Pages that link to "Q28510698"
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The following pages link to Mvwf, a dominant modifier of murine von Willebrand factor, results from altered lineage-specific expression of a glycosyltransferase (Q28510698):
Displaying 50 items.
- Beta-1,4-N-acetyl-galactosaminyl transferase 2 (Q21499144) (← links)
- High von Willebrand Factor Levels Increase the Risk of First Ischemic Stroke: Influence of ADAMTS13, Inflammation, and Genetic Variability (Q22299317) (← links)
- Animal models for thrombotic thrombocytopenic purpura (Q26851228) (← links)
- Loss of fibrinogen in zebrafish results in symptoms consistent with human hypofibrinogenemia (Q27306700) (← links)
- Expression of the Blood-Group-Related Gene B4galnt2 Alters Susceptibility to Salmonella Infection (Q27318788) (← links)
- Shigatoxin triggers thrombotic thrombocytopenic purpura in genetically susceptible ADAMTS13-deficient mice (Q28594414) (← links)
- Lessons Learned from Animal Models of Inherited Bleeding Disorders (Q30409863) (← links)
- Modifiers of von Willebrand factor identified by natural variation in inbred strains of mice (Q30433859) (← links)
- Expression of the blood-group-related glycosyltransferase B4galnt2 influences the intestinal microbiota in mice (Q30517268) (← links)
- Long-term balancing selection at the blood group-related gene B4galnt2 in the genus Mus (Rodentia; Muridae). (Q30627326) (← links)
- Sialyltransferase ST3Gal-IV operates as a dominant modifier of hemostasis by concealing asialoglycoprotein receptor ligands (Q33343091) (← links)
- Role of sialic acid for platelet life span: exposure of beta-galactose results in the rapid clearance of platelets from the circulation by asialoglycoprotein receptor-expressing liver macrophages and hepatocytes (Q33384971) (← links)
- A novel role for von Willebrand factor in the pathogenesis of experimental cerebral malaria (Q33427139) (← links)
- The molecular basis of von Willebrand disease (Q33651554) (← links)
- A von Willebrand factor fragment containing the D'D3 domains is sufficient to stabilize coagulation factor VIII in mice (Q33917215) (← links)
- The intestinal stem cell niche: there grows the neighborhood (Q33947648) (← links)
- Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor (Q33998293) (← links)
- Third Åland islands conference on von Willebrand disease, 26-28 September 2012: meeting report. (Q34185963) (← links)
- In vivo analysis of the role of O-glycosylations of von Willebrand factor. (Q34278082) (← links)
- The diagnosis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization. (Q34313804) (← links)
- The molecular biology of von Willebrand disease (Q34421530) (← links)
- Molecular and cellular biology of von Willebrand factor (Q34529616) (← links)
- Von Willebrand factor and von Willebrand disease (Q34530389) (← links)
- von Willebrand disease: still an intriguing disorder in the era of molecular medicine (Q34637001) (← links)
- Cloning and expression of porcine β1,4 N-acetylgalactosaminyl transferase encoding a new xenoreactive antigen (Q34674815) (← links)
- Beyond Mendel: an evolving view of human genetic disease transmission (Q34932051) (← links)
- The highly prolific phenotype of Lacaune sheep is associated with an ectopic expression of the B4GALNT2 gene within the ovary (Q35004518) (← links)
- Von Willebrand factor inhibits mature smooth muscle gene expression through impairment of Notch signaling (Q35005989) (← links)
- An apparently silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand disease (Q35018544) (← links)
- Genetic dissection of quantitative trait Loci for hemostasis and thrombosis on mouse chromosomes 11 and 5 using congenic and subcongenic strains (Q35023208) (← links)
- How to roll an endothelial cigar: the biogenesis of Weibel-Palade bodies (Q35613686) (← links)
- Contrasting genetic architectures in different mouse reference populations used for studying complex traits. (Q35664102) (← links)
- Cholera toxin activates nonconventional adjuvant pathways that induce protective CD8 T-cell responses after epicutaneous vaccination (Q35750997) (← links)
- Modeling Disorders of Blood Coagulation in the Zebrafish (Q35801753) (← links)
- Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival. (Q35848737) (← links)
- Enhanced VWF biosynthesis and elevated plasma VWF due to a natural variant in the murine Vwf gene (Q35849025) (← links)
- Clinical diagnosis of von Willebrand disease (Q35915740) (← links)
- Identifying novel genetic determinants of hemostatic balance (Q36230809) (← links)
- The endothelial-specific regulatory mutation, Mvwf1, is a common mouse founder allele (Q36428412) (← links)
- von Willebrand factor, endothelial dysfunction, and cardiovascular disease (Q36481209) (← links)
- ABO blood group determines plasma von Willebrand factor levels: a biologic function after all? (Q36604393) (← links)
- A guide to murine coagulation factor structure, function, assays, and genetic alterations (Q36777940) (← links)
- Clearance mechanisms of von Willebrand factor and factor VIII. (Q36787433) (← links)
- Genetic regulation of plasma von Willebrand factor levels: quantitative trait loci analysis in a mouse model (Q36846397) (← links)
- Relationship between ABO blood group and von Willebrand factor levels: from biology to clinical implications (Q36951311) (← links)
- Animal models of hemophilia and related bleeding disorders (Q37091290) (← links)
- Sensitized mutagenesis screen in Factor V Leiden mice identifies thrombosis suppressor loci. (Q38615493) (← links)
- Evaluating the maintenance of disease-associated variation at the blood group-related gene B4galnt2 in house mice. (Q38625566) (← links)
- N-linked glycan truncation causes enhanced clearance of plasma-derived von Willebrand factor. (Q39299024) (← links)
- An experimental model to study the in vivo survival of von Willebrand factor. Basic aspects and application to the R1205H mutation. (Q40616991) (← links)