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The A391E mutation enhances FGFR3 activation in the absence of ligand
The A391E mutation in the transmembrane domain of FGFR3 leads to aberrant development of the cranium. It has been hypothesized that the mutant glutamic acid in the membrane enhances FGFR3 ligand-independent activation by over-stabilizing the FGFR3 dimer due to hydrogen bonding. We previously tested...
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| Main Authors: | , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2011
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3110564/ https://ncbi.nlm.nih.gov/pubmed/21536014 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbamem.2011.04.007 |
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