tyrosine has been researched along with Marfan Syndrome in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 2 (66.67) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Adcock, EW; Butler, IJ; Caprioli, RM; Denson, SE; Howell, RR; Morriss, FH; Seifert, WE; Stoerner, JW | 1 |
| Byers, PH; McInnes, RR | 1 |
| Doering, K; Downing, AK; Handford, PA; Smallridge, RS; Whiteman, P | 1 |
1 review(s) available for tyrosine and Marfan Syndrome
| Article | Year |
|---|---|
Biochemical genetics: examples of life after cloning.
Topics: Animals; Choroideremia; Cloning, Molecular; Fibrillins; Humans; Marfan Syndrome; Microfilament Proteins; Protein Processing, Post-Translational; Tyrosine | 1993 |
2 other study(ies) available for tyrosine and Marfan Syndrome
| Article | Year |
|---|---|
CSF neurotransmitter studies. An infant with ascorbic acid-responsive tyrosinemia.
Topics: Ascorbic Acid; Female; Glycols; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Infant, Newborn; Infant, Premature; Marfan Syndrome; Methoxyhydroxyphenylglycol; Phenylacetates; Tyrosine | 1980 |
EGF-like domain calcium affinity modulated by N-terminal domain linkage in human fibrillin-1.
Topics: Binding Sites; Calcium; Epidermal Growth Factor; Fibrillin-1; Fibrillins; Humans; Magnetic Resonance Spectroscopy; Marfan Syndrome; Microfilament Proteins; Mutation; Phenotype; Protein Binding; Protein Structure, Secondary; Spectrometry, Fluorescence; Tyrosine | 1999 |