arginine has been researched along with Eye Abnormalities 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 | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Andley, UP; Reilly, MA | 1 |
| Billingsley, G; Glaser, T; Heon, E; Levin, A; Oliver, E; Priston, M; Ritch, R; Vincent, A; Walter, M | 1 |
| Eiberg, H; Hansen, L; Rosenberg, T | 1 |
3 other study(ies) available for arginine and Eye Abnormalities
| Article | Year |
|---|---|
Quantitative biometric phenotype analysis in mouse lenses.
Topics: Aging; alpha-Crystallin A Chain; Animals; Arginine; Biometry; Cataract; Cysteine; Eye Abnormalities; Genotype; Heterozygote; Homozygote; Image Processing, Computer-Assisted; Lens, Crystalline; Mice; Mice, Knockout; Mice, Transgenic; Mutation; Organ Size; Phenotype; Solubility | 2010 |
Further support of the role of CYP1B1 in patients with Peters anomaly.
Topics: Arginine; Aryl Hydrocarbon Hydroxylases; Case-Control Studies; Child; Cytochrome P-450 CYP1B1; Cytochrome P-450 Enzyme System; Eye Abnormalities; Female; Glaucoma; Histidine; Humans; Methionine; Mutation, Missense; Proline; Threonine | 2006 |
Novel MAF mutation in a family with congenital cataract-microcornea syndrome.
Topics: Amino Acid Substitution; Arginine; Cataract; Cornea; DNA; Eye Abnormalities; Female; Humans; Infant, Newborn; Leucine Zippers; Male; Mutation; Pedigree; Phenotype; Proto-Oncogene Proteins c-maf; Serine | 2007 |