Detalhe da pesquisa
1.
Modulation of factor VIII pharmacokinetics by genetic components in factor VIII receptors.
Haemophilia
; 29(2): 479-487, 2023 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-36533781
2.
Whole-Exome Sequencing in a Family with an Unexplained Tendency for Venous Thromboembolism: Multicomponent Prediction of Low-Frequency Variant Deleteriousness and of Individual Protein Interaction.
Int J Mol Sci
; 24(18)2023 Sep 07.
Artigo
Inglês
| MEDLINE | ID: mdl-37762110
3.
Combination of Genomic and Transcriptomic Approaches Highlights Vascular and Circadian Clock Components in Multiple Sclerosis.
Int J Mol Sci
; 23(1)2021 Dec 28.
Artigo
Inglês
| MEDLINE | ID: mdl-35008743
4.
Performance prediction models based on anthropometric, genetic and psychological traits of Croatian sprinters.
Biol Sport
; 36(1): 17-23, 2019 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-30899135
5.
Changes in expression profiles of internal jugular vein wall and plasma protein levels in multiple sclerosis.
Mol Med
; 24(1): 42, 2018 08 09.
Artigo
Inglês
| MEDLINE | ID: mdl-30134823
6.
Severe bleeding and absent ADP-induced platelet aggregation associated with inherited combined CalDAG-GEFI and P2Y12 deficiencies.
Haematologica
; 105(7): e361-e364, 2020 07.
Artigo
Inglês
| MEDLINE | ID: mdl-31649128
7.
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
Inglês
| MEDLINE | ID: mdl-37866515
8.
Polymorphisms at LDLR locus may be associated with coronary artery disease through modulation of coagulation factor VIII activity and independently from lipid profile.
Blood
; 116(25): 5688-97, 2010 Dec 16.
Artigo
Inglês
| MEDLINE | ID: mdl-20810930
9.
Combination of CLEC4M rs868875 G-Carriership and ABO O Genotypes May Predict Faster Decay of FVIII Infused in Hemophilia A Patients.
J Clin Med
; 11(3)2022 Jan 29.
Artigo
Inglês
| MEDLINE | ID: mdl-35160186
10.
The Asialoglycoprotein Receptor Minor Subunit Gene Contributes to Pharmacokinetics of Factor VIII Concentrates in Hemophilia A.
Thromb Haemost
; 122(5): 715-725, 2022 05.
Artigo
Inglês
| MEDLINE | ID: mdl-34407556
11.
F9 missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypes.
J Thromb Haemost
; 20(1): 69-81, 2022 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34626083
12.
The p.P1127S pathogenic variant lowers von Willebrand factor levels through higher affinity for the macrophagic scavenger receptor LRP1: Clinical phenotype and pathogenic mechanisms.
J Thromb Haemost
; 20(8): 1818-1829, 2022 08.
Artigo
Inglês
| MEDLINE | ID: mdl-35596664
13.
Cis-Segregation of c.1171C>T Stop Codon (p.R391*) in SERPINC1 Gene and c.1691G>A Transition (p.R506Q) in F5 Gene and Selected GWAS Multilocus Approach in Inherited Thrombophilia.
Genes (Basel)
; 12(6)2021 06 18.
Artigo
Inglês
| MEDLINE | ID: mdl-34207366
14.
In vivo modulation of a dominant-negative variant in mouse models of von Willebrand disease type 2A.
J Thromb Haemost
; 19(1): 139-146, 2021 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33047469
15.
Aptamer-modified FXa generation assays to investigate hypercoagulability in plasma from patients with ischemic heart disease.
Thromb Res
; 189: 140-146, 2020 05.
Artigo
Inglês
| MEDLINE | ID: mdl-32224381
16.
Expression profiles of the internal jugular and saphenous veins: Focus on hemostasis genes.
Thromb Res
; 191: 113-124, 2020 07.
Artigo
Inglês
| MEDLINE | ID: mdl-32438216
17.
Functional polymorphisms in the LDLR and pharmacokinetics of Factor VIII concentrates.
J Thromb Haemost
; 17(8): 1288-1296, 2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31055871
18.
Apolipoprotein C-III Strongly Correlates with Activated Factor VII-Anti-Thrombin Complex: An Additional Link between Plasma Lipids and Coagulation.
Thromb Haemost
; 119(2): 192-202, 2019 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-30602199
19.
C6orf10 Low-Frequency and Rare Variants in Italian Multiple Sclerosis Patients.
Front Genet
; 10: 573, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-31297130
20.
Evaluation of factor V mRNA to define the residual factor V expression levels in severe factor V deficiency.
Haematologica
; 93(3): 477-8, 2008 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-18310546