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Journal of Medical Genetics|July 24, 2017
Identification of the first dominant mutation of LAMA5 gene causing a complex multisystem syndrome due to dysfunction of the extracellular matrixSimone Sampaolo, Filomena Napolitano, Alfonsina Tirozzi, et al.Human Molecular Genetics|January 30, 2022
Deregulation of microtubule organization and RNA metabolism in Arx models for lissencephaly and developmental epileptic encephalopathyDenise Drongitis, Marianna Caterino, Lucia Verrillo, et al.Human Molecular Genetics|November 7, 2019
Histone demethylase KDM5C is a SAHA-sensitive central hub at the crossroads of transcriptional axes involved in multiple neurodevelopmental disordersLoredana Poeta, Agnese Padula, Benedetta Attianese, et al.Bone Research|April 2, 2026
ADAR2 induces the differentiation of osteosarcoma cells by editing activity on IGFBP7: new implications for therapyMichela Rossi, Federica Scotto di Carlo, Jacopo Di Gregorio, et al.Pageof 7