VWF wt Allele

Known as: VDW, Type 1 Gene, von Willebrand Disease, Type 1 Gene, Von Willebrand Factor wt Allele 
Human VWF wild-type allele is located in the vicinity of 12p13.3 and is approximately 176 kb in length. This allele, which encodes Von Willebrand… (More)
National Institutes of Health

Papers overview

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Highly Cited
2008
Highly Cited
2008
OBJECTIVE Outcomes after ventricular assist device (VAD) implantation have significantly improved during the last decade. However… (More)
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Highly Cited
2008
Highly Cited
2008
BACKGROUND Type 1 von Willebrand disease (VWD) is a congenital bleeding disorder characterized by a partial quantitative… (More)
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Highly Cited
2006
Highly Cited
2006
Type 1 von Willebrand disease (VWD) is characterized by a partial quantitative deficiency of von Willebrand factor (VWF). Few VWF… (More)
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Highly Cited
2006
Highly Cited
2006
In order to evaluate the changes within the VWF gene that might contribute to the pathogenesis of type 1 von Willebrand disease… (More)
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Highly Cited
2006
Highly Cited
2006
BACKGROUND A quantitative description of bleeding symptoms in type 1 von Willebrand disease (VWD) has never been reported… (More)
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Review
2006
Review
2006
von Willebrand disease (VWD) is a bleeding disorder caused by inherited defects in the concentration, structure, or function of… (More)
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Highly Cited
2005
Highly Cited
2005
OBJECTIVE The aim of this study was the validation of the criteria defining a significant mucocutaneous-bleeding history in type… (More)
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Review
2005
Review
2005
Everyone experiences minor bleeding and clotting, and many illnesses feature extremes of hemorrhage or thrombosis. Recent… (More)
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Review
2003
Review
2003
Von Willebrand disease (VWD) type 1 is reported to be common but frequently is difficult to diagnose. Many people have… (More)
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Highly Cited
1998
Highly Cited
1998
We have evaluated the performance of a new analyzer using high shear stress, the PFA-100 (Platelet Function Analyzer, Dade… (More)
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