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Mirko Pinotti

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Mario Lapecorella; A Lucchesi; Mariasanta Napolitano; Mirko Pinotti; F Pisani; V Rizza; L Aloisio; F Bernardi; K Clemente; Antonio Famulari; P Ferraresi; Pierpaolo Di Cocco
Management of kidney transplantation in a factor VII-deficient patient: case report.
Mirko Pinotti; Giuseppe Tagariello; Donata Belvini; Matteo Campioni; Alessandro Canella; Pierpaolo Caruso; Giancarlo Castaman; Sofia Giacomelli; Francesco Bernardi
Ribosome readthrough accounts for secreted full-length factor IX in hemophilia B patients with nonsense mutations.
Rita Cortesi; Andrea Costenaro; Markus Drechsler; Paola Bergamini; Matteo Campioni; Lorenza Marvelli; Mirko Pinotti; Laura Ravani; Elisabetta Esposito
Long-chain cationic derivatives of PTA (1,3,5-triaza-7-phosphaadamantane) as new components of potential non-viral vectors.

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All Publications

2012: Mario Lapecorella; A Lucchesi; Mariasanta Napolitano; Mirko Pinotti; F Pisani; V Rizza; L Aloisio; F Bernardi; K Clemente; Antonio Famulari; P Ferraresi; Pierpaolo Di Cocco
Management of kidney transplantation in a factor VII-deficient patient: case report.
Transplantation proceedings 2012;44(7):2033-5.
2012: Mirko Pinotti; Giuseppe Tagariello; Donata Belvini; Matteo Campioni; Alessandro Canella; Pierpaolo Caruso; Giancarlo Castaman; Sofia Giacomelli; Francesco Bernardi
Ribosome readthrough accounts for secreted full-length factor IX in hemophilia B patients with nonsense mutations.
Human mutation 2012;33(9):1373-6.
2012: Rita Cortesi; Andrea Costenaro; Markus Drechsler; Paola Bergamini; Matteo Campioni; Lorenza Marvelli; Mirko Pinotti; Laura Ravani; Elisabetta Esposito
Long-chain cationic derivatives of PTA (1,3,5-triaza-7-phosphaadamantane) as new components of potential non-viral vectors.
International journal of pharmaceutics 2012;431(1-2):176-82.
2012: Nicola Cavallari; Ampaiwan Chuamsunrit; Iva Maestri; Guglielmo Mariani; Franco Pagani; Dario Balestra; Francesco Bernardi; Alessio Branchini; Werasak Sasanakul; Mirko Pinotti
Activation of a cryptic splice site in a potentially lethal coagulation defect accounts for a functional protein variant.
Biochimica et biophysica acta 2012;1822(7):1109-13.
2012: Alessio Branchini; Alessandro Canella; Muriel Giansily-Blaizot; Mario Lapecorella; Rosella Mari; Guglielmo Mariani; Mariasanta Napolitano; Mirko Pinotti; Lara Rizzotto; Francesco Bernardi
Natural and engineered carboxy-terminal variants: decreased secretion and gain-of-function result in asymptomatic coagulation factor VII deficiency.
Haematologica 2012;97(5):705-9.
2012: Simonetta Friso; Domenico Girelli; Pasquale Guarini; Valentina Lotto; Nicola Martinelli; Patrizia Pattini; Mirko Pinotti; Francesca Pizzolo; Silvia Udali; Francesco Bernardi; Sang-Woon Choi; Roberto Corrocher; Oliviero Olivieri
Promoter methylation in coagulation F7 gene influences plasma FVII concentrations and relates to coronary artery disease.
Journal of medical genetics 2012;49(3):192-9.
2011: Mirko Pinotti; francesco bernardi; A Dal Mas; F Pagani
RNA-based therapeutic approaches for coagulation factor deficiencies.
Journal of thrombosis and haemostasis : JTH 2011;9(11):2143-52.
2010: Nicola Martinelli; Domenico Girelli; Barbara Lunghi; Mirko Pinotti; Giovanna Marchetti; Giovanni Malerba; Pier Franco Pignatti; Roberto Corrocher; Oliviero Olivieri; Francesco Bernardi
Polymorphisms at LDLR locus may be associated with coronary artery disease through modulation of coagulation factor VIII activity and independently from lipid profile.
