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Concetta Federico

Showing results (91-100 of 102) with videos related to

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Neuromolecular Medicine|September 21, 2023
Fibroblast Growth Factor Receptor 2 (FGFR2), a New Gene Involved in the Genesis of Autism Spectrum DisorderAntonio Gennaro Nicotera, Greta Amore, Maria Concetta Saia, et al.
Genes|January 8, 2025
Exploring the Role of <i>FICD</i>, a New Potential Gene Involved in Borderline Intellectual Functioning, Psychological and Metabolic DisordersMirella Vinci, Donatella Greco, Maria Grazia Figura, et al.
International Journal of Molecular Sciences|December 23, 2022
<i>PHF21A</i> Related Disorder: Description of a New CaseAmbra Butera, Antonio Gennaro Nicotera, Gabriella Di Rosa, et al.
Cell Death & Disease|October 6, 2021
Targeting the miRNA-155/TNFSF10 network restrains inflammatory response in the retina in a mouse model of Alzheimer's diseaseChiara Burgaletto, Chiara Bianca Maria Platania, Giulia Di Benedetto, et al.
Antioxidants (Basel, Switzerland)|January 21, 2022
Activity-Dependent Neuroprotective Protein (ADNP)-Derived Peptide (NAP) Counteracts UV-B Radiation-Induced ROS Formation in Corneal EpitheliumGrazia Maugeri, Agata Grazia D'Amico, Salvatore Giunta, et al.
Biomedicines|September 23, 2022
Identification of a Novel Missense Mutation of <i>POLR3A</i> Gene in a Cohort of Sicilian Patients with LeukodystrophyAntonino Musumeci, Francesco Calì, Carmela Scuderi, et al.
Genes|August 29, 2024
<i>PLEKHG1</i>: New Potential Candidate Gene for Periventricular White Matter AbnormalitiesFrancesco Calì, Mirella Vinci, Simone Treccarichi, et al.
Journal of Molecular Neuroscience : MN|June 11, 2026
A de novo Loss-of-function Variant in RAPGEF6 Supports its Role in Neuropsychiatric DisordersSimone Treccarichi, Mirella Vinci, Maria Grazia Figura, et al.
Cancers|April 28, 2019
Deletions of Chromosome 7q Affect Nuclear Organization and <i>HLXB9</i>Gene Expression in Hematological DisordersConcetta Federico, Temitayo Owoka, Denise Ragusa, et al.
Medicina (Kaunas, Lithuania)|August 26, 2023
Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex FamiliesFrancesco Calì, Francesco Domenico Di Blasi, Emanuela Avola, et al.
Pageof 11

Showing results (91-100 of 102) with videos related to

Sort By:
Pageof 11
Neuromolecular Medicine|September 21, 2023
Fibroblast Growth Factor Receptor 2 (FGFR2), a New Gene Involved in the Genesis of Autism Spectrum DisorderAntonio Gennaro Nicotera, Greta Amore, Maria Concetta Saia, et al.
Genes|January 8, 2025
Exploring the Role of <i>FICD</i>, a New Potential Gene Involved in Borderline Intellectual Functioning, Psychological and Metabolic DisordersMirella Vinci, Donatella Greco, Maria Grazia Figura, et al.
International Journal of Molecular Sciences|December 23, 2022
<i>PHF21A</i> Related Disorder: Description of a New CaseAmbra Butera, Antonio Gennaro Nicotera, Gabriella Di Rosa, et al.
Cell Death & Disease|October 6, 2021
Targeting the miRNA-155/TNFSF10 network restrains inflammatory response in the retina in a mouse model of Alzheimer's diseaseChiara Burgaletto, Chiara Bianca Maria Platania, Giulia Di Benedetto, et al.
Antioxidants (Basel, Switzerland)|January 21, 2022
Activity-Dependent Neuroprotective Protein (ADNP)-Derived Peptide (NAP) Counteracts UV-B Radiation-Induced ROS Formation in Corneal EpitheliumGrazia Maugeri, Agata Grazia D'Amico, Salvatore Giunta, et al.
Biomedicines|September 23, 2022
Identification of a Novel Missense Mutation of <i>POLR3A</i> Gene in a Cohort of Sicilian Patients with LeukodystrophyAntonino Musumeci, Francesco Calì, Carmela Scuderi, et al.
Genes|August 29, 2024
<i>PLEKHG1</i>: New Potential Candidate Gene for Periventricular White Matter AbnormalitiesFrancesco Calì, Mirella Vinci, Simone Treccarichi, et al.
Journal of Molecular Neuroscience : MN|June 11, 2026
A de novo Loss-of-function Variant in RAPGEF6 Supports its Role in Neuropsychiatric DisordersSimone Treccarichi, Mirella Vinci, Maria Grazia Figura, et al.
Cancers|April 28, 2019
Deletions of Chromosome 7q Affect Nuclear Organization and <i>HLXB9</i>Gene Expression in Hematological DisordersConcetta Federico, Temitayo Owoka, Denise Ragusa, et al.
Medicina (Kaunas, Lithuania)|August 26, 2023
Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex FamiliesFrancesco Calì, Francesco Domenico Di Blasi, Emanuela Avola, et al.
Pageof 11