Direct assessment of the effect of the Gly380Arg achondroplasia mutation on FGFR3 dimerization using quantitative imaging FRET.
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A Genetic-Pathophysiological Framework for CraniosynostosisFluorophores, environments, and quantification techniques in the analysis of transmembrane helix interaction using FRETStructural and physico-chemical effects of disease and non-disease nsSNPs on proteinsCharacterization of membrane protein interactions in plasma membrane derived vesicles with quantitative imaging Förster resonance energy transferCoupling of transmembrane helix orientation to membrane release of the juxtamembrane region in FGFR3Experimental verification of the kinetic theory of FRET using optical microspectroscopy and obligate oligomers.Analytical characterization of plasma membrane-derived vesicles produced via osmotic and chemical vesiculation.Unliganded EphA3 dimerization promoted by the SAM domain.FGFR3 transmembrane domain interactions persist in the presence of its extracellular domain.Mapping the self-association domains of ataxin-1: identification of novel non overlapping motifs.The FRET signatures of noninteracting proteins in membranes: simulations and experiments.The safety dance: biophysics of membrane protein folding and misfolding in a cellular contextApplications of Single-Molecule Methods to Membrane Protein Folding Studies.Effect of the achondroplasia mutation on FGFR3 dimerization and FGFR3 structural response to fgf1 and fgf2: A quantitative FRET study in osmotically derived plasma membrane vesicles.On human disease-causing amino acid variants: statistical study of sequence and structural patterns.Unliganded fibroblast growth factor receptor 1 forms density-independent dimers.Strong dimerization of wild-type ErbB2/Neu transmembrane domain and the oncogenic Val664Glu mutant in mammalian plasma membranes.Glycophorin A transmembrane domain dimerization in plasma membrane vesicles derived from CHO, HEK 293T, and A431 cells.Analysis of the clinical and molecular characteristics of a child with achondroplasia: A case report.Effect of thanatophoric dysplasia type I mutations on FGFR3 dimerization.Crouzon syndrome and Bent bone dysplasia associated with mutations at the same Tyr-381 residue in FGFR2 gene.Multichannel wide-field microscopic FRET imaging based on simultaneous spectral unmixing of excitation and emission spectra.A New Method to Study Heterodimerization of Membrane Proteins and Its Application to Fibroblast Growth Factor Receptors.Association of achondroplasia with sagittal synostosis and scaphocephaly in two patients, an underestimated condition?Postnatal soluble FGFR3 therapy rescues achondroplasia symptoms and restores bone growth in mice.FGFR3 mutation causes abnormal membranous ossification in achondroplasia
P2860
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P2860
Direct assessment of the effect of the Gly380Arg achondroplasia mutation on FGFR3 dimerization using quantitative imaging FRET.
description
2012 nî lūn-bûn
@nan
2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Direct assessment of the effec ...... ing quantitative imaging FRET.
@ast
Direct assessment of the effec ...... ing quantitative imaging FRET.
@en
Direct assessment of the effec ...... ing quantitative imaging FRET.
@nl
type
label
Direct assessment of the effec ...... ing quantitative imaging FRET.
@ast
Direct assessment of the effec ...... ing quantitative imaging FRET.
@en
Direct assessment of the effec ...... ing quantitative imaging FRET.
@nl
prefLabel
Direct assessment of the effec ...... ing quantitative imaging FRET.
@ast
Direct assessment of the effec ...... ing quantitative imaging FRET.
@en
Direct assessment of the effec ...... ing quantitative imaging FRET.
@nl
P2860
P1433
P1476
Direct assessment of the effec ...... ing quantitative imaging FRET.
@en
P2093
Jesse Placone
P2860
P304
P356
10.1371/JOURNAL.PONE.0046678
P407
P577
2012-10-09T00:00:00Z