Page last updated: 2024-11-02

pd 98059 and Acrocephalosyndactylia

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.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chen, P1
Zhang, L2
Weng, T1
Zhang, S1
Sun, S1
Chang, M1
Li, Y1
Zhang, B1
Lomri, A1
Lemonnier, J1
Delannoy, P1
Marie, PJ1

Other Studies

2 other studies available for pd 98059 and Acrocephalosyndactylia

ArticleYear
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.
    PloS one, 2014, Volume: 9, Issue:1

    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.
    Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2001, Volume: 16, Issue:4

    Topics: Acrocephalosyndactylia; Amino Acid Substitution; Cell Line, Transformed; DNA, Complementary; Enzyme

2001