Mitro, Nico

Lipids in the nervous system: From biochemistry and molecular biology to patho-physiology

Cermenati, G., Mitro, N., Audano, M., Melcangi, R. C., Crestani, M., De Fabiani, E., & Caruso, D. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids

Sphingolipid Metabolism and SignalingLipid metabolism and biosynthesis

Cited by 137

The ATP-binding cassette transporter A1 regulates phosphoantigen release and Vγ9Vδ2 T cell activation by dendritic cells

Castella, B., Kopecka, J., Sciancalepore, P., Mandili, G., Foglietta, M., Mitro, N., Caruso, D., Novelli, F., Riganti, C., & Massaia, M. (2017) · Nature Communications

Immunotherapy and Immune ResponsesT-cell and B-cell Immunology

Cited by 82

Epigenome modifiers and metabolic rewiring: New frontiers in therapeutics

Ferrari, A., Longo, R., Silva, R., Mitro, N., Caruso, D., De Fabiani, E., & Crestani, M. (2019) · Pharmacology & Therapeutics

Epigenetics and DNA MethylationMetabolomics and Mass Spectrometry Studies

Cited by 19

Sustained activation of detoxification pathways promotes liver carcinogenesis in response to chronic bile acid-mediated damage

Collino, A., Termanini, A., Nicoli, P., Diaferia, G., Polletti, S., Recordati, C., Castiglioni, V., Caruso, D., Mitro, N., Natoli, G., et al. (2018) · PLOS Genetics

Drug Transport and Resistance MechanismsLiver physiology and pathology

Cited by 13

Spinocerebellar ataxia 38: structure–function analysis shows ELOVL5 G230V is proteotoxic, conformationally altered and a mutational hotspot

Ferrero, E., Di Gregorio, E., Ferrero, M., Ortolan, E., Moon, Y.-A., Di Campli, A., Pavinato, L., Mancini, C., Tripathy, D., Manes, M., et al. (2023) · Human Genetics

Genetic Neurodegenerative DiseasesHereditary Neurological Disorders

Cited by 9

Spinocerebellar ataxia 38: structure-function analysis shows ELOVL5 G230V is proteotoxic, conformationally altered and a mutational hotspot

Ferrero, E., Gregorio, E. D., Ferrero, M., Ortolan, E., Moon, Y.-A., Campli, A. D., Pavinato, L., Mancini, C., Tripathy, D., Manes, M., et al. (2023) · Human Genetics

Genetic Neurodegenerative DiseasesHereditary Neurological Disorders

Cited by 9