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Journal Articles

The Chemical Chaperone 4-Phenylbutyrate Increases Secretion and Activity of Missense and Elongated Factor VII Mutants

Elisabeth Andersen, MSc, Maria Eugenia Chollet, Marcello Baroni, Mirko Pinotti, Francesco Bernardi, Ellen Skarpen, Per Morten Sandset, Grethe Skretting

Blood (2018) 132 (Supplement 1): 3777.

https://doi.org/10.1182/blood-2018-99-118246

Published: 2018

Journal Articles

Specific factor IX mRNA and protein features favor drug-induced readthrough over recurrent nonsense mutations

Alessio Branchini, Mattia Ferrarese, Matteo Campioni, Giancarlo Castaman, Rosella Mari, Francesco Bernardi, Mirko Pinotti

Blood (2017) 129 (16): 2303–2307.

https://doi.org/10.1182/blood-2016-09-738641

Published: 2017

Journal Articles

Delivery of a Modified U1 Small Nuclear RNA Alleviates Splicing-Defective Coagulation Factor VII Expression in Mouse Models

Dario Balestra, PhD, Armida Faella, Nicola Cavallari, PhD, Paris Margaritis, PhD, Franco Pagani, MD, Francesco Bernardi, PhD, Valder R Arruda, MD, PhD, Mirko Pinotti, PhD

Blood (2012) 120 (21): 754.

https://doi.org/10.1182/blood.V120.21.754.754

Published: 2012

Journal Articles

Polymorphisms at LDLR locus may be associated with coronary artery disease through modulation of coagulation factor VIII activity and independently from lipid profile

Nicola Martinelli, Domenico Girelli, Barbara Lunghi, Mirko Pinotti, Giovanna Marchetti, Giovanni Malerba, Pier Franco Pignatti, Roberto Corrocher, Oliviero Olivieri, Francesco Bernardi

Blood (2010) 116 (25): 5688–5697.

https://doi.org/10.1182/blood-2010-03-277079

Published: 2010

Includes: Supplemental data

Journal Articles

The dominant-negative von Willebrand factor gene deletion p.P1127_C1948delinsR: molecular mechanism and modulation

Caterina Casari, Mirko Pinotti, Stefano Lancellotti, Elena Adinolfi, Alessandra Casonato, Raimondo De Cristofaro, Francesco Bernardi

Blood (2010) 116 (24): 5371–5376.

https://doi.org/10.1182/blood-2010-02-268920

Published: 2010

Includes: Supplemental data

Journal Articles

Rescue of coagulation factor VII function by the U1+5A snRNA

Mirko Pinotti, Dario Balestra, Lara Rizzotto, Iva Maestri, Franco Pagani, Francesco Bernardi

Blood (2009) 113 (25): 6461–6464.

https://doi.org/10.1182/blood-2009-03-207613

Published: 2009

Journal Articles

U1-snRNA–mediated rescue of mRNA processing in severe factor VII deficiency

Mirko Pinotti, Lara Rizzotto, Dario Balestra, Marzena Anna Lewandowska, Nicola Cavallari, Giovanna Marchetti, Francesco Bernardi, Franco Pagani

Blood (2008) 111 (5): 2681–2684.

https://doi.org/10.1182/blood-2007-10-117440

Published: 2008

Journal Articles

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

Elisabetta Castoldi, José W. P. Govers-Riemslag, Mirko Pinotti, Debora Bindini, Guido Tans, Mauro Berrettini, Maria Gabriella Mazzucconi, Francesco Bernardi, Jan Rosing

Blood (2003) 102 (12): 4014–4020.

https://doi.org/10.1182/blood-2003-04-1199

Published: 2003

Journal Articles

Residual factor VII activity and different hemorrhagic phenotypes in CRM + factor VII deficiencies (Gly331Ser and Gly283Ser)

Mirko Pinotti, Daniela Etro, Debora Bindini, Maria Luisa Papa, Giuseppina Rodorigo, Angiola Rocino, Guglielmo Mariani, Nicola Ciavarella, Francesco Bernardi

Blood (2002) 99 (4): 1495–1497.

https://doi.org/10.1182/blood.V99.4.1495

Published: 2002

Journal Articles

Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studies

Mirko Pinotti, Raffaella Toso, Domenico Girelli, Debora Bindini, Paolo Ferraresi, Maria L. Papa, Roberto Corrocher, Giovanna Marchetti, Francesco Bernardi

Blood (2000) 95 (11): 3423–3428.

https://doi.org/10.1182/blood.V95.11.3423

Published: 2000

NARROW

The Chemical Chaperone 4-Phenylbutyrate Increases Secretion and Activity of Missense and Elongated Factor VII Mutants

Specific factor IX mRNA and protein features favor drug-induced readthrough over recurrent nonsense mutations

Delivery of a Modified U1 Small Nuclear RNA Alleviates Splicing-Defective Coagulation Factor VII Expression in Mouse Models

Polymorphisms at LDLR locus may be associated with coronary artery disease through modulation of coagulation factor VIII activity and independently from lipid profile

The dominant-negative von Willebrand factor gene deletion p.P1127_C1948delinsR: molecular mechanism and modulation

Rescue of coagulation factor VII function by the U1+5A snRNA

U1-snRNA–mediated rescue of mRNA processing in severe factor VII deficiency

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

Residual factor VII activity and different hemorrhagic phenotypes in CRM + factor VII deficiencies (Gly331Ser and Gly283Ser)

Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studies

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American Society of Hematology

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American Society of Hematology

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