SARA is dispensable for functional TGF-β signaling

FEBS Letters

Volumn 586, Issue 19, 2012, Pages 3367-3372

  Bakkebo, Maren ^a,b   Huse, Kanutte ^a,b   Hilden, Vera I ^a,b   Forfang, Lise ^a,b   Myklebust, June H ^a,b   Smeland, Erlend B ^a,b   Oksvold, Morten P ^a,b  

^a OSLO UNIVERSITY HOSPITAL   (Norway)

^b UNIVERSITY OF OSLO   (Norway)

Author keywords

R Smad; SARA; TGF signaling

Indexed keywords

SMAD ANCHOR FOR RECEPTOR ACTIVATION; SMAD PROTEIN; TRANSFORMING GROWTH FACTOR BETA; TRANSFORMING GROWTH FACTOR BETA RECEPTOR;

ARTICLE; B CELL LYMPHOMA; CELL NUCLEUS; CONTROLLED STUDY; GENE TARGETING; HELA CELL; IMMUNOPRECIPITATION; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; PROTEIN TRANSPORT; SIGNAL TRANSDUCTION; TRANSCRIPTION INITIATION;

CELL LINE, TUMOR; GENE KNOCKDOWN TECHNIQUES; HELA CELLS; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; LYMPHOMA, B-CELL; PHOSPHORYLATION; RECEPTORS, TRANSFORMING GROWTH FACTOR BETA; RECOMBINANT PROTEINS; RNA, SMALL INTERFERING; SERINE ENDOPEPTIDASES; SIGNAL TRANSDUCTION; SMAD PROTEINS, RECEPTOR-REGULATED; TRANSFORMING GROWTH FACTOR BETA1;

EID: 84866627933     PISSN: 00145793     EISSN: 18733468     Source Type: Journal    
DOI: 10.1016/j.febslet.2012.07.027     Document Type: Article

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