pd 98059 has been researched along with Acrocephalosyndactylia in 2 studies
2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one: inhibits MAP kinase kinase (MEK) activity, p42 MAPK and p44 MAPK; structure in first source
2-(2-amino-3-methoxyphenyl)chromen-4-one : A member of the class of monomethoxyflavones that is 3'-methoxyflavone bearing an additional amino substituent at position 2'.
Acrocephalosyndactylia: Congenital craniostenosis with syndactyly.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chen, P | 1 |
Zhang, L | 2 |
Weng, T | 1 |
Zhang, S | 1 |
Sun, S | 1 |
Chang, M | 1 |
Li, Y | 1 |
Zhang, B | 1 |
Lomri, A | 1 |
Lemonnier, J | 1 |
Delannoy, P | 1 |
Marie, PJ | 1 |
2 other studies available for pd 98059 and Acrocephalosyndactylia
Article | Year |
---|---|
A Ser252Trp mutation in fibroblast growth factor receptor 2 (FGFR2) mimicking human Apert syndrome reveals an essential role for FGF signaling in the regulation of endochondral bone formation.
Topics: Acrocephalosyndactylia; Animals; Cell Differentiation; Embryonic Development; Flavonoids; Gene Knock | 2014 |
Increased expression of protein kinase Calpha, interleukin-1alpha, and RhoA guanosine 5'-triphosphatase in osteoblasts expressing the Ser252Trp fibroblast growth factor 2 receptor Apert mutation: identification by analysis of complementary DNA microarray.
Topics: Acrocephalosyndactylia; Amino Acid Substitution; Cell Line, Transformed; DNA, Complementary; Enzyme | 2001 |