Bile acids modulate signaling by functional perturbation of plasma membrane domains

Journal of Biological Chemistry

Volumn 288, Issue 50, 2013, Pages 35660-35670

  Zhou, Yong ^a   Maxwell, Kelsey N ^a   Sezgin, Erdinc ^b   Lu, Maryia ^a   Liang, Hong ^a   Hancock, John F ^a   Dial, Elizabeth J ^a   Lichtenberger, Lenard M ^a   Levental, Ilya ^a  

^a UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^b MAX PLANCK INSTITUTE OF MOLECULAR CELL BIOLOGY AND GENETICS   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CELLULAR TOXICITIES; FUNCTIONAL PERTURBATION; LATERAL SEGREGATION; MEMBRANE FUNCTIONS; MEMBRANE VESICLES; PLASMA MEMBRANE DOMAINS; PRIMARY FUNCTIONS; PROTEIN PARTITIONING;

BIOMIMETICS; BODY FLUIDS; CELL MEMBRANES; CYTOLOGY; LIPOSOMES; MEMBRANES; PROTEINS; SIGNAL TRANSDUCTION;

CELL SIGNALING;

BILE ACID; EPIDERMAL GROWTH FACTOR; H RAS PROTEIN; K RAS PROTEIN; LIPOSOME; RAS PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CELL MEMBRANE; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; CYTOTOXICITY; MEMBRANE DAMAGE; MEMBRANE VESICLE; MISCIBILITY; NONHUMAN; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DOMAIN; PROTEIN LOCALIZATION; RAT; SIGNAL TRANSDUCTION;

BILE ACID; LIPID RAFT; MEMBRANE BILAYER; MEMBRANE BIOPHYSICS; MEMBRANE LIPIDS; MEMBRANE STRUCTURE; RAS;

ANIMALS; CELL LINE, TUMOR; CELL SURVIVAL; DEOXYCHOLIC ACID; DOSE-RESPONSE RELATIONSHIP, DRUG; LIPOSOMES; MAP KINASE SIGNALING SYSTEM; MEMBRANE MICRODOMAINS; MEMBRANE PROTEINS; MICELLES; NANOSTRUCTURES; RAS PROTEINS; RATS; SIGNAL TRANSDUCTION; SOLUBILITY;

EID: 84890339661     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M113.519116     Document Type: Article

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