Profilo personale

Claudia Provenzano

Le informazioni pubblicate in questa pagina sono gestite in completa autonomia da CLAUDIA PROVENZANO il/la quale se ne assume ogni responsabilità

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Telefono: 06 90091361

Prodotti della ricerca

B. Cardinali (1), C. Provenzano (1), Mariapaola Izzo (1), C. Voellenkle (2), J. Battistini (1), G. Strimpakos (1), E. Golini (1), S. Mandillo (1), F. Scavizzi (1), M. Raspa (1), A. Perfetti (2), D. Baci (2), D. Lazarevic (3), J. Garcia-Manteiga (3), G. Gourdon (4) F. Martelli (2), G. Falcone (1)

Inducible CRISPR/Cas9 strategy mediates efficient gene editing of trinucleotide repeat expansion in DMPK locus

(2021) Pathogenesis and Therapies of Neuromuscular Diseases, 18th Interuniversitary Institute of Myology (IIM) Meeting, On-line, 22-24 Ottobre 2021
Beatrice Cardinali 1, Claudia Provenzano 1, Mariapaola Izzo 1, Jonathan Battistini 1, Georgios Strimpakos 1, Elisabetta Golini 1, Silvia Mandillo*1, Ferdinando Scavizzi 1, Marcello Raspa 1, Christine Voellenkle 2, Alessandra Perfetti 2, Denisa Baci 2, Fabio Martelli 2, Genevieve Gourdon 3, Germana Falcone 1

Gene Therapy Strategies For Myotonic Dystrophy Type 1

(2021) "Mechanistic Insights into Neurological Disorders and New Therapeutic Strategies", DSB Conference, CNR Rome, Italy, 07-08/07/2021
Raul Ondono , Ángel Lirio , Carlos Elvira , Elena Álvarez-Marimon , Claudia Provenzano , Beatrice Cardinali , Manuel Pérez-Alonso, Alex Perálvarez-Marín , José I. Borrell , Germana Falcone , Roger Estrada-Tejedor

Design of novel small molecule base-pair recognizers of toxic CUG RNA transcripts characteristics of DM1

Raul Ondono , Ángel Lirio , Carlos Elvira , Elena Álvarez-Marimon , Claudia Provenzano , Beatrice Cardinali , Manuel Pérez-Alonso, Alex Perálvarez-Marín , José I. Borrell , Germana Falcone , (2020) in Computational and Structural Biotechnology Journal
Provenzano C.[1], Cardinali B.[1], Perfetti A.[2], Mandillo S.[1], Golini E.[1], Strimpakos G.[1], Voellenkle C.[2], Longo M.[2], Martelli F.[2], Falcone G. [1]

GENE EDITING IN MYOTONIC DYSTROPHY TYPE 1: ASSESSMENT OF EFFICIENCY, SAFETY AND THERAPEUTIC EFFECT OF CTG-REPEAT DELETION IN A MOUSE MODEL OF DISEASE

(2019) XX Scientific Convention Telethon, Riva del Garda (TN), 28-30/10/2019
Cappella, Marisa; Perfetti, Alessandra; Cardinali, Beatrice; Garcia-Manteiga, Jose Manuel; Carrara, Matteo; Provenzano, Claudia; Fuschi, Paola; Cardani, Rosanna; Renna, Laura Valentina; Meola, Giovanni; Falcone, Germana; Martelli, Fabio

High-throughput analysis of the RNAinduced silencing complex in myotonic dystrophy type 1 patients identifies the dysregulation of miR-29c and its target ASB2

(2018) in Cell death and disease
Claudia Provenzano (1,8), Marisa Cappella (1,2,8), Rea Valaperta (3), Rosanna Cardani (4), Giovanni Meola (5,6), Fabio Martelli (7) Beatrice Cardinali (1) and Germana Falcone(1)

CRISPR/Cas9-MediatedDeletion ofCTGExpansions Recovers Normal Phenotype in Myogenic Cells Derived from Myotonic Dystrophy 1 Patients

Claudia Provenzano (1,8), Marisa Cappella (1,2,8), Rea Valaperta (3), Rosanna Cardani (4), Giovanni Meola (5,6), Fabio Martelli (7) (2017) in MOLECULAR THERAPY-NUCLEIC ACIDS
C. Provenzano (1) M. Cappella (1) (2) R. Valaperta (3) R. Cardani (3) G. Meola (3) (4) F. Martelli (3) B. Cardinali (1) G. Falcone (1)

CRISPR/Cas9-mediated genomic deletions of trinucleotide repeats in Myotonic Dystrophy type 1: a new tool for gene therapy?

C. Provenzano (1) M. Cappella (1) (2) R. Valaperta (3) R. Cardani (3) G. Meola (3) (4) F. Martelli (3) B. Cardinali (1) (2017) CRISPR: From Biology to Technology and Novel Therapeutics, 22-24/10/2017
Claudia Provenzano a, Michela Zamboni a, Liana Venezianob, Elide Mantuano b, Barbara Garavaglia c, Giovanna Zorzi d, Javier Pagonabarraga e, Paola Giunti f, Donato Civitareale a

Functional characterization of two novel mutations in TTF-1/NKX2.1 homeodomain in patients with benign hereditary chorea

(2016) in Journal of the neurological sciences
Cardinali B, Cappella M, Provenzano C, Garcia-Manteiga JM, Lazarevic D, Cittaro D, Martelli F, Falcone G.

MicroRNA-222 regulates muscle alternative splicing through Rbm24 during differentiation of skeletal muscle cells

(2016) in Cell death and disease
Montalban E.; Mattugini N.; Ciarapica R.; Provenzano C.; Savino M.; Scagnoli F.; Prosperini G.; Carissimi C.; Fulci V.; Matrone C.; Calissano P.; Nasi S.

MiR-21 is an Ngf-modulated MicroRNA That supports Ngf signaling and regulates neuronal degeneration in PC12 cells

(2014) in Neuromolecular medicine
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