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S Duga

Showing results (21-30 of 40) with videos related to

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Molecular Reproduction and Development|December 24, 1997
Identification and spatial distribution of the mRNA encoding the gp49 component of the gilthead sea bream, Sparus aurata, egg envelopeL Del Giacco, C Vanoni, D Bonsignorio, et al.
European Journal of Biochemistry|July 15, 1996
L-aspartate oxidase from Escherichia coli. I. Characterization of coenzyme binding and product inhibitionM Mortarino, A Negri, G Tedeschi, et al.
Thrombosis Research|September 20, 2001
Identification of four novel polymorphisms in the Aalpha and gamma fibrinogen genes and analysis of association with plasma levels of the proteinM Menegatti, R Asselta, S Duga, et al.
Journal of Human Genetics|November 28, 2001
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphismsS Duga, G Soldà, R Asselta, et al.
European Journal of Biochemistry|January 23, 1999
A new exon in the 5' untranslated region of the connexin32 geneS Duga, R Asselta, L Del Giacco, et al.
Journal of Thrombosis and Haemostasis : JTH|July 23, 2003
Severe factor V deficiency: exon skipping in the factor V gene causing a partial deletion of the C1 domainR Asselta, M C Montefusco, S Duga, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 23, 2011
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiencyE M Paraboschi, S M Kayiran, N Özbek, et al.
Blood|February 9, 2000
Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretionS Duga, R Asselta, E Santagostino, et al.
Journal of Thrombosis and Haemostasis : JTH|April 22, 2005
Liver histology of an afibrinogenemic patient with the Bbeta-L353R mutation showing no evidence of hepatic endoplasmic reticulum storage disease (ERSD); comparative study in COS-1 cells of the intracellular processing of the Bbeta-L353R fibrinogen vs. the ERSD-associated gamma-G284R mutantS Duga, P Braidotti, R Asselta, et al.
Blood|September 26, 2000
Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncationR Asselta, S Duga, T Simonic, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
Molecular Reproduction and Development|December 24, 1997
Identification and spatial distribution of the mRNA encoding the gp49 component of the gilthead sea bream, Sparus aurata, egg envelopeL Del Giacco, C Vanoni, D Bonsignorio, et al.
European Journal of Biochemistry|July 15, 1996
L-aspartate oxidase from Escherichia coli. I. Characterization of coenzyme binding and product inhibitionM Mortarino, A Negri, G Tedeschi, et al.
Thrombosis Research|September 20, 2001
Identification of four novel polymorphisms in the Aalpha and gamma fibrinogen genes and analysis of association with plasma levels of the proteinM Menegatti, R Asselta, S Duga, et al.
Journal of Human Genetics|November 28, 2001
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphismsS Duga, G Soldà, R Asselta, et al.
European Journal of Biochemistry|January 23, 1999
A new exon in the 5' untranslated region of the connexin32 geneS Duga, R Asselta, L Del Giacco, et al.
Journal of Thrombosis and Haemostasis : JTH|July 23, 2003
Severe factor V deficiency: exon skipping in the factor V gene causing a partial deletion of the C1 domainR Asselta, M C Montefusco, S Duga, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 23, 2011
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiencyE M Paraboschi, S M Kayiran, N Özbek, et al.
Blood|February 9, 2000
Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretionS Duga, R Asselta, E Santagostino, et al.
Journal of Thrombosis and Haemostasis : JTH|April 22, 2005
Liver histology of an afibrinogenemic patient with the Bbeta-L353R mutation showing no evidence of hepatic endoplasmic reticulum storage disease (ERSD); comparative study in COS-1 cells of the intracellular processing of the Bbeta-L353R fibrinogen vs. the ERSD-associated gamma-G284R mutantS Duga, P Braidotti, R Asselta, et al.
Blood|September 26, 2000
Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncationR Asselta, S Duga, T Simonic, et al.
Pageof 4