FGFR3 heterodimerization in achondroplasia, the most common form of human dwarfism

Journal of Biological Chemistry

Volumn 286, Issue 15, 2011, Pages 13272-13281

  He, Lijuan ^a   Shobnam, Nadia ^a   Wimley, William C ^b   Hristova, Kalina ^a  

^a Johns Hopkins University   (United States)

^b TULANE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELLULAR MEMBRANES; FIBROBLAST GROWTH FACTOR RECEPTORS; HETERODIMERIZATION; HETERODIMERS; HOMODIMERS; KINASE DOMAINS; LIGAND CONCENTRATION; LOWER PROBABILITIES; TRANS-MEMBRANE DOMAINS; WILD TYPES;

ACTIVATION ANALYSIS; CELL CULTURE; LAKES;

PHOSPHORYLATION;

FIBROBLAST GROWTH FACTOR RECEPTOR 3; HETERODIMER; HOMODIMER; MUTANT PROTEIN;

ACHONDROPLASIA; ARTICLE; CELL MEMBRANE; COMPLEX FORMATION; CONTROLLED STUDY; DIMERIZATION; DOWN REGULATION; DWARFISM; EMBRYO; ENZYME LOCALIZATION; ENZYME PHOSPHORYLATION; HUMAN; HUMAN CELL; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; WILD TYPE;

ACHONDROPLASIA; AMINO ACID SUBSTITUTION; HEK293 CELLS; HUMANS; MUTATION, MISSENSE; PHOSPHORYLATION; PROTEIN MULTIMERIZATION; PROTEIN STRUCTURE, TERTIARY; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 3;

EID: 79953856862     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.205583     Document Type: Article

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