Editorial: Inherited and acquired ribosomopathies: missing puzzle pieces

by Roberto Valli, Marianna Penzo
Published 2023-04-01

Soybean Meal-Dependent Intestinal Inflammation Induces Different Patterns of Bone-Loss in Adult Zebrafish Scale

by Marta Carnovali, Roberto Valli, Giuseppe Banfi, Giovanni Porta, Massimo Mariotti
Published 2021-04-01

The Potential Role of the T2 Ribonucleases in TME-Based Cancer Therapy

by Paola Campomenosi, Lorenzo Mortara, Barbara Bassani, Roberto Valli, Giovanni Porta, Antonino Bruno, Francesco Acquati
Published 2023-08-01

Human RNASET2: A Highly Pleiotropic and Evolutionary Conserved Tumor Suppressor Gene Involved in the Control of Ovarian Cancer Pathogenesis

by Antonino Bruno, Douglas M. Noonan, Roberto Valli, Giovanni Porta, Roberto Taramelli, Lorenzo Mortara, Francesco Acquati
Published 2022-08-01

Counteracting the Common Shwachman–Diamond Syndrome-Causing <i>SBDS</i> c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing

by Laura Peretto, Elena Tonetto, Iva Maestri, Valentino Bezzerri, Roberto Valli, Marco Cipolli, Mirko Pinotti, Dario Balestra
Published 2023-02-01

A Cell-Autonomous Oncosuppressive Role of Human RNASET2 Affecting ECM-Mediated Oncogenic Signaling

by Francesca Roggiani, Cristina Riva, Francesco Raspagliesi, Giovanni Porta, Roberto Valli, Roberto Taramelli, Francesco Acquati, Delia Mezzanzanica, Antonella Tomassetti
Published 2019-02-01

Chromosome Missegregation in Single Human Oocytes Is Related to the Age and Gene Expression Profile

by Stefano Barone, Patrizia Sarogni, Roberto Valli, Maria Michela Pallotta, Gazzi Silvia, Annalisa Frattini, Abdul Waheed Khan, Erika Rapalini, Cristiana Parri, Antonio Musio
Published 2020-03-01

Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia

by Claudio Azzolini, Simone Donati, Giovanni Micheloni, Vittoria Moretti, Roberto Valli, Francesco Acquati, Lucy Costantino, Fulvio Ferrara, Davide Borroni, Elias Premi, Francesco Testa, Francesca Simonelli, Giovanni Porta
Published 2021-01-01

<i>OTX</i> Genes in Adult Tissues

by Alessandro Terrinoni, Giovanni Micheloni, Vittoria Moretti, Sabrina Caporali, Sergio Bernardini, Marilena Minieri, Massimo Pieri, Cristina Giaroni, Francesco Acquati, Lucy Costantino, Fulvio Ferrara, Roberto Valli, Giovanni Porta
Published 2023-11-01

The synergism of SMC1A cohesin gene silencing and bevacizumab against colorectal cancer

by Maddalena Di Nardo, Simonetta Astigiano, Silvia Baldari, Maria Michela Pallotta, Giovanni Porta, Simona Pigozzi, Annalisa Antonini, Laura Emionite, Annalisa Frattini, Roberto Valli, Gabriele Toietta, Silvia Soddu, Antonio Musio
Published 2024-02-01

Case Report: Heterozygous Germline Variant in EIF6 Additional to Biallelic SBDS Pathogenic Variants in a Patient With Ribosomopathy Shwachman–Diamond Syndrome

by Ibrahim Taha, Selena Foroni, Roberto Valli, Annalisa Frattini, Annalisa Frattini, Pamela Roccia, Giovanni Porta, Marco Zecca, Elena Bergami, Marco Cipolli, Francesco Pasquali, Cesare Danesino, Claudia Scotti, Antonella Minelli
Published 2022-08-01

DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation.

