Associated Papers
Characterization of Novel Variants in P2YRY12, GP6 and TBXAS1 in Patients with Lifelong History of Bleeding.
Zamora-Cánovas A et al.
Biomolecules, 2025
41463295 (PubMed )
Supplement: biomolecules-15-01639-s001.zip › biomolecules-3972089-supplementary.pdf
Molecular Pathogenesis of Inherited Platelet Dysfunction.
Rodríguez-Alén A et al.
Biomolecules, 2025
The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants.
Stefanucci L et al.
Blood, 2023
37647632 (PubMed )
Supplement: BLOOD_BLD-2023-020118-mmc3.xlsx › ST3.3
Inherited platelet diseases with normal platelet count: phenotypes, genotypes and diagnostic strategy.
Nurden P et al.
Haematologica, 2021
Receptor homodimerization plays a critical role in a novel dominant negative P2RY12 variant identified in a family with severe bleeding.
Mundell SJ et al.
Journal of Thrombosis and Haemostasis : Jth, 2018
P2Y₁₂ receptor gene mutations associated with bleeding.
Scavone M et al.
Platelets, 2017
Inherited dysfunctional platelet P2Y12 receptor mutations associated with bleeding disorders.
Lecchi A et al.
Hamostaseologie, 2016
Identification of a new dysfunctional platelet P2Y12 receptor variant associated with bleeding diathesis.
Lecchi A et al.
Blood, 2015
Molecular bases of defective signal transduction in the platelet P2Y12 receptor of a patient with congenital bleeding.
Cattaneo M et al.
Proceedings of the National Academy of Sciences of the United States of America, 2003
Select a paper to view details