Page last updated: 2024-08-17

aspartic acid and Pigmentary Retinopathy

aspartic acid has been researched along with Pigmentary Retinopathy in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19902 (28.57)18.7374
1990's1 (14.29)18.2507
2000's3 (42.86)29.6817
2010's0 (0.00)24.3611
2020's1 (14.29)2.80

Authors

AuthorsStudies
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, ES1
Chou, CL; Lin, CS; Palmer, N; Tsang, SH; Tsui, I1
Baracca, A; Casalena, GA; DiMauro, S; Lenaz, G; Sgarbi, G; Solaini, G1
Airaksinen, EM; Marnela, KM; Oja, SS; Sihvola, P1
Fuchs, S; Gal, A; Millán, JM; Nájera, C; Paricio, N; Prieto, F; Wedemann, H1
Fletcher, EL1
Lee, TY; Onisawa, J1

Reviews

1 review(s) available for aspartic acid and Pigmentary Retinopathy

ArticleYear
Alterations in neurochemistry during retinal degeneration.
    Microscopy research and technique, 2000, Jul-15, Volume: 50, Issue:2

    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

Other Studies

6 other study(ies) available for aspartic acid and Pigmentary Retinopathy

ArticleYear
A budding yeast model for human disease mutations in the
    RNA (New York, N.Y.), 2021, Volume: 27, Issue:9

    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.
    Current eye research, 2008, Volume: 33, Issue:11

    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.
    Archives of neurology, 2009, Volume: 66, Issue:8

    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.
    Annals of clinical research, 1980, Volume: 12, Issue:2

    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.
    Molecular and cellular probes, 1995, Volume: 9, Issue:1

    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.
    Biochemical medicine, 1970, Volume: 3, Issue:5

    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