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Federica Sangiuolo

Showing results (1-10 of 101) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|February 22, 2014
Small Fragment Homologous Replacement (SFHR): sequence-specific modification of genomic DNA in eukaryotic cells by small DNA fragmentsAndrea Luchetti, Arianna Malgieri, Federica Sangiuolo
Expert Opinion on Medical Diagnostics|March 15, 2013
Diagnostic CFTR mutation analysisMaria Rosaria D'Apice, Giuseppe Novelli, Federica Sangiuolo
Human Mutation|March 17, 2004
Biochemical characterization of two GALK1 mutations in patients with galactokinase deficiencyFederica Sangiuolo, Mauro Magnani, Dwight Stambolian, et al.
Frontiers in Cell and Developmental Biology|January 26, 2023
Organoid factory: The recent role of the human induced pluripotent stem cells (hiPSCs) in precision medicineGiuseppe Novelli, Paola Spitalieri, Michela Murdocca, et al.
Frontiers in Genetics|March 19, 2015
Application of Next Generation Sequencing for personalized medicine for sudden cardiac deathElena Morini, Federica Sangiuolo, Daniela Caporossi, et al.
Frontiers in Cell and Developmental Biology|May 22, 2023
Editorial: Reviews in induced pluripotent stem cellsMirella Dottori, Wan-Ju Li, Gabriella Minchiotti, et al.
Pharmacogenomics|April 23, 2002
Towards the pharmacogenomics of cystic fibrosisFederica Sangiuolo, Maria Rosaria D'Apice, Emanuela Bruscia, et al.
World Journal of Stem Cells|April 27, 2016
Human induced pluripotent stem cells for monogenic disease modelling and therapyPaola Spitalieri, Valentina Rosa Talarico, Michela Murdocca, et al.
Human Genomics|June 28, 2020
Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discoveryClaudia De Masi, Paola Spitalieri, Michela Murdocca, et al.
Genetic Testing and Molecular Biomarkers|March 25, 2009
Prenatal diagnosis of Cockayne syndrome type A based on the identification of two novel mutations in the ERCC8 geneChiara Conte, Maria Rosaria D'Apice, Annalisa Botta, et al.
Pageof 11

Showing results (1-10 of 101) with videos related to

Sort By:
Pageof 11
Methods in Molecular Biology (Clifton, N.J.)|February 22, 2014
Small Fragment Homologous Replacement (SFHR): sequence-specific modification of genomic DNA in eukaryotic cells by small DNA fragmentsAndrea Luchetti, Arianna Malgieri, Federica Sangiuolo
Expert Opinion on Medical Diagnostics|March 15, 2013
Diagnostic CFTR mutation analysisMaria Rosaria D'Apice, Giuseppe Novelli, Federica Sangiuolo
Human Mutation|March 17, 2004
Biochemical characterization of two GALK1 mutations in patients with galactokinase deficiencyFederica Sangiuolo, Mauro Magnani, Dwight Stambolian, et al.
Frontiers in Cell and Developmental Biology|January 26, 2023
Organoid factory: The recent role of the human induced pluripotent stem cells (hiPSCs) in precision medicineGiuseppe Novelli, Paola Spitalieri, Michela Murdocca, et al.
Frontiers in Genetics|March 19, 2015
Application of Next Generation Sequencing for personalized medicine for sudden cardiac deathElena Morini, Federica Sangiuolo, Daniela Caporossi, et al.
Frontiers in Cell and Developmental Biology|May 22, 2023
Editorial: Reviews in induced pluripotent stem cellsMirella Dottori, Wan-Ju Li, Gabriella Minchiotti, et al.
Pharmacogenomics|April 23, 2002
Towards the pharmacogenomics of cystic fibrosisFederica Sangiuolo, Maria Rosaria D'Apice, Emanuela Bruscia, et al.
World Journal of Stem Cells|April 27, 2016
Human induced pluripotent stem cells for monogenic disease modelling and therapyPaola Spitalieri, Valentina Rosa Talarico, Michela Murdocca, et al.
Human Genomics|June 28, 2020
Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discoveryClaudia De Masi, Paola Spitalieri, Michela Murdocca, et al.
Genetic Testing and Molecular Biomarkers|March 25, 2009
Prenatal diagnosis of Cockayne syndrome type A based on the identification of two novel mutations in the ERCC8 geneChiara Conte, Maria Rosaria D'Apice, Annalisa Botta, et al.
Pageof 11