Showing results (21-30 of 59) with videos related to
Sort By:
Pageof 6
Clinical Chemistry and Laboratory Medicine|June 5, 2013
Prenatal molecular diagnosis of inherited neuromuscular diseases: Duchenne/Becker muscular dystrophy, myotonic dystrophy type 1 and spinal muscular atrophyGabriella Esposito, Raffaella Ruggiero, Maria Savarese, et al.Antioxidants (Basel, Switzerland)|February 24, 2024
Formyl Peptide Receptor 2-Dependent cPLA2 and 5-LOX Activation Requires a Functional NADPH OxidaseTiziana Pecchillo Cimmino, Iolanda Panico, Simona Scarano, et al.Journal of Human Genetics|September 8, 2017
Precise mapping of 17 deletion breakpoints within the central hotspot deletion region (introns 50 and 51) of the DMD geneGabriella Esposito, Maria Roberta Tremolaterra, Evelina Marsocci, et al.Diagnostics (Basel, Switzerland)|December 1, 2020
Multi-Gene Next-Generation Sequencing for Molecular Diagnosis of Autosomal Recessive Congenital Ichthyosis: A Genotype-Phenotype Study of Four Italian PatientsTiziana Fioretti, Luigi Auricchio, Angelo Piccirillo, et al.International Journal of Molecular Sciences|April 30, 2021
Nuclear FGFR2 Interacts with the MLL-AF4 Oncogenic Chimera and Positively Regulates HOXA9 Gene Expression in t(4;11) Leukemia CellsTiziana Fioretti, Armando Cevenini, Mariateresa Zanobio, et al.The Biochemical Journal|May 18, 2011
Protein network study of human AF4 reveals its central role in RNA Pol II-mediated transcription and in phosphorylation-dependent regulatory mechanismsGabriella Esposito, Armando Cevenini, Alessandro Cuomo, et al.Scientific Reports|December 1, 2019
Phosphoproteomic analysis sheds light on intracellular signaling cascades triggered by Formyl-Peptide Receptor 2Fabio Cattaneo, Rosita Russo, Martina Castaldo, et al.The Biochemical Journal|February 10, 2004
Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme functionGabriella Esposito, Luigi Vitagliano, Paola Costanzo, et al.Cell Biochemistry and Function|August 18, 2022
MiR-27a downregulates 14-3-3θ, RUNX1, AF4, and MLL-AF4, crucial drivers of blast transformation in t(4;11) leukemia cellsTiziana Fioretti, Mariateresa Zanobio, Maddalena Raia, et al.Genes|November 27, 2025
Clinical and Molecular Findings in PROM1-Associated Inherited Retinal DystrophiesFabiana D'Esposito, Caterina Gagliano, Sabrina Vallone, et al.Pageof 6