Blood 2010;116(25):5688-97.
2010: Caterina Casari; Mirko Pinotti; Stefano Lancellotti; Elena Adinolfi; Alessandra Casonato; Raimondo De Cristofaro; Francesco Bernardi
The dominant-negative von Willebrand factor gene deletion p.P1127_C1948delinsR: molecular mechanism and modulation.
Blood 2010;116(24):5371-6.
2010: Marcello Baroni; Giulia Pavani; Diego Marescotti; Tahar Kaabache; Delphine Borgel; Sophie Gandrille; Giovanna Marchetti; Cristina Legnani; Armando D'Angelo; Mirko Pinotti; francesco bernardi
Membrane binding and anticoagulant properties of protein S natural variants.
Thrombosis research 2010;125(2):e33-9.
2009: francesco bernardi; Alberto Dolce; Mirko Pinotti; Amy D Shapiro; E Santagostino; F Peyvandi; A Batorova; M Lapecorella; J F Schved; Jørgen Ingerslev; Guglielmo Mariani
Major differences in bleeding symptoms between factor VII deficiency and hemophilia B.
Journal of thrombosis and haemostasis : JTH 2009;7(5):774-9.
2009: Monia Monti; Keren S Borensztajn; Mirko Pinotti; Alessandro Canella; Alessio Branchini; Giovanna Marchetti; Pieter H Reitsma; francesco bernardi; C Arnold Spek
Characterization of the intracellular signalling capacity of natural FXa mutants with reduced pro-coagulant activity.
Thrombosis research 2009;123(6):914-8.
2009: Paolo Ferraresi; Gianluca Campo; Giovanna Marchetti; Mirko Pinotti; Marco Valgimigli; Donato Gemmati; Roberto Ferrari; francesco bernardi
Temporal and genotype-driven variation of factor VII levels in patients with acute myocardial infarction.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2009;15(1):119-22.
2008: Cristiano Bertolucci; Nicola Cavallari; Ilaria Colognesi; Jacopo Aguzzi; zheng chen; Pierpaolo Caruso; Augusto Foá; Gianluca Tosini; francesco bernardi; Mirko Pinotti
Evidence for an overlapping role of CLOCK and NPAS2 transcription factors in liver circadian oscillators.
Molecular and cellular biology 2008;28(9):3070-5.
2008: Giovanna Marchetti; P Caruso; Barbara Lunghi; Mirko Pinotti; M Lapecorella; M Napolitano; Alessandro Canella; Guglielmo Mariani; francesco bernardi
Vitamin K-induced modification of coagulation phenotype in VKORC1 homozygous deficiency.
Journal of thrombosis and haemostasis : JTH 2008;6(5):797-803.
2008: Mirko Pinotti; Lara Rizzotto; Dario Balestra; Marzena Anna Lewandowska; Nicola Cavallari; Giovanna Marchetti; francesco bernardi; Franco Pagani
U1-snRNA-mediated rescue of mRNA processing in severe factor VII deficiency.
Blood 2008;111(5):2681-4.
2008: Nicola Martinelli; Elisabetta Trabetti; Mirko Pinotti; Oliviero Olivieri; Marco Sandri; Simonetta Friso; Francesca Pizzolo; Claudia Bozzini; Pier Paolo Caruso; Ugo Cavallari; Suzanne Cheng; Pier Franco Pignatti; francesco bernardi; Roberto Corrocher; Domenico Girelli
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis.
PloS one 2008;3(2):e1523.
2007: Monia Monti; Mirko Pinotti; Giovanni Appendino; Franco Dallocchio; Tiziana Bellini; Fabiana Antognoni; Ferruccio Poli; francesco bernardi
Characterization of anti-coagulant properties of prenylated coumarin ferulenol.
Biochimica et biophysica acta 2007;1770(10):1437-40.
