aspartic acid has been researched along with Pigmentary Retinopathy in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (28.57) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 3 (42.86) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (14.29) | 2.80 |
Authors | Studies |
---|---|
Baker, RE; Basrai, MA; Corbett, AH; Enyenihi, L; Farchi, D; Fasken, MB; Hess, L; Kremsky, I; Lee, RS; Leung, SW; Sterrett, MC; Strassler, SE; van Hoof, A; Withers, ES | 1 |
Chou, CL; Lin, CS; Palmer, N; Tsang, SH; Tsui, I | 1 |
Baracca, A; Casalena, GA; DiMauro, S; Lenaz, G; Sgarbi, G; Solaini, G | 1 |
Airaksinen, EM; Marnela, KM; Oja, SS; Sihvola, P | 1 |
Fuchs, S; Gal, A; Millán, JM; Nájera, C; Paricio, N; Prieto, F; Wedemann, H | 1 |
Fletcher, EL | 1 |
Lee, TY; Onisawa, J | 1 |
1 review(s) available for aspartic acid and Pigmentary Retinopathy
Article | Year |
---|---|
Alterations in neurochemistry during retinal degeneration.
Topics: Animals; Animals, Newborn; Aspartic Acid; gamma-Aminobutyric Acid; Glutamic Acid; Glutamine; Glycine; Humans; Immunohistochemistry; Neurotransmitter Agents; Photoreceptor Cells, Vertebrate; Rats; Retina; Retinal Degeneration; Retinitis Pigmentosa; Time Factors | 2000 |
6 other study(ies) available for aspartic acid and Pigmentary Retinopathy
Article | Year |
---|---|
A budding yeast model for human disease mutations in the
Topics: Amino Acid Sequence; Amino Acid Substitution; Aspartic Acid; Dwarfism; Exoribonucleases; Exosome Multienzyme Ribonuclease Complex; Facies; Gene Expression; Glycine; Hearing Loss; Humans; Models, Biological; Models, Molecular; Mutation, Missense; Protein Conformation; Retinitis Pigmentosa; RNA-Binding Proteins; RNA, Fungal; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Sequence Homology, Amino Acid; Syndrome | 2021 |
Phenotype-genotype correlations in autosomal dominant retinitis pigmentosa caused by RHO, D190N.
Topics: Adolescent; Adult; Asparagine; Aspartic Acid; Child; Electroretinography; Fluorescence; Fundus Oculi; Genes, Dominant; Genotype; Humans; Male; Middle Aged; Mutation; Pedigree; Phenotype; Retinal Pigment Epithelium; Retinitis Pigmentosa; Rhodopsin; Visual Acuity; Visual Fields; Young Adult | 2008 |
Human NARP mitochondrial mutation metabolism corrected with alpha-ketoglutarate/aspartate: a potential new therapy.
Topics: Adenosine Triphosphate; Anti-Infective Agents, Local; Aspartic Acid; C-Reactive Protein; Cell Line; Cell Survival; DNA, Mitochondrial; Energy Metabolism; Gramicidin; Humans; Ketoglutaric Acids; Leigh Disease; Mitochondria; Mitochondrial Proton-Translocating ATPases; Mutation; Nerve Tissue Proteins; Oligomycins; Oxidative Phosphorylation; Retinitis Pigmentosa; Spinocerebellar Degenerations | 2009 |
Taurine and other amino acids of platelets and plasma in retinitis pigmentosa.
Topics: Adolescent; Adult; Aged; Amino Acids; Aspartic Acid; Blood Platelets; Female; Humans; Male; Middle Aged; Retinitis Pigmentosa; Taurine | 1980 |
Gly114Asp mutation of rhodopsin in autosomal dominant retinitis pigmentosa.
Topics: Adolescent; Adult; Amino Acid Sequence; Aspartic Acid; Base Sequence; Codon; Female; Genes, Dominant; Glycine; Humans; Male; Middle Aged; Molecular Sequence Data; Pedigree; Point Mutation; Polymorphism, Genetic; Retinitis Pigmentosa; Rhodopsin | 1995 |
Biochemical studies of urinary acid mucopolysaccharide--peptide complexes in Hurler's syndrome.
Topics: Amino Acids; Aspartic Acid; Bone and Bones; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chondroitin; Chromatography, Ion Exchange; Female; Galactosamine; Glucosamine; Glutamates; Glycine; Glycosaminoglycans; Humans; Hypertrichosis; Joint Diseases; Male; Mucopolysaccharidosis I; Retinitis Pigmentosa; Serine; Uronic Acids | 1970 |