Page 1 | Search Results | Blood | American Society of Hematology

1-19 of 19

Sort by

Sort Order Select

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

Activated Factor VII–Antithrombin Complex Plasma Concentration Is An Independent Predictor Of Total and Cardiovascular Mortality In Patients With Coronary Artery Disease and Its Prognostic Significance Is Improved By Using Factor VII Genotype-Specific Threshold Levels

Nicola Martinelli, MD, PhD, Domenico Girelli, MD, Marcello Baroni, Patrizia Guarini, Federica Tosi, Barbara Lunghi, Barry J Woodhams, Ph.D., Francesco Bernardi, Oliviero Olivieri, MD

Blood (2013) 122 (21): 2339.

https://doi.org/10.1182/blood.V122.21.2339.2339

Published: 2013

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

At Disease Presentation, Severity of the Bleeding Symptom Predicts the Following Bleeds in Patients with FVII Deficiency

Matteo ND Di Minno, Angelika Batorova, MD, PhD, Mariasanta Napolitano, MD, Alberto Dolce, PhD, Giovanni Di Minno, MD, Francesco Bernardi, PhD, Jean-Francois Schved, Jørgen Ingerslev, MD, Muriel Giansily-Blaizot, MD, PhD, Guenter K.H. Auerswald, Sr., MD, Guglielmo Mariani, MD

Blood (2011) 118 (21): 30.

https://doi.org/10.1182/blood.V118.21.30.30

Published: 2011

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

An underestimated combination of opposites resulting in enhanced thrombotic tendency

Paolo Simioni, Elisabetta Castoldi, Barbara Lunghi, Daniela Tormene, Jan Rosing, Francesco Bernardi

Blood (2005) 106 (7): 2363–2365.

https://doi.org/10.1182/blood-2005-04-1461

Published: 2005

Journal Articles

Gain-of-function proteins for gene transfer in hemophilia

Francesco Bernardi

Blood (2005) 105 (6): 2243.

https://doi.org/10.1182/blood-2004-12-4912

Published: 2005

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

Phenotype and genotype expression in pseudohomozygous R2 factor V

Michael Kalafatis, Paolo Simioni, Francesco Bernardi

Blood (2001) 98 (6): 1988–1990.

https://doi.org/10.1182/blood.V98.6.1988

Published: 2001

Journal Articles

Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family

Elisabetta Castoldi, Paolo Simioni, Michael Kalafatis, Barbara Lunghi, Daniela Tormene, Domenico Girelli, Antonio Girolami, Francesco Bernardi

Blood (2000) 96 (4): 1443–1448.

https://doi.org/10.1182/blood.V96.4.1443

Published: 2000

Journal Articles

Clinical manifestations, management, and molecular genetics in congenital factor VII deficiency: the International Registry on Congenital Factor VII Deficiency (IRF7)

Guglielmo Mariani, Falko H. Herrmann, Francesco Bernardi, Jean-Francois Schved, Gunther Auerswald, Jorgen Ingerslev, The Factor VII Deficiency Study Group

Blood (2000) 96 (1): 374.

https://doi.org/10.1182/blood.V96.1.374

Published: 2000

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

Journal Articles

A Novel Factor V Null Mutation Detected in a Thrombophilic Patient With Pseudo-Homozygous APC Resistance and in an Asymptomatic Unrelated Subject

Barbara Lunghi, Elisabetta Castoldi, Federico Mingozzi, Francesco Bernardi, Giancarlo Castaman

Blood (1998) 92 (4): 1463–1465.

https://doi.org/10.1182/blood.V92.4.1463

Published: 1998

Journal Articles

A New Factor V Gene Polymorphism (His 1254 Arg) Present in Subjects of African Origin Mimics the R2 Polymorphism (His 1299 Arg)

Barbara Lunghi, Elisabetta Castoldi, Federico Mingozzi, Francesco Bernardi

Blood (1998) 91 (1): 364–365.

https://doi.org/10.1182/blood.V91.1.364

Published: 1998

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

Activated Factor VII–Antithrombin Complex Plasma Concentration Is An Independent Predictor Of Total and Cardiovascular Mortality In Patients With Coronary Artery Disease and Its Prognostic Significance Is Improved By Using Factor VII Genotype-Specific Threshold Levels

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

At Disease Presentation, Severity of the Bleeding Symptom Predicts the Following Bleeds in Patients with FVII Deficiency

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

An underestimated combination of opposites resulting in enhanced thrombotic tendency

Gain-of-function proteins for gene transfer in hemophilia

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)

Phenotype and genotype expression in pseudohomozygous R2 factor V

Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family

Clinical manifestations, management, and molecular genetics in congenital factor VII deficiency: the International Registry on Congenital Factor VII Deficiency (IRF7)

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

A Novel Factor V Null Mutation Detected in a Thrombophilic Patient With Pseudo-Homozygous APC Resistance and in an Asymptomatic Unrelated Subject

A New Factor V Gene Polymorphism (His 1254 Arg) Present in Subjects of African Origin Mimics the R2 Polymorphism (His 1299 Arg)

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only