Associated Papers
Bioinformatic analysis of rare endothelial protein C receptor missense variants associated with coagulation and thrombophilia risk.
Unar A et al.
Scientific Reports, 2025
Multipopulation GWAS for venous thromboembolism identifies novel loci followed by experimental validation in zebrafish.
Wolford BN et al.
Blood Advances, 2025
Impact of nonsynonymous single nucleotide polymorphisms in PROCR gene on protein stability and thrombotic risk: a molecular dynamic approach.
Abuagla HA et al.
Frontiers in Genetics, 2025
40370698 (PubMed )
Supplement: DataSheet1.pdf
Thrombotic Risk Determined by Protein C Receptor (PROCR) Variants among Middle-Aged and Older Adults: A Population-Based Cohort Study.
Manderstedt E et al.
Thrombosis and Haemostasis, 2022
Targeted gene sequencing identifies variants in the protein C and endothelial protein C receptor genes in patients with unprovoked venous thromboembolism.
Wu C et al.
Arteriosclerosis, Thrombosis, and Vascular Biology, 2013
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