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R Asselta

Showing results (11-20 of 34) with videos related to

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Thrombosis and Haemostasis|January 12, 2001
Concerns about the mutations identified in a case of familial coagulation factor V deficiency: factor V StanfordM C Montefusco, R Asselta, R van Wijk, et al.
Molecular and Cellular Probes|September 4, 1998
Analysis of the 16S rRNA gene sequence of the coryneform bacterium associated with hyperkeratotic dermatitis of athymic nude mice and development of a PCR-based detection assayS Duga, A Gobbi, R Asselta, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 28, 2017
Molecular investigation of 41 patients affected by coagulation factor XI deficiencyV Rimoldi, E M Paraboschi, M Menegatti, 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.
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.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 22, 2014
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 womenE Biguzzi, F Franchi, B Acaia, 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.
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.
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.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Thrombosis and Haemostasis|January 12, 2001
Concerns about the mutations identified in a case of familial coagulation factor V deficiency: factor V StanfordM C Montefusco, R Asselta, R van Wijk, et al.
Molecular and Cellular Probes|September 4, 1998
Analysis of the 16S rRNA gene sequence of the coryneform bacterium associated with hyperkeratotic dermatitis of athymic nude mice and development of a PCR-based detection assayS Duga, A Gobbi, R Asselta, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 28, 2017
Molecular investigation of 41 patients affected by coagulation factor XI deficiencyV Rimoldi, E M Paraboschi, M Menegatti, 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.
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.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 22, 2014
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 womenE Biguzzi, F Franchi, B Acaia, 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.
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.
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.
Pageof 4