MicroRNA-424 predicts a role for β-1,4 branched glycosylation in cell cycle progression

Journal of Biological Chemistry

Volumn 291, Issue 3, 2016, Pages 1529-1537

  Vaiana, Christopher A ^a   Kurcon, Tomasz ^a   Mahal, Lara K ^a  

^a NEW YORK UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL CULTURE; CELL DEATH; CELL PROLIFERATION; CELLS; GLYCOSYLATION; POLYSACCHARIDES; RNA;

ANTI-PROLIFERATIVE; BRANCHING PATTERNS; CELL-CYCLE ARREST; CELL-CYCLE PROGRESSION; MAMMARY EPITHELIAL CELLS; N-LINKED GLYCOSYLATION; PROTEIN EXPRESSIONS; TRANSFORMING GROWTH FACTOR BETA;

CYTOLOGY;

BETA 1,4 N GLYCAN; CYCLIN D1; GALECTIN 3; GLYCAN; GLYCOSYLTRANSFERASE; MICRORNA; MICRORNA 424; PHOSPHATASE; PROTEIN CDC25A; PROTEIN GALNT13; PROTEIN MGAT4A; PROTEIN OGT; TRANSFORMING GROWTH FACTOR BETA; UNCLASSIFIED DRUG; CCND1 PROTEIN, HUMAN; GALNT13 PROTEIN, HUMAN; LUCIFERASE; MGAT4A PROTEIN, HUMAN; MIRN424 MICRORNA, HUMAN; N ACETYLGALACTOSAMINYLTRANSFERASE; N ACETYLGLUCOSAMINYLTRANSFERASE; RECOMBINANT PROTEIN; SMALL INTERFERING RNA; UDP-N-ACETYLGLUCOSAMINE-PEPTIDE BETA-N-ACETYLGLUCOSAMINYLTRANSFERASE;

ARTICLE; BREAST EPITHELIUM CELL; CELL CYCLE ARREST; CELL CYCLE PROGRESSION; CELL CYCLE REGULATION; CELL PROLIFERATION; CONTROLLED STUDY; DOWN REGULATION; GENE SILENCING; GLYCOSYLATION; LUCIFERASE ASSAY; MCF 7 CELL LINE; PREDICTION; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; PROTEIN TARGETING; AGONISTS; ANTAGONISTS AND INHIBITORS; CELL CYCLE; CELL LINE; CYTOLOGY; ENZYME REPRESSION; ENZYMOLOGY; GENETICS; HEK293 CELL LINE; HUMAN; MAMMARY GLAND; METABOLISM; REPORTER GENE; RNA INTERFERENCE;

CELL CYCLE; CELL LINE; CELL PROLIFERATION; CYCLIN D1; ENZYME REPRESSION; GENES, REPORTER; GLYCOSYLATION; HEK293 CELLS; HUMANS; LUCIFERASES; MAMMARY GLANDS, HUMAN; MICRORNAS; N-ACETYLGALACTOSAMINYLTRANSFERASES; N-ACETYLGLUCOSAMINYLTRANSFERASES; RECOMBINANT PROTEINS; RNA INTERFERENCE; RNA, SMALL INTERFERING; TRANSFORMING GROWTH FACTOR BETA;

EID: 84954493500     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M115.672220     Document Type: Article

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