Publications by authors named "Francesca Di Leva"

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SINEUP RNA rescues molecular phenotypes associated with CHD8 suppression in autism spectrum disorder model systems.
Francesca Di Leva, Michele Arnoldi, Stefania Santarelli, Mathieu Massonot, Marianne Victoria Lemée

Mol Ther· March 2025

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CAG repeat expansion in the Huntington's disease gene shapes linear and circular RNAs biogenesis.
Dilara Ayyildiz, Guendalina Bergonzoni, Alan Monziani, Takshashila Tripathi, Jessica Döring, Francesca Di Leva

PLoS Genet· October 2023

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Increased Levels of the Parkinson's Disease-Associated Gene ITPKB Correlate with Higher Expression Levels of α-Synuclein, Independent of Mutation Status.
Francesca Di Leva, Michele Filosi, Lisa Oyston, Erica Silvestri, Anne Picard

Int J Mol Sci· January 2023

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CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing.
Emanuela Kerschbamer, Michele Arnoldi, Takshashila Tripathi, Miguel Pellegrini, Samuele Maturi, Francesca Di Leva

Nucleic Acids Res· December 2022

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Induced Pluripotent Stem Cell (iPSC) Lines from a Family with Resistant Epileptic Encephalopathy Caused by Compound Heterozygous Mutations in Gene.
Cecilia Cattelani, Ingrid Battistella, Francesca Di Leva, Giulia Fioravanti, Francesco Benedicenti

Int J Mol Sci· October 2022

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Design and Delivery of SINEUP: A New Modular Tool to Increase Protein Translation.
Michele Arnoldi, Giulia Zarantonello, Stefano Espinoza, Stefano Gustincich, Francesca Di Leva

Methods Mol Biol· March 2022

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Natural SINEUP RNAs in Autism Spectrum Disorders: Dysregulation in a Neuronal Suppression Model Leads to RAB11B Protein Increase.
Giulia Zarantonello, Michele Arnoldi, Michele Filosi, Toma Tebaldi, Giovanni Spirito, Francesca Di Leva

Front Genet· November 2021

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The Unexpected Tuners: Are LncRNAs Regulating Host Translation during Infections?
Primoz Knap, Toma Tebaldi, Francesca Di Leva, Marta Biagioli, Mauro Dalla Serra

Toxins (Basel)· November 2017

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Epigenetics of Huntington's Disease.
Silvia Bassi, Takshashila Tripathi, Alan Monziani, Francesca Di Leva, Marta Biagioli

Adv Exp Med Biol· September 2017

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Arnica montana Stimulates Extracellular Matrix Gene Expression in a Macrophage Cell Line Differentiated to Wound-Healing Phenotype.
Marta Marzotto, Clara Bonafini, Debora Olioso, Anna Baruzzi, Laura Bettinetti, Francesca Di Leva

PLoS One· June 2017

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Transcriptomic Profiling Discloses Molecular and Cellular Events Related to Neuronal Differentiation in SH-SY5Y Neuroblastoma Cells.
Francesco Pezzini, Laura Bettinetti, Francesca Di Leva, Marzia Bianchi, Elisa Zoratti

Cell Mol Neurobiol· May 2017

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Characterization of 17 strains belonging to the Mycobacterium simiae complex and description of Mycobacterium paraense sp. nov.
Ana R Fusco da Costa, Tarcisio Fedrizzi, Maria L Lopes, Monica Pecorari, Wana L Oliveira da Costa, Francesca Di Leva

Int J Syst Evol Microbiol· February 2015

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The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in mice.
Mario Bortolozzi, Marisa Brini, Nick Parkinson, Giulia Crispino, Pietro Scimemi, Francesca Di Leva

J Biol Chem· November 2010

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Deletions and mutations in the acidic lipid-binding region of the plasma membrane Ca2+ pump: a study on different splicing variants of isoform 2.
Marisa Brini, Francesca Di Leva, Claudia K Ortega, Teuta Domi, Denis Ottolini

J Biol Chem· October 2010

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Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss.
Viviana Chinetti, Sandra Iossa, Gennaro Auletta, Carla Laria, Maria De Luca, Francesca Di Leva

Int J Audiol· April 2010

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Mammalian Pumilio 2 regulates dendrite morphogenesis and synaptic function.
John P Vessey, Lucia Schoderboeck, Ewald Gingl, Ettore Luzi, Julia Riefler, Francesca Di Leva

Proc Natl Acad Sci U S A· February 2010

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The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss.
Sarah L Spiden, Mario Bortolozzi, Francesca Di Leva, Martin Hrabé de Angelis, Helmut Fuchs

PLoS Genet· October 2008

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The plasma membrane Ca2+ ATPase of animal cells: structure, function and regulation.
Francesca Di Leva, Teuta Domi, Laura Fedrizzi, Dmitry Lim, Ernesto Carafoli

Arch Biochem Biophys· August 2008

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Inhibitory interaction of the 14-3-3 proteins with ubiquitous (PMCA1) and tissue-specific (PMCA3) isoforms of the plasma membrane Ca2+ pump.
Cristina I Linde, Francesca Di Leva, Teuta Domi, Silvio C E Tosatto, Marisa Brini

Cell Calcium· June 2008

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Functional specificity of PMCA isoforms?
Teuta Domi, Francesca Di Leva, Laura Fedrizzi, Alessandro Rimessi, Marisa Brini

Ann N Y Acad Sci· March 2007

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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, Angela D'Eustacchio, Monica Errichiello

Audiol Neurootol· May 2006

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Audiometric evaluation of carriers of the connexin 26 mutation 35delG.
Annamaria Franzé, Antonella Caravelli, Francesca Di Leva, Elio Marciano, Gennaro Auletta

Eur Arch Otorhinolaryngol· November 2005

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Down-regulation of otospiralin mRNA in response to acoustic stress in guinea pig.
Antonella Caravelli, Luigi Pianese, Claudio Saulino, Francesca Di Leva, Luigi Sequino

Hear Res· December 2004

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Human synaptobrevin-like 1 gene basal transcription is regulated through the interaction of selenocysteine tRNA gene transcription activating factor-zinc finger 143 factors with evolutionary conserved cis-elements.
Francesca Di Leva, Maria Immacolata Ferrante, Francesca Demarchi, Antonella Caravelli, Maria Rosaria Matarazzo

J Biol Chem· February 2004

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Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian families.
Francesca Di Leva, Adamo Pio D'Adamo, Luiaino Strollo, Gennaro Auletta, Antonella Caravelli

Int J Audiol· December 2003

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