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Journal of Thrombosis and Haemostasis : JTH|August 23, 2011
RNA-based therapeutic approaches for coagulation factor deficienciesM Pinotti, F Bernardi, A Dal Mas, et al.Journal of Thrombosis and Haemostasis : JTH|April 17, 2014
An engineered U1 small nuclear RNA rescues splicing defective coagulation F7 gene expression in miceD Balestra, A Faella, P Margaritis, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 18, 1998
Molecular and clinical aspects of factor VII deficiencyG Mariani, L Lo Coco, F Bernardi, et al.Blood|August 26, 1998
Molecular mechanisms of FVII deficiency: expression of mutations clustered in the IVS7 donor splice site of factor VII geneM Pinotti, R Toso, R Redaelli, et al.Thrombosis and Haemostasis|August 28, 2002
Reduced activation of the Gla19Ala FX variant via the extrinsic coagulation pathway results in symptomatic CRMred FX deficiencyM Pinotti, G Marchetti, M Baroni, et al.Journal of Thrombosis and Haemostasis : JTH|August 12, 2016
Differential functional readthrough over homozygous nonsense mutations contributes to the bleeding phenotype in coagulation factor VII deficiencyA Branchini, M Ferrarese, S Lombardi, et al.Biochimica Et Biophysica Acta|May 28, 2015
Asymmetric processing of mutant factor X Arg386Cys reveals differences between intrinsic and extrinsic pathway activationM Baroni, G Pavani, M Pinotti, et al.Human Molecular Genetics|May 1, 1993
In-frame deletion of von Willebrand factor A domains in a dominant type of von Willebrand diseaseF Bernardi, P Patracchini, D Gemmati, et al.Thrombosis and Haemostasis|May 1, 1995
Protein S mRNA in patients with protein S deficiencyE Sacchi, M Pinotti, G Marchetti, et al.Journal of Thrombosis and Haemostasis : JTH|June 18, 2015
The carboxyl-terminal region is NOT essential for secreted and functional levels of coagulation factor XA Branchini, M Baroni, F Burini, et al.Pageof 45