cysteine has been researched along with Amaurosis in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (57.14) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 2 (28.57) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Gentleman, S; Lu, Z; Poliakov, E; Redmond, TM; Tsai, JY; Yu, S | 1 |
Capone, A; Dailey, W; Drenser, K; Trese, M; Wu, WC | 1 |
Sturman, JA | 1 |
Achatz, H; Berger, W; Cremers, F; Dörner, C; Gal, A; Haasemann, M; Hellebrand, H; Meindl, A; Meitinger, T; van de Pol, D | 1 |
Vullings, HG | 2 |
Chavez, Y; Cobo, A; Lisker, R; Zavala, C | 1 |
7 other study(ies) available for cysteine and Amaurosis
Article | Year |
---|---|
Mutation of key residues of RPE65 abolishes its enzymatic role as isomerohydrolase in the visual cycle.
Topics: Acyltransferases; Amino Acid Substitution; Animals; Blindness; Carrier Proteins; Cattle; Cell Line; cis-trans-Isomerases; Cysteine; Dogs; Eye Proteins; Humans; Iron; Isomerases; Mice; Oxygenases; Point Mutation; Protein Processing, Post-Translational; Retina; Retinaldehyde; Transfection; Vision, Ocular | 2005 |
Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene.
Topics: Amino Acid Sequence; Blindness; Child, Preschool; Cysteine; Deafness; DNA Mutational Analysis; Eye Diseases, Hereditary; Eye Proteins; Female; Genotype; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Molecular Sequence Data; Mutation; Nerve Tissue Proteins; Phenotype; Polymerase Chain Reaction; Retina; Vitreoretinopathy, Proliferative | 2007 |
Taurine in nutrition.
Topics: Animals; Blindness; Brain; Cysteine; Epilepsy; Female; Humans; Infant; Infant Nutritional Physiological Phenomena; Infant, Newborn; Myocardium; Nutritional Physiological Phenomena; Nutritional Requirements; Pregnancy; Retina; Retinal Degeneration; Taurine | 1977 |
Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins.
Topics: Adult; Amino Acid Sequence; Base Sequence; Blindness; Child; Child, Preschool; Chromosome Mapping; Cysteine; Deafness; DNA; DNA Mutational Analysis; Exons; Genetic Linkage; Humans; Infant; Intellectual Disability; Introns; Male; Molecular Sequence Data; Mucins; Point Mutation; Sequence Homology, Amino Acid; X Chromosome | 1992 |
Influence of light and darkness on the hypothalamo-hypophysial system of blinded and unilaterally blinded frogs (Rana temporaria).
Topics: Animals; Anura; Autoradiography; Blindness; Cell Nucleus; Cysteine; Darkness; Hypothalamo-Hypophyseal System; Hypothalamus; Light; Optic Nerve; Rana temporaria; Retina; Sulfur Isotopes; Time Factors | 1973 |
Influence of light and darkness on the hypothalamo-hypophysial system of Rana esculenta and the involvement of the pineal complex.
Topics: Adaptation, Physiological; Animals; Anura; Autoradiography; Blindness; Cerebral Ventricles; Cysteine; Darkness; Hypothalamo-Hypophyseal System; Hypothalamus; Light; Neurosecretion; Pineal Gland; Rana esculenta; Rana temporaria; Sulfur Radioisotopes; Time Factors | 1973 |
Frequency of homocystinuria amongst the blind.
Topics: Adolescent; Adult; Aged; Blindness; Child, Preschool; Chromatography, Paper; Cysteine; Cystinuria; False Positive Reactions; Female; Homocystine; Homocystinuria; Humans; Male; Mexico; Middle Aged | 1973 |