glutamic acid has been researched along with Corneal Dystrophies in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Bollati, M; de Rosa, M; Drnovšek-Olup, B; Fakin, A; Gornik, A; Hawlina, M; Hočevar, A; Jaklič, H; Maver, A; Peterlin, B; Pfeifer, V; Pižem, J; Potrč, M; Teran, N; Vogelnik, K; Volk, M | 1 |
| Andresson, T; Bosley, AD; Brandt, W; Dean, M; Esposito, D; Hirota, Y; Kinoshita, S; Kostiha, BN; Kruth, HS; Morham, SG; Nickerson, ML; Okano, T; Weiss, JS; Wessjohann, L | 1 |
| Bateman, JB; Bhattacharya, SS; Deery, EC; Garibaldi, D; Hunt, DM; Li, Y; Lin, W; Newbold, RJ; Warren, MJ; Wilkie, SE; Zack, DJ; Zhang, H; Zhang, K | 1 |
3 other study(ies) available for glutamic acid and Corneal Dystrophies
| Article | Year |
|---|---|
Clinical and Histopathological Features of Gelsolin Amyloidosis Associated with a Novel
Topics: Adult; Aged; Amyloid Neuropathies, Familial; Amyloidosis; Amyloidosis, Familial; Corneal Diseases; Corneal Dystrophies, Hereditary; Exome; Family Health; Female; Fundus Oculi; Gelsolin; Genetic Association Studies; Glutamic Acid; Humans; Lysine; Male; Middle Aged; Mutation; Optic Nerve; Optic Nerve Diseases; Phenotype; Protein Folding; Tomography, Optical Coherence | 2021 |
The UBIAD1 prenyltransferase links menaquinone-4 [corrected] synthesis to cholesterol metabolic enzymes.
Topics: Aged; Aged, 80 and over; Amino Acid Sequence; Cholesterol; Cornea; Corneal Dystrophies, Hereditary; Dimethylallyltranstransferase; Female; Finland; Genetic Variation; Glutamic Acid; Glycine; Humans; Hydroxymethylglutaryl CoA Reductases; Immunoprecipitation; Japan; Lipid Metabolism; Male; Middle Aged; Models, Molecular; Molecular Sequence Data; Mutation, Missense; Pedigree; Protein Conformation; Sequence Analysis, DNA; Sterol O-Acyltransferase; Turkey; Vitamin K 2 | 2013 |
Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy.
Topics: Amino Acid Sequence; Amino Acid Substitution; Calcium-Binding Proteins; Corneal Dystrophies, Hereditary; DNA; Female; Glutamic Acid; Glycine; Guanylate Cyclase-Activating Proteins; Humans; Male; Models, Molecular; Molecular Sequence Data; Mutation; Pedigree; Protein Conformation; Pyrimidines; Sequence Homology, Amino Acid | 2001 |