UCP2 transports C4 metabolites out of mitochondria, regulating glucose and glutamine oxidation A Vozza, G Parisi, F De Leonardis, FM Lasorsa, A Castegna, D Amorese, ... Proceedings of the National Academy of Sciences 111 (3), 960-965, 2014 | 396 | 2014 |
A fourth ADP/ATP carrier isoform in man: identification, bacterial expression, functional characterization and tissue distribution V Dolce, P Scarcia, D Iacopetta, F Palmieri FEBS letters 579 (3), 633-637, 2005 | 289 | 2005 |
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1 L Palmieri, V Papaleo, V Porcelli, P Scarcia, L Gaita, R Sacco, J Hager, ... Molecular psychiatry 15 (1), 38-52, 2010 | 242 | 2010 |
Identification and functional reconstitution of the yeast peroxisomal adenine nucleotide transporter L Palmieri, H Rottensteiner, W Girzalsky, P Scarcia, F Palmieri, ... The EMBO journal, 2001 | 229 | 2001 |
Complete loss-of-function of the heart/muscle-specific adenine nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathy L Palmieri, S Alberio, I Pisano, T Lodi, M Meznaric-Petrusa, J Zidar, ... Human molecular genetics 14 (20), 3079-3088, 2005 | 206 | 2005 |
Identification of mitochondrial carriers in Saccharomyces cerevisiae by transport assay of reconstituted recombinant proteins F Palmieri, G Agrimi, E Blanco, A Castegna, MA Di Noia, V Iacobazzi, ... Biochimica et biophysica acta (BBA)-Bioenergetics 1757 (9-10), 1249-1262, 2006 | 181 | 2006 |
The human gene SLC25A17 encodes a peroxisomal transporter of coenzyme A, FAD and NAD+ G Agrimi, A Russo, P Scarcia, F Palmieri Biochemical Journal 443 (1), 241-247, 2012 | 161 | 2012 |
Identification and functional characterization of a novel mitochondrial carrier for citrate and oxoglutarate in Saccharomyces cerevisiae A Castegna, P Scarcia, G Agrimi, L Palmieri, H Rottensteiner, I Spera, ... Journal of Biological Chemistry 285 (23), 17359-17370, 2010 | 138 | 2010 |
Epistasis-driven identification of SLC25A51 as a regulator of human mitochondrial NAD import E Girardi, G Agrimi, U Goldmann, G Fiume, S Lindinger, V Sedlyarov, ... Nature communications 11 (1), 6145, 2020 | 93 | 2020 |
Mutations in AAC2, equivalent to human adPEO-associated ANT1 mutations, lead to defective oxidative phosphorylation in Saccharomyces cerevisiae and affect … F Fontanesi, L Palmieri, P Scarcia, T Lodi, C Donnini, A Limongelli, ... Human Molecular Genetics 13 (9), 923-934, 2004 | 92 | 2004 |
Diseases Caused by Mutations in Mitochondrial Carrier Genes SLC25: A Review F Palmieri, P Scarcia, M Monné Biomolecules 10 (4), 655, 2020 | 90 | 2020 |
Mutations in the mitochondrial citrate carrier SLC25A1 are associated with impaired neuromuscular transmission A Chaouch, V Porcelli, D Cox, S Edvardson, P Scarcia, A De Grassi, ... Journal of neuromuscular diseases 1 (1), 75-90, 2014 | 85 | 2014 |
KRAS-regulated glutamine metabolism requires UCP2-mediated aspartate transport to support pancreatic cancer growth S Raho, L Capobianco, R Malivindi, A Vozza, C Piazzolla, F De Leonardis, ... Nature Metabolism 2 (12), 1373-1381, 2020 | 81 | 2020 |
The mitochondrial citrate carrier in Yarrowia lipolytica: Its identification, characterization and functional significance for the production of citric acid EY Yuzbasheva, G Agrimi, TV Yuzbashev, P Scarcia, EB Vinogradova, ... Metabolic engineering 54, 264-274, 2019 | 70 | 2019 |
Agenesis of corpus callosum and optic nerve hypoplasia due to mutations in SLC25A1 encoding the mitochondrial citrate transporter S Edvardson, V Porcelli, C Jalas, D Soiferman, Y Kellner, A Shaag, ... Journal of Medical Genetics 50 (4), 240-245, 2013 | 69 | 2013 |
Peroxisomes as novel players in cell calcium homeostasis FM Lasorsa, P Pinton, L Palmieri, P Scarcia, H Rottensteiner, R Rizzuto, ... Journal of Biological Chemistry 283 (22), 15300-15308, 2008 | 64 | 2008 |
The yeast peroxisomal adenine nucleotide transporter: characterization of two transport modes and involvement in ΔpH formation across peroxisomal membranes FM Lasorsa, P Scarcia, R Erdmann, F Palmieri, H Rottensteiner, ... Biochemical Journal 381 (Pt 3), 581, 2004 | 51 | 2004 |
SLC25A10 biallelic mutations in intractable epileptic encephalopathy with complex I deficiency G Punzi, V Porcelli, M Ruggiu, MF Hossain, A Menga, P Scarcia, ... Human Molecular Genetics 27 (3), 499-504, 2018 | 46 | 2018 |
Statins, fibrates and retinoic acid upregulate mitochondrial acylcarnitine carrier gene expression V Iacobazzi, P Convertini, V Infantino, P Scarcia, S Todisco, F Palmieri Biochemical and Biophysical Research Communications 388 (4), 643-647, 2009 | 43 | 2009 |
Identification of a novel Sp1 splice variant as a strong transcriptional activator V Infantino, P Convertini, F Iacobazzi, I Pisano, P Scarcia, V Iacobazzi Biochemical and biophysical research communications 412 (1), 86-91, 2011 | 38 | 2011 |