2007: Marcello Baroni; Cinzia Pizzirani; Mirko Pinotti; Davide Ferrari; Elena Adinolfi; Sara Calzavarini; Pierpaolo Caruso; francesco bernardi; Francesco Di Virgilio
Stimulation of P2 (P2X7) receptors in human dendritic cells induces the release of tissue factor-bearing microparticles.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2007;21(8):1926-33.
2007: Ilaria Colognesi; Vittorio Pasquali; Augusto Foà; Paolo Renzi; francesco bernardi; Cristiano Bertolucci; Mirko Pinotti
Temporal variations of coagulation factor VII activity in mice are influenced by lighting regime.
Chronobiology international 2007;24(2):305-13.
2006: Giovanna Marchetti; Barbara Lunghi; Cristina Legnani; Michela Cini; Mirko Pinotti; Francesco Mascoli; Francesco Bernard
Contribution of low density lipoprotein receptor-related protein genotypes to coagulation factor VIII levels in thrombotic women.
Haematologica 2006;91(9):1261-3.
2006: Mirko Pinotti; Lara Rizzotto; Ampaiwan Chuansumrit; Guglielmo Mariani; francesco bernardi
Gentamicin induces sub-therapeutic levels of coagulation factor VII in patients with nonsense mutations.
Journal of thrombosis and haemostasis : JTH 2006;4(8):1828-30.
2006: Lara Rizzotto; Mirko Pinotti; Paolo Pinton; Rosario Rizzuto; francesco bernardi
Intracellular evaluation of ER targeting elucidates a mild form of inherited coagulation deficiency.
Molecular medicine (Cambridge, Mass.) 2006;12(7-8):137-42.
2006: Mirko Pinotti; Lara Rizzotto; Paolo Pinton; Paolo Ferraresi; Ampaiwan Chuansumrit; Pimlak Charoenkwan; Giovanna Marchetti; Rosario Rizzuto; Guglielmo Mariani; francesco bernardi
Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII.
Journal of thrombosis and haemostasis : JTH 2006;4(6):1308-14.
2006: M Baroni; G Mazzola; Tahar Kaabache; Delphine Borgel; Sophie Gandrille; S Vigano' D'Angelo; Giovanna Marchetti; Maria Grazia di Iasio; Mirko Pinotti; A D'Angelo; francesco bernardi
Molecular bases of type II protein S deficiency: the I203-D204 deletion in the EGF4 domain alters GLA domain function.
Journal of thrombosis and haemostasis : JTH 2006;4(1):186-91.
2005: Barbara Lunghi; Daniela Scanavini; Elisabetta Castoldi; Donato Gemmati; Silvia Tognazzo; Rosaria Redaelli; A Ghirarduzzi; M Ieran; Mirko Pinotti; francesco bernardi
The factor V Glu1608Lys mutation is recurrent in familial thrombophilia.
Journal of thrombosis and haemostasis : JTH 2005;3(9):2032-8.
2005: Cristiano Bertolucci; Mirko Pinotti; Ilaria Colognesi; Augusto Foà; francesco bernardi; Francesco Portaluppi
Circadian rhythms in mouse blood coagulation.
Journal of biological rhythms 2005;20(3):219-24.
2005: Mirko Pinotti; Cristiano Bertolucci; Francesco Portaluppi; Ilaria Colognesi; Elena Frigato; Augusto Foà; francesco bernardi
Daily and circadian rhythms of tissue factor pathway inhibitor and factor VII activity.
Arteriosclerosis, thrombosis, and vascular biology 2005;25(3):646-9.
2004: Christian Furlan Freguia; Raffaella Toso; Eleanor S Pollak; Valder R Arruda; Mirko Pinotti; francesco bernardi
Characterization of mild coagulation factor VII deficiency: activity and clearance of the Arg315Trp and Arg315Lys variants in the Cys310-Cys329 loop (c170s).
Haematologica 2004;89(12):1504-9.
2004: Claudia Bozzini; Domenico Girelli; francesco bernardi; Paolo Ferraresi; Oliviero Olivieri; Mirko Pinotti; Nicola Martinelli; Franco Manzato; Simonetta Friso; Giuliano Villa; Francesca Pizzolo; Federico Beltrame; Roberto Corrocher
Influence of polymorphisms in the factor VII gene promoter on activated factor VII levels and on the risk of myocardial infarction in advanced coronary atherosclerosis.
