Compounds > tryptophan

tryptophan and Corneal Dystrophies

tryptophan has been researched along with Corneal Dystrophies in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's0 (0.00)18.2507
2000's2 (33.33)29.6817
2010's3 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chang, AA; Grothe, HL; Little, MR; Nelson, EF; Sjogren, PP; Yuan, C1
Fernandez-Godino, R; Garland, DL; Harnly, JM; Kaur, I; Lambris, JD; Pierce, EA; Speicher, DW; Speicher, KD1
Hulleman, JD; Nguyen, A1
Chen, L; Gu, Y; Hu, R; Jin, F; Qi, M; Yan, X; Yang, Y; Yu, P1
Aldave, AJ; Hwang, DG; Yellore, VS1
Garner, A1

Other Studies

6 other study(ies) available for tryptophan and Corneal Dystrophies

ArticleYear
Altered protein conformation and lower stability of the dystrophic transforming growth factor beta-induced protein mutants.
    Molecular vision, 2013, Volume: 19

    Topics: Anilino Naphthalenesulfonates; Benzothiazoles; Circular Dichroism; Corneal Dystrophies, Hereditary; Extracellular Matrix Proteins; Humans; Mutant Proteins; Protein Conformation; Protein Stability; Proteolysis; Recombinant Proteins; Spectrometry, Fluorescence; Thiazoles; Transforming Growth Factor beta; Tryptophan

2013
Mouse genetics and proteomic analyses demonstrate a critical role for complement in a model of DHRD/ML, an inherited macular degeneration.
    Human molecular genetics, 2014, Jan-01, Volume: 23, Issue:1

    Topics: Animals; Arginine; Bruch Membrane; Cell Adhesion; Complement C3; Complement System Proteins; Corneal Dystrophies, Hereditary; Disease Models, Animal; Extracellular Matrix Proteins; Gene Knock-In Techniques; Humans; Mice; Mice, Transgenic; Optic Disk Drusen; Point Mutation; Proteomics; Reproducibility of Results; Retinal Drusen; Tryptophan

2014
Differential tolerance of 'pseudo-pathogenic' tryptophan residues in calcium-binding EGF domains of short fibulin proteins.
    Experimental eye research, 2015, Volume: 130

    Topics: Amino Acid Sequence; Blotting, Western; Calcium-Binding Proteins; Cell Line; Corneal Dystrophies, Hereditary; Epidermal Growth Factor; Extracellular Matrix Proteins; Gene Expression; Humans; Mutagenesis, Site-Directed; Mutation; Optic Disk Drusen; Plasmids; Protein Folding; Protein Structure, Tertiary; Real-Time Polymerase Chain Reaction; Sequence Homology; Transfection; Tryptophan

2015
p.Ala546 > Asp and p.Arg555 > Trp mutations of TGFBI gene and their clinical manifestations in two large Chinese families with granular corneal dystrophy type I.
    Genetic testing, 2008, Volume: 12, Issue:3

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Asian People; Aspartic Acid; Case-Control Studies; Corneal Dystrophies, Hereditary; DNA Mutational Analysis; Extracellular Matrix Proteins; Family; Female; Humans; Male; Middle Aged; Mutation, Missense; Pedigree; Transforming Growth Factor beta; Tryptophan; Young Adult

2008
Atypical vortex pattern of corneal deposits in granular corneal dystrophy.
    Cornea, 2003, Volume: 22, Issue:8

    Topics: Adult; Arginine; Child; Cornea; Corneal Dystrophies, Hereditary; Female; Humans; Mutation, Missense; Pedigree; Transforming Growth Factor beta; Transforming Growth Factor beta1; Tryptophan

2003
Histochemistry of corneal granular dystrophy.
    The British journal of ophthalmology, 1969, Volume: 53, Issue:12

    Topics: Adult; Aged; Amyloid; Arginine; Cornea; Corneal Dystrophies, Hereditary; Epithelium; Eye Proteins; Female; Fibroblasts; Histocytochemistry; Humans; Male; Microscopy, Electron; Middle Aged; Sulfhydryl Compounds; Tryptophan; Tyrosine

1969