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Dario Balestra

Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 14

Top Venues

International journal of molecular sciences

Molecular medicine (Cambridge, Mass.)

Human mutation

PLoS genetics

Università degli Studi di Ferrara (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Università degli Studi di Ferrara Jan 1o 2009 - Dec 31o 2011

Italy

PHD :: Department of Molecular Biology

Publications

Laura Peretto, Elena Tonetto, Iva Maestri, Valentino Bezzerri, Roberto Valli, Marco Cipolli, Mirko Pinotti, Dario Balestra
Counteracting the Common Shwachman-Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing. International journal of molecular sciences 24 (4) (2023)
Laura Peretto, Elena Tonetto, Iva Maestri, Valentino Bezzerri, Roberto Valli, Marco Cipolli, Mirko Pinotti, Dario Balestra
Counteracting the Common Shwachman-Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing. International journal of molecular sciences 24 (4) (2023)
Laura Peretto, Elena Tonetto, Iva Maestri, Valentino Bezzerri, Roberto Valli, Marco Cipolli, Mirko Pinotti, Dario Balestra
Counteracting the Common Shwachman-Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing. International journal of molecular sciences 24 (4) (2023)
Barbara Lunghi, Nicole Ziliotto, Dario Balestra, Lucrezia Rossi, Patrizia Della Valle, Pasquale Pignatelli, Mirko Pinotti, Armando D'Angelo, Giovanna Marchetti, Francesco Bernardi
Whole-Exome Sequencing in a Family with an Unexplained Tendency for Venous Thromboembolism: Multicomponent Prediction of Low-Frequency Variant Deleteriousness and of Individual Protein Interaction. International journal of molecular sciences 24 (18) (2023)
Laura Peretto, Elena Tonetto, Iva Maestri, Valentino Bezzerri, Roberto Valli, Marco Cipolli, Mirko Pinotti, Dario Balestra
Counteracting the Common Shwachman-Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing. International journal of molecular sciences 24 (4) (2023)
Laura Peretto, Elena Tonetto, Iva Maestri, Valentino Bezzerri, Roberto Valli, Marco Cipolli, Mirko Pinotti, Dario Balestra
Counteracting the Common Shwachman-Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing. International journal of molecular sciences 24 (4) (2023)
Angelisa Frasca, Efterpi Pavlidou, Matteo Bizzotto, Yunan Gao, Dario Balestra, Mirko Pinotti, Hans Atli Dahl, Nicholas D Mazarakis, Nicoletta Landsberger, Maria Kinali
Not Just Loss-of-Function Variations: Identification of a Hypermorphic Variant in a Patient With a CDKL5 Missense Substitution. Neurology. Genetics 8 (2) (2022)
Claudia Sacchetto, Laura Peretto, Francisco Baralle, Iva Maestri, Francesca Tassi, Francesco Bernardi, Stan F J van de Graaf, Franco Pagani, Mirko Pinotti, Dario Balestra
OTC intron 4 variations mediate pathogenic splicing patterns caused by the c.386G>A mutation in humans and spf ash mice, and govern susceptibility to RNA-based therapies. Molecular medicine (Cambridge, Mass.) 27 (1) (2021)
Dario Balestra, Daniela Scalet, Mattia Ferrarese, Silvia Lombardi, Nicole Ziliotto, Chrystal C Croes, Naomi Petersen, Piter Bosma, Federico Riccardi, Franco Pagani, Mirko Pinotti, Stan F J van de Graaf
A Compensatory U1snRNA Partially Rescues FAH Splicing and Protein Expression in a Splicing-Defective Mouse Model of Tyrosinemia Type I. International journal of molecular sciences 21 (6) (2020)
Dario Balestra, Mattia Ferrarese, Silvia Lombardi, Nicole Ziliotto, Alessio Branchini, Naomi Petersen, Piter Bosma, Mirko Pinotti, Stan F J van de Graaf
An Exon-Specific Small Nuclear U1 RNA (ExSpeU1) Improves Hepatic OTC Expression in a Splicing-Defective spf/ash Mouse Model of Ornithine Transcarbamylase Deficiency. International journal of molecular sciences 21 (22) (2020)
Dario Balestra, Alessio Branchini
Molecular Mechanisms and Determinants of Innovative Correction Approaches in Coagulation Factor Deficiencies. International journal of molecular sciences 20 (12) (2019)
Dario Balestra, Domenico Giorgio, Matteo Bizzotto, Sandro Sonnino, Bruria Ben Zeev, Mirko Pinotti, Nicoletta Landsberger, Angelisa Frasca
Splicing Mutations Impairing CDKL5 Expression and Activity Can be Efficiently Rescued by U1snRNA-Based Therapy. International journal of molecular sciences 20 (17) (2019)
Daniela Scalet, Iva Maestri, Alessio Branchini, Francesco Bernardi, Mirko Pinotti, Dario Balestra
Disease-causing variants of the conserved +2T of 5' splice sites can be rescued by engineered U1snRNAs. Human mutation 40 (1) (2018)
Mojca Tajnik, Malgorzata Ewa Rogalska, Erica Bussani, Elena Barbon, Dario Balestra, Mirko Pinotti, Franco Pagani
Molecular Basis and Therapeutic Strategies to Rescue Factor IX Variants That Affect Splicing and Protein Function. PLoS genetics 12 (5) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Dario Balestra