4-phosphonomethylphenylalanine has been researched along with Eye Abnormalities in 1 studies
*Eye Abnormalities: Congenital absence of or defects in structures of the eye; may also be hereditary. [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Englert, C; Imhof, D; Landgraf, K; Markschies, N; Musharraf, A; Pankratz, S; Teichmann, K | 1 |
1 other study(ies) available for 4-phosphonomethylphenylalanine and Eye Abnormalities
| Article | Year |
|---|---|
Eyes absent proteins: characterization of substrate specificity and phosphatase activity of mutants associated with branchial, otic and renal anomalies.
Topics: Animals; Arabidopsis Proteins; Branchio-Oto-Renal Syndrome; Eye Abnormalities; Humans; Intracellular Signaling Peptides and Proteins; Kinetics; Mice; Mutant Proteins; Nuclear Proteins; Peptide Library; Phenylalanine; Phosphorylation; Point Mutation; Protein Structure, Tertiary; Protein Tyrosine Phosphatases; Substrate Specificity | 2008 |