glycine has been researched along with Corneal Dystrophies in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (66.67) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Li, D | 1 |
| Qi, Y | 1 |
| Wang, L | 1 |
| Lin, H | 2 |
| Zhou, N | 1 |
| Zhao, L | 1 |
| Auw-Haedrich, C | 1 |
| Agostini, H | 1 |
| Clausen, I | 1 |
| Reinhard, T | 1 |
| Eberwein, P | 1 |
| Schorderet, DF | 1 |
| Gruenauer-Kloevekorn, C | 1 |
| Li, DD | 1 |
| Qi, YH | 1 |
| Han, Q | 1 |
| Zhao, LM | 1 |
| Zhang, CM | 1 |
| Piao, MZ | 1 |
| Zhou, XT | 1 |
| Wu, LC | 1 |
| Chu, RY | 1 |
| Nickerson, ML | 1 |
| Bosley, AD | 1 |
| Weiss, JS | 1 |
| Kostiha, BN | 1 |
| Hirota, Y | 1 |
| Brandt, W | 1 |
| Esposito, D | 1 |
| Kinoshita, S | 1 |
| Wessjohann, L | 1 |
| Morham, SG | 1 |
| Andresson, T | 1 |
| Kruth, HS | 1 |
| Okano, T | 1 |
| Dean, M | 1 |
| Wilkie, SE | 1 |
| Li, Y | 1 |
| Deery, EC | 1 |
| Newbold, RJ | 1 |
| Garibaldi, D | 1 |
| Bateman, JB | 1 |
| Zhang, H | 1 |
| Lin, W | 1 |
| Zack, DJ | 1 |
| Bhattacharya, SS | 1 |
| Warren, MJ | 1 |
| Hunt, DM | 1 |
| Zhang, K | 1 |
6 other studies available for glycine and Corneal Dystrophies
| Article | Year |
|---|---|
An atypical phenotype of Reis-Bücklers corneal dystrophy caused by the G623D mutation in TGFBI.
Topics: Adult; Amino Acid Sequence; Amino Acid Substitution; Aspartic Acid; Base Sequence; Cornea; Corneal D | 2008 |
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 Mutati | 2009 |
[Analysis of TGFBI gene mutation in a Chinese family with atypical Reis-Buckler corneal dystrophy].
Topics: Asian People; Aspartic Acid; Corneal Dystrophies, Hereditary; Corneal Stroma; Exons; Extracellular M | 2009 |
Arg555Gln mutation of TGFBI gene in geographical-type Reis-Bücklers corneal dystrophy in a Chinese family.
Topics: Arginine; Base Sequence; China; Corneal Dystrophies, Hereditary; DNA Primers; Exons; Female; Glycine | 2012 |
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; | 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, Heredit | 2001 |