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Maria Guarnaccia

Showing results (21-30 of 36) with videos related to

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Cells|September 28, 2023
Transcriptomic Analysis in the Hippocampus and Retina of Tg2576 AD Mice Reveals Defective Mitochondrial Oxidative Phosphorylation and Recovery by Tau 12A12mAb TreatmentGiovanna Morello, Maria Guarnaccia, Valentina La Cognata, et al.
Cells|July 29, 2023
A Diagnostic Gene-Expression Signature in Fibroblasts of Amyotrophic Lateral SclerosisGiovanna Morello, Valentina La Cognata, Maria Guarnaccia, et al.
Cellular and Molecular Life Sciences : CMLS|July 27, 2024
Increased copy-number variant load of associated risk genes in sporadic cases of amyotrophic lateral sclerosisMaria Guarnaccia, Giovanna Morello, Valentina La Cognata, et al.
International Journal of Molecular Sciences|August 2, 2019
A Systems Biology Approach for Personalized Medicine in Refractory EpilepsyGiuseppina Daniela Naimo, Maria Guarnaccia, Teresa Sprovieri, et al.
European Journal of Medical Genetics|March 17, 2016
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent featuresPiero Pavone, Andrea Domenico Praticò, Giulia Gentile, et al.
Scientific Reports|July 12, 2019
Integrative multi-omic analysis identifies new drivers and pathways in molecularly distinct subtypes of ALSGiovanna Morello, Maria Guarnaccia, Antonio Gianmaria Spampinato, et al.
Cells|July 29, 2023
CXCR2 Is Deregulated in ALS Spinal Cord and Its Activation Triggers Apoptosis in Motor Neuron-Like Cells Overexpressing hSOD1-G93AValentina La Cognata, Agata Grazia D'Amico, Grazia Maugeri, et al.
Journal of Personalized Medicine|December 5, 2020
Genomic Portrait of a Sporadic Amyotrophic Lateral Sclerosis Case in a Large Spinocerebellar Ataxia Type 1 FamilyGiovanna Morello, Giulia Gentile, Rossella Spataro, et al.
Life (Basel, Switzerland)|July 27, 2022
A Targeted Next-Generation Sequencing Panel to Genotype GliomasMaria Guarnaccia, Laura Guarnaccia, Valentina La Cognata, et al.
Biomedicines|July 29, 2023
Detection of Single-Nucleotide and Copy Number Defects Underlying Hyperphenylalaninemia by Next-Generation SequencingElisabetta Anna Tendi, Giovanna Morello, Maria Guarnaccia, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Cells|September 28, 2023
Transcriptomic Analysis in the Hippocampus and Retina of Tg2576 AD Mice Reveals Defective Mitochondrial Oxidative Phosphorylation and Recovery by Tau 12A12mAb TreatmentGiovanna Morello, Maria Guarnaccia, Valentina La Cognata, et al.
Cells|July 29, 2023
A Diagnostic Gene-Expression Signature in Fibroblasts of Amyotrophic Lateral SclerosisGiovanna Morello, Valentina La Cognata, Maria Guarnaccia, et al.
Cellular and Molecular Life Sciences : CMLS|July 27, 2024
Increased copy-number variant load of associated risk genes in sporadic cases of amyotrophic lateral sclerosisMaria Guarnaccia, Giovanna Morello, Valentina La Cognata, et al.
International Journal of Molecular Sciences|August 2, 2019
A Systems Biology Approach for Personalized Medicine in Refractory EpilepsyGiuseppina Daniela Naimo, Maria Guarnaccia, Teresa Sprovieri, et al.
European Journal of Medical Genetics|March 17, 2016
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent featuresPiero Pavone, Andrea Domenico Praticò, Giulia Gentile, et al.
Scientific Reports|July 12, 2019
Integrative multi-omic analysis identifies new drivers and pathways in molecularly distinct subtypes of ALSGiovanna Morello, Maria Guarnaccia, Antonio Gianmaria Spampinato, et al.
Cells|July 29, 2023
CXCR2 Is Deregulated in ALS Spinal Cord and Its Activation Triggers Apoptosis in Motor Neuron-Like Cells Overexpressing hSOD1-G93AValentina La Cognata, Agata Grazia D'Amico, Grazia Maugeri, et al.
Journal of Personalized Medicine|December 5, 2020
Genomic Portrait of a Sporadic Amyotrophic Lateral Sclerosis Case in a Large Spinocerebellar Ataxia Type 1 FamilyGiovanna Morello, Giulia Gentile, Rossella Spataro, et al.
Life (Basel, Switzerland)|July 27, 2022
A Targeted Next-Generation Sequencing Panel to Genotype GliomasMaria Guarnaccia, Laura Guarnaccia, Valentina La Cognata, et al.
Biomedicines|July 29, 2023
Detection of Single-Nucleotide and Copy Number Defects Underlying Hyperphenylalaninemia by Next-Generation SequencingElisabetta Anna Tendi, Giovanna Morello, Maria Guarnaccia, et al.
Pageof 4