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FEBS Letters|November 6, 2002
Structural and functional analysis of aldolase B mutants related to hereditary fructose intoleranceGabriella Esposito, Luigi Vitagliano, Rita Santamaria, et al.
Molecular Genetics & Genomic Medicine|September 19, 2020
A putative frameshift variant in the CHM gene is associated with an unexpected splicing alteration in a choroideremia patientTiziana Fioretti, Silvana Ungari, Maria Savarese, et al.
International Journal of Molecular Sciences|May 31, 2020
Phosphorylation Sites in Protein Kinases and Phosphatases Regulated by Formyl Peptide Receptor 2 SignalingMaria Carmela Annunziata, Melania Parisi, Gabriella Esposito, et al.
Journal of Paediatrics and Child Health|May 27, 2010
Aminotransferases and muscular diseases: a disregarded lesson. Case reports and review of the literatureClaudio Veropalumbo, Ennio Del Giudice, Gabriella Esposito, et al.
Open Biology|October 24, 2023
Formyl-peptide receptor 2 signalling triggers aerobic metabolism of glucose through Nox2-dependent modulation of pyruvate dehydrogenase activityTiziana Pecchillo Cimmino, Ester Pagano, Mariano Stornaiuolo, et al.
Antioxidants (Basel, Switzerland)|September 23, 2022
Formyl-Peptide Receptor 2 Signaling Redirects Glucose and Glutamine into Anabolic Pathways in Metabolic Reprogramming of Lung Cancer CellsTiziana Pecchillo Cimmino, Ester Pagano, Mariano Stornaiuolo, et al.
Italian Journal of Pediatrics|November 2, 2012
Fatty liver disease and hypertransaminasemia hiding the association of clinically silent Duchenne muscular dystrophy and hereditary fructose intoleranceGiulia Paolella, Pasquale Pisano, Raffaele Albano, et al.
Cellular Oncology (Dordrecht, Netherlands)|September 8, 2019
Crosstalk between 14-3-3θ and AF4 enhances MLL-AF4 activity and promotes leukemia cell proliferationTiziana Fioretti, Armando Cevenini, Mariateresa Zanobio, et al.
Diagnostics (Basel, Switzerland)|October 23, 2021
Comprehensive Molecular Analysis of DMD Gene Increases the Diagnostic Value of Dystrophinopathies: A Pilot Study in a Southern Italy Cohort of PatientsFatima Domenica Elisa De Palma, Marcella Nunziato, Valeria D'Argenio, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 3, 2013
A 15-year case-mix experience for fragile X syndrome molecular diagnosis and comparison between conventional and alternative techniques leading to a novel diagnostic procedureGabriella Esposito, Raffaella Ruggiero, Giovanni Savarese, et al.
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