arginine and Retinal Degeneration

arginine has been researched along with Retinal Degeneration in 37 studies

Research

Studies (37)

Timeframe	Studies, this research(%)	All Research%
pre-1990	11 (29.73)	18.7374
1990's	14 (37.84)	18.2507
2000's	9 (24.32)	29.6817
2010's	2 (5.41)	24.3611
2020's	1 (2.70)	2.80

Authors

Authors	Studies
Chen, Q; Ding, LJ; Huang, XF; Lu, F; Rao, FQ; Xiang, L; Xie, BT; Yan, T; Yang, QL; Zeng, HY	1
Defoort-Dhellemmes, S; Dhaenens, CM; Smirnov, VM; Vincent-Delorme, C	1
Arsenijevic, Y; Bemelmans, AP; Crippa, SV; Grimm, C; Kostic, C; Pignat, V; Samardzija, M; Wenzel, A	1
Itabashi, T; Kawamura, M; Kunikata, H; Sato, H; Tamai, M; Wada, Y	1
Abrahamson, M; Andréasson, S; Eksandh, L; Ponjavic, V; Schatz, P	1
Ding, X; Feathers, KL; Feng, W; Gal, A; Liu, Y; McHenry, CL; Nair, AR; Sieving, PA; Thompson, DA; Vollrath, D	1
Fiona, WJ; Santos, L; Walter, JH	1
Bandello, F; Garrè, C; Interlandi, E; Marini, V; Pognuz, DR; Rossi, S; Simonelli, F; Testa, F; Virgili, G	1
Arshinoff, SA; Bell, L; Marliss, EB; McCulloch, JC; McInnes, RR	1
Brusilow, S; de Monasterio, F; Kaiser-Kupfer, MI; Valle, D; Walser, M	1
Kaiser-Kupfer, M; Valle, D	1
Berson, EL; Shih, VE; Sullivan, PL	1
Brusilow, S; Kaiser-Kupfer, MI; Takki, K; Valle, D; Walser, M	1
Berson, EL; Gargiulo, M; Shih, VE	1
Brusilow, SW; Kaiser-Kupfer, M; Valle, D; Walser, M	1
Brusilow, S; de Monasterio, FM; Kaiser-Kupfer, MI; Valle, D; Walser, M	1
Becquet, F; Courtois, Y; Goureau, O; Hartmann, MP; Jeanny, JC	1
Feist, RM; Skalka, H; Stone, EM; White, MF	1
Lawler, AM; Milam, AH; Sipila, I; Steel, G; Valle, D; Wang, T	1
Lam, BL; Sheffield, VC; Stone, EM; Vandenburgh, K	1
Ferrell, RE; Gass, JD; Gorin, MB; Jackson, KE; Jacobson, SG; Mitchell, E; Sheffield, VC; Stone, EM	1
Blankenagel, A; Fuchs, S; Gal, A; Grüning, G; Krastel, H; Meins, M; Reck, B; Schwinger, E	1
Arden, G; Bhattacharya, S; Eckstein, A; Fitzke, F; Inglehearn, C; Jay, M; Jubb, C; Keen, J; Wells, J; Wroblewski, J	1
Benlian, P; Coscas, GJ; Gerber, S; Kaplan, J; Munnich, A; Soubrane, G; Souied, E	1
Deutman, AF; Heutink, P; Hoyng, CB; Oostra, BA; Pinckers, A; Testers, L	1
Fletcher, EL; Kalloniatis, M	1
Hejtmancik, FJ; Shastry, BS; Trese, MT	1
Bingham, EL; Hiriyanna, K; Kemp, J; Richards, J; Sieving, PA	1
Duda, T; Koch, KW; Krishnan, A; Lange, C; Sharma, RK; Venkataraman, V	1
Milam, AH; Steel, G; Valle, D; Wang, T	1
Arnaud, B; Bareil, C; Claustres, M; Delague, V; Demaille, J; Hamel, C	1
Birch, DG; Bowne, SJ; Daiger, SP; Heckenlively, JR; Lewis, RA; Mintz-Hittner, H; Northrup, H; Rodriquez, JA; Ruiz, RS; Saperstein, DA; Sohocki, MM; Sullivan, LS	1
Ayuso, C; Bueno, J; Carballo, M; García-Sandoval, B; Giménez, A; Lorda, I; Martinez-Gimeno, M; Ramos, C; Trujillo, MJ	1
Caruso, RC; Kaiser-Kupfer, MI; Valle, D	1
Brody, LC; Engelhardt, JF; Kaiser-Kupfer, M; Looney, JE; Mitchell, GA; Obie, C; Patel, AS; Sipila, I; Steel, G; Wong, C	1
Jones, ME	1
Visek, WJ	1

