about
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis.Chronic sleep deprivation markedly reduces coagulation factor VII expressionActivation of a cryptic splice site in a potentially lethal coagulation defect accounts for a functional protein variant.Functional genetics.Intracellular evaluation of ER targeting elucidates a mild form of inherited coagulation deficiencyLong-chain cationic derivatives of PTA (1,3,5-triaza-7-phosphaadamantane) as new components of potential non-viral vectors.Characterization of the intracellular signalling capacity of natural FXa mutants with reduced pro-coagulant activity.U1-snRNA-mediated rescue of mRNA processing in severe factor VII deficiency.Characterization of anti-coagulant properties of prenylated coumarin ferulenol.Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII.Factor VII mutant V154G models a zymogen-like form of factor VIIa.An exon-specific U1 small nuclear RNA (snRNA) strategy to correct splicing defects.An engineered U1 small nuclear RNA rescues splicing defective coagulation F7 gene expression in mice.A frequent human coagulation Factor VII mutation (A294V, c152) in loop 140s affects the interaction with activators, tissue factor and substrates.The dominant-negative von Willebrand factor gene deletion p.P1127_C1948delinsR: molecular mechanism and modulation.Cationic lipid nanosystems as carriers for nucleic acids.Polymorphisms at LDLR locus may be associated with coronary artery disease through modulation of coagulation factor VIII activity and independently from lipid profile.Inhibitors to factor VII in congenital factor VII deficiency.Ribosome readthrough accounts for secreted full-length factor IX in hemophilia B patients with nonsense mutations.Effective hemostasis during minor surgery in a case of hereditary combined deficiency of vitamin K-dependent clotting factors.Major differences in bleeding symptoms between factor VII deficiency and hemophilia B.Rescue of coagulation factor VII function by the U1+5A snRNA.Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster.Daily and circadian rhythms of tissue factor pathway inhibitor and factor VII activity.Coinheritance of Factor V (FV) Leiden enhances thrombin formation and is associated with a mild bleeding phenotype in patients homozygous for the FVII 9726+5G>A (FVII Lazio) mutation.The factor V Glu1608Lys mutation is recurrent in familial thrombophilia.Modulation of factor V levels in plasma by polymorphisms in the C2 domain.Circadian Rhythms in Mouse Blood CoagulationDisease-causing variants of the conserved +2T of 5' splice sites can be rescued by engineered U1snRNAsTemporal Variations of Coagulation Factor VII Activity in Mice Are Influenced by Lighting RegimeTemporal and Genotype-Driven Variation of Factor VII Levels in Patients With Acute Myocardial InfarctionStimulation of P2 (P2X7) receptors in human dendritic cells induces the release of tissue factor-bearing microparticlesMolecular bases of type II protein S deficiency: the I203-D204 deletion in the EGF4 domain alters GLA domain functionMutation pattern in clinically asymptomatic coagulation factor VII deficiencyPolymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery diseaseComparison among natural (Arg304Gln, Arg304Trp) and artificial (Arg290His, Arg290Lys) mutations in coagulation factor VII loopsGentamicin induces sub-therapeutic levels of coagulation factor VII in patients with nonsense mutationsInfluence of polymorphisms in the factor VII gene promoter on activated factor VII levels and on the risk of myocardial infarction in advanced coronary atherosclerosisEvaluation of factor V mRNA to define the residual factor V expression levels in severe factor V deficiencyVitamin K-induced modification of coagulation phenotype in VKORC1 homozygous deficiency
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Mirko Pinotti
@ast
Mirko Pinotti
@en
Mirko Pinotti
@es
Mirko Pinotti
@nl
Mirko Pinotti
@sl
type
label
Mirko Pinotti
@ast
Mirko Pinotti
@en
Mirko Pinotti
@es
Mirko Pinotti
@nl
Mirko Pinotti
@sl
prefLabel
Mirko Pinotti
@ast
Mirko Pinotti
@en
Mirko Pinotti
@es
Mirko Pinotti
@nl
Mirko Pinotti
@sl
P106
P1153
7006026567
P21
P31
P496
0000-0002-4114-7055