Platelet microparticles are heterogeneous and highly dependent on the activation mechanism: Studies using a new digital flow cytometer

Cytometry Part A

Volumn 71, Issue 1, 2007, Pages 38-45

  Perez Pujol, Sílvia ^a   Marker, Paul H ^a   Key, Nigel S ^b  

^a UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

Flow cytometry; Microparticle; Phosphatidylserine; Platelet; Sorting

Indexed keywords

CELL ANTIBODY; GLYCOPROTEIN; IONOPHORE; MEMBRANE PROTEIN; PADGEM PROTEIN; PHOSPHATIDYLSERINE; PROCOAGULANT; THROMBIN RECEPTOR ACTIVATING PEPTIDE;

AGONIST; ARTICLE; BLOOD CLOTTING; CELL SELECTION; CELL SUBPOPULATION; DIGITAL IMAGING; FLOW CYTOMETRY; HUMAN; HUMAN CELL; METHODOLOGY; MICROVASCULATURE; PARTICLE SIZE; PRIORITY JOURNAL; PROTEIN EXPRESSION; THROMBOCYTE; THROMBOCYTE ACTIVATION;

ACID PHOSPHATASE; ANNEXIN A5; BLOOD PLATELETS; CALCIMYCIN; FLOW CYTOMETRY; INTEGRIN BETA3; ISOENZYMES; P-SELECTIN; PLATELET ACTIVATION; PLATELET GLYCOPROTEIN GPIB-IX COMPLEX;

EID: 33846828571     PISSN: 15524922     EISSN: 15524930     Source Type: Journal    
DOI: 10.1002/cyto.a.20354     Document Type: Article

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