Compounds > methionine

Page last updated: 2024-08-17

methionine and Pigmentary Retinopathy

methionine has been researched along with Pigmentary Retinopathy in 11 studies

Research

Studies (11)

Timeframe	Studies, this research(%)	All Research%
pre-1990	4 (36.36)	18.7374
1990's	4 (36.36)	18.2507
2000's	1 (9.09)	29.6817
2010's	2 (18.18)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Almansa, I; Benlloch-Navarro, S; López-Pedrajas, R; Miranda, M; Romero, FJ; Sánchez-Vallejo, V; Trachsel-Moncho, L	1
Gaillard, MC; Munier, FL; Schorderet, DF; Tiab, L; Vaclavik, V	1
Jacobson, SG; Li, ZY; Milam, AH	1
Antich, J; Ayuso, C; Carballo, M; Garcia-Sandoval, B; Gean, E; Ramos, C; Reig, C	1
al-Maghtheh, M; Bhattacharya, S; Bird, A; Inglehearn, C; Jay, M; Lunt, P	1
Attardi, G; Henderson, NS; Holt, IJ; Nijtmans, LG	1
Berson, EL	1
Berson, EL; Dryja, TP; Sandberg, MA	1
Herron, WL; Riegel, BW	1
Herron, WL; Myers, OE; Riegel, BW; Rubin, ML	1
Matsuura, K	1

Reviews

1 review(s) available for methionine and Pigmentary Retinopathy

Article	Year
Hereditary and nutritionally induced retinal degenerations: electrophysiologic and biochemical studies. Birth defects original article series, 1976, Volume: 12, Issue:3 Topics: Adolescent; Adult; Animals; Caseins; Child; Cysteine; Electrophysiology; Electroretinography; Humans; Metabolism, Inborn Errors; Methionine; Photoreceptor Cells; Retinal Degeneration; Retinitis Pigmentosa; Taurine	1976

Other Studies

10 other study(ies) available for methionine and Pigmentary Retinopathy

Article	Year
Alterations in glutamate cysteine ligase content in the retina of two retinitis pigmentosa animal models. Free radical biology & medicine, 2016, Volume: 96 Topics: Animals; Cysteine; Disease Models, Animal; Glutamate-Cysteine Ligase; Glutathione Disulfide; Humans; Methionine; Mice; Oxidative Stress; Retina; Retinal Degeneration; Retinitis Pigmentosa; Sulfoxides	2016
Variable phenotypic expressivity in a Swiss family with autosomal dominant retinitis pigmentosa due to a T494M mutation in the PRPF3 gene. Molecular vision, 2010, Mar-19, Volume: 16 Topics: Adult; Aged; Amino Acid Substitution; Base Sequence; Child; Child, Preschool; DNA Mutational Analysis; Electroretinography; Family; Female; Fluorescence; Fundus Oculi; Genes, Dominant; Humans; Male; Methionine; Middle Aged; Molecular Sequence Data; Mutation; Nuclear Proteins; Phenotype; Retinitis Pigmentosa; Ribonucleoprotein, U4-U6 Small Nuclear; Switzerland; Threonine; Young Adult	2010
Autosomal dominant retinitis pigmentosa caused by the threonine-17-methionine rhodopsin mutation: retinal histopathology and immunocytochemistry. Experimental eye research, 1994, Volume: 58, Issue:4 Topics: Aged; Fluorescent Antibody Technique; Genes, Dominant; Humans; Male; Methionine; Microscopy, Electron; Microscopy, Immunoelectron; Mutation; Photoreceptor Cells; Retina; Retinitis Pigmentosa; Rhodopsin; Threonine; Vision, Ocular	1994
Identification of a novel rhodopsin mutation (Met-44-Thr) in a simplex case of retinitis pigmentosa. Human genetics, 1994, Volume: 94, Issue:3 Topics: Adolescent; Aged; DNA Mutational Analysis; Electrophoresis, Agar Gel; Exons; Female; Humans; Male; Methionine; Middle Aged; Pedigree; Point Mutation; Polymerase Chain Reaction; Retinitis Pigmentosa; Rhodopsin; Threonine	1994
Two new rhodopsin transversion mutations (L40R; M216K) in families with autosomal dominant retinitis pigmentosa. Human mutation, 1994, Volume: 3, Issue:4 Topics: Arginine; Genes, Dominant; Humans; Leucine; Lysine; Methionine; Point Mutation; Protein Conformation; Retinitis Pigmentosa; Rhodopsin	1994
Impaired ATP synthase assembly associated with a mutation in the human ATP synthase subunit 6 gene. The Journal of biological chemistry, 2001, Mar-02, Volume: 276, Issue:9 Topics: Adenosine Triphosphate; Ataxia; DNA, Mitochondrial; Humans; Methionine; Muscle Weakness; Mutation; Protein Subunits; Proton-Translocating ATPases; Retinitis Pigmentosa	2001
Autosomal dominant retinitis pigmentosa with rhodopsin, valine-345-methionine. Transactions of the American Ophthalmological Society, 1991, Volume: 89 Topics: Adult; Amino Acid Sequence; Child; Dark Adaptation; Electroretinography; Female; Fundus Oculi; Humans; Male; Methionine; Middle Aged; Molecular Sequence Data; Mutagenesis, Site-Directed; Pedigree; Retinitis Pigmentosa; Rhodopsin; Valine; Visual Fields	1991
Production rate and removal of rod outer segment material in vitamin A deficiency. Investigative ophthalmology, 1974, Volume: 13, Issue:1 Topics: Animals; Autoradiography; Diagnosis, Differential; Diet; Disease Models, Animal; Electroretinography; Epithelium; Eye Proteins; Methionine; Phagocytosis; Photoreceptor Cells; Rats; Retina; Retinal Diseases; Retinitis Pigmentosa; Time Factors; Tritium; Vitamin A Deficiency	1974
Retinal dystrophy in the rat--a pigment epithelial disease. Investigative ophthalmology, 1969, Volume: 8, Issue:6 Topics: Age Factors; Animals; Autoradiography; Epithelium; Methionine; Microscopy, Electron; Phagocytosis; Photoreceptor Cells; Pigments, Biological; Rats; Retina; Retinal Degeneration; Retinitis Pigmentosa; Time Factors; Tritium	1969
[Biochemical studies on the pathogenesis on retinitis pigmentosa. 2. The concentration of GSH in blood of patients with retinitis pigmentosa]. Nippon Ganka Gakkai zasshi, 1969, Volume: 73, Issue:9 Topics: Adult; Aged; Alloxan; Dark Adaptation; Female; Glutathione; Humans; Male; Methionine; Methods; Middle Aged; Oxidation-Reduction; Retinitis Pigmentosa; Veins; Visual Acuity	1969