Jean-claude C. Bordet

Groupement Hospitalier Est, Hospices Civils De Lyon
Bron, 69500, France

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 41 publications

Corrigendum to 'Platelet dense granule defect: experience in the French population' [Research and Practice in Thrombosis and Haemostasis Volume 10, Issue 2, February 2026, 103364].

Corrigendum to 'Platelet dense granule defect: experience in the French population' [Research and Practice in Thrombosis and Haemostasis Volume 10, Issue 2, February 2026, 103364].

Journal: Research and practice in thrombosis and haemostasis

Published: July 28, 2026

Platelet dense granule defect: experience in the French population.

Platelet dense granule defect: experience in the French population.

Journal: Research and practice in thrombosis and haemostasis

Published: December 21, 2025

F-actin disassembly by the oxidoreductase MICAL1 promotes mechano-dependent VWF-GPIbα interaction in platelets.

F-actin disassembly by the oxidoreductase MICAL1 promotes mechano-dependent VWF-GPIbα interaction in platelets.

Journal: Nature communications

Published: February 06, 2025

Shear Forces Induced Platelet Clearance Is a New Mechanism of Thrombocytopenia.

Shear Forces Induced Platelet Clearance Is a New Mechanism of Thrombocytopenia.

Journal: Circulation research

Published: October 26, 2023

Somatic RAP1B gain-of-function variant underlies isolated thrombocytopenia and immunodeficiency.

Somatic RAP1B gain-of-function variant underlies isolated thrombocytopenia and immunodeficiency.

Journal: The Journal of clinical investigation

Published: March 07, 2023

MAGT1 deficiency in XMEN disease is associated with severe platelet dysfunction and impaired platelet glycoprotein N-glycosylation.

MAGT1 deficiency in XMEN disease is associated with severe platelet dysfunction and impaired platelet glycoprotein N-glycosylation.

Journal: Journal of thrombosis and haemostasis : JTH

Published: January 11, 2023

DOCK11 deficiency in patients with X-linked actinopathy and autoimmunity.

DOCK11 deficiency in patients with X-linked actinopathy and autoimmunity.

Journal: Blood

Published: October 11, 2022

Multicolor flow cytometry in clinical samples for platelet signaling assessment.

Multicolor flow cytometry in clinical samples for platelet signaling assessment.

Journal: Research and practice in thrombosis and haemostasis

Published: September 25, 2022

Platelet function studies in myeloproliferative neoplasms patients with Calreticulin or JAK2 V617F mutation.

Platelet function studies in myeloproliferative neoplasms patients with Calreticulin or JAK2 V617F mutation.

Journal: Research and practice in thrombosis and haemostasis

Published: September 12, 2022

APOLD1 loss causes endothelial dysfunction involving cell junctions, cytoskeletal architecture, and Weibel-Palade bodies, while disrupting hemostasis.

APOLD1 loss causes endothelial dysfunction involving cell junctions, cytoskeletal architecture, and Weibel-Palade bodies, while disrupting hemostasis.

Journal: Haematologica

Published: May 27, 2022

Cyclic thrombocytopenia related to erythropoietin-dependent anti-platelet anti-GPIV/IIIb antibody in hemodialysis.

Cyclic thrombocytopenia related to erythropoietin-dependent anti-platelet anti-GPIV/IIIb antibody in hemodialysis.

Journal: Journal of nephrology

Published: March 14, 2022

Recombinant porcine factor VIII corrects thrombin generation in vitro in plasma from patients with congenital hemophilia A and inhibitors.

Recombinant porcine factor VIII corrects thrombin generation in vitro in plasma from patients with congenital hemophilia A and inhibitors.

Journal: Research and practice in thrombosis and haemostasis

Published: August 09, 2021

Showing 1-12 of 41

Last Updated: 09/26/2026