FGFR3 heterodimerization in achondroplasia, the most common form of human dwarfism.
about
Transmembrane helix dimerization: beyond the search for sequence motifsMultiple consequences of a single amino acid pathogenic RTK mutation: the A391E mutation in FGFR3Effect of the G375C and G346E achondroplasia mutations on FGFR3 activation.Pathogenic Cysteine Removal Mutations in FGFR Extracellular Domains Stabilize Receptor Dimers and Perturb the TM Dimer Structure.Direct assessment of the effect of the Gly380Arg achondroplasia mutation on FGFR3 dimerization using quantitative imaging FRET.FGFR3 transmembrane domain interactions persist in the presence of its extracellular domain.Bilateral ossiculoplasty in 1 case of achondroplasia.Physical-chemical principles underlying RTK activation, and their implications for human disease.Achondroplasia: Development, pathogenesis, and therapy.The physical basis of FGFR3 response to fgf1 and fgf2.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.Consequences of replacing EGFR juxtamembrane domain with an unstructured sequence.The A391E mutation enhances FGFR3 activation in the absence of ligand.Skeletal Characterization of the Fgfr3 Mouse Model of Achondroplasia Using Micro-CT and MRI Volumetric Imaging.Quantifying the Interaction between EGFR Dimers and Grb2 in Live Cells.A New Method to Study Heterodimerization of Membrane Proteins and Its Application to Fibroblast Growth Factor Receptors.Fibroblast growth factor receptor 3 isoforms: Novel therapeutic targets for hepatocellular carcinoma?Postnatal soluble FGFR3 therapy rescues achondroplasia symptoms and restores bone growth in mice.
P2860
Q26865109-9E00F259-C7CF-4F71-8E04-845053C3ADEEQ28486282-B4BCC80F-CECD-418E-8247-C01A3AD96A61Q31056899-EE08EA37-0001-40D7-A058-3EC745A89AA7Q33810258-B1178F82-052E-47A0-8B48-B682EE3EB262Q34441834-32E2C7CE-EBDE-4645-B4C1-C192A26A59AAQ36977147-0FFCAE8A-5AA3-4A45-A71A-8193D35CF8BAQ37606527-22351F76-7F04-4FAE-AF56-46F268A57044Q37917164-651D73F5-BE70-4BFD-B632-18A22B49D57EQ39041957-06DA71D2-8E3E-439A-9DA9-014FD9123F43Q39479116-398C5D29-2439-46E9-9E50-BB326BB011F7Q39867428-39F544E9-EA69-4080-AE93-AAA60390AC69Q41188895-308E0EA3-0D5A-45BC-9669-9EA3234E03C8Q42749671-74113E2D-F5E6-4CBC-9A78-4D57916B45F1Q47738835-7D5AEEFC-7E70-4454-AC49-CFAB6CA6DBA5Q47892855-AC517E26-8CFE-45A9-9851-CBBFE7EA0745Q50293429-A336F558-6BA6-4848-A36C-878D4F726992Q52926888-1BB8DA0F-9388-4B37-BD23-C330249A65B9Q54408207-BD9A1145-3EB0-483D-ADF4-DEF73606BD61
P2860
FGFR3 heterodimerization in achondroplasia, the most common form of human dwarfism.
description
2011 nî lūn-bûn
@nan
2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
FGFR3 heterodimerization in achondroplasia, the most common form of human dwarfism.
@ast
FGFR3 heterodimerization in achondroplasia, the most common form of human dwarfism.
@en
FGFR3 heterodimerization in achondroplasia, the most common form of human dwarfism.
@nl
type
label
FGFR3 heterodimerization in achondroplasia, the most common form of human dwarfism.
@ast
FGFR3 heterodimerization in achondroplasia, the most common form of human dwarfism.
@en
FGFR3 heterodimerization in achondroplasia, the most common form of human dwarfism.
@nl
prefLabel
FGFR3 heterodimerization in achondroplasia, the most common form of human dwarfism.
@ast
FGFR3 heterodimerization in achondroplasia, the most common form of human dwarfism.
@en
FGFR3 heterodimerization in achondroplasia, the most common form of human dwarfism.
@nl
P2093
P2860
P356
P1476
FGFR3 heterodimerization in achondroplasia, the most common form of human dwarfism.
@en
P2093
Nadia Shobnam
William C Wimley
P2860
P304
13272-13281
P356
10.1074/JBC.M110.205583
P407
P577
2011-02-15T00:00:00Z