tryptophan and Retinal Degeneration

tryptophan has been researched along with Retinal Degeneration in 10 studies

Research

Studies (10)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (10.00)	18.7374
1990's	4 (40.00)	18.2507
2000's	4 (40.00)	29.6817
2010's	1 (10.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
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
Aartsen, WM; Kamphuis, W; Malysheva, A; McCabe, CJ; Meuleman, J; Seeliger, MW; Tonagel, F; van de Pavert, SA; Versteeg, I; Wijnholds, J	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
Bingham, EL; Hiriyanna, K; Kemp, J; Richards, J; Sieving, PA	1
Arnaud, B; Bareil, C; Claustres, M; Delague, V; Demaille, J; Hamel, C	1
Ayuso, C; Bueno, J; Carballo, M; García-Sandoval, B; Giménez, A; Lorda, I; Martinez-Gimeno, M; Ramos, C; Trujillo, MJ	1
Francois, J	1

Reviews

1 review(s) available for tryptophan and Retinal Degeneration

Article	Year
Hereditary chorioretinal degeneration and metabolic disturbances. International ophthalmology clinics, 1968,Winter, Volume: 8, Issue:4 Topics: Abetalipoproteinemia; Amino Acid Metabolism, Inborn Errors; Animals; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Cystinosis; Cystinuria; Female; Growth Disorders; Humans; Lipid Metabolism, Inborn Errors; Lipids; Lipoproteins; Metabolism, Inborn Errors; Mice; Mucopolysaccharidoses; Rabbits; Rats; Refsum Disease; Retinal Degeneration; Retinal Pigments; Tryptophan	1968

Article

Year

Hereditary chorioretinal degeneration and metabolic disturbances.

International ophthalmology clinics, 1968,Winter, Volume: 8, Issue:4

Topics: Abetalipoproteinemia; Amino Acid Metabolism, Inborn Errors; Animals; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Cystinosis; Cystinuria; Female; Growth Disorders; Humans; Lipid Metabolism, Inborn Errors; Lipids; Lipoproteins; Metabolism, Inborn Errors; Mice; Mucopolysaccharidoses; Rabbits; Rats; Refsum Disease; Retinal Degeneration; Retinal Pigments; Tryptophan

1968

Other Studies

9 other study(ies) available for tryptophan and Retinal Degeneration

Article	Year
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
A single amino acid substitution (Cys249Trp) in Crb1 causes retinal degeneration and deregulates expression of pituitary tumor transforming gene Pttg1. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2007, Jan-17, Volume: 27, Issue:3 Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Cysteine; Eye Proteins; Gene Expression Regulation; Humans; Membrane Proteins; Mice; Mice, Knockout; Molecular Sequence Data; Neoplasm Proteins; Nerve Tissue Proteins; Protein Structure, Tertiary; Retinal Degeneration; Retinitis Pigmentosa; Securin; Tryptophan	2007
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
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
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
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