Page last updated: 2024-08-26

paxilline and Achondroplasia

paxilline has been researched along with Achondroplasia in 1 studies

Research

Studies (1)

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	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Baruzzi, A; Ferrarini, F; Liboi, E; Lievens, PM; Montone, R; Romanelli, MG	1

Other Studies

1 other study(ies) available for paxilline and Achondroplasia

Article	Year
Mutant FGFR3 associated with SADDAN disease causes cytoskeleton disorganization through PLCγ1/Src-mediated paxillin hyperphosphorylation. The international journal of biochemistry & cell biology, 2018, Volume: 95 Topics: Achondroplasia; Amino Acid Substitution; Animals; Cell Line, Transformed; Cell Line, Tumor; Chondrocytes; Cytoskeleton; Humans; Mice; Mutation; Paxillin; Phospholipase C gamma; Phosphorylation; Protein Kinase Inhibitors; Protein Processing, Post-Translational; Protein Transport; Receptor, Fibroblast Growth Factor, Type 3; Recombinant Fusion Proteins; Signal Transduction; src-Family Kinases; Thanatophoric Dysplasia; Tyrosine	2018

Article

Year

Mutant FGFR3 associated with SADDAN disease causes cytoskeleton disorganization through PLCγ1/Src-mediated paxillin hyperphosphorylation.

The international journal of biochemistry & cell biology, 2018, Volume: 95

Topics: Achondroplasia; Amino Acid Substitution; Animals; Cell Line, Transformed; Cell Line, Tumor; Chondrocytes; Cytoskeleton; Humans; Mice; Mutation; Paxillin; Phospholipase C gamma; Phosphorylation; Protein Kinase Inhibitors; Protein Processing, Post-Translational; Protein Transport; Receptor, Fibroblast Growth Factor, Type 3; Recombinant Fusion Proteins; Signal Transduction; src-Family Kinases; Thanatophoric Dysplasia; Tyrosine

2018