by Elizabeth Nacheva, Katya Mokretar, Aynur Soenmez, Alan M Pittman, Colin Grace, Roberto Valli, Ayesha Ejaz, Selina Vattathil, Emanuela Maserati, Henry Houlden, Jan-Willem Taanman, Anthony H Schapira, Christos Proukakis
Published 2017-01-01

Homeoprotein OTX1 and OTX2 involvement in rat myenteric neuron adaptation after DNBS-induced colitis

by Michela Bistoletti, Giovanni Micheloni, Nicolò Baranzini, Annalisa Bosi, Andrea Conti, Viviana Filpa, Cristina Pirrone, Giorgia Millefanti, Elisabetta Moro, Annalisa Grimaldi, Roberto Valli, Andreina Baj, Francesca Crema, Cristina Giaroni, Giovanni Porta
Published 2020-02-01

Enhanced p53 Levels Are Involved in the Reduced Mineralization Capacity of Osteoblasts Derived from Shwachman–Diamond Syndrome Subjects

by Annalisa Frattini, Simona Bolamperti, Roberto Valli, Marco Cipolli, Rita Maria Pinto, Elena Bergami, Maria Rita Frau, Simone Cesaro, Michela Signo, Valentino Bezzerri, Giovanni Porta, Abdul Waheed Khan, Alessandro Rubinacci, Isabella Villa
Published 2021-12-01

Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)

by Emanuela Maserati, Claudio Panarello, Cristina Morerio, Roberto Valli, Barbara Pressato, Francesco Patitucci, Elisa Tassano, Alessandra Di Cesare-Merlone, Chiara Cugno, Carlo L. Balduini, Francesco Lo Curto, Carlo Dufour, Franco Locatelli, Francesco Pasquali
Published 2008-08-01

Occurrence of L1M Elements in Chromosomal Rearrangements Associated to Chronic Myeloid Leukemia (CML): Insights from Patient-Specific Breakpoints Characterization

by Alberto L’Abbate, Vittoria Moretti, Ester Pungolino, Giovanni Micheloni, Roberto Valli, Annalisa Frattini, Matteo Barcella, Francesco Acquati, Rolland A Reinbold, Lucy Costantino, Fulvio Ferrara, Alessandra Trojani, Mario Ventura, Giovanni Porta, Roberto Cairoli
Published 2023-06-01

The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations

by Abdul Waheed Khan, Alyssa Kennedy, Elissa Furutani, Kasiani Myers, Annalisa Frattini, Francesco Acquati, Pamela Roccia, Giovanni Micheloni, Antonella Minelli, Giovanni Porta, Marco Cipolli, Simone Cesaro, Cesare Danesino, Francesco Pasquali, Akiko Shimamura, Roberto Valli
Published 2021-11-01

Donor Cell Acute Myeloid Leukemia after Hematopoietic Stem Cell Transplantation for Chronic Granulomatous Disease: A Case Report and Literature Review

by Giovanni Micheloni, Annalisa Frattini, Marta Donini, Stefano Dusi, Anna Leszl, Annamaria Di Meglio, Martina Pigazzi, Antonio Musio, Marco Zecca, Tommaso Mina, Marco Rabusin, Pamela Roccia, Paolo Bernasconi, Irene Dambruoso, Antonella Minelli, Giuseppe Montalbano, Francesco Acquati, Giovanni Porta, Roberto Valli, Francesco Pasquali
Published 2023-11-01

Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or nor...

by Abdul Waheed Khan, Antonella Minelli, Annalisa Frattini, Giuseppe Montalbano, Alessia Bogni, Marco Fabbri, Giovanni Porta, Francesco Acquati, Rita Maria Pinto, Elena Bergami, Rossella Mura, Anna Pegoraro, Simone Cesaro, Marco Cipolli, Marco Zecca, Cesare Danesino, Franco Locatelli, Emanuela Maserati, Francesco Pasquali, Roberto Valli
Published 2020-01-01