Search Results - "DI LEVA, Francesca"

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

“…Arnica montana (Arnica m.) is used for its purported anti-inflammatory and tissue healing actions after trauma, bruises, or tissue injuries, but its cellular…”
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The plasma membrane Ca2+ ATPase of animal cells: structure, function and regulation by Di Leva, Francesca, Domi, Teuta, Fedrizzi, Laura, Lim, Dmitry, Carafoli, Ernesto

“…Most important processes in cell life are regulated by calcium (Ca2+). A number of mechanisms have thus been developed to maintain the concentration of free…”
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Transcriptomic Profiling Discloses Molecular and Cellular Events Related to Neuronal Differentiation in SH-SY5Y Neuroblastoma Cells by Pezzini, Francesco, Bettinetti, Laura, Di Leva, Francesca, Bianchi, Marzia, Zoratti, Elisa, Carrozzo, Rosalba, Santorelli, Filippo M., Delledonne, Massimo, Lalowski, Maciej, Simonati, Alessandro

“…Human SH-SY5Y neuroblastoma cells are widely utilized in in vitro studies to dissect out pathogenetic mechanisms of neurodegenerative disorders. These cells…”
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CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing by Kerschbamer, Emanuela, Arnoldi, Michele, Tripathi, Takshashila, Pellegrini, Miguel, Maturi, Samuele, Erdin, Serkan, Salviato, Elisa, Di Leva, Francesca, Sebestyén, Endre, Dassi, Erik, Zarantonello, Giulia, Benelli, Matteo, Campos, Eric, Basson, M Albert, Gusella, James F, Gustincich, Stefano, Piazza, Silvano, Demichelis, Francesca, Talkowski, Michael E, Ferrari, Francesco, Biagioli, Marta

“…Disruptive mutations in the chromodomain helicase DNA-binding protein 8 gene (CHD8) have been recurrently associated with autism spectrum disorders (ASDs)…”
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CAG repeat expansion in the Huntington’s disease gene shapes linear and circular RNAs biogenesis by Ayyildiz, Dilara, Bergonzoni, Guendalina, Monziani, Alan, Tripathi, Takshashila, Döring, Jessica, Kerschbamer, Emanuela, Di Leva, Francesca, Pennati, Elia, Donini, Luisa, Kovalenko, Marina, Zasso, Jacopo, Conti, Luciano, Wheeler, Vanessa C, Dieterich, Christoph, Piazza, Silvano, Dassi, Erik, Biagioli, Marta

“…Alternative splicing (AS) appears to be altered in Huntington’s disease (HD), but its significance for early, pre-symptomatic disease stages has not been…”
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D12 Faulty linear and back-splicing in Huntington’s disease: novel players in the pathologic process hint at innovative RNA biomarkers by Pellegrini, Miguel, Ayyildiz, Dilara, Bergonzoni, Guendalina, Monziani, Alan, Tripathi, Takshashila, Döring, Jessica, Cardamone, Giulia, Kerschbamer, Emanuela, Di Leva, Francesca, Perrone, F, Abruzzese, MP, Busi, LC, Asselta, Rosanna, Pennati, Elia, Donini, Luisa, Zasso, Jacopo, Conti, Luciano, Wheeler, Vanessa C, Dieterich, Christoph, Piazza, Silvano, Dassi, Erik, Squitieri, Ferdinando, Biagioli, Marta

“…Alternative Splicing (AS) is crucial for generating protein-coding isoforms and circular RNAs (circRNAs), stable non-coding RNA’s produced by circularization…”
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Induced Pluripotent Stem Cell (iPSC) Lines from a Family with Resistant Epileptic Encephalopathy Caused by Compound Heterozygous Mutations in SZT2 Gene by Cattelani, Cecilia, Battistella, Ingrid, Di Leva, Francesca, Fioravanti, Giulia, Benedicenti, Francesco, Stanzial, Franco, Schwienbacher, Christine, Fanelli, Francesca, Pramstaller, Peter P, Hicks, Andrew A, Conti, Luciano, Corti, Corrado

“…Mutations in the SZT2 gene have been associated with developmental and epileptic encephalopathy-18, a rare severe autosomal recessive neurologic disorder,…”
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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 by Di Leva, Francesca, Filosi, Michele, Oyston, Lisa, Silvestri, Erica, Picard, Anne, Lavdas, Alexandros A, Lobbestael, Evy, Baekelandt, Veerle, Neely, G Gregory, Pramstaller, Peter P, Hicks, Andrew A, Corti, Corrado

“…Autosomal dominant mutations in the gene encoding α-synuclein ( ) were the first to be linked with hereditary Parkinson's disease (PD). Duplication and…”
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Mammalian Pumilio 2 regulates dendrite morphogenesis and synaptic function by Vessey, John P, Schoderboeck, Lucia, Gingl, Ewald, Luzi, Ettore, Riefler, Julia, Di Leva, Francesca, Karra, Daniela, Thomas, Sabine, Kiebler, Michael A, Macchi, Paolo

“…In Drosophila, Pumilio (Pum) is important for neuronal homeostasis as well as learning and memory. We have recently characterized a mammalian homolog of Pum,…”
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Functional Specificity of PMCA Isoforms? by DOMI, TEUTA, LEVA, FRANCESCA DI, FEDRIZZI, LAURA, RIMESSI, ALESSANDRO, BRINI, MARISA

