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Stefano Duga

Showing results (51-60 of 141) with videos related to

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Chemmedchem|June 7, 2017
2,6-Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ: Design, Synthesis, and Structure-Activity RelationshipsValentina Straniero, Carlo Zanotto, Letizia Straniero, et al.
Haematologica|November 9, 2004
Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patientsGiorgia Zadra, Rosanna Asselta, Massimo Malcovati, et al.
Plos One|June 2, 2017
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysisChiara Chiereghin, Michela Robusto, Antonio Mastrangelo, et al.
Blood|October 24, 2002
Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency: molecular characterization by expression of the recombinant proteinStefano Duga, Maria Claudia Montefusco, Rosanna Asselta, et al.
Haematologica|September 24, 2009
Premature termination codon mutations in the von Willebrand factor gene are associated with allele-specific and position-dependent mRNA decayManuela Platè, Stefano Duga, Luciano Baronciani, et al.
Thrombosis and Haemostasis|September 1, 2009
Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiencySilvia Spena, Rosanna Asselta, Sonia Caccia, et al.
Haematologica|August 11, 2019
Profiling the mutational landscape of coagulation factor V deficiencyElvezia Maria Paraboschi, Marzia Menegatti, Valeria Rimoldi, et al.
Blood|June 21, 2003
Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V: Broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutationsMaria Claudia Montefusco, Stefano Duga, Rosanna Asselta, et al.
Parkinsonism & Related Disorders|September 25, 2014
Glucocerebrosidase mutations in primary parkinsonismRosanna Asselta, Valeria Rimoldi, Chiara Siri, et al.
Parkinsonism & Related Disorders|November 23, 2011
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian populationLuca Trotta, Ilaria Guella, Giulia Soldà, et al.
Pageof 15

Showing results (51-60 of 141) with videos related to

Sort By:
Pageof 15
Chemmedchem|June 7, 2017
2,6-Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ: Design, Synthesis, and Structure-Activity RelationshipsValentina Straniero, Carlo Zanotto, Letizia Straniero, et al.
Haematologica|November 9, 2004
Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patientsGiorgia Zadra, Rosanna Asselta, Massimo Malcovati, et al.
Plos One|June 2, 2017
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysisChiara Chiereghin, Michela Robusto, Antonio Mastrangelo, et al.
Blood|October 24, 2002
Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency: molecular characterization by expression of the recombinant proteinStefano Duga, Maria Claudia Montefusco, Rosanna Asselta, et al.
Haematologica|September 24, 2009
Premature termination codon mutations in the von Willebrand factor gene are associated with allele-specific and position-dependent mRNA decayManuela Platè, Stefano Duga, Luciano Baronciani, et al.
Thrombosis and Haemostasis|September 1, 2009
Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiencySilvia Spena, Rosanna Asselta, Sonia Caccia, et al.
Haematologica|August 11, 2019
Profiling the mutational landscape of coagulation factor V deficiencyElvezia Maria Paraboschi, Marzia Menegatti, Valeria Rimoldi, et al.
Blood|June 21, 2003
Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V: Broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutationsMaria Claudia Montefusco, Stefano Duga, Rosanna Asselta, et al.
Parkinsonism & Related Disorders|September 25, 2014
Glucocerebrosidase mutations in primary parkinsonismRosanna Asselta, Valeria Rimoldi, Chiara Siri, et al.
Parkinsonism & Related Disorders|November 23, 2011
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian populationLuca Trotta, Ilaria Guella, Giulia Soldà, et al.
Pageof 15