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Volumn 249, Issue 4971, 1990, Pages 915-918

A β3 integrin mutation abolishes ligand binding and alters divalent cation-dependent conformation

(6) Loftus, Joseph C a O'Toole, Timothy E a Plow, Edward F a Glass, Alison a Frelinger III, Andrew L a Ginsberg, Mark H a

a SCRIPPS RESEARCH INSTITUTE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

INTEGRIN;

ARTICLE; GENE MUTATION; GLANZMANN DISEASE; HEREDITY; HUMAN; HUMAN CELL; LIGAND BINDING; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; ANIMAL; ASPARTIC ACID; BASE SEQUENCE; BINDING SITES; CELL LINE; COMPARATIVE STUDY; INTEGRINS; LIGANDS; MACROMOLECULAR SYSTEMS; MOLECULAR SEQUENCE DATA; MUTATION; OLIGONUCLEOTIDE PROBES; PLATELET MEMBRANE GLYCOPROTEINS; POLYMERASE CHAIN REACTION; PROTEIN CONFORMATION; SEQUENCE HOMOLOGY, NUCLEIC ACID; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; TYROSINE;

EID: 0025062149 PISSN: 00368075 EISSN: None Source Type: Journal
DOI: 10.1126/science.2392682 Document Type: Article

Times cited : (327)

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