Thrombosis and haemostasis 2004;92(3):541-9.
2004: Mirko Pinotti; Monia Monti; Marcello Baroni; Giovanna Marchetti; Francesco Bernardi
Molecular characterization of factor X deficiency associated with borderline plasma factor X level.
Haematologica 2004;89(4):501-2.
2004: Daniela Scanavini; Domenico Girelli; Barbara Lunghi; Nicola Martinelli; Cristina Legnani; Mirko Pinotti; Gualtiero Palareti; francesco bernardi
Modulation of factor V levels in plasma by polymorphisms in the C2 domain.
Arteriosclerosis, thrombosis, and vascular biology 2004;24(1):200-6.
2003: Daniela Etro; Mirko Pinotti; Karin Wulff; Giovanna Marchetti; Angiola Rocino; Falko H Herrmann; francesco bernardi
The Gly331Ser mutation in factor VII in Europe and the Middle East.
Haematologica 2003;88(12):1434-6.
2003: Christian Furlan Freguia; Raffaella Toso; Paolo Ferraresi; Mirko Pinotti; francesco bernardi
Variation of factor VII 140s and 170s loops in fishes: evolutionary aspects and comparison with mutations found in FVII deficiency.
Thrombosis and haemostasis 2003;90(6):1220-2.
2003: Elisabetta Castoldi; José W P Govers-Riemslag; Mirko Pinotti; Debora Bindini; Guido Tans; Mauro Berrettini; Maria Gabriella Mazzucconi; francesco bernardi; Jan Rosing
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.
Blood 2003;102(12):4014-20.
2003: Christian Furlan Freguia; Raffaella Toso; Mirko Pinotti; Donato Gemmati; francesco bernardi
Comparison among natural (Arg304Gln, Arg304Trp) and artificial (Arg290His, Arg290Lys) mutations in coagulation factor VII loops.
Journal of thrombosis and haemostasis : JTH 2003;1(11):2455-7.
2003: Giovanna Marchetti; Paolo Ferraresi; Cristina Legnani; Mirko Pinotti; Barbara Lunghi; Chiara Scapoli; Donato Gemmati; Sergio Coccheri; Gualtiero Palareti; francesco bernardi
Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster.
British journal of haematology 2003;121(4):632-8.
2003: Mirko Pinotti; Rodney M Camire; Marcello Baroni; Anna Rajab; Giovanna Marchetti; francesco bernardi
Impaired prothrombinase activity of factor X Gly381Asp results in severe familial CRM+ FX deficiency.
Thrombosis and haemostasis 2003;89(2):243-8.
2003: Raffaella Toso; francesco bernardi; Theresa Tidd; Mirko Pinotti; Rodney M Camire; Giovanna Marchetti; Katherine A High; Eleanor S Pollak
Factor VII mutant V154G models a zymogen-like form of factor VIIa.
The Biochemical journal 2003;369(Pt 3):563-71.
2002: Rama Kudaravalli; Theresa Tidd; Mirko Pinotti; Antonia Ratti; Rosa Santacroce; Maurizio Margaglione; Bruno Dallapiccola; francesco bernardi; Paolo Fortina; Marcella Devoto; Eleanor S Pollak
Polymorphic changes in the 5' flanking region of factor VII have a combined effect on promoter strength.
Thrombosis and haemostasis 2002;88(5):763-7.
2002: Mirko Pinotti; Giovanna Marchetti; M Baroni; F Cinotti; M Morfini; francesco bernardi
Reduced activation of the Gla19Ala FX variant via the extrinsic coagulation pathway results in symptomatic CRMred FX deficiency.
Thrombosis and haemostasis 2002;88(2):236-41.
2002: Raffaella Toso; Mirko Pinotti; Katherine A High; Eleanor S Pollak; francesco bernardi
A frequent human coagulation Factor VII mutation (A294V, c152) in loop 140s affects the interaction with activators, tissue factor and substrates.
The Biochemical journal 2002;363(Pt 2):411-6.
