PLAU wt Allele

Known as: RP11-417O11.1, BDPLT5, Plasminogen Activator, Urokinase wt Allele 
Human PLAU wild-type allele is located within 10q24 and is approximately 6 kb in length. This allele, which encodes urokinase-type plasminogen… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1992-2018
0246819922018

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2012
2012
Platelet aggregometry and dense granule adenosine triphosphate (ATP) release assays are helpful to diagnose platelet disorders… (More)
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2011
2011
Quebec platelet disorder (QPD) is an autosomal dominant bleeding disorder associated with a unique gain-of-function defect in… (More)
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2010
2010
Quebec platelet disorder (QPD) is an autosomal dominant bleeding disorder linked to a region on chromosome 10 that includes PLAU… (More)
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2009
2009
Quebec platelet disorder (QPD) is an autosomal dominant disorder with high penetrance that is associated with increased risks for… (More)
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2009
2009
Quebec platelet disorder (QPD) is an inherited bleeding disorder associated with increased urokinase plasminogen activator (uPA… (More)
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2007
2007
Monoclonal antibodies (mAbs) specific for the human macrophage galactose-type calcium-type lectin (MGL) were established. The… (More)
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2006
2006
BACKGROUND The Quebec platelet disorder (QPD) is inherited and characterized by delayed-onset bleeding following hemostatic… (More)
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2004
2004
Quebec platelet disorder (QPD) is an autosomal dominant bleeding disorder associated with increased urokinase-type plasminogen… (More)
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2003
2003
The Quebec Platelet Disorder (QPD) is an unusual bleeding disorder associated with increased platelet stores of urokinase-type… (More)
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2001
2001
The Quebec platelet disorder (QPD) is an autosomal dominant platelet disorder associated with delayed bleeding and alpha-granule… (More)
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