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Francesca Puppo

Showing results (11-20 of 35) with videos related to

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Physiological Genomics|September 8, 2005
Comparative genomic sequence analysis coupled to chromatin immunoprecipitation: a screening procedure applied to search for regulatory elements at the RET locusFrancesca Puppo, Marco Musso, Doroti Pirulli, et al.
IEEE Transactions on Nanobioscience|March 6, 2014
Memristive biosensors under varying humidity conditionsFrancesca Puppo, Akshat Dave, Marie-Agnès Doucey, et al.
Human Mutation|July 16, 2020
Splicing impact of deep exonic missense variants in CAPN3 explored systematically by minigene functional assayEugénie Dionnet, Aurélia Defour, Nathalie Da Silva, et al.
Methods (San Diego, Calif.)|June 11, 2017
A bimetallic nanocoral Au decorated with Pt nanoflowers (bio)sensor for H<sub>2</sub>O<sub>2</sub> detection at low potentialGabriella Sanzò, Irene Taurino, Francesca Puppo, et al.
American Journal of Human Genetics|September 6, 2002
A rare haplotype of the RET proto-oncogene is a risk-modifying allele in hirschsprung diseasePaola Griseri, Barbara Pesce, Giovanna Patrone, et al.
Frontiers in Bioengineering and Biotechnology|February 6, 2026
A cross-correction gene therapy approach for CDKL5 deficiency disorder improves the pathological phenotype of CDD patient-derived cortical organoidsGiorgio Medici, Angelica M Bove, Stefania Trazzi, et al.
Biomaterials|May 28, 2025
Graphene-polymer nanofibers enable optically induced electrical responses in stem cell-derived electrically excitable cells and brain organoidsErin LaMontagne, Alex Savchenko, Gisselle Gonzalez, et al.
Cells|January 26, 2021
Using iPSC Models to Understand the Role of Estrogen in Neuron-Glia Interactions in Schizophrenia and Bipolar DisorderDenis Reis de Assis, Attila Szabo, Jordi Requena Osete, et al.
Plos Genetics|June 21, 2013
Deregulation of the protocadherin gene FAT1 alters muscle shapes: implications for the pathogenesis of facioscapulohumeral dystrophyNathalie Caruso, Balàzs Herberth, Marc Bartoli, et al.
Human Mutation|July 27, 2017
Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophyKarine Nguyen, Francesca Puppo, Stéphane Roche, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Physiological Genomics|September 8, 2005
Comparative genomic sequence analysis coupled to chromatin immunoprecipitation: a screening procedure applied to search for regulatory elements at the RET locusFrancesca Puppo, Marco Musso, Doroti Pirulli, et al.
IEEE Transactions on Nanobioscience|March 6, 2014
Memristive biosensors under varying humidity conditionsFrancesca Puppo, Akshat Dave, Marie-Agnès Doucey, et al.
Human Mutation|July 16, 2020
Splicing impact of deep exonic missense variants in CAPN3 explored systematically by minigene functional assayEugénie Dionnet, Aurélia Defour, Nathalie Da Silva, et al.
Methods (San Diego, Calif.)|June 11, 2017
A bimetallic nanocoral Au decorated with Pt nanoflowers (bio)sensor for H<sub>2</sub>O<sub>2</sub> detection at low potentialGabriella Sanzò, Irene Taurino, Francesca Puppo, et al.
American Journal of Human Genetics|September 6, 2002
A rare haplotype of the RET proto-oncogene is a risk-modifying allele in hirschsprung diseasePaola Griseri, Barbara Pesce, Giovanna Patrone, et al.
Frontiers in Bioengineering and Biotechnology|February 6, 2026
A cross-correction gene therapy approach for CDKL5 deficiency disorder improves the pathological phenotype of CDD patient-derived cortical organoidsGiorgio Medici, Angelica M Bove, Stefania Trazzi, et al.
Biomaterials|May 28, 2025
Graphene-polymer nanofibers enable optically induced electrical responses in stem cell-derived electrically excitable cells and brain organoidsErin LaMontagne, Alex Savchenko, Gisselle Gonzalez, et al.
Cells|January 26, 2021
Using iPSC Models to Understand the Role of Estrogen in Neuron-Glia Interactions in Schizophrenia and Bipolar DisorderDenis Reis de Assis, Attila Szabo, Jordi Requena Osete, et al.
Plos Genetics|June 21, 2013
Deregulation of the protocadherin gene FAT1 alters muscle shapes: implications for the pathogenesis of facioscapulohumeral dystrophyNathalie Caruso, Balàzs Herberth, Marc Bartoli, et al.
Human Mutation|July 27, 2017
Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophyKarine Nguyen, Francesca Puppo, Stéphane Roche, et al.
Pageof 4