Reviews

1 review(s) available for arginine and Retinal Degeneration

Article	Year
Gyrate atrophy of the choroid and retina. Progress in clinical and biological research, 1982, Volume: 82 Topics: Arginine; Choroid; Creatine; Diet; Genes, Recessive; Humans; Ornithine; Ornithine-Oxo-Acid Transaminase; Pyridoxine; Retinal Degeneration; Uveal Diseases	1982

Other Studies

36 other study(ies) available for arginine and Retinal Degeneration

Article	Year
Dysregulated Arginine Metabolism Is Linked to Retinal Degeneration in Cep250 Knockout Mice. Investigative ophthalmology & visual science, 2023, 09-01, Volume: 64, Issue:12 Topics: Animals; Arginine; Ciliopathies; Mice; Mice, Knockout; Retina; Retinal Degeneration	2023
[Triple hyperautofluorescent retinal ring. Pathognomonic appearance of c.166G>A NR2E3-related inherited retinal degeneration]. Journal francais d'ophtalmologie, 2019, Volume: 42, Issue:3 Topics: Adolescent; Amino Acid Substitution; Arginine; Female; Fluorescence; Glycine; Humans; Optical Imaging; Orphan Nuclear Receptors; Polymorphism, Single Nucleotide; Retina; Retinal Degeneration; Retinal Dystrophies; Tomography, Optical Coherence	2019
Gene therapy regenerates protein expression in cone photoreceptors in Rpe65(R91W/R91W) mice. PloS one, 2011, Feb-03, Volume: 6, Issue:2 Topics: Amino Acid Substitution; Animals; Arginine; Carrier Proteins; Cells, Cultured; cis-trans-Isomerases; Eye Proteins; Gene Expression; Genetic Therapy; Homozygote; Humans; Mice; Mice, Transgenic; Mutant Proteins; Mutation, Missense; Proteins; Retinal Cone Photoreceptor Cells; Retinal Degeneration; Tryptophan	2011
Ocular findings in a Japanese family with an Arg41Trp mutation of the CRX gene. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2003, Volume: 241, Issue:7 Topics: Adult; Aged; Aged, 80 and over; Arginine; Asian People; Base Sequence; Electroretinography; Female; Fluorescein Angiography; Fundus Oculi; Genes, Dominant; Homeodomain Proteins; Humans; Male; Middle Aged; Mutation; Pedigree; Retinal Cone Photoreceptor Cells; Retinal Degeneration; Retinal Rod Photoreceptor Cells; Trans-Activators; Tryptophan; Visual Fields	2003
Macular appearance by means of OCT and electrophysiology in members of two families with different mutations in RDS (the peripherin/RDS gene). Acta ophthalmologica Scandinavica, 2003, Volume: 81, Issue:5 Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Arginine; Codon, Terminator; Electroretinography; Female; Humans; Intermediate Filament Proteins; Leucine; Macula Lutea; Male; Membrane Glycoproteins; Middle Aged; Molecular Biology; Nerve Tissue Proteins; Pedigree; Peripherins; Phenotype; Retinal Degeneration; Serine; Tomography, Optical Coherence; Visual Acuity; Visual Fields	2003
MERTK arginine-844-cysteine in a patient with severe rod-cone dystrophy: loss of mutant protein function in transfected cells. Investigative ophthalmology & visual science, 2004, Volume: 45, Issue:5 Topics: Adolescent; Arginine; Blotting, Western; c-Mer Tyrosine Kinase; Cysteine; Female; Gene Expression Regulation; Genetic Variation; Humans; Kidney; Mutation, Missense; Phosphorylation; Photoreceptor Cells, Vertebrate; Polymorphism, Single-Stranded Conformational; Proto-Oncogene Proteins; Receptor Protein-Tyrosine Kinases; Retinal Degeneration; Reverse Transcriptase Polymerase Chain Reaction; Transfection; Tyrosine	2004
