Lorena Travaglini
Bambino Gesù Children's Hospital(IT)
Publications by Year
Research Areas
Hereditary Neurological Disorders, RNA modifications and cancer, Genomics and Rare Diseases, Neurogenetic and Muscular Disorders Research, RNA regulation and disease
Most-Cited Works
- → Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies(2009)409 cited
- → Epigenetic Silencing of the Myelopoiesis Regulator microRNA-223 by the AML1/ETO Oncoprotein(2007)384 cited
- → Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes(2010)282 cited
- → CEP290 Mutations Are Frequently Identified in the Oculo-Renal Form of Joubert Syndrome–Related Disorders(2007)156 cited
- → MEDNIK syndrome: a novel defect of copper metabolism treatable by zinc acetate therapy(2013)152 cited
- → Polycombs and microRNA-223 regulate human granulopoiesis by transcriptional control of target gene expression(2012)146 cited
- → Sequential Valproic Acid/All- trans Retinoic Acid Treatment Reprograms Differentiation in Refractory and High-Risk Acute Myeloid Leukemia(2006)121 cited
- → Exposure of normal and transformed cells to nevirapine, a reverse transcriptase inhibitor, reduces cell growth and promotes differentiation(2003)114 cited
- → MKS3/TMEM67mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement(2008)105 cited
- → Oxidative stress in Duchenne muscular dystrophy: focus on the NRF2 redox pathway(2017)101 cited