Zobrazeno 1 - 10
of 350
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75334f7646b294781c6be7aa2dd31d34
https://doi.org/10.1182/blood.v82.7.1985.bloodjournal8271985
https://doi.org/10.1182/blood.v82.7.1985.bloodjournal8271985
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62948c7afd07f079eee5ef2a79e73abf
https://doi.org/10.1182/blood.v77.4.694.bloodjournal774694
https://doi.org/10.1182/blood.v77.4.694.bloodjournal774694
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98e0d30b3049b9fff0ccb08e8e96d5fb
https://doi.org/10.1182/blood.v75.6.1220.bloodjournal7561220
https://doi.org/10.1182/blood.v75.6.1220.bloodjournal7561220
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61c657548fe112713390f86161ef5edc
https://pubmed.ncbi.nlm.nih.gov/7693034
https://pubmed.ncbi.nlm.nih.gov/7693034
Publikováno v:
Blood. 75(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84ab908a572dbf660df018278eff19ea
https://pubmed.ncbi.nlm.nih.gov/2180491
https://pubmed.ncbi.nlm.nih.gov/2180491
Publikováno v:
médecine/sciences. 11:1021
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec4672c059f8c836c20708be0f338cea
https://doi.org/10.4267/10608/2402
https://doi.org/10.4267/10608/2402
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b34aeed5125f9786669ec68b3e77efa7
https://doi.org/10.1182/blood.v68.3.774.bloodjournal683774
https://doi.org/10.1182/blood.v68.3.774.bloodjournal683774
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ea95b12a3e10440809de7bf80e66811
https://pubmed.ncbi.nlm.nih.gov/6460535
https://pubmed.ncbi.nlm.nih.gov/6460535
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