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Francesca Di Leva

Showing results (11-20 of 26) with videos related to

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European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|May 17, 2005
Audiometric evaluation of carriers of the connexin 26 mutation 35delGAnnamaria Franzé, Antonella Caravelli, Francesca Di Leva, et al.
Cellular and Molecular Neurobiology|July 17, 2016
Transcriptomic Profiling Discloses Molecular and Cellular Events Related to Neuronal Differentiation in SH-SY5Y Neuroblastoma CellsFrancesco Pezzini, Laura Bettinetti, Francesca Di Leva, et al.
Frontiers in Genetics|December 9, 2021
Natural SINEUP RNAs in Autism Spectrum Disorders: <i>RAB11B-AS1</i> Dysregulation in a Neuronal <i>CHD8</i> Suppression Model Leads to RAB11B Protein IncreaseGiulia Zarantonello, Michele Arnoldi, Michele Filosi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2010
Mammalian Pumilio 2 regulates dendrite morphogenesis and synaptic functionJohn P Vessey, Lucia Schoderboeck, Ewald Gingl, et al.
International Journal of Audiology|March 18, 2010
Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing lossViviana Chinetti, Sandra Iossa, Gennaro Auletta, et al.
The Journal of Biological Chemistry|June 11, 2002
Physical and functional interaction of HIV-1 Tat with E2F-4, a transcriptional regulator of mammalian cell cycleConcetta Ambrosino, Camillo Palmieri, Antimina Puca, et al.
International Journal of Molecular Sciences|November 11, 2022
Induced Pluripotent Stem Cell (iPSC) Lines from a Family with Resistant Epileptic Encephalopathy Caused by Compound Heterozygous Mutations in <i>SZT2</i> GeneCecilia Cattelani, Ingrid Battistella, Francesca Di Leva, et al.
International Journal of Audiology|December 9, 2003
Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian familiesFrancesca Di Leva, Adamo Pio D'Adamo, Luiaino Strollo, et al.
Audiology & Neuro-Otology|February 2, 2006
Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11)Francesca Di Leva, Pio D'Adamo, Maria Vittoria Cubellis, et al.
International Journal of Molecular Sciences|February 11, 2023
Increased Levels of the Parkinson's Disease-Associated Gene ITPKB Correlate with Higher Expression Levels of α-Synuclein, Independent of Mutation StatusFrancesca Di Leva, Michele Filosi, Lisa Oyston, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|May 17, 2005
Audiometric evaluation of carriers of the connexin 26 mutation 35delGAnnamaria Franzé, Antonella Caravelli, Francesca Di Leva, et al.
Cellular and Molecular Neurobiology|July 17, 2016
Transcriptomic Profiling Discloses Molecular and Cellular Events Related to Neuronal Differentiation in SH-SY5Y Neuroblastoma CellsFrancesco Pezzini, Laura Bettinetti, Francesca Di Leva, et al.
Frontiers in Genetics|December 9, 2021
Natural SINEUP RNAs in Autism Spectrum Disorders: <i>RAB11B-AS1</i> Dysregulation in a Neuronal <i>CHD8</i> Suppression Model Leads to RAB11B Protein IncreaseGiulia Zarantonello, Michele Arnoldi, Michele Filosi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2010
Mammalian Pumilio 2 regulates dendrite morphogenesis and synaptic functionJohn P Vessey, Lucia Schoderboeck, Ewald Gingl, et al.
International Journal of Audiology|March 18, 2010
Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing lossViviana Chinetti, Sandra Iossa, Gennaro Auletta, et al.
The Journal of Biological Chemistry|June 11, 2002
Physical and functional interaction of HIV-1 Tat with E2F-4, a transcriptional regulator of mammalian cell cycleConcetta Ambrosino, Camillo Palmieri, Antimina Puca, et al.
International Journal of Molecular Sciences|November 11, 2022
Induced Pluripotent Stem Cell (iPSC) Lines from a Family with Resistant Epileptic Encephalopathy Caused by Compound Heterozygous Mutations in <i>SZT2</i> GeneCecilia Cattelani, Ingrid Battistella, Francesca Di Leva, et al.
International Journal of Audiology|December 9, 2003
Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian familiesFrancesca Di Leva, Adamo Pio D'Adamo, Luiaino Strollo, et al.
Audiology & Neuro-Otology|February 2, 2006
Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11)Francesca Di Leva, Pio D'Adamo, Maria Vittoria Cubellis, et al.
International Journal of Molecular Sciences|February 11, 2023
Increased Levels of the Parkinson's Disease-Associated Gene ITPKB Correlate with Higher Expression Levels of α-Synuclein, Independent of Mutation StatusFrancesca Di Leva, Michele Filosi, Lisa Oyston, et al.
Pageof 3