Pages that link to "Q24318690"
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The following pages link to Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels (Q24318690):
Displaying 28 items.
- Terminal nucleotidyltransferase 5A (Q21118130) (← links)
- Genetic Drivers of von Willebrand Factor Levels in an Ischemic Stroke Population and Association With Risk for Recurrent Stroke (Q30252447) (← links)
- Single nucleotide polymorphisms in an intergenic chromosome 2q region associated with tissue factor pathway inhibitor plasma levels and venous thromboembolism. (Q30275601) (← links)
- Syntaxin-binding protein STXBP5 inhibits endothelial exocytosis and promotes platelet secretion. (Q30590837) (← links)
- A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis (Q31113588) (← links)
- Sex-specific effect of CPB2 Ala147Thr but not Thr325Ile variants on the risk of venous thrombosis: A comprehensive meta-analysis (Q33731941) (← links)
- Genome-wide investigation of DNA methylation marks associated with FV Leiden mutation. (Q34263842) (← links)
- Elevated factor VIII levels and risk of venous thrombosis. (Q34270700) (← links)
- Platelet secretion and hemostasis require syntaxin-binding protein STXBP5. (Q34311741) (← links)
- Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association (Q34319603) (← links)
- FcRn Rescues Recombinant Factor VIII Fc Fusion Protein from a VWF Independent FVIII Clearance Pathway in Mouse Hepatocytes (Q35612397) (← links)
- Dissecting the genetic determinants of hemostasis and thrombosis (Q36259417) (← links)
- Epigenetic basis of regeneration: analysis of genomic DNA methylation profiles in the MRL/MpJ mouse (Q37383801) (← links)
- von Willebrand factor: at the crossroads of bleeding and thrombosis. (Q38000162) (← links)
- The secretion of von Willebrand factor from endothelial cells; an increasingly complicated story. (Q38117737) (← links)
- Clearance of von Willebrand factor. (Q38117738) (← links)
- Maximizing the power of principal-component analysis of correlated phenotypes in genome-wide association studies (Q38205644) (← links)
- Leveraging cell type specific regulatory regions to detect SNPs associated with tissue factor pathway inhibitor plasma levels. (Q38728512) (← links)
- Blood triglyceride levels are associated with DNA methylation at the serine metabolism gene PHGDH. (Q40046496) (← links)
- Syntaxin-binding protein 5 exocytosis regulation: differential role in endothelial cells and platelets (Q42936873) (← links)
- Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients (Q48123953) (← links)
- Novel Thrombotic Function of a Human SNP in STXBP5 Revealed by CRISPR/Cas9 Gene Editing in Mice (Q50291228) (← links)
- Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project (Q57611749) (← links)
- The common single nucleotide variants c.2365A>G and c.2385T>C modify VWF biosynthesis and clearance (Q59511557) (← links)
- Significantly altered peripheral blood cell DNA methylation profile as a result of immediate effect of metformin use in healthy individuals (Q60044954) (← links)
- [The research progress of Von Willebrand disease] (Q85963378) (← links)
- Targeting von Willebrand Factor in Ischaemic Stroke: Focus on Clinical Evidence (Q88920978) (← links)
- Genetic regulation of plasma von Willebrand factor levels in health and disease (Q91675224) (← links)