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Isabella Ceccherini

Showing results (11-20 of 180) with videos related to

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The Journal of Molecular Diagnostics : JMD|October 27, 2006
Betaine, dimethyl sulfoxide, and 7-deaza-dGTP, a powerful mixture for amplification of GC-rich DNA sequencesMarco Musso, Renata Bocciardi, Sara Parodi, et al.
BMC Proceedings|May 10, 2008
Incorporating prior biological information in linkage studies increases power and limits multiple testingFrancesca Lantieri, Halfdan Rydbeck, Paola Griseri, et al.
Frontiers in Neurology|April 5, 2021
A Common 3'UTR Variant of the <i>PHOX2B</i> Gene Is Associated With Infant Life-Threatening and Sudden Death Events in the Italian PopulationTiziana Bachetti, Simona Bagnasco, Raffaele Piumelli, et al.
Italian Journal of Pediatrics|August 25, 2019
PAPA and FMF in two siblings: possible amplification of clinical presentation? A case reportMaria Cristina Maggio, Isabella Ceccherini, Alice Grossi, et al.
Molecular Cancer Research : MCR|September 13, 2006
Nuclear factor Y drives basal transcription of the human TLX3, a gene overexpressed in T-cell acute lymphocytic leukemiaSilvia Borghini, Manuela Vargiolu, Marco Di Duca, et al.
Experimental Cell Research|April 18, 2015
Identification of novel pathways and molecules able to down-regulate PHOX2B gene expression by in vitro drug screening approaches in neuroblastoma cellsEleonora Di Zanni, Diego Fornasari, Roberto Ravazzolo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 9, 2016
Unusual presentations and intrafamilial phenotypic variability in infantile onset Alexander diseaseDavide Tonduti, Anna Ardissone, Isabella Ceccherini, et al.
Scientific Reports|October 17, 2024
A systematic review and meta-analysis of GFAP gene variants in Alexander diseaseAlice Grossi, Francesca Rosamilia, Silvia Carestiato, et al.
Methods in Molecular Biology (Clifton, N.J.)|August 14, 2023
A Knock-In Mouse Model of Cryopyrin-Associated Periodic SyndromesArinna Bertoni, Ignazia Prigione, Sabrina Chiesa, et al.
International Journal of Molecular Sciences|March 14, 2017
Custom Array Comparative Genomic Hybridization: the Importance of DNA Quality, an Expert Eye, and Variant ValidationFrancesca Lantieri, Michela Malacarne, Stefania Gimelli, et al.
Pageof 18

Showing results (11-20 of 180) with videos related to

Sort By:
Pageof 18
The Journal of Molecular Diagnostics : JMD|October 27, 2006
Betaine, dimethyl sulfoxide, and 7-deaza-dGTP, a powerful mixture for amplification of GC-rich DNA sequencesMarco Musso, Renata Bocciardi, Sara Parodi, et al.
BMC Proceedings|May 10, 2008
Incorporating prior biological information in linkage studies increases power and limits multiple testingFrancesca Lantieri, Halfdan Rydbeck, Paola Griseri, et al.
Frontiers in Neurology|April 5, 2021
A Common 3'UTR Variant of the <i>PHOX2B</i> Gene Is Associated With Infant Life-Threatening and Sudden Death Events in the Italian PopulationTiziana Bachetti, Simona Bagnasco, Raffaele Piumelli, et al.
Italian Journal of Pediatrics|August 25, 2019
PAPA and FMF in two siblings: possible amplification of clinical presentation? A case reportMaria Cristina Maggio, Isabella Ceccherini, Alice Grossi, et al.
Molecular Cancer Research : MCR|September 13, 2006
Nuclear factor Y drives basal transcription of the human TLX3, a gene overexpressed in T-cell acute lymphocytic leukemiaSilvia Borghini, Manuela Vargiolu, Marco Di Duca, et al.
Experimental Cell Research|April 18, 2015
Identification of novel pathways and molecules able to down-regulate PHOX2B gene expression by in vitro drug screening approaches in neuroblastoma cellsEleonora Di Zanni, Diego Fornasari, Roberto Ravazzolo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 9, 2016
Unusual presentations and intrafamilial phenotypic variability in infantile onset Alexander diseaseDavide Tonduti, Anna Ardissone, Isabella Ceccherini, et al.
Scientific Reports|October 17, 2024
A systematic review and meta-analysis of GFAP gene variants in Alexander diseaseAlice Grossi, Francesca Rosamilia, Silvia Carestiato, et al.
Methods in Molecular Biology (Clifton, N.J.)|August 14, 2023
A Knock-In Mouse Model of Cryopyrin-Associated Periodic SyndromesArinna Bertoni, Ignazia Prigione, Sabrina Chiesa, et al.
International Journal of Molecular Sciences|March 14, 2017
Custom Array Comparative Genomic Hybridization: the Importance of DNA Quality, an Expert Eye, and Variant ValidationFrancesca Lantieri, Michela Malacarne, Stefania Gimelli, et al.
Pageof 18