2000: Domenico Girelli; C Russo; Paolo Ferraresi; Oliviero Olivieri; Mirko Pinotti; Simonetta Friso; Franco Manzato; Alessandro Mazzucco; francesco bernardi; Roberto Corrocher
Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease.
The New England journal of medicine 2000;343(11):774-80.
2000: Mirko Pinotti; Raffaella Toso; Domenico Girelli; Debora Bindini; Paolo Ferraresi; Maria Luisa Papa; Roberto Corrocher; Giovanna Marchetti; francesco bernardi
Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studies.
Blood 2000;95(11):3423-8.
1998: Mirko Pinotti; Raffaella Toso; Rosaria Redaelli; M Berrettini; Giovanna Marchetti; francesco bernardi
Molecular mechanisms of FVII deficiency: expression of mutations clustered in the IVS7 donor splice site of factor VII gene.
Blood 1998;92(5):1646-51.
1997: francesco bernardi; P Arcieri; RM Bertina; F Chiarotti; J Corral; Mirko Pinotti; H Prydz; M Samama; PM Sandset; R Strom; V V Garcia; Guglielmo Mariani
Contribution of factor VII genotype to activated FVII levels. Differences in genotype frequencies between northern and southern European populations.
Arteriosclerosis, thrombosis, and vascular biology 1997;17(11):2548-53.
1996: francesco bernardi; Giancarlo Castaman; Mirko Pinotti; Paolo Ferraresi; M G Di Iasio; Barbara Lunghi; F Rodeghiero; Giovanna Marchetti
Mutation pattern in clinically asymptomatic coagulation factor VII deficiency.
Human mutation 1996;8(2):108-15.
1996: Barbara Lunghi; Licia Iacoviello; Donato Gemmati; M G Dilasio; Elisabetta Castoldi; Mirko Pinotti; Giancarlo Castaman; Rosaria Redaelli; Guglielmo Mariani; Giovanna Marchetti; francesco bernardi
Detection of new polymorphic markers in the factor V gene: association with factor V levels in plasma.
Thrombosis and haemostasis 1996;75(1):45-8.
1996: francesco bernardi; Giovanna Marchetti; Mirko Pinotti; P Arcieri; C Baroncini; M Papacchini; E Zepponi; N Ursicino; F Chiarotti; Guglielmo Mariani
Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasma.
Arteriosclerosis, thrombosis, and vascular biology 1996;16(1):72-6.
1995: Giovanna Marchetti; Giancarlo Castaman; Mirko Pinotti; Barbara Lunghi; M G Di Iasio; M Ruggieri; F Rodeghiero; francesco bernardi
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domain.
British journal of haematology 1995;90(4):910-5.
1994: francesco bernardi; Giancarlo Castaman; Rosaria Redaelli; Mirko Pinotti; Barbara Lunghi; F Rodeghiero; Giovanna Marchetti
Topologically equivalent mutations causing dysfunctional coagulation factors VII (294Ala-->Val) and X (334Ser-->Pro).
Human molecular genetics 1994;3(7):1175-7.
1994: francesco bernardi; D L Liney; P Patracchini; Donato Gemmati; Cristina Legnani; P Arcieri; Mirko Pinotti; Rosaria Redaelli; G Ballerini; S Pemberton
Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII.
British journal of haematology 1994;86(3):610-8.
1993: francesco bernardi; P Patracchini; Donato Gemmati; Mirko Pinotti; C Schwienbacher; G Ballerini; Giovanna Marchetti
In-frame deletion of von Willebrand factor A domains in a dominant type of von Willebrand disease.
Human molecular genetics 1993;2(5):545-8.
1992: Giovanna Marchetti; P Patracchini; Donato Gemmati; V DeRosa; Mirko Pinotti; G Rodorigo; Alessandra Casonato; A Girolami; francesco bernardi
Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7).
Human genetics 1992;89(5):497-502.
1991: Giovanna Marchetti; Donato Gemmati; P Patracchini; Mirko Pinotti; francesco bernardi
PCR detection of a repeat polymorphism within the F7 gene.
Nucleic acids research 1991;19(16):4570.