Detalhe da pesquisa
1.
Analysis of the role of von Willebrand factor, platelet glycoprotein VI-, and α2ß1-mediated collagen binding in thrombus formation.
Blood;
124(11): 1799-807, 2014 Sep 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25051961
2.
Omental implantation of BOECs in hemophilia dogs results in circulating FVIII antigen and a complex immune response.
Blood;
123(26): 4045-53, 2014 Jun 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24829206
3.
Pathologic mechanisms of type 1 VWD mutations R1205H and Y1584C through in vitro and in vivo mouse models.
Blood;
117(16): 4358-66, 2011 Apr 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21346256
4.
Mutation-specific hemostatic variability in mice expressing common type 2B von Willebrand disease substitutions.
Blood;
115(23): 4862-9, 2010 Jun 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20371742
5.
A microRNA-regulated and GP64-pseudotyped lentiviral vector mediates stable expression of FVIII in a murine model of Hemophilia A.
Mol Ther;
19(4): 723-30, 2011 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21285959
6.
A murine model for induction of long-term immunologic tolerance to factor VIII does not require persistent detectable levels of plasma factor VIII and involves contributions from Foxp3+ T regulatory cells.
Blood;
114(3): 677-85, 2009 Jul 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19458355
7.
ADAMTS13 cleavage efficiency is altered by mutagenic and, to a lesser extent, polymorphic sequence changes in the A1 and A2 domains of von Willebrand factor.
Br J Haematol;
143(4): 552-8, 2008 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18986390
8.
Ex vivo gene therapy for hemophilia A that enhances safe delivery and sustained in vivo factor VIII expression from lentivirally engineered endothelial progenitors.
Stem Cells;
25(10): 2660-9, 2007 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17615271
9.
Transgene-host cell interactions mediate significant influences on the production, stability, and function of recombinant canine FVIII.
Mol Ther Methods Clin Dev;
2: 15033, 2015.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26636112
10.
Quantitative and qualitative changes of von Willebrand factor and their impact on mortality in patients with end-stage kidney disease.
Blood Coagul Fibrinolysis;
24(7): 719-26, 2013 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23846000
11.
The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study.
Blood;
109(1): 145-54, 2007 Jan 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17190853
12.
Cell type-specific regulation of von Willebrand factor expression by the E4BP4 transcriptional repressor.
Blood;
105(4): 1531-9, 2005 Feb 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15498853
13.
A novel type 2A von Willebrand factor mutation located at the last nucleotide of exon 26 (3538G>A) causes skipping of 2 nonadjacent exons.
Blood;
104(9): 2739-45, 2004 Nov 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15226181
14.
Founder von Willebrand factor haplotype associated with type 1 von Willebrand disease.
Blood;
102(2): 549-57, 2003 Jul 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-12649144