histidine has been researched along with Retinal Degeneration in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (15.38) | 18.7374 |
| 1990's | 3 (23.08) | 18.2507 |
| 2000's | 5 (38.46) | 29.6817 |
| 2010's | 3 (23.08) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| 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 |
| Conley, SM; Naash, MI; Stricker, HM | 1 |
| Ferrell, WD; Jones, BW; Lee, DC; Marc, RE; Moritz, OL; Tam, BM; Vazquez-Chona, FR | 1 |
| Boonstra, FN; Brunner, HG; Cremers, FP; Koenekoop, RK; Kroes, HY; Schuil, J; van den Born, LI; van den Helm, B; van Genderen, MM; Yzer, S | 1 |
| Geller, S; LaVail, M; Lee, D; Matthes, M; Stone, J; Valter, K; Walsh, N; Yasumura, D | 1 |
| Chida, Y; Kikawa, E; Nakazawa, M; Shiono, T; Tamai, M; Wada, Y | 1 |
| Bush, RA; Kononen, L; Machida, S; Sieving, PA | 1 |
| Ayuso, C; Bueno, J; Carballo, M; García-Sandoval, B; Giménez, A; Lorda, I; Martinez-Gimeno, M; Ramos, C; Trujillo, MJ | 1 |
| Frens, DB; Jacobson, DM; Johnson, R | 1 |
| Fishman, GA; Khadivi, P; Kimura, AE; Nichols, BE; Sheffield, VC; Stone, EM | 1 |
| Holmgren, G; Nordström, S; Thorburn, W | 1 |
| Ionasescu, V; Mueller, S; Stegink, L; Weinstein, M | 1 |
13 other study(ies) available for histidine and Retinal Degeneration
| Article | Year |
|---|---|
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 |
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 |
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 |
A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population.
Topics: Amino Acid Substitution; Carrier Proteins; cis-trans-Isomerases; Disease Progression; DNA; DNA Mutational Analysis; Eye Proteins; Family Health; Female; Founder Effect; Genetic Variation; Heterozygote; Histidine; Homozygote; Humans; Male; Mutation; Netherlands; Pedigree; Proteins; Retinal Degeneration; Tyrosine | 2003 |
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 |
Autosomal dominant cone-rod dystrophy associated with mutations in codon 244 (Asn244His) and codon 184 (Tyr184Ser) of the peripherin/RDS gene.
Topics: Adult; Aged; Amino Acid Sequence; Asparagine; Base Sequence; Codon; DNA; Electroretinography; Eye Proteins; Female; Fluorescein Angiography; Histidine; Humans; Intermediate Filament Proteins; Male; Membrane Glycoproteins; Middle Aged; Molecular Sequence Data; Nerve Tissue Proteins; Pedigree; Peripherins; Photoreceptor Cells; Point Mutation; Polymorphism, Single-Stranded Conformational; Retinal Degeneration; Serine; Tyrosine; Visual Fields | 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 |
Two novel mutations (Y141H; C214Y) and previously published mutation (R142W) in the RDS-peripherin gene in autosomal dominant macular dystrophies in Spanish families.
Topics: Amino Acid Substitution; Arginine; Cysteine; Electrophoresis, Polyacrylamide Gel; Eye Proteins; Genes, Dominant; Histidine; Humans; Intermediate Filament Proteins; Macular Degeneration; Membrane Glycoproteins; Mutation, Missense; Nerve Tissue Proteins; Peripherins; Polymerase Chain Reaction; Retinal Degeneration; Tryptophan; Tyrosine | 2001 |
Joubert's syndrome, ocular fibrosis, and normal histidine levels.
Topics: Cerebellum; Female; Fibrosis; Histidine; Humans; Infant; Magnetic Resonance Imaging; Nystagmus, Pathologic; Retinal Degeneration; Strabismus; Syndrome | 1992 |
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 |
Urinary metabolic studies in hereditary macular degeneration.
Topics: Albuminuria; Amino Acids; Carbohydrates; Cystinuria; Electrophoresis, Paper; Female; Glycosuria; Histidine; Humans; Keto Acids; Male; Pedigree; Phenylketonurias; Retinal Degeneration; Syndrome; Tyrosine | 1974 |
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 |