scholarly article | Q13442814 |
P356 | DOI | 10.1111/J.1365-2141.1977.TB00649.X |
P698 | PubMed publication ID | 871437 |
P2093 | author name string | P N Walsh | |
J G White | |||
D C Mills | |||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 287-296 | |
P577 | publication date | 1977-06-01 | |
P1433 | published in | British Journal of Haematology | Q4970200 |
P1476 | title | Metabolism and function of human platelets washed by albumin density gradient separation | |
P478 | volume | 36 |
Q40983690 | 2-Methylthioadenosine[beta-32P]diphosphate. An agonist and radioligand for the receptor that inhibits the accumulation of cyclic AMP in intact blood platelets |
Q72961006 | 29 Receptors for PGI2 and PGD2 on human platelets |
Q36867848 | A catalytic domain exosite (Cys527-Cys542) in factor XIa mediates binding to a site on activated platelets |
Q72833834 | A method to minimize platelet activation during platelet isolation |
Q74171423 | Activated platelets but not endothelial cells participate in the initiation of the consolidation phase of blood coagulation |
Q37034062 | Active release of human platelet factor VIII-related antigen by adenosine diphosphate, collagen, and thrombin |
Q73295898 | Affinity of Fibrinogen Binding to Platelet Membrane Glycoprotein IIb/IIIa Increases with RGDS and gamma Chain Fibrinogen Peptide Hybrid |
Q74088680 | Characterization of the initial alpha-thrombin interaction with glycoprotein Ib alpha in relation to platelet activation |
Q72069270 | Disulfide bond requirements for assembly of the platelet glycoprotein Ib-binding domain of von Willebrand factor |
Q34564820 | Fibrinogen-independent platelet adhesion and thrombus formation on subendothelium mediated by glycoprotein IIb-IIIa complex at high shear rate |
Q33380132 | Flow cytometric analysis of anti-platelet antibodies in patients with chronic idiopathic thrombocytopenic purpura (ITP) using acid-treated, formalin-fixed platelets |
Q67775135 | Function of glycoprotein Ib alpha in platelet activation induced by alpha-thrombin |
Q36314768 | Glanzmann thrombasthenia: deficient binding of von Willebrand factor to thrombin-stimulated platelets |
Q35207304 | High-molecular weight kininogen. A secreted platelet protein |
Q37038202 | Human platelets and factor XI. Localization in platelet membranes of factor XI-like activity and its functional distinction from plasma factor XI |
Q71143448 | Identification of a novel binding site to the integrin alphaIIbbeta3 located in the C-terminal heparin-binding domain of human plasma fibronectin |
Q34565552 | Independent modulation of von Willebrand factor and fibrinogen binding to the platelet membrane glycoprotein IIb/IIIa complex as demonstrated by monoclonal antibody |
Q50791515 | Inhibition of cytokine‐induced nitric oxide production by transforming growth factor‐beta 1 in human smooth muscle cells |
Q33479095 | Inhibition of platelet-aggregating activity in thrombotic thrombocytopenic purpura plasma by normal adult immunoglobulin G |
Q34624945 | Interaction of asialo von Willebrand factor with glycoprotein Ib induces fibrinogen binding to the glycoprotein IIb/IIIa complex and mediates platelet aggregation |
Q37554183 | Interaction of purified type IIB von Willebrand factor with the platelet membrane glycoprotein Ib induces fibrinogen binding to the glycoprotein IIb/IIIa complex and initiates aggregation |
Q34705232 | Isolated deficiency of platelet procoagulant activity |
Q71244316 | Isolated recombinant domain of von Willebrand factor displaying increased sensitivity to ristocetin |
Q71103977 | Leucocyte-dependent platelet activation: an alternative pathway for initiation of blood clotting in inflammation |
Q44408524 | Novel effect of cyclicization of the Arg-Gly-Asp-containing peptide on vitronectin binding to platelets |
Q33458561 | Novel platelet-agglutinating protein from a thrombotic thrombocytopenic purpura plasma |
Q63973106 | On the Mechanism of the Spermine-Exerted Inhibition on α-Thrombin-Induced Platelet Activation* |
Q33455870 | Platelet aggregation in chronic idiopathic thrombocytopenic purpura |
Q66971028 | Platelets and Surface-Mediated Clotting Activity |
Q33821754 | Platelets have more than one binding site for von Willebrand factor |
Q57704398 | Reversible activation defect of the platelet glycoprotein IIb-IIIa complex in patients with uremia |
Q35903946 | Role of Purinergic Receptor Expression and Function for Reduced Responsiveness to Adenosine Diphosphate in Washed Human Platelets |
Q33489289 | Soluble P‐selectin is present in normal circulation and its plasma level is elevated in patients with thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome |
Q61778578 | Structural and Functional Characterization of Platelet Receptor-mediated Factor VIII Binding |
Q102059065 | Superiority of albumin-globulin ratio over albumin to predict mortality in patients undergoing peritoneal dialysis |
Q71843085 | Synergistic effect of epinephrine and shearing on platelet activation |
Q39903313 | The ability of fibrinogen fragments to support ADP-induced platelet aggregation |
Q34102427 | The factor IXa second epidermal growth factor (EGF2) domain mediates platelet binding and assembly of the factor X activating complex. |
Q74588342 | The interaction of factor XIa with activated platelets but not endothelial cells promotes the activation of factor IX in the consolidation phase of blood coagulation |
Q35863726 | The prostanoids in hemostasis and thrombosis: a review |
Q35577294 | Type IIB von Willebrand factor with normal sialic acid content induces platelet aggregation in the absence of ristocetin. Role of platelet activation, fibrinogen, and two distinct membrane receptors |
Q36206114 | Ultrastructure of clots during isometric contraction |
Q37023086 | Variant von Willebrand's disease: characterization of two subtypes by analysis of multimeric composition of factor VIII/von Willebrand factor in plasma and platelets |
Q34208569 | von Willebrand factor binding to platelet GpIb initiates signals for platelet activation |
Q33478102 | von Willebrand factor binds to platelets and induces aggregation in platelet-type but not type IIB von Willebrand disease |
Q34574601 | von Willebrand factor interaction with the glycoprotein IIb/IIa complex. Its role in platelet function as demonstrated in patients with congenital afibrinogenemia |
Search more.