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Volumn 7, Issue 5, 2001, Pages 284-293

Synthesis and biological evaluation of analogues of the tetrapeptide N-Acetyl-Ser-Asp-Lys-Pro (AcSDKP), an inhibitor of primitive haematopoietic cell proliferation

(6) Thierry, Josiane a Grillon, Catherine a Gaudron, Sandrine a Potier, Pierre a Riches, Andrew b Wdzieczak Bakala, Joanna a

a CNRS (France)

b UNIVERSITY OF ST ANDREWS (United Kingdom)

Author keywords

AcSDKP; AcSDKP analogues; CFU GM; HPP CFC; Proliferation inhibitor; Pseudopeptides

Indexed keywords

ANTINEOPLASTIC AGENT; SERASPENIDE; TETRAPEPTIDE;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; BIOLOGY; BONE MARROW; CARBOXY TERMINAL SEQUENCE; CELL COMPARTMENTALIZATION; CELL CYCLE S PHASE; CELL DAMAGE; CELL PROLIFERATION; COLONY FORMING CELL; COLONY FORMING UNIT GM; CONTROLLED STUDY; DRUG STRUCTURE; DRUG SYNTHESIS; HEMATOPOIETIC STEM CELL; IN VITRO STUDY; IN VIVO STUDY; IONIZING RADIATION; MOUSE; NONHUMAN; PREVENTION; PRIORITY JOURNAL; PROTECTION; PROTEIN EXPRESSION; TOXICITY;

ANIMALS; ASPARTIC ACID; CELL DIVISION; CELLS, CULTURED; HEMATOPOIETIC STEM CELLS; LYSINE; MICE; MODELS, CHEMICAL; OLIGOPEPTIDES; PEPTIDES; S PHASE; SERINE;

MURINAE;

EID: 0034949548 PISSN: 10752617 EISSN: None Source Type: Journal
DOI: 10.1002/psc.322 Document Type: Article

Times cited : (12)

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