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Journal of Cellular and Molecular Medicine|April 24, 2020
Dysregulation of NIPBL leads to impaired RUNX1 expression and haematopoietic defectsMara Mazzola, Alex Pezzotta, Grazia Fazio, et al.
Human Genetics|May 16, 2024
Characterization of a novel HDAC2 pathogenetic variant: a missing puzzle piece for chromatinopathiesElisabetta Di Fede, Antonella Lettieri, Esi Taci, et al.
American Journal of Medical Genetics. Part A|March 10, 2022
Identical EP300 variant leading to Rubinstein-Taybi syndrome with different clinical and immunologic phenotypeFrancesco Saettini, Grazia Fazio, Maria Teresa Bonati, et al.
International Journal of Molecular Sciences|April 3, 2021
Insights into the Role of the Microbiota and of Short-Chain Fatty Acids in Rubinstein-Taybi SyndromeElisabetta Di Fede, Emerenziana Ottaviano, Paolo Grazioli, et al.
Journal of Cellular Physiology|July 25, 2015
CyclinD1 Down-Regulation and Increased Apoptosis Are Common Features of CohesinopathiesGrazia Fazio, Carles Gaston-Massuet, Laura Rachele Bettini, et al.
Haematologica|January 12, 2019
NIPBL: a new player in myeloid cell differentiationMara Mazzola, Gianluca Deflorian, Alex Pezzotta, et al.
Molecular Cancer Research : MCR|July 26, 2014
Cytoskeletal regulatory gene expression and migratory properties of B-cell progenitors are affected by the ETV6-RUNX1 rearrangementChiara Palmi, Grazia Fazio, Angela M Savino, et al.
Npj Aging|July 10, 2025
p300 inhibition delays premature cellular senescenceElisabetta Di Fede, Esi Taci, Silvia Castiglioni, et al.
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