Detalhe da pesquisa
1.
Sialylation on O-linked glycans protects von Willebrand factor from macrophage galactose lectin-mediated clearance.
Haematologica
; 107(3): 668-679, 2022 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33763999
2.
Screening for von Willebrand disease does not impact posttonsillectomy bleeding in a low-risk population.
Pediatr Blood Cancer
; 68(12): e29371, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34606172
3.
The role of genetics in the pathogenesis and diagnosis of type 1 Von Willebrand disease.
Curr Opin Hematol
; 26(5): 331-335, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31261173
4.
Gut microbiota regulate hepatic von Willebrand factor synthesis and arterial thrombus formation via Toll-like receptor-2.
Blood
; 130(4): 542-553, 2017 07 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-28572286
5.
Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States.
Blood
; 127(20): 2481-8, 2016 05 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-26862110
6.
von Willebrand factor propeptide: biology and clinical utility.
Blood
; 126(15): 1753-61, 2015 Oct 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26215113
7.
VWF propeptide in defining VWD subtypes.
Blood
; 125(19): 2882-3, 2015 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25953977
8.
Variable content of von Willebrand factor mutant monomer drives the phenotypic variability in a family with von Willebrand disease.
Blood
; 126(2): 262-9, 2015 Jul 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26019279
9.
Crucial role for the VWF A1 domain in binding to type IV collagen.
Blood
; 125(14): 2297-304, 2015 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25662333
10.
Allosteric activation of ADAMTS13 by von Willebrand factor.
Proc Natl Acad Sci U S A
; 111(52): 18584-9, 2014 Dec 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-25512528
11.
G protein-dependent basal and evoked endothelial cell vWF secretion.
Blood
; 123(3): 442-50, 2014 Jan 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-24081657
12.
No increase in bleeding identified in type 1 VWD subjects with D1472H sequence variation.
Blood
; 121(18): 3742-4, 2013 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23520336
13.
The B subunits of Shiga-like toxins induce regulated VWF secretion in a phospholipase D1-dependent manner.
Blood
; 120(5): 1143-9, 2012 Aug 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-22718838
14.
Intersection of mechanisms of type 2A VWD through defects in VWF multimerization, secretion, ADAMTS-13 susceptibility, and regulated storage.
Blood
; 119(19): 4543-53, 2012 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22431572
15.
VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population.
Blood
; 119(9): 2135-40, 2012 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22197721
16.
The common VWF variant p.Y1584C: detailed pathogenic examination of an enigmatic sequence change.
J Thromb Haemost
; 22(3): 666-675, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38040335
17.
Distinguishing ASH clinical practice guidelines from other forms of ASH clinical advice.
Blood Adv
; 8(11): 2960-2963, 2024 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38593461
18.
Collagen binding provides a sensitive screen for variant von Willebrand disease.
Clin Chem
; 59(4): 684-91, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23340442
19.
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
20.
Gain-of-function GPIb ELISA assay for VWF activity in the Zimmerman Program for the Molecular and Clinical Biology of VWD.
Blood
; 117(6): e67-74, 2011 Feb 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-21148813