tyrosine has been researched along with Cardio-Cutaneous Syndrome 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 | 0 (0.00) | 29.6817 |
2010's | 2 (66.67) | 24.3611 |
2020's | 1 (33.33) | 2.80 |
Authors | Studies |
---|---|
Bennett, AM; Enyenihi, L; Perla, S; Yi, JS | 1 |
Chen, C; Wang, DW; Wang, Y | 1 |
Iwers, L; Majdani, O; Maser, F | 1 |
3 other study(ies) available for tyrosine and Cardio-Cutaneous Syndrome
Article | Year |
---|---|
Tyrosyl phosphorylation of PZR promotes hypertrophic cardiomyopathy in PTPN11-associated Noonan syndrome with multiple lentigines.
Topics: Animals; Cardiomyopathy, Hypertrophic; Disease Models, Animal; Female; Intracellular Signaling Peptides and Proteins; LEOPARD Syndrome; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Mutation; Myocytes, Cardiac; Phosphoproteins; Phosphorylation; Protein Tyrosine Phosphatase, Non-Receptor Type 11; Tyrosine | 2020 |
Leopard syndrome caused by heterozygous missense mutation of Tyr 279 Cys in the PTPN11 gene in a sporadic case of Chinese Han.
Topics: Adolescent; Asian People; Cysteine; Heterozygote; Humans; LEOPARD Syndrome; Male; Mutation, Missense; Protein Tyrosine Phosphatase, Non-Receptor Type 11; Tyrosine | 2014 |
[The LEOPARD-syndrome].
Topics: Adolescent; Amino Acid Substitution; Chromosomes, Human, Pair 12; Cochlear Implantation; Cysteine; Deafness; Diagnosis, Differential; DNA Mutational Analysis; Exons; Female; Humans; LEOPARD Syndrome; Point Mutation; Protein Tyrosine Phosphatase, Non-Receptor Type 12; Tyrosine | 2010 |