Compounds > lysine
Page last updated: 2024-08-17

lysine and Pigmentary Retinopathy

lysine has been researched along with Pigmentary Retinopathy in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's6 (75.00)18.2507
2000's1 (12.50)29.6817
2010's1 (12.50)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Akiyama, M; Fujiwara, K; Funatsu, J; Hisatomi, T; Ikeda, Y; Ishibashi, T; Ishizu, M; Koyanagi, Y; Momozawa, Y; Murakami, Y; Nakatake, S; Shimokawa, S; Sonoda, KH; Tachibana, T1
Bleeker-Wagemakers, EM; de Jong, LA; de Jong, PT; Gal, A; Riemslag, FC; van den Born, LI; van Schooneveld, MJ1
Akeo, K; Kudoh, J; Mashima, Y; Oguchi, Y; Saga, M; Shimizu, N1
Chida, Y; Kamio, K; Kikawa, E; Nakazawa, M; Shiono, T; Tamai, M1
Arden, GB; Bhattacharya, SS; Bird, AC; Fitzke, FW; Inglehearn, CF; Jay, M; Keen, TJ; Owens, SL1
al-Maghtheh, M; Bhattacharya, S; Bird, A; Inglehearn, C; Jay, M; Lunt, P1
Govardhan, CP; Oprian, DD1
Hwa, J; Khorana, HG; Klein-Seetharaman, J1

Other Studies

8 other study(ies) available for lysine and Pigmentary Retinopathy

ArticleYear
Relationships Between Serum Antioxidant and Oxidant Statuses and Visual Function in Retinitis Pigmentosa.
    Investigative ophthalmology & visual science, 2019, 10-01, Volume: 60, Issue:13

    Topics: Adult; Antioxidants; Biomarkers; Female; Glutathione Peroxidase; Glutathione Peroxidase GPX1; Humans; Lysine; Male; Oxidants; Oxidoreductases Acting on CH-NH Group Donors; Retinitis Pigmentosa; Superoxide Dismutase; Visual Acuity; Visual Field Tests; Visual Fields; Young Adult

2019
Thr4Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family.
    Ophthalmic genetics, 1994, Volume: 15, Issue:2

    Topics: Adult; Codon; Electroretinography; Female; Fundus Oculi; Humans; Lysine; Middle Aged; Netherlands; Pedigree; Photoreceptor Cells; Point Mutation; Retinitis Pigmentosa; Rhodopsin; Threonine; Vision Tests; Visual Fields

1994
Autosomal dominant retinitis pigmentosa. A mutation in codon 181 (Glu-->Lys) of the rhodopsin gene in a Japanese family.
    Ophthalmic genetics, 1994, Volume: 15, Issue:2

    Topics: Adult; Base Sequence; Codon; DNA Mutational Analysis; Female; Fluorescein Angiography; Fundus Oculi; Glutamic Acid; Humans; Japan; Lysine; Molecular Sequence Data; Photoreceptor Cells; Point Mutation; Polymerase Chain Reaction; Retinitis Pigmentosa; Rhodopsin; Visual Fields

1994
Ocular findings in patients with autosomal dominant retinitis pigmentosa and transversion mutation in codon 244 (Asn244Lys) of the peripherin/RDS gene.
    Archives of ophthalmology (Chicago, Ill. : 1960), 1994, Volume: 112, Issue:12

    Topics: Adult; Asparagine; Base Sequence; Child; Codon; Female; Genes, Dominant; Humans; Intermediate Filament Proteins; Lysine; Male; Membrane Glycoproteins; Middle Aged; Molecular Sequence Data; Mutation; Nerve Tissue Proteins; Neuropeptides; Pedigree; Peripherins; Retinitis Pigmentosa

1994
Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding site.
    The British journal of ophthalmology, 1994, Volume: 78, Issue:5

    Topics: Adolescent; Adult; Aged; Binding Sites; Dark Adaptation; Electroretinography; Female; Fundus Oculi; Genes, Dominant; Humans; Lysine; Male; Middle Aged; Mutation; Night Blindness; Pedigree; Retinaldehyde; Retinitis Pigmentosa; Rhodopsin; Vision Disorders; Visual Fields

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
Active site-directed inactivation of constitutively active mutants of rhodopsin.
    The Journal of biological chemistry, 1994, Mar-04, Volume: 269, Issue:9

    Topics: Amines; Amino Acid Sequence; Animals; Binding Sites; Cattle; Humans; Kinetics; Lysine; Molecular Structure; Point Mutation; Retinaldehyde; Retinitis Pigmentosa; Rhodopsin; Structure-Activity Relationship; Transducin

1994
Structure and function in rhodopsin: Mass spectrometric identification of the abnormal intradiscal disulfide bond in misfolded retinitis pigmentosa mutants.
    Proceedings of the National Academy of Sciences of the United States of America, 2001, Apr-24, Volume: 98, Issue:9

    Topics: Amino Acid Sequence; Animals; COS Cells; Cysteine; Disulfides; Endopeptidase K; Humans; Lysine; Maleimides; Models, Molecular; Molecular Sequence Data; Mutation; Protein Denaturation; Protein Folding; Protein Structure, Secondary; Retinitis Pigmentosa; Rhodopsin; Rod Opsins; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Structure-Activity Relationship

2001