Dietary compliance in ornithine aminotransferase deficiency. Journal of inherited metabolic disease, 2006, Volume: 29, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Female; Humans; Lysine; Male; Ornithine-Oxo-Acid Transaminase; Patient Compliance; Retinal Degeneration	2006
Intrafamilial clinical heterogeneity associated with a novel mutation of the retinal degeneration slow/peripherin gene. Ophthalmic research, 2007, Volume: 39, Issue:5 Topics: Aged; Arginine; Cysteine; Electrooculography; Electroretinography; Fluorescence; Fundus Oculi; Genetic Heterogeneity; Humans; Intermediate Filament Proteins; Membrane Glycoproteins; Middle Aged; Mutation; Nerve Tissue Proteins; Pedigree; Peripherins; Phenotype; Retinal Degeneration; Visual Acuity	2007
Hyperornithinaemia and gyrate atrophy of the retina: improvement of vision during treatment with a low-arginine diet. Lancet (London, England), 1981, Mar-07, Volume: 1, Issue:8219 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Arginine; Atrophy; Depression, Chemical; Humans; Male; Ornithine; Ornithine-Oxo-Acid Transaminase; Retinal Degeneration; Visual Acuity	1981
Visual results of a long-term trial of a low-arginine diet in gyrate atrophy of choroid and retina. Ophthalmology, 1981, Volume: 88, Issue:4 Topics: Adult; Arginine; Atrophy; Choroid; Color Vision Defects; Dark Adaptation; Electroretinography; Female; Humans; Middle Aged; Retinal Degeneration; Uveal Diseases; Vision Disorders	1981
Ocular findings in patients with gyrate atrophy on pyridoxine and low-protein, low-arginine diets. Ophthalmology, 1981, Volume: 88, Issue:4 Topics: Adolescent; Adult; Arginine; Atrophy; Child; Choroid; Dark Adaptation; Dietary Proteins; Electroretinography; Female; Humans; Male; Ornithine; Pyridoxine; Retinal Degeneration; Uveal Diseases; Vision Disorders; Visual Acuity; Visual Fields	1981
Gyrate atrophy of the choroid and retina. Biochemical considerations and experience with an arginine-restricted diet. Ophthalmology, 1981, Volume: 88, Issue:4 Topics: Adolescent; Adult; Aminoisobutyric Acids; Arginine; Atrophy; Child; Choroid; Female; Humans; Male; Middle Aged; Ornithine; Ornithine-Oxo-Acid Transaminase; Retinal Degeneration; Uveal Diseases	1981
Reduction of hyperornithinemia with a low protein, low arginine diet and pyridoxine in patients with a deficiency of ornithine-ketoacid transaminase (OKT) activity and gyrate atrophy of the choroid and retina. Clinica chimica acta; international journal of clinical chemistry, 1981, Jul-01, Volume: 113, Issue:3 Topics: Adolescent; Adult; Amino Acids, Essential; Arginine; Child; Choroid; Dietary Proteins; Female; Humans; Male; Ornithine; Ornithine-Oxo-Acid Transaminase; Pyridoxine; Retinal Degeneration; Transaminases; Uveal Diseases	1981
Gyrate atrophy of the choroid and retina: amino acid metabolism and correction of hyperornithinemia with an arginine-deficient diet. The Journal of clinical investigation, 1980, Volume: 65, Issue:2 Topics: Adult; Amino Acids; Arginine; Choroid; Diet; Female; Humans; Male; Middle Aged; Ornithine; Retinal Degeneration; Retinal Detachment; Time Factors; Uveal Diseases	1980
Gyrate atrophy of the choroid and retina: improved visual function following reduction of plasma ornithine by diet. Science (New York, N.Y.), 1980, Dec-05, Volume: 210, Issue:4474 Topics: Adult; Arginine; Choroid; Color Perception; Dark Adaptation; Dietary Proteins; Female; Humans; Ornithine; Photoreceptor Cells; Retinal Degeneration; Uveal Diseases; Vision, Ocular	1980