“…:  In mammals, four different genes encode four PMCA isoforms. PMCA1 and PMCA4 are expressed ubiquitously. PMCA2 and PMCA3 are expressed prevalently in the…”
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Natural SINEUP RNAs in Autism Spectrum Disorders: RAB11B-AS1 Dysregulation in a Neuronal CHD8 Suppression Model Leads to RAB11B Protein Increase by Zarantonello, Giulia, Arnoldi, Michele, Filosi, Michele, Tebaldi, Toma, Spirito, Giovanni, Barbieri, Anna, Gustincich, Stefano, Sanges, Remo, Domenici, Enrico, Di Leva, Francesca, Biagioli, Marta

“…CHD8 represents one of the highest confidence genetic risk factors implied in Autism Spectrum Disorders, with most mutations leading to CHD8 haploinsufficiency…”
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Characterization of 17 strains belonging to the Mycobacterium simiae complex and description of Mycobacterium paraense sp. nov by Fusco da Costa, Ana R, Fedrizzi, Tarcisio, Lopes, Maria L, Pecorari, Monica, Oliveira da Costa, Wana L, Giacobazzi, Elisabetta, da Costa Bahia, Jeann R, De Sanctis, Veronica, Batista Lima, Karla V, Bertorelli, Roberto, Grottola, Antonella, Fabio, Anna, Mariottini, Alessandro, Ferretti, Pamela, Di Leva, Francesca, Fregni Serpini, Giulia, Tagliazucchi, Sara, Rumpianesi, Fabio, Jousson, Olivier, Segata, Nicola, Tortoli, Enrico

“…Fourteen mycobacterial strains isolated from pulmonary samples of independent patients in the state of Pará (Brazil), and three strains isolated in Italy, were…”
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The Unexpected Tuners: Are LncRNAs Regulating Host Translation during Infections? by Knap, Primoz, Tebaldi, Toma, Di Leva, Francesca, Biagioli, Marta, Dalla Serra, Mauro, Viero, Gabriella

“…Pathogenic bacteria produce powerful virulent factors, such as pore-forming toxins, that promote their survival and cause serious damage to the host. Host…”
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Physical and Functional Interaction of HIV-1 Tat with E2F-4, a Transcriptional Regulator of Mammalian Cell Cycle by Ambrosino, Concetta, Palmieri, Camillo, Puca, Antimina, Trimboli, Francesca, Schiavone, Marco, Olimpico, Francesco, Ruocco, Maria R, di Leva, Francesca, Toriello, Mario, Quinto, Ileana, Venuta, Salvatore, Scala, Giuseppe

“…Tat protein of the human immunodeficiency virus type-1 (HIV-1) plays a critical role in the regulation of viral transcription and replication. In addition, Tat…”
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The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss by Spiden, Sarah L, Bortolozzi, Mario, Di Leva, Francesca, de Angelis, Martin Hrabé, Fuchs, Helmut, Lim, Dmitry, Ortolano, Saida, Ingham, Neil J, Brini, Marisa, Carafoli, Ernesto, Mammano, Fabio, Steel, Karen P

“…Progressive hearing loss is common in the human population, but we have few clues to the molecular basis. Mouse mutants with progressive hearing loss offer…”
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Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss by Chinetti, Viviana, Iossa, Sandra, Auletta, Gennaro, Laria, Carla, de Luca, Maria, Di Leva, Francesca, Riccardi, Pasquale, Giannini, Pasquale, Gasparini, Paolo, Ciccodicola, Alfredo, Marciano, Elio, Franzè, Annamaria

“…Abstract The aim of this study was to screen 349 patients affected by sensorineural hearing loss (SNHL), mostly from the Campania region (southern Italy), for…”
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The new phylogenesis of the genus Mycobacterium by Tortoli, Enrico, Fedrizzi, Tarcisio, Pecorari, Monica, Giacobazzi, Elisabetta, De Sanctis, Veronica, Bertorelli, Roberto, Grottola, Antonella, Fabio, Anna, Ferretti, Pamela, Di Leva, Francesca, Serpini, Giulia Fregni, Tagliazucchi, Sara, Rumpianesi, Fabio, Jousson, Olivier, Segata, Nicola

“…Abstract Phylogenetic knowledge of the genus Mycobacterium is based on comparative analysis of their genetic sequences. The 16S rRNA has remained for many…”
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Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11) by Di Leva, Francesca, D'Adamo, Pio, Cubellis, Maria Vittoria, D'Eustacchio, Angela, Errichiello, Monica, Saulino, Claudio, Auletta, Gennaro, Giannini, Pasquale, Donaudy, Francesca, Ciccodicola, Alfredo, Gasparini, Paolo, Franzè, Annamaria, Marciano, Elio

“…We ascertained a large Italian family with an autosomal dominant form of non-syndromic sensorineural hearing loss with vestibular involvement. A genome-wide…”
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Design and Delivery of SINEUP: A New Modular Tool to Increase Protein Translation by Arnoldi, Michele, Zarantonello, Giulia, Espinoza, Stefano, Gustincich, Stefano, Di Leva, Francesca, Biagioli, Marta

“…SINEUP is a new class of long non-coding RNAs (lncRNAs) which contain an inverted Short Interspersed Nuclear Element (SINE) B2 element (invSINEB2) necessary to…”
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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 by Di Leva, Francesca, Ferrante, Maria Immacolata, Demarchi, Francesca, Caravelli, Antonella, Matarazzo, Maria Rosaria, Giacca, Mauro, D'Urso, Michele, D'Esposito, Maurizio, Franzé, Annamaria

“…The synaptobrevin-like 1 (SYBL1) gene is ubiquitously expressed and codes for an unusual member of the v-SNAREs molecules implicated in cellular exocytosis…”
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