asparagine has been researched along with Corneal Dystrophies in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Agostini, H; Auw-Haedrich, C; Clausen, I; Eberwein, P; Gruenauer-Kloevekorn, C; Reinhard, T; Schorderet, DF | 1 |
| Aldave, AJ; Bourla, N; Chen, MC; Gorin, MB; Khan, MA; Momi, RS; Rayner, SA; Sampat, KM; Sonmez, B; Yellore, VS | 1 |
2 other study(ies) available for asparagine and Corneal Dystrophies
| Article | Year |
|---|---|
A corneal dystrophy associated with transforming growth factor beta-induced Gly623Asp mutation an amyloidogenic phenotype.
Topics: Adult; Aged; Amyloid; Amyloidosis, Familial; Asparagine; Corneal Dystrophies, Hereditary; DNA Mutational Analysis; Extracellular Matrix Proteins; Female; Glycine; Humans; Male; Middle Aged; Mutation, Missense; Pedigree; Phenotype; Polymerase Chain Reaction; Transforming Growth Factor beta; Transforming Growth Factor beta1; Visual Acuity | 2009 |
Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy.
Topics: Amino Acid Substitution; Asparagine; Corneal Dystrophies, Hereditary; Dimethylallyltranstransferase; Female; Humans; Leucine; Male; Mutation; Mutation, Missense; Polymorphism, Single Nucleotide; Proteins; Serine; Valine | 2007 |