Elisabetta Flex
Istituto Superiore di Sanità(IT)
Publications by Year
Research Areas
Protein Tyrosine Phosphatases, Galectins and Cancer Biology, RNA modifications and cancer, PI3K/AKT/mTOR signaling in cancer, Cellular transport and secretion
Most-Cited Works
- → Diversity and Functional Consequences of Germline and Somatic PTPN11 Mutations in Human Disease(2006)425 cited
- → Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair(2009)413 cited
- → Somatically acquired JAK1 mutations in adult acute lymphoblastic leukemia(2008)326 cited
- → Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome(2015)216 cited
- → Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases(2019)157 cited
- → Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis(2014)142 cited
- → Mutations ofZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot(2003)139 cited
- → A Functional Variant of the Adipocyte Glycerol Channel Aquaporin 7 Gene Is Associated With Obesity and Related Metabolic Abnormalities(2007)110 cited
- → A homozygousGJA1 gene mutation causes a Hallermann-Streiff/ODDD spectrum phenotype(2004)107 cited
- → The Functional Q84R Polymorphism of Mammalian Tribbles Homolog TRB3 Is Associated With Insulin Resistance and Related Cardiovascular Risk in Caucasians From Italy(2005)103 cited