 |
| Merin, S; Shapira, Y; Statter, M; Yarom, R; Yatziv, S | 1 |
| Kennaway, NG; Weleber, RG | 1 |
| Behrens-Baumann, W; Hansmann, I; König, U; Langenbeck, U; Schröder, K | 1 |
| Lawler, AM; Milam, AH; Sipila, I; Steel, G; Valle, D; Wang, T | 1 |
| Lee, CC; Lin, HJ; Tsai, CH; Tsai, FJ; Wu, JY; Yang, C | 1 |
| Berson, EL; Rabin, AR; Schmidt, SY | 1 |
| Ionasescu, V; Mueller, S; Stegink, L; Weinstein, M | 1 |
15 other study(ies) available for lysine and Retinal Degeneration
| Article | Year |
|---|---|
DZNep inhibits H3K27me3 deposition and delays retinal degeneration in the rd1 mice.
Topics: Adenosine; Amino Acid Motifs; Animals; Calpain; Disease Models, Animal; Epigenesis, Genetic; Female; Histones; Humans; Lysine; Male; Methylation; Mice; Mice, Inbred ICR; Phosphatidylinositol 3-Kinases; Proto-Oncogene Proteins c-akt; Retina; Retinal Degeneration | 2018 |
Acetylation: a lysine modification with neuroprotective effects in ischemic retinal degeneration.
Topics: Acetylation; Animals; Blotting, Western; Caspase 3; Cell Survival; Electroretinography; Female; Histone Deacetylase Inhibitors; Histone Deacetylases; Histones; Hydroxamic Acids; Lysine; Male; Neuroprotective Agents; Rats, Inbred BN; Reperfusion Injury; Retinal Degeneration; Retinal Neurons; Valproic Acid | 2014 |
Biochemical analysis of phenotypic diversity associated with mutations in codon 244 of the retinal degeneration slow gene.
Topics: Amino Acid Substitution; Animals; Asparagine; Chlorocebus aethiops; Codon; COS Cells; Eye Proteins; Genetic Variation; Histidine; Intermediate Filament Proteins; Lysine; Membrane Glycoproteins; Membrane Proteins; Mice; Nerve Tissue Proteins; Peripherins; Phenotype; Retinal Degeneration; Tetraspanins | 2010 |
The separation of the diastereoisomers of isoleucine and hydroxylysine by ion exchange chromatography.
Topics: Chromatography; Chromatography, Ion Exchange; Hydroxylysine; Ion Exchange Resins; Isoleucine; Leucine; Lysine; Retinal Degeneration; Retinal Detachment | 1954 |
A three base pair deletion encoding the amino acid (lysine-270) in the alpha-cone transducin gene.
Topics: Adult; Amino Acid Sequence; Base Pairing; Base Sequence; Genotype; Humans; Lysine; Male; Models, Molecular; Molecular Sequence Data; Mutation; Pedigree; Photoreceptor Cells, Vertebrate; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Retinal Degeneration; Sequence Deletion; Transducin | 2004 |
Dietary compliance in ornithine aminotransferase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Female; Humans; Lysine; Male; Ornithine-Oxo-Acid Transaminase; Patient Compliance; Retinal Degeneration | 2006 |
Arrestin translocation in rod photoreceptors.
Topics: Animals; Arrestin; Cattle; Cycloheximide; Green Fluorescent Proteins; Light; Lysine; Microscopy, Confocal; Neurons; Protein Transport; Proto-Oncogene Proteins c-myc; Retinal Degeneration; Retinal Rod Photoreceptor Cells; Rhodopsin; Xenopus | 2006 |
Possible syndrome of high myopia with retinal degeneration, cataract, manic depression, and elevated plasma amino acids.
Topics: Aged; Amino Acids; Bipolar Disorder; Cataract; Female; Humans; Lysine; Male; Middle Aged; Myopia; Ornithine; Ornithine-Oxo-Acid Transaminase; Retinal Degeneration; Serine; Syndrome | 1980 |
Myopathy in hyperornithinemic gyrate atrophy of choroid and retina.
Topics: Adolescent; Adult; Biopsy; Child; Choroid; Female; Humans; Lysine; Male; Muscular Atrophy; Ornithine; Retinal Degeneration; Uveal Diseases | 1981 |
Clinical trial of vitamin B6 for gyrate atrophy of the choroid and retina.
Topics: Analysis of Variance; Atrophy; Choroid; Dose-Response Relationship, Drug; Electroretinography; Humans; Lysine; Ornithine; Pyridoxine; Retinal Degeneration; Uveal Diseases | 1981 |
Biochemical and therapeutical studies in a case of atrophia gyrata.
Topics: Adult; Atrophy; Choroid; Humans; Lysine; Male; Ornithine; Ornithine-Oxo-Acid Transaminase; Pedigree; Pyridoxine; Retina; Retinal Degeneration; Transaminases | 1982 |
Mice lacking ornithine-delta-aminotransferase have paradoxical neonatal hypoornithinaemia and retinal degeneration.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Animals; Animals, Newborn; Arginine; Base Sequence; DNA Primers; Food, Fortified; Genotype; Gyrate Atrophy; Humans; Infant; Lysine; Mammals; Mice; Mice, Mutant Strains; Molecular Sequence Data; Ornithine; Ornithine-Oxo-Acid Transaminase; Phenotype; Polymerase Chain Reaction; Retina; Retinal Degeneration | 1995 |
A novel mutation K167X of the XLRS1 gene (RS1) in a Taiwanese family with X-linked juvenile retinoschisis.
Topics: Amino Acid Substitution; Codon, Nonsense; Eye Proteins; Genetic Linkage; Humans; Lysine; Mutation; Retinal Degeneration; Taiwan; X Chromosome | 2000 |
Plasma amino-acids in hereditary retinal disease. Ornithine, lysine, and taurine.
Topics: Adolescent; Adult; Amino Acids; Atrophy; Child; Female; Humans; Lysine; Male; Middle Aged; Ornithine; Retinal Degeneration; Taurine | 1976 |
Amino acid abnormality in Sjögren-Larsson syndrome.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Dental Enamel Hypoplasia; Epilepsy; Ethylamines; Glutamine; Glycine; Histidine; Humans; Ichthyosis; Intellectual Disability; Isoleucine; Leucine; Lysine; Male; Muscle Spasticity; Retinal Degeneration; Serine; Syndrome; Valine | 1973 |