Protection against light-induced retinal degeneration by an inhibitor of NO synthase. Neuroreport, 1993, Dec-13, Volume: 5, Issue:3 Topics: Amino Acid Oxidoreductases; Animals; Arginine; Injections, Intraperitoneal; Light; Male; NG-Nitroarginine Methyl Ester; Nitric Oxide Synthase; Photoreceptor Cells; Rats; Retinal Degeneration	1993
Choroidal neovascularization in a patient with adult foveomacular dystrophy and a mutation in the retinal degeneration slow gene (Pro 210 Arg) American journal of ophthalmology, 1994, Aug-15, Volume: 118, Issue:2 Topics: Arginine; Choroid; Eye Proteins; Fovea Centralis; Humans; Intermediate Filament Proteins; Macular Degeneration; Male; Membrane Glycoproteins; Middle Aged; Mutation; Neovascularization, Pathologic; Nerve Tissue Proteins; Peripherins; Proline; Retinal Degeneration	1994
Mice lacking ornithine-delta-aminotransferase have paradoxical neonatal hypoornithinaemia and retinal degeneration. Nature genetics, 1995, Volume: 11, Issue:2 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Animals; Animals, Newborn; Arginine; Base Sequence; DNA Primers; Food, Fortified; Genotype; Gyrate Atrophy; Humans; Infant; Lysine; Mammals; Mice; Mice, Mutant Strains; Molecular Sequence Data; Ornithine; Ornithine-Oxo-Acid Transaminase; Phenotype; Polymerase Chain Reaction; Retina; Retinal Degeneration	1995
Retinitis pigmentosa associated with a dominant mutation in codon 46 of the peripherin/RDS gene (arginine-46-stop). American journal of ophthalmology, 1995, Volume: 119, Issue:1 Topics: Adult; Amino Acid Sequence; Arginine; Base Sequence; Codon; DNA; Electroretinography; Fundus Oculi; Genes, Dominant; Humans; Intermediate Filament Proteins; Male; Membrane Glycoproteins; Middle Aged; Molecular Sequence Data; Mutation; Nerve Tissue Proteins; Neuropeptides; Pedigree; Peripherins; Polymerase Chain Reaction; Prospective Studies; Retinal Degeneration; Retinitis Pigmentosa; Rhodopsin	1995
A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration. Ophthalmology, 1995, Volume: 102, Issue:2 Topics: Adolescent; Adult; Aged; Amino Acid Sequence; Arginine; Base Sequence; Chromosome Deletion; DNA Mutational Analysis; Electrophoresis, Polyacrylamide Gel; Eye Proteins; Female; Fluorescein Angiography; Fundus Oculi; Humans; Intermediate Filament Proteins; Macular Degeneration; Male; Membrane Glycoproteins; Middle Aged; Molecular Sequence Data; Nerve Tissue Proteins; Pedigree; Peripherins; Phenotype; Point Mutation; Polymerase Chain Reaction; Proline; Retinal Degeneration; Visual Fields	1995
Heterozygous 'null allele' mutation in the human peripherin/RDS gene. Human molecular genetics, 1993, Volume: 2, Issue:12 Topics: Alleles; Animals; Arginine; Base Sequence; Exons; Genetic Carrier Screening; Humans; Intermediate Filament Proteins; Male; Membrane Glycoproteins; Mice; Middle Aged; Mutation; Nerve Tissue Proteins; Neuropeptides; Peripherins; Polymerase Chain Reaction; Retinal Degeneration	1993
Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy. Nature genetics, 1993, Volume: 3, Issue:3 Topics: Adult; Amino Acid Sequence; Arginine; Base Sequence; Cysteine; DNA; Exons; Eye Proteins; Female; Fluorescein Angiography; Genes, Dominant; Glutamine; Humans; Intermediate Filament Proteins; Macular Degeneration; Male; Membrane Glycoproteins; Molecular Sequence Data; Nerve Tissue Proteins; Oligodeoxyribonucleotides; Pedigree; Peripherins; Point Mutation; Polymerase Chain Reaction; Retinal Degeneration; Retinitis Pigmentosa; Sequence Deletion; Tryptophan	1993
