tryptophan and Macular Degeneration

tryptophan has been researched along with Macular Degeneration in 13 studies

Research

Studies (13)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	5 (38.46)	18.2507
2000's	4 (30.77)	29.6817
2010's	3 (23.08)	24.3611
2020's	1 (7.69)	2.80

Authors

Authors	Studies
Chen, TY; Chi, ZL; Hu, ZX; Lin, K; Lin, Z; Tang, YP; Wu, RH; Zhang, XB	1
Cheu, R; Danis, RP; Hunt, PW; Jabs, DA; Jones, NG; Klatt, NR; Milush, JM; Trang, G; Van Natta, ML	1
Azadi, S; Burnett, JL; Chakraborty, D; Conley, SM; Fliesler, SJ; Naash, MI; Stuck, MW	1
Bradley, DT; Hughes, AE; Mullan, GM	1
Ayuso, C; Baiget, M; Carballo, M; Gamundi, MJ; García-Sandoval, B; Hernan, I; Muntanyola, M; Trujillo, MJ	1
Marmorstein, AD; Marmorstein, LY; McLaughlin, PJ; Peachey, NS; Sasaki, T	1
Fu, L; Garland, D; Pearson, E; Pierce, EA; Rajendran, A; Shukla, D; Stone, EM; Yang, Z; Zhang, K	1
Arden, G; Bhattacharya, S; Eckstein, A; Fitzke, F; Inglehearn, C; Jay, M; Jubb, C; Keen, J; Wells, J; Wroblewski, J	1
Nakazawa, M; Tamai, M; Wada, Y	1
Butler, N; Grounauer, PA; Héon, E; Munier, FL; Niemeyer, G; Piguet, B; Schorderet, DF; Sheffield, VC; Stone, EM	1
Felbor, U; Schilling, H; Weber, BH	1
Borberg, H; Brunner, R; Engels, B; Oette, K; Widder, RA	1
Ayuso, C; Bueno, J; Carballo, M; García-Sandoval, B; Giménez, A; Lorda, I; Martinez-Gimeno, M; Ramos, C; Trujillo, MJ	1

Reviews

1 review(s) available for tryptophan and Macular Degeneration

Article	Year
Complement factor B polymorphism 32W protects against age-related macular degeneration. Molecular vision, 2011, Apr-20, Volume: 17 Topics: Aged; Aged, 80 and over; Arginine; Case-Control Studies; Complement Activation; Complement Factor B; Complement Factor H; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Haplotypes; High-Temperature Requirement A Serine Peptidase 1; Humans; Linkage Disequilibrium; Macular Degeneration; Male; Middle Aged; Odds Ratio; Polymorphism, Single Nucleotide; Retina; Risk Factors; Serine Endopeptidases; Smoking; Tryptophan	2011

Article

Year

Complement factor B polymorphism 32W protects against age-related macular degeneration.

Molecular vision, 2011, Apr-20, Volume: 17

Topics: Aged; Aged, 80 and over; Arginine; Case-Control Studies; Complement Activation; Complement Factor B; Complement Factor H; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Haplotypes; High-Temperature Requirement A Serine Peptidase 1; Humans; Linkage Disequilibrium; Macular Degeneration; Male; Middle Aged; Odds Ratio; Polymorphism, Single Nucleotide; Retina; Risk Factors; Serine Endopeptidases; Smoking; Tryptophan

