Cozzi, Anna

Overexpression of Wild Type and Mutated Human Ferritin H-chain in HeLa Cells

Cozzi, A., Corsi, B., Levi, S., Santambrogio, P., Albertini, A., & Arosio, P. (2000) · Journal of Biological Chemistry

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 242

Mitochondrial ferritin limits oxidative damage regulating mitochondrial iron availability: hypothesis for a protective role in Friedreich ataxia

Campanella, A., Rovelli, E., Santambrogio, P., Cozzi, A., Taroni, F., & Levi, S. (2008) · Human Molecular Genetics

Mitochondrial Function and PathologyIron Metabolism and Disorders

Cited by 162

Analysis of the biologic functions of H- and L-ferritins in HeLa cells by transfection with siRNAs and cDNAs: evidence for a proliferative role of L-ferritin

Cozzi, A., Corsi, B., Levi, S., Santambrogio, P., Biasiotto, G., & Arosio, P. (2004) · Blood

Iron Metabolism and DisordersFerroptosis and cancer prognosis

Cited by 132

Characterization of nuclear ferritin and mechanism of translocation

SURGULADZE, N., PATTON, S., COZZI, A., FRIED, M. G., & CONNOR, J. R. (2005) · Biochemical Journal

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 81

Mutant Ferritin L-chains That Cause Neurodegeneration Act in a Dominant-negative Manner to Reduce Ferritin Iron Incorporation

Luscieti, S., Santambrogio, P., Langlois d'Estaintot, B., Granier, T., Cozzi, A., Poli, M., Gallois, B., Finazzi, D., Cattaneo, A., Levi, S., et al. (2010) · Journal of Biological Chemistry

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 51

Human L-ferritin deficiency is characterized by idiopathic generalized seizures and atypical restless leg syndrome

Cozzi, A., Santambrogio, P., Privitera, D., Broccoli, V., Rotundo, L. I., Garavaglia, B., Benz, R., Altamura, S., Goede, J. S., Muckenthaler, M. U., et al. (2013) · Journal of Experimental Medicine

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 47

Characterization of the l-ferritin variant 460InsA responsible of a hereditary ferritinopathy disorder

Cozzi, A., Santambrogio, P., Corsi, B., Campanella, A., Arosio, P., & Levi, S. (2006) · Neurobiology of Disease

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 38