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Davide Cacchiarelli

Showing results (31-40 of 71) with videos related to

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Stem Cell Reports|April 23, 2021
Automatic identification of small molecules that promote cell conversion and reprogrammingFrancesco Napolitano, Trisevgeni Rapakoulia, Patrizia Annunziata, et al.
The EMBO Journal|September 15, 2023
TFEB and TFE3 control glucose homeostasis by regulating insulin gene expressionAdrien Pasquier, Nunzia Pastore, Luca D'Orsi, et al.
Cell Reports Methods|February 19, 2026
Human neuromuscular organoids mimic cancer-induced muscle cachexiaPietro Chiolerio, Beatrice Auletta, Camilla Pezzini, et al.
Nature Cell Biology|April 27, 2023
Esrrb guides naive pluripotent cells through the formative transcriptional programmeElena Carbognin, Valentina Carlini, Francesco Panariello, et al.
Journal of Molecular Cell Biology|February 2, 2024
Identification of druggable host dependency factors shared by multiple SARS-CoV-2 variants of concernIlaria Frasson, Linda Diamante, Manuela Zangrossi, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
Excitatory Cortical Neurons from CDKL5 Deficiency Disorder Patient-Derived Organoids Show Early Hyperexcitability Not Identified in Neurogenin2 Induced NeuronsMadison R Glass, Dosh Whye, Nickesha C Anderson, et al.
Nature Communications|May 29, 2023
Multi-omic approach characterises the neuroprotective role of retromer in regulating lysosomal healthJames L Daly, Chris M Danson, Philip A Lewis, et al.
Nature Communications|February 11, 2018
Genome-wide tracking of dCas9-methyltransferase footprintsChristina Galonska, Jocelyn Charlton, Alexandra L Mattei, et al.
Neurobiology of Disease|September 10, 2025
Excitatory cortical neurons from CDKL5 deficiency disorder patient-derived organoids show early hyperexcitability not identified in neurogenin2 induced neuronsMadison R Glass, Dosh Whye, Nickesha C Anderson, et al.
European Journal of Human Genetics : EJHG|December 12, 2024
Heterozygous variants disrupting the interaction of ERF with activated ERK1/2 cause microcephaly, developmental delay, and skeletal anomaliesLucia Micale, Aikaterini Vourlia, Carmela Fusco, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
Stem Cell Reports|April 23, 2021
Automatic identification of small molecules that promote cell conversion and reprogrammingFrancesco Napolitano, Trisevgeni Rapakoulia, Patrizia Annunziata, et al.
The EMBO Journal|September 15, 2023
TFEB and TFE3 control glucose homeostasis by regulating insulin gene expressionAdrien Pasquier, Nunzia Pastore, Luca D'Orsi, et al.
Cell Reports Methods|February 19, 2026
Human neuromuscular organoids mimic cancer-induced muscle cachexiaPietro Chiolerio, Beatrice Auletta, Camilla Pezzini, et al.
Nature Cell Biology|April 27, 2023
Esrrb guides naive pluripotent cells through the formative transcriptional programmeElena Carbognin, Valentina Carlini, Francesco Panariello, et al.
Journal of Molecular Cell Biology|February 2, 2024
Identification of druggable host dependency factors shared by multiple SARS-CoV-2 variants of concernIlaria Frasson, Linda Diamante, Manuela Zangrossi, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
Excitatory Cortical Neurons from CDKL5 Deficiency Disorder Patient-Derived Organoids Show Early Hyperexcitability Not Identified in Neurogenin2 Induced NeuronsMadison R Glass, Dosh Whye, Nickesha C Anderson, et al.
Nature Communications|May 29, 2023
Multi-omic approach characterises the neuroprotective role of retromer in regulating lysosomal healthJames L Daly, Chris M Danson, Philip A Lewis, et al.
Nature Communications|February 11, 2018
Genome-wide tracking of dCas9-methyltransferase footprintsChristina Galonska, Jocelyn Charlton, Alexandra L Mattei, et al.
Neurobiology of Disease|September 10, 2025
Excitatory cortical neurons from CDKL5 deficiency disorder patient-derived organoids show early hyperexcitability not identified in neurogenin2 induced neuronsMadison R Glass, Dosh Whye, Nickesha C Anderson, et al.
European Journal of Human Genetics : EJHG|December 12, 2024
Heterozygous variants disrupting the interaction of ERF with activated ERK1/2 cause microcephaly, developmental delay, and skeletal anomaliesLucia Micale, Aikaterini Vourlia, Carmela Fusco, et al.
Pageof 8