Pubblicazioni


2018

Colabufo NA, Contino M, Cantore M, Berardi F, Perrone R, Tonazzi A, Console L, Panaro MA, Savolainen H and Luurtsema G.

An innovative small molecule for promoting neuroreparative strategie. RSC Adv. (2018) 8: 5451-5458

2018

Scalera V, Giangregorio N, De Leonardis S, Console L, Carulli ES, Tonazzi A.

Characterization of a novel Mitochondrial Ascorbate Transporter from rat liver and potato mitochondria. Front Mol Biosci (2018) 5: 1-9

2018

Console L, Scalise M, Tonazzi A, Giangregorio N, Indiveri C,

Characterization of Exosomal SLC22A5 (OCTN2) carnitine transporter. Sci Rep (2018) 8, 3758

2018

Pisani L, De Palma A, Giangregorio N, Miniero DV, Pesce P, Nicolotti O, Campagna F, Altomare CD, Catto M,

Mannich base approach to 5-methoxyisatin 3-(4-isopropylphenyl)hydrazone: A water-soluble prodrug for a multitarget inhibition of cholinesterases, beta-amyloid fibrillization and oligomer-induced cytotoxicity, Eu J Pharm Sci (2017) 109: 381-388

2018

Caracausi M, Ghini V, Locatelli C, Mericio M, Piovesan A, Antonaros F, Pelleri MC, Vitale L, Vacca RA, Bedetti F, Mimmi MC, Luchinat C, Turano P, Strippoli P, Cocchi G.

Plasma and urinary metabolomic profiles of Down syndrome correlate with alteration of mitochondrial metabolism. Sci Rep. 8:2977.

2018

Nabavi SF, Sureda A, Dehpour AR, Shirooie S, Silva AS, Devi KP, Ahmed T, Ishaq N, Hashim R, Sobarzo-S�nchez E, Daglia M, Braidy N, Volpicella M, Vacca RA, Nabavi SM.

Regulation of autophagy by polyphenols: Paving the road for treatment of neurodegeneration. Biotechnol Adv. (2018) pii: S0734-9750(17)30153-2.

2018

Volpicella M, Leoni C, Manzari C, Chiara M, Picardi E, Piancone E, Italiano F, D'Erchia A, Trotta M, Horner DS, Pesole G, Ceci LR.

Transcriptomic analysis of nickel exposure in Sphingobium sp. ba1 cells using RNA-seq. Sci Rep. 2017, 7: 8262.

2018

Chiara M, Placido A, Picardi E, Ceci LR, Horner DS, Pesole G.

A-GAME: improving the assembly of pooled functional metagenomics sequence data. BMC Genomics. 2018, 19: 44.

2018

Torraco A, Stehling O, Stümpfig C, Rösser R, De Rasmo D, Fiermonte G, Verrigni D, Rizza T, Vozza A, Di Nottia M, Diodato D, Martinelli D, Piemonte F, Dionisi-Vici C, Bertini E, Lill R, Carrozzo R.

ISCA1 Mutation In A Patient With Infantile-Onset Leukodystrophy Causes Defects In Mitochondrial [4Fe-4S] Proteins. Hum Mol Genet. (2018)

2018

de Bari L, Atlante A.

Including the mitochondrial metabolism of L-lactate in cancer metabolic reprogramming. Cell Mol Life Sci. (2018) doi: 10.1007/s00018-018-2831-y.

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