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
D121 Located within the DRY Motif of P2Y12 Is Essential for P2Y12-Mediated Platelet Function.
Dangelmaier C et al.
International Journal of Molecular Sciences, 2022
Inherited platelet diseases with normal platelet count: phenotypes, genotypes and diagnostic strategy.
Nurden P et al.
Haematologica, 2021
Strengths and Weaknesses of Light Transmission Aggregometry in Diagnosing Hereditary Platelet Function Disorders.
Alessi MC et al.
Journal of Clinical Medicine, 2020
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
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