threonine has been researched along with Corneal Dystrophies in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 3 (60.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ji, YW; Kim, EK; Kim, TI; Lee, J; Park, SY; Seo, KY | 1 |
| Chen, L; Ge, Z; Gu, Y; Guo, L; Qi, M; Si, J; Yan, X; Yang, Y; Yu, P | 1 |
| Al-Rajhi, A; Brandt, JD; Fingert, JH; Mannis, MJ; Roos, B; Shah, SS; Sheffield, VC; Stone, EM; Syed, NA | 1 |
| Ayala-Ramirez, R; Graue-Wiechers, F; Zenteno, JC | 1 |
| Bennett, K; Dota, A; Kawasaki, S; Kinoshita, S; Nishida, K; Quantock, AJ | 1 |
5 other study(ies) available for threonine and Corneal Dystrophies
| Article | Year |
|---|---|
Delayed Onset of Lattice Corneal Dystrophy Type IIIA Due to a Novel T621P Mutation in TGFBI.
Topics: Adult; Cornea; Corneal Dystrophies, Hereditary; DNA Mutational Analysis; Exons; Extracellular Matrix Proteins; Female; Humans; Male; Middle Aged; Pedigree; Point Mutation; Proline; Threonine; Tomography, Optical Coherence; Transforming Growth Factor beta; Visual Acuity | 2016 |
A clinical and molecular-genetic analysis of Chinese patients with lattice corneal dystrophy and novel Thr538Pro mutation in the TGFBI (BIGH3) gene.
Topics: China; Corneal Dystrophies, Hereditary; Female; Humans; Male; Mutation; Pedigree; Polymerase Chain Reaction; Proline; Threonine; Transforming Growth Factor beta; Transforming Growth Factor beta1 | 2006 |
Mutation in the SLC4A11 gene associated with autosomal recessive congenital hereditary endothelial dystrophy in a large Saudi family.
Topics: Anion Transport Proteins; Antiporters; Arabs; Cohort Studies; Corneal Dystrophies, Hereditary; Endothelium, Corneal; Female; Genes, Recessive; Homozygote; Humans; Male; Methionine; Mutation; Pedigree; Saudi Arabia; Threonine | 2008 |
Novel CYP4V2 gene mutation in a Mexican patient with Bietti's crystalline corneoretinal dystrophy.
Topics: Aged; Amino Acid Substitution; Corneal Dystrophies, Hereditary; Cytochrome P-450 Enzyme System; Cytochrome P450 Family 4; Cytosine; Diagnostic Techniques, Ophthalmological; Female; Fundus Oculi; Humans; Indians, North American; Isoleucine; Mexico; Mutation; Retinal Diseases; Threonine; Thymine | 2008 |
Amyloid and Pro501 Thr-mutated (beta)ig-h3 gene product colocalize in lattice corneal dystrophy type IIIA.
Topics: Aged; Amyloid; Congo Red; Corneal Dystrophies, Hereditary; DNA; Exons; Extracellular Matrix Proteins; Humans; Immunoenzyme Techniques; Male; Neoplasm Proteins; Point Mutation; Polymerase Chain Reaction; Proline; Threonine; Transforming Growth Factor beta | 1999 |