Retinitis punctata albescens associated with the Arg135Trp mutation in the rhodopsin gene. American journal of ophthalmology, 1996, Volume: 121, Issue:1 Topics: Adolescent; Adult; Amino Acid Sequence; Apolipoproteins E; Arginine; Base Sequence; DNA; Eye Proteins; Female; Fundus Oculi; Humans; Infant; Intermediate Filament Proteins; Male; Membrane Glycoproteins; Membrane Proteins; Molecular Sequence Data; Mutation; Nerve Tissue Proteins; Pedigree; Peripherins; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Retinal Degeneration; Retinitis Pigmentosa; Rhodopsin; Rod Cell Outer Segment; Tetraspanins; Tryptophan	1996
Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS gene. American journal of ophthalmology, 1996, Volume: 121, Issue:6 Topics: Adult; Aged; Amino Acid Sequence; Arginine; Base Sequence; Choroid Diseases; Codon; DNA; DNA Mutational Analysis; DNA Primers; Eye Proteins; Female; Fluorescein Angiography; Fundus Oculi; Humans; Intermediate Filament Proteins; Male; Membrane Glycoproteins; Middle Aged; Molecular Sequence Data; Nerve Tissue Proteins; Pedigree; Peripherins; Point Mutation; Polymerase Chain Reaction; Retinal Degeneration; Tryptophan	1996
Neurochemical development of the degenerating rat retina. The Journal of comparative neurology, 1997, Nov-10, Volume: 388, Issue:1 Topics: Aging; Amino Acids; Animals; Animals, Newborn; Arginine; Aspartic Acid; gamma-Aminobutyric Acid; Glutamine; Glycine; Immunohistochemistry; Neurotransmitter Agents; Rats; Rats, Inbred BUF; Rats, Mutant Strains; Retina; Retinal Degeneration; Taurine	1997
Recurrent missense (R197C) and nonsense (Y89X) mutations in the XLRS1 gene in families with X-linked retinoschisis. Biochemical and biophysical research communications, 1999, Mar-16, Volume: 256, Issue:2 Topics: Amino Acid Substitution; Arginine; Base Sequence; Codon, Terminator; Conserved Sequence; DNA Mutational Analysis; Exons; Eye Diseases, Hereditary; Eye Proteins; Female; Genes, Recessive; Genetic Linkage; Humans; Male; Mutation, Missense; Pedigree; Peptide Fragments; Point Mutation; Retinal Degeneration; X Chromosome	1999
Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave. American journal of ophthalmology, 1999, Volume: 128, Issue:2 Topics: Adolescent; Adult; Arginine; Diagnosis, Differential; DNA; Electroretinography; Exons; Eye Diseases, Hereditary; Eye Proteins; Genetic Linkage; Humans; Male; Middle Aged; Mutation, Missense; Pedigree; Polymerase Chain Reaction; Retina; Retinal Degeneration; Tryptophan; X Chromosome	1999
Mutations in the rod outer segment membrane guanylate cyclase in a cone-rod dystrophy cause defects in calcium signaling. Biochemistry, 1999, Oct-19, Volume: 38, Issue:42 Topics: Animals; Arginine; Aspartic Acid; Calcium Signaling; Calcium-Binding Proteins; Cattle; Cysteine; Enzyme Activation; Glutamic Acid; Guanylate Cyclase; Guanylate Cyclase-Activating Proteins; Humans; Mutagenesis, Insertional; Protein Binding; Receptors, Cell Surface; Retinal Degeneration; Rod Cell Outer Segment; S100 Proteins	1999
