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Direct Assessment of the Effect of the Gly380Arg Achondroplasia Mutation on FGFR3 Dimerization Using Quantitative Imaging FRET

The Gly380Arg mutation in FGFR3 is the genetic cause for achondroplasia (ACH), the most common form of human dwarfism. The mutation has been proposed to increase FGFR3 dimerization, but the dimerization propensities of wild-type and mutant FGFR3 have not been compared. Here we use quantitative imagi...

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Detalhes bibliográficos
Main Authors: Placone, Jesse, Hristova, Kalina
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3467271/
https://ncbi.nlm.nih.gov/pubmed/23056398
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0046678
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