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Maria Vittoria Cubellis

Showing results (1-10 of 66) with videos related to

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Nature Genetics|June 28, 2012
Gain of function in CDKN1CAndrea Riccio, Maria Vittoria Cubellis
International Journal of Molecular Sciences|May 27, 2023
Rare Diseases: Implementation of Molecular Diagnosis, Pathogenesis Insights and Precision Medicine TreatmentLidia Larizza, Maria Vittoria Cubellis
Biochimie|April 6, 2015
Taming molecular flexibility to tackle rare diseasesMaria Vittoria Cubellis, Marc Baaden, Giuseppina Andreotti
Drug Testing and Analysis|April 8, 2015
Looking for protein stabilizing drugs with thermal shift assayGiuseppina Andreotti, Maria Monticelli, Maria Vittoria Cubellis
BMC Bioinformatics|December 15, 2005
Secondary structure assignment that accurately reflects physical and evolutionary characteristicsMaria Vittoria Cubellis, Fabien Cailliez, Simon C Lovell
Biochimica Et Biophysica Acta|December 24, 2013
A thermodynamic assay to test pharmacological chaperones for Fabry diseaseGiuseppina Andreotti, Valentina Citro, Antonella Correra, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Biochemical phenotype of a common disease-causing mutation and a possible therapeutic approach for the phosphomannomutase 2-associated disorder of glycosylationGiuseppina Andreotti, Emilia Pedone, Assunta Giordano, et al.
BMC Bioinformatics|July 3, 2013
Identification and analysis of conserved pockets on protein surfacesMarco Cammisa, Antonella Correra, Giuseppina Andreotti, et al.
Orphanet Journal of Rare Diseases|July 26, 2013
Fabry_CEP: a tool to identify Fabry mutations responsive to pharmacological chaperonesMarco Cammisa, Antonella Correra, Giuseppina Andreotti, et al.
Gene|December 3, 2002
An intron-less betagamma-crystallin-type gene from the sponge Geodia cydoniumAntimo Di Maro, Elio Pizzo, Maria Vittoria Cubellis, et al.
Pageof 7

Showing results (1-10 of 66) with videos related to

Sort By:
Pageof 7
Nature Genetics|June 28, 2012
Gain of function in CDKN1CAndrea Riccio, Maria Vittoria Cubellis
International Journal of Molecular Sciences|May 27, 2023
Rare Diseases: Implementation of Molecular Diagnosis, Pathogenesis Insights and Precision Medicine TreatmentLidia Larizza, Maria Vittoria Cubellis
Biochimie|April 6, 2015
Taming molecular flexibility to tackle rare diseasesMaria Vittoria Cubellis, Marc Baaden, Giuseppina Andreotti
Drug Testing and Analysis|April 8, 2015
Looking for protein stabilizing drugs with thermal shift assayGiuseppina Andreotti, Maria Monticelli, Maria Vittoria Cubellis
BMC Bioinformatics|December 15, 2005
Secondary structure assignment that accurately reflects physical and evolutionary characteristicsMaria Vittoria Cubellis, Fabien Cailliez, Simon C Lovell
Biochimica Et Biophysica Acta|December 24, 2013
A thermodynamic assay to test pharmacological chaperones for Fabry diseaseGiuseppina Andreotti, Valentina Citro, Antonella Correra, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Biochemical phenotype of a common disease-causing mutation and a possible therapeutic approach for the phosphomannomutase 2-associated disorder of glycosylationGiuseppina Andreotti, Emilia Pedone, Assunta Giordano, et al.
BMC Bioinformatics|July 3, 2013
Identification and analysis of conserved pockets on protein surfacesMarco Cammisa, Antonella Correra, Giuseppina Andreotti, et al.
Orphanet Journal of Rare Diseases|July 26, 2013
Fabry_CEP: a tool to identify Fabry mutations responsive to pharmacological chaperonesMarco Cammisa, Antonella Correra, Giuseppina Andreotti, et al.
Gene|December 3, 2002
An intron-less betagamma-crystallin-type gene from the sponge Geodia cydoniumAntimo Di Maro, Elio Pizzo, Maria Vittoria Cubellis, et al.
Pageof 7