Correction of ornithine accumulation prevents retinal degeneration in a mouse model of gyrate atrophy of the choroid and retina. Proceedings of the National Academy of Sciences of the United States of America, 2000, Feb-01, Volume: 97, Issue:3 Topics: Amino Acids; Animals; Arginine; Choroid; Disease Models, Animal; Electroretinography; Gyrate Atrophy; Mice; Mice, Knockout; Ornithine; Ornithine-Oxo-Acid Transaminase; Retina; Retinal Degeneration	2000
W179R: a novel missense mutation in the peripherin/RDS gene in a family with autosomal dominant retinitis pigmentosa. Human mutation, 2000, Volume: 15, Issue:6 Topics: Arginine; Genes, Dominant; Humans; Intermediate Filament Proteins; Membrane Glycoproteins; Mutation, Missense; Nerve Tissue Proteins; Peripherins; Retinal Degeneration; Retinitis Pigmentosa; Tryptophan	2000
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies. Human mutation, 2001, Volume: 17, Issue:1 Topics: Amino Acid Substitution; Animals; Arginine; Cysteine; Genetic Variation; Glutamine; Homeodomain Proteins; Humans; Intermediate Filament Proteins; Leucine; Membrane Glycoproteins; Mutation; Nerve Tissue Proteins; Optic Atrophies, Hereditary; Peripherins; Prevalence; Proline; Retinal Degeneration; Retinal Diseases; Retinitis Pigmentosa; Rhodopsin; Trans-Activators; Tyrosine	2001
Two novel mutations (Y141H; C214Y) and previously published mutation (R142W) in the RDS-peripherin gene in autosomal dominant macular dystrophies in Spanish families. Human mutation, 2001, Volume: 17, Issue:1 Topics: Amino Acid Substitution; Arginine; Cysteine; Electrophoresis, Polyacrylamide Gel; Eye Proteins; Genes, Dominant; Histidine; Humans; Intermediate Filament Proteins; Macular Degeneration; Membrane Glycoproteins; Mutation, Missense; Nerve Tissue Proteins; Peripherins; Polymerase Chain Reaction; Retinal Degeneration; Tryptophan; Tyrosine	2001
Gyrate atrophy of the choroid and retina. Long-term reduction of ornithine slows retinal degeneration. Archives of ophthalmology (Chicago, Ill. : 1960), 1991, Volume: 109, Issue:11 Topics: Adult; Arginine; Child; Child, Preschool; Female; Follow-Up Studies; Fundus Oculi; Genetic Variation; Gyrate Atrophy; Humans; Infant; Longitudinal Studies; Male; Middle Aged; Ornithine; Ornithine-Oxo-Acid Transaminase; Retinal Degeneration; Treatment Outcome	1991
At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns. Proceedings of the National Academy of Sciences of the United States of America, 1989, Volume: 86, Issue:1 Topics: Alleles; Arginine; Atrophy; Choroid; DNA; Female; Finland; Genes; Humans; Leucine; Male; Mutation; Ornithine-Oxo-Acid Transaminase; Pedigree; Proline; Retina; Retinal Degeneration; Threonine; Transaminases; Uveal Diseases	1989
Conversion of glutamate to ornithine and proline: pyrroline-5-carboxylate, a possible modulator of arginine requirements. The Journal of nutrition, 1985, Volume: 115, Issue:4 Topics: Amino Acids; Animals; Arginine; Biotransformation; Glutamates; Glutamic Acid; Humans; Intestinal Mucosa; Kidney; Liver; Ornithine; Ornithine-Oxo-Acid Transaminase; Proline; Proline Oxidase; Pyrroles; Retinal Degeneration; Spleen	1985
Arginine and disease states. The Journal of nutrition, 1985, Volume: 115, Issue:4 Topics: Ammonia; Animals; Arginine; Blood Glucose; Humans; Insulin; Lipid Metabolism; Liver Diseases; Male; Nutritional Requirements; Orotic Acid; Retinal Degeneration; Reye Syndrome; Spermatogenesis; Urea	1985