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Literature DB >> 10669143

High levels of factor VIII and venous thrombosis.

F R Rosendaal¹.

Abstract

Entities: Disease

Mesh：

Substances：
Factor VIII

Year: 2000 PMID： 10669143

Source DB: PubMed Journal: Thromb Haemost ISSN： 0340-6245 Impact factor: 5.249

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Cited

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9 in total

1. Circumventing furin enhances factor VIII biological activity and ameliorates bleeding phenotypes in hemophilia models.

Authors: Joshua I Siner; Benjamin J Samelson-Jones; Julie M Crudele; Robert A French; Benjamin J Lee; Shanzhen Zhou; Elizabeth Merricks; Robin Raymer; Timothy C Nichols; Rodney M Camire; Valder R Arruda
Journal: JCI Insight Date: 2016-10-06

2. Genetic regulation of plasma von Willebrand factor levels: quantitative trait loci analysis in a mouse model.

Authors: H L Lemmerhirt; K W Broman; J A Shavit; D Ginsburg
Journal: J Thromb Haemost Date: 2006-11-28 Impact factor: 5.824

3. Henoch-Schonlein purpura with high factor VIII levels and deep venous thrombosis: an association or coincidence?

Authors: Rezan Topaloglu; Umut Selda Bayrakci; Barbaros Cil; Diclehan Orhon; Aysin Bakkaloglu
Journal: Rheumatol Int Date: 2008-02-19 Impact factor: 2.631

4. Modifiers of von Willebrand factor identified by natural variation in inbred strains of mice.

Authors: Jordan A Shavit; Ani Manichaikul; Heidi L Lemmerhirt; Karl W Broman; David Ginsburg
Journal: Blood Date: 2009-09-29 Impact factor: 22.113

5. Sialyltransferase ST3Gal-IV operates as a dominant modifier of hemostasis by concealing asialoglycoprotein receptor ligands.

Authors: Lesley G Ellies; David Ditto; Gallia G Levy; Mark Wahrenbrock; David Ginsburg; Ajit Varki; Dzung T Le; Jamey D Marth
Journal: Proc Natl Acad Sci U S A Date: 2002-07-03 Impact factor: 11.205

High levels of factor VIII and venous thrombosis.

1. Circumventing furin enhances factor VIII biological activity and ameliorates bleeding phenotypes in hemophilia models.

2. Genetic regulation of plasma von Willebrand factor levels: quantitative trait loci analysis in a mouse model.

3. Henoch-Schonlein purpura with high factor VIII levels and deep venous thrombosis: an association or coincidence?

4. Modifiers of von Willebrand factor identified by natural variation in inbred strains of mice.

5. Sialyltransferase ST3Gal-IV operates as a dominant modifier of hemostasis by concealing asialoglycoprotein receptor ligands.

Review 6. Dissecting the genetic determinants of hemostasis and thrombosis.

Review 7. Emerging therapies for hemophilia: controversies and unanswered questions.

8. Rational Diagnosis of Cardiovascular Disease.

Review 9. Gene Therapy for Hemophilia: Facts and Quandaries in the 21st Century.