Zobrazeno 1 - 10
of 99
pro vyhledávání: '"JP Caen"'
Publikováno v:
Blood. 82:1985-1988
Bernard-Soulier syndrome (BSS) platelets, which lack the membrane glycoprotein complex Ib-IX, do not adhere to subendothelium. The adhesion of platelets from two patients with BSS to subendothelial microfibrils (MFs) and type I collagen was compared
Publikováno v:
Blood. 77:694-699
The subcellular localization of the platelet membrane receptors glycoproteins (GP) Ib and IIb/IIIa [corrected] has been studied within resting platelets by a combination of biochemical and cytochemical techniques. While both GPIb and GPIIb/IIIa are l
Autor:
Em, Cramer, Gf, Savidge, Vainchenker W, Mc, Berndt, Dominique Pidard, Jp, Caen, Jm, Massé, Breton-Gorius J
Publikováno v:
Europe PubMed Central
Using an immunogold staining technique and electron microscopy, we investigated the localization of the alpha-granule pool of glycoprotein (GP) IIb-IIIa in normal platelets and maturing megakaryocytes (MK), in pathologic platelets from a patient with
Publikováno v:
Blood. 82(10)
CD36 (glycoprotein [GP] IV) is a membrane GP of 88 kD found on monocytes, endothelial cells, and platelets. It may serve as a receptor for collagen and is also able to bind thrombospondin (TSP), because a monoclonal antibody to CD36 inhibits TSP bind
Publikováno v:
Blood. 75(7)
Publikováno v:
médecine/sciences. 11:1021
Publikováno v:
Blood. 68:774-778
The electron microscopic localization of von Willebrand factor (vWF) was studied in platelets from normal and von Willebrand disease (vWD) pigs. In normal pig platelets, immunolabeling for vWF was far more intense and extensive than in human platelet
Publikováno v:
Blood. 59(4)
The gray platelet syndrome is a rare inherited platelet disorder characterized by the absence of alp ha-granules as observed by electron microscopy. Analysis of the glycoprotein composition of the platelets of 2 such patients by SDS-polyacrylamide ge
Publikováno v:
Europe PubMed Central
Studies have been carried out with cultured human megakaryocytes derived from Gray Platelet Syndrome blood and have demonstrated that MK-DGF and MK-F4 are present in the early stages of megakaryocyte maturation (day 5-6) but disappear in the late pha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ba2b4638f8d737cab2e52343ba4abe25
http://europepmc.org/abstract/med/3615193
http://europepmc.org/abstract/med/3615193
Autor:
Soria J, Soria C, Mirshahi M, Claude Boucheix, Pujade E, Jy, Perrot, Samama M, Bernadou A, Jp, Caen
Publikováno v:
Europe PubMed Central
A specific determination of fibrin degradation product (FbDP) is essential for the monitoring of thrombolytic therapy. In patients under thrombolytic therapy, even with tpA (tissue type plasminogen activator) fibrinogen is degraded, and fragment D de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::11735dbf0c69bcbb12204b6a58f8f31e
http://europepmc.org/abstract/med/3103876
http://europepmc.org/abstract/med/3103876