Search research articles
Contact Us
Filters
Showing results (1-10 of 66) with videos related to
Page
of 7
Sort By:
Nature Genetics
|
June 28, 2012
Gain of function in CDKN1C
Andrea Riccio, Maria Vittoria Cubellis
International Journal of Molecular Sciences
|
May 27, 2023
Rare Diseases: Implementation of Molecular Diagnosis, Pathogenesis Insights and Precision Medicine Treatment
Lidia Larizza, Maria Vittoria Cubellis
Biochimie
|
April 6, 2015
Taming molecular flexibility to tackle rare diseases
Maria Vittoria Cubellis, Marc Baaden, Giuseppina Andreotti
Drug Testing and Analysis
|
April 8, 2015
Looking for protein stabilizing drugs with thermal shift assay
Giuseppina Andreotti, Maria Monticelli, Maria Vittoria Cubellis
BMC Bioinformatics
|
December 15, 2005
Secondary structure assignment that accurately reflects physical and evolutionary characteristics
Maria Vittoria Cubellis, Fabien Cailliez, Simon C Lovell
Biochimica Et Biophysica Acta
|
December 24, 2013
A thermodynamic assay to test pharmacological chaperones for Fabry disease
Giuseppina 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 glycosylation
Giuseppina Andreotti, Emilia Pedone, Assunta Giordano, et al.
BMC Bioinformatics
|
July 3, 2013
Identification and analysis of conserved pockets on protein surfaces
Marco 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 chaperones
Marco Cammisa, Antonella Correra, Giuseppina Andreotti, et al.
Gene
|
December 3, 2002
An intron-less betagamma-crystallin-type gene from the sponge Geodia cydonium
Antimo Di Maro, Elio Pizzo, Maria Vittoria Cubellis, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 66) with videos related to
Sort By:
Page
of 7
Nature Genetics
|
June 28, 2012
Gain of function in CDKN1C
Andrea Riccio, Maria Vittoria Cubellis
International Journal of Molecular Sciences
|
May 27, 2023
Rare Diseases: Implementation of Molecular Diagnosis, Pathogenesis Insights and Precision Medicine Treatment
Lidia Larizza, Maria Vittoria Cubellis
Biochimie
|
April 6, 2015
Taming molecular flexibility to tackle rare diseases
Maria Vittoria Cubellis, Marc Baaden, Giuseppina Andreotti
Drug Testing and Analysis
|
April 8, 2015
Looking for protein stabilizing drugs with thermal shift assay
Giuseppina Andreotti, Maria Monticelli, Maria Vittoria Cubellis
BMC Bioinformatics
|
December 15, 2005
Secondary structure assignment that accurately reflects physical and evolutionary characteristics
Maria Vittoria Cubellis, Fabien Cailliez, Simon C Lovell
Biochimica Et Biophysica Acta
|
December 24, 2013
A thermodynamic assay to test pharmacological chaperones for Fabry disease
Giuseppina 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 glycosylation
Giuseppina Andreotti, Emilia Pedone, Assunta Giordano, et al.
BMC Bioinformatics
|
July 3, 2013
Identification and analysis of conserved pockets on protein surfaces
Marco 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 chaperones
Marco Cammisa, Antonella Correra, Giuseppina Andreotti, et al.
Gene
|
December 3, 2002
An intron-less betagamma-crystallin-type gene from the sponge Geodia cydonium
Antimo Di Maro, Elio Pizzo, Maria Vittoria Cubellis, et al.
Page
of 7