Detalhe da pesquisa
1.
Partial F8 gene duplication (factor VIII Padua) associated with high factor VIII levels and familial thrombophilia.
Blood
; 137(17): 2383-2393, 2021 04 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33275657
2.
Molecular basis of anticoagulant and anticomplement activity of the tick salivary protein Salp14 and its homologs.
J Biol Chem
; 297(1): 100865, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34118237
3.
Making sense of FV short.
Blood
; 141(26): 3134-3135, 2023 06 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37383004
4.
Characterization of an autosomal dominant bleeding disorder caused by a thrombomodulin mutation.
Blood
; 125(9): 1497-501, 2015 Feb 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-25564403
5.
Survival protein anoctamin-6 controls multiple platelet responses including phospholipid scrambling, swelling, and protein cleavage.
FASEB J
; 30(2): 727-37, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26481309
6.
Endocytosis of exogenous factor V by ex-vivo differentiated megakaryocytes from patients with severe parahaemophilia.
Br J Haematol
; 175(3): 517-524, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27443583
7.
FV and APC resistance: the plot thickens.
Blood
; 123(15): 2288-9, 2014 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-24723678
8.
Fibrinogen γ' increases the sensitivity to activated protein C in normal and factor V Leiden plasma.
Blood
; 124(9): 1531-8, 2014 Aug 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-24951429
9.
Antisense-based RNA therapy of factor V deficiency: in vitro and ex vivo rescue of a F5 deep-intronic splicing mutation.
Blood
; 122(23): 3825-31, 2013 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-24085767
10.
Factor V variants in bleeding and thrombosis.
Res Pract Thromb Haemost
; 8(1): 102330, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38404937
11.
In vitro and ex vivo rescue of a nonsense mutation responsible for severe coagulation factor V deficiency.
J Thromb Haemost
; 22(2): 410-422, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37866515
12.
Plasma levels of Complement components C5 and C9 are associated with thrombin generation.
J Thromb Haemost
; 2024 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38838952
13.
Post-transcriptional control of haemostatic genes: mechanisms and emerging therapeutic concepts in thrombo-inflammatory disorders.
Cardiovasc Res
; 119(8): 1624-1640, 2023 07 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36943786
14.
Factor V Leiden-independent activated protein C resistance: Communication from the plasma coagulation inhibitors subcommittee of the International Society on Thrombosis and Haemostasis Scientific and Standardisation Committee.
J Thromb Haemost
; 21(1): 164-174, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36695379
15.
High incidence of intracranial bleeding in factor V-deficient patients with homozygous F5 splicing mutations.
Br J Haematol
; 179(1): 163-166, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27351627
16.
Residual platelet factor V ensures thrombin generation in patients with severe congenital factor V deficiency and mild bleeding symptoms.
Blood
; 115(4): 879-86, 2010 Jan 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-19861681
17.
Effect of five therapeutic strategies on the coagulation defect induced by the thrombomodulin c.1611C>A mutation.
Br J Haematol
; 174(6): 993-6, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26517807
18.
Pleiotropic anticoagulant functions of protein S, consequences for the clinical laboratory. Communication from the SSC of the ISTH.
J Thromb Haemost
; 19(1): 281-286, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33405384
19.
Severe thrombophilia in a factor V-deficient patient homozygous for the Ala2086Asp mutation (FV Besançon).
J Thromb Haemost
; 19(5): 1186-1199, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33605529
20.
Low plasma levels of tissue factor pathway inhibitor in patients with congenital factor V deficiency.
Blood
; 112(9): 3615-23, 2008 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18695002