[HTML][HTML] Proteome-wide mendelian randomization identifies causal plasma proteins in venous thromboembolism development
Genome-wide association studies (GWAS) have identified numerous risk loci for venous
thromboembolism (VTE), but it is challenging to decipher the underlying mechanisms. We …
thromboembolism (VTE), but it is challenging to decipher the underlying mechanisms. We …
[HTML][HTML] Association between uric acid and risk of venous thromboembolism in East Asian populations: a cohort and Mendelian randomization study
Background Serum uric acid (SUA) levels have been associated with an increased risk and
recurrence of venous thromboembolism (VTE) in European populations, but the potential …
recurrence of venous thromboembolism (VTE) in European populations, but the potential …
[HTML][HTML] Thrombosis prophylaxis in surgical patients using the Caprini Risk Score
S Wilson, X Chen, MA Cronin, N Dengler… - Current Problems in …, 2022 - Elsevier
Venous thromboembolism (VTE), which encompasses deep venous thrombosis (DVT) and
pulmonary embolism (PE), is associated with significant mortality and morbidity among …
pulmonary embolism (PE), is associated with significant mortality and morbidity among …
The association of the prothrombin A19911G single-nucleotide polymorphism and the risk of venous thromboembolism: A systematic review and meta-analysis
K Xiang, H Xu, Y Zhang, Q Leng, F Zhang - Phlebology, 2024 - journals.sagepub.com
Background The study employed meta-analysis to provide a comprehensive synthesis of
evidence regarding the association between the prothrombin A19911G polymorphism and …
evidence regarding the association between the prothrombin A19911G polymorphism and …
[HTML][HTML] Rapid identification of a pathogenic variant of PROS1 in a thrombophilic family by whole exome sequencing: A case report
W Zhang, C Huang, W Zhou - Medicine, 2021 - journals.lww.com
Interventions: Whole exome sequencing (WES) of the proband was performed to identify
disease-causing variants. Subsequently, Sanger sequencing was performed to validate the …
disease-causing variants. Subsequently, Sanger sequencing was performed to validate the …
[HTML][HTML] Human induced pluripotent stem cells derived from a patient with a mutation of SERPINC1 c. 236G> A (p. R79H)
W Chen, Y Wang, L Shen, S Huang, X Yang, D Wu - Stem Cell Research, 2023 - Elsevier
Mutation of SERPINC1 is related to the incidence of Inherited antithrombin (AT) deficiency.
In this study, we generated a human induced pluripotent stem cell (iPSC) line from …
In this study, we generated a human induced pluripotent stem cell (iPSC) line from …
Prevalence of Factor V Leiden Mutation in Healthy Females of Sindh, Pakistan and Comparison of Three Detection Methods in Resource-Limited Settings: Prevalence …
FF Khidri, H Riaz, YM Waryah, R Nigar… - Pakistan Journal of …, 2023 - thejas.com.pk
Abstract Factor V Leiden (FVL) mutation is related to venous thromboembolism and
pregnancy complications. It is highly prevalent among Caucasians; however, few studies …
pregnancy complications. It is highly prevalent among Caucasians; however, few studies …
Hospital-Acquired Venous Thromboembolism or Bleeding Following Total Joint Arthroplasty: A Systematic Review and meta-analysis for the Association of the Gene …
M Debeau - 2021 - digitalcommons.wayne.edu
This review seeks to understand the current existing literature on genetic polymorphisms to
VTE following orthopedic surgery. Using PRISMA guidelines, 234 studies were retrieved …
VTE following orthopedic surgery. Using PRISMA guidelines, 234 studies were retrieved …