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S Lucioli

Showing results (1-10 of 6) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992). Supplement|June 5, 2004
A mitochondrial ATPase 6 mutation is associated with Leigh syndrome in a family and affects proton flow and adenosine triphosphate output when modeled in Escherichia coliR Carrozzo, T Rizza, S Lucioli, et al.
Journal of Virology|September 1, 1997
Poliovirus Sabin type 1 neutralization epitopes recognized by immunoglobulin A monoclonal antibodiesL Fiore, B Ridolfi, D Genovese, et al.
Plant Physiology and Biochemistry : PPB|November 19, 2013
Characterization of the response of in vitro cultured Myrtus communis L. plants to high concentrations of NaClP Di Cori, S Lucioli, A Frattarelli, et al.
Human Mutation|March 26, 2003
Mutation analysis in 16 patients with mtDNA depletionR Carrozzo, B Bornstein, S Lucioli, et al.
Neurology|June 16, 2005
Detection of common and private mutations in the COL6A1 gene of patients with Bethlem myopathyS Lucioli, B Giusti, E Mercuri, et al.
Human Mutation|January 22, 2008
Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinaseD P Dimmock, Q Zhang, C Dionisi-Vici, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Acta Paediatrica (Oslo, Norway : 1992). Supplement|June 5, 2004
A mitochondrial ATPase 6 mutation is associated with Leigh syndrome in a family and affects proton flow and adenosine triphosphate output when modeled in Escherichia coliR Carrozzo, T Rizza, S Lucioli, et al.
Journal of Virology|September 1, 1997
Poliovirus Sabin type 1 neutralization epitopes recognized by immunoglobulin A monoclonal antibodiesL Fiore, B Ridolfi, D Genovese, et al.
Plant Physiology and Biochemistry : PPB|November 19, 2013
Characterization of the response of in vitro cultured Myrtus communis L. plants to high concentrations of NaClP Di Cori, S Lucioli, A Frattarelli, et al.
Human Mutation|March 26, 2003
Mutation analysis in 16 patients with mtDNA depletionR Carrozzo, B Bornstein, S Lucioli, et al.
Neurology|June 16, 2005
Detection of common and private mutations in the COL6A1 gene of patients with Bethlem myopathyS Lucioli, B Giusti, E Mercuri, et al.
Human Mutation|January 22, 2008
Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinaseD P Dimmock, Q Zhang, C Dionisi-Vici, et al.
Pageof 1