Compounds > cysteine

cysteine and Amaurosis

cysteine has been researched along with Amaurosis in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19904 (57.14)18.7374
1990's1 (14.29)18.2507
2000's2 (28.57)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gentleman, S; Lu, Z; Poliakov, E; Redmond, TM; Tsai, JY; Yu, S1
Capone, A; Dailey, W; Drenser, K; Trese, M; Wu, WC1
Sturman, JA1
Achatz, H; Berger, W; Cremers, F; Dörner, C; Gal, A; Haasemann, M; Hellebrand, H; Meindl, A; Meitinger, T; van de Pol, D1
Vullings, HG2
Chavez, Y; Cobo, A; Lisker, R; Zavala, C1

Other Studies

7 other study(ies) available for cysteine and Amaurosis

ArticleYear
Mutation of key residues of RPE65 abolishes its enzymatic role as isomerohydrolase in the visual cycle.
    Proceedings of the National Academy of Sciences of the United States of America, 2005, Sep-20, Volume: 102, Issue:38

    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.
    Archives of ophthalmology (Chicago, Ill. : 1960), 2007, Volume: 125, Issue:2

    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.
    Comprehensive therapy, 1977, Volume: 3, Issue:10

    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.
    Nature genetics, 1992, Volume: 2, Issue:2

    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).
    Zeitschrift fur Zellforschung und mikroskopische Anatomie (Vienna, Austria : 1948), 1973, Volume: 136, Issue:3

    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.
    Zeitschrift fur Zellforschung und mikroskopische Anatomie (Vienna, Austria : 1948), 1973, Volume: 146, Issue:4

    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.
    Clinical genetics, 1973, Volume: 4, Issue:2

    Topics: Adolescent; Adult; Aged; Blindness; Child, Preschool; Chromatography, Paper; Cysteine; Cystinuria; False Positive Reactions; Female; Homocystine; Homocystinuria; Humans; Male; Mexico; Middle Aged

1973