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International Journal of Molecular Sciences|July 9, 2022
LAM Cells as Potential Drivers of Senescence in Lymphangioleiomyomatosis MicroenvironmentClara Bernardelli, Silvia Ancona, Melania Lazzari, et al.
Genes, Chromosomes & Cancer|October 12, 2011
T-cell lymphoblastic lymphoma shows differences and similarities with T-cell acute lymphoblastic leukemia by genomic and gene expression analysesKatia Basso, Lara Mussolin, Antonella Lettieri, et al.
Birth Defects Research|July 10, 2024
Intrauterine growth in chromatinopathies: A long road for better understanding and for improving clinical managementLaura Avagliano, Silvia Castiglioni, Antonella Lettieri, et al.
Frontiers in Cell and Developmental Biology|October 13, 2022
Epigenetic disorders: Lessons from the animals-animal models in chromatinopathiesElisabetta Di Fede, Paolo Grazioli, Antonella Lettieri, et al.
Molecular and Cellular Endocrinology|June 27, 2017
Iron overload induces hypogonadism in male mice via extrahypothalamic mechanismsChiara Macchi, Liliana Steffani, Roberto Oleari, et al.
American Journal of Medical Genetics. Part A|April 5, 2025
Cohesins: Crossroad Between Cornelia de Lange Spectrum and Cancer PredispositionLaura Rigotti, Stefano Rebellato, Antonella Lettieri, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 19, 2022
Lack of ApoA-I in ApoEKO Mice Causes Skin Xanthomas, Worsening of Inflammation, and Increased Coronary Atherosclerosis in the Absence of HyperlipidemiaMarco Busnelli, Stefano Manzini, Alice Colombo, 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.
Genes|March 25, 2022
<i>KMT2A</i>: Umbrella Gene for Multiple DiseasesSilvia Castiglioni, Elisabetta Di Fede, Clara Bernardelli, et al.
Orphanet Journal of Rare Diseases|December 20, 2024
Expanding the clinical spectrum of PPP3CA variants - alternative isoforms matterSilvia Castiglioni, Laura Pezzoli, Lidia Pezzani, et al.
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