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M Pinotti

Showing results (31-40 of 51) with videos related to

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Human Genetics|July 1, 1992
Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7)G Marchetti, P Patracchini, D Gemmati, et al.
Journal of Thrombosis and Haemostasis : JTH|March 5, 2008
Vitamin K-induced modification of coagulation phenotype in VKORC1 homozygous deficiencyG Marchetti, P Caruso, B Lunghi, et al.
Human Mutation|January 1, 1996
Mutation pattern in clinically asymptomatic coagulation factor VII deficiencyF Bernardi, G Castaman, M Pinotti, et al.
Blood|May 29, 2000
Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studiesM Pinotti, R Toso, D Girelli, et al.
The New England Journal of Medicine|September 14, 2000
Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery diseaseD Girelli, C Russo, P Ferraresi, et al.
Journal of Thrombosis and Haemostasis : JTH|July 12, 2018
The chaperone-like sodium phenylbutyrate improves factor IX intracellular trafficking and activity impaired by the frequent p.R294Q mutationS Pignani, A Todaro, M Ferrarese, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 1, 1996
Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasmaF Bernardi, G Marchetti, M Pinotti, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|June 28, 2008
[Acute acalculous cholecystitis as a complication of hepatitis A: report of 2 pediatric cases]M Fuoti, M Pinotti, V Miceli, et al.
Journal of Thrombosis and Haemostasis : JTH|May 19, 2006
Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VIIM Pinotti, L Rizzotto, P Pinton, et al.
Journal of Thrombosis and Haemostasis : JTH|June 25, 2005
The factor V Glu1608Lys mutation is recurrent in familial thrombophiliaB Lunghi, D Scanavini, E Castoldi, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Human Genetics|July 1, 1992
Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7)G Marchetti, P Patracchini, D Gemmati, et al.
Journal of Thrombosis and Haemostasis : JTH|March 5, 2008
Vitamin K-induced modification of coagulation phenotype in VKORC1 homozygous deficiencyG Marchetti, P Caruso, B Lunghi, et al.
Human Mutation|January 1, 1996
Mutation pattern in clinically asymptomatic coagulation factor VII deficiencyF Bernardi, G Castaman, M Pinotti, et al.
Blood|May 29, 2000
Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studiesM Pinotti, R Toso, D Girelli, et al.
The New England Journal of Medicine|September 14, 2000
Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery diseaseD Girelli, C Russo, P Ferraresi, et al.
Journal of Thrombosis and Haemostasis : JTH|July 12, 2018
The chaperone-like sodium phenylbutyrate improves factor IX intracellular trafficking and activity impaired by the frequent p.R294Q mutationS Pignani, A Todaro, M Ferrarese, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 1, 1996
Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasmaF Bernardi, G Marchetti, M Pinotti, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|June 28, 2008
[Acute acalculous cholecystitis as a complication of hepatitis A: report of 2 pediatric cases]M Fuoti, M Pinotti, V Miceli, et al.
Journal of Thrombosis and Haemostasis : JTH|May 19, 2006
Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VIIM Pinotti, L Rizzotto, P Pinton, et al.
Journal of Thrombosis and Haemostasis : JTH|June 25, 2005
The factor V Glu1608Lys mutation is recurrent in familial thrombophiliaB Lunghi, D Scanavini, E Castoldi, et al.
Pageof 6