2011

Other Studies

12 other study(ies) available for tryptophan and Macular Degeneration

Article	Year
Vitreous metabolomic signatures of pathological myopia with complications. Eye (London, England), 2023, Volume: 37, Issue:14 Topics: Biomarkers; Humans; Macular Degeneration; Myopia, Degenerative; Retinal Detachment; Retinal Perforations; Retinoschisis; Retrospective Studies; Tryptophan; Uric Acid	2023
Association of Age-related Macular Degeneration With Mortality in Patients With Acquired Immunodeficiency Syndrome; Role of Systemic Inflammation. American journal of ophthalmology, 2019, Volume: 199 Topics: Acquired Immunodeficiency Syndrome; Adult; Antigens, CD; Biomarkers; C-Reactive Protein; Case-Control Studies; Chemokine CXCL10; Female; Humans; Inflammation; Interleukin-6; Kynurenine; Longitudinal Studies; Macular Degeneration; Male; Middle Aged; Proportional Hazards Models; Prospective Studies; Risk Factors; Tryptophan	2019
Insights into the mechanisms of macular degeneration associated with the R172W mutation in RDS. Human molecular genetics, 2014, Jun-15, Volume: 23, Issue:12 Topics: Amino Acid Substitution; Animals; Arginine; Basic-Leucine Zipper Transcription Factors; Disease Models, Animal; Eye Proteins; Fundus Oculi; Humans; Macular Degeneration; Membrane Proteins; Mice; Mice, Transgenic; Peripherins; Retinal Cone Photoreceptor Cells; Tetraspanins; Tryptophan	2014
High prevalence of mutations in peripherin/RDS in autosomal dominant macular dystrophies in a Spanish population. Molecular vision, 2007, Jun-28, Volume: 13 Topics: Adult; Aged; Amino Acid Substitution; Arginine; Codon, Nonsense; Cytosine; Fundus Oculi; Gene Frequency; Genes, Dominant; Humans; Intermediate Filament Proteins; Introns; Macular Degeneration; Membrane Glycoproteins; Middle Aged; Mutation; Mutation, Missense; Nerve Tissue Proteins; Pedigree; Peripherins; Protein Splicing; Spain; Thymine; Tryptophan	2007
Formation and progression of sub-retinal pigment epithelium deposits in Efemp1 mutation knock-in mice: a model for the early pathogenic course of macular degeneration. Human molecular genetics, 2007, Oct-15, Volume: 16, Issue:20 Topics: Animals; Arginine; Bruch Membrane; Disease Models, Animal; Disease Progression; Extracellular Matrix Proteins; Female; Humans; Macular Degeneration; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mice, Transgenic; Mutagenesis, Site-Directed; Optic Nerve; Pigment Epithelium of Eye; Point Mutation; Retina; Time Factors; Tryptophan	2007
The R345W mutation in EFEMP1 is pathogenic and causes AMD-like deposits in mice. Human molecular genetics, 2007, Oct-15, Volume: 16, Issue:20 Topics: Adolescent; Adult; Aged; Animals; Arginine; Child; DNA Mutational Analysis; Extracellular Matrix Proteins; Female; Humans; Macular Degeneration; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Middle Aged; Pedigree; Point Mutation; 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
Macular dystrophy associated with monogenic Arg172Trp mutation of the peripherin/RDS gene in a Japanese family. Retina (Philadelphia, Pa.), 1995, Volume: 15, Issue:6 Topics: Adolescent; Amino Acid Sequence; Arginine; Base Sequence; Electroretinography; Eye Proteins; Fluorescein Angiography; Fundus Oculi; Humans; Intermediate Filament Proteins; Japan; Macular Degeneration; Male; Membrane Glycoproteins; Membrane Proteins; Middle Aged; Molecular Sequence Data; Nerve Tissue Proteins; Neuropeptides; Pedigree; Peripherins; Photoreceptor Cells; Point Mutation; Tetraspanins; Tryptophan; Visual Acuity; Visual Fields	1995
Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the RDS/peripherin gene. Ophthalmic genetics, 1996, Volume: 17, Issue:4 Topics: Adult; Aged; Arginine; DNA Mutational Analysis; Eye Proteins; Female; Fluorescein Angiography; Fundus Oculi; Genotype; Humans; Intermediate Filament Proteins; Macular Degeneration; Male; Membrane Glycoproteins; Middle Aged; Nerve Tissue Proteins; Pedigree; Peripherins; Phenotype; Point Mutation; Rhodopsin; Switzerland; Tryptophan	1996
Adult vitelliform macular dystrophy is frequently associated with mutations in the peripherin/RDS gene. Human mutation, 1997, Volume: 10, Issue:4 Topics: Aged; Female; Glycine; Humans; Intermediate Filament Proteins; Macular Degeneration; Male; Membrane Glycoproteins; Methionine; Middle Aged; Mutation; Nerve Tissue Proteins; Peripherins; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Serine; Threonine; Tryptophan; Valine	1997
Changes of hemorheological and biochemical parameters after plasma perfusion using a tryptophan-polyvinyl alcohol adsorber leading to clinical improvement in patients suffering from maculopathy. Blood purification, 1998, Volume: 16, Issue:1 Topics: Blood Viscosity; Erythrocyte Aggregation; Hematocrit; Humans; Macular Degeneration; Membranes, Artificial; Plasmapheresis; Polyvinyl Alcohol; Tryptophan	1998
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