von Willebrand factor: the complex molecular genetics of a multidomain and multifunctional protein

The mutation N528S in the von Willebrand factor (VWF) propeptide causes defective multimerization and storage of VWF

(2010) S. L. Haberichter et al.   BLOOD

A cluster of mutations in the D3 domain of von Willebrand factor correlates with a distinct subgroup of von Willebrand disease: type 2A/IIE

(2010) R. Schneppenheim et al.   BLOOD

Common VWF exon 28 polymorphisms in African Americans affecting the VWF activity assay by ristocetin cofactor

(2010) V. H. Flood et al.   BLOOD

Absent collagen binding in a VWF A3 domain mutant: utility of the VWF:CB in diagnosis of VWD

(2010) V. H. FLOOD et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

A novel binding site for ADAMTS13 constitutively exposed on the surface of globular VWF

(2009) S. Zanardelli et al.   BLOOD

Genetic testing for von Willebrand disease: the case for

(2009) I. R. PEAKE et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Genetic testing for von Willebrand disease: the case against

(2009) E. J. FAVALORO   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

ANO2 is the cilial calcium-activated chloride channel that may mediate olfactory amplification

(2009) Aaron B. Stephan et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Correction of Bleeding Symptoms in von Willebrand Factor–Deficient Mice by Liver-Expressed von Willebrand Factor Mutants

(2008) Isabelle Marx et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD)

(2008) U. BUDDE et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS