IRIS

FIERMONTE, Giuseppe

FIERMONTE, Giuseppe  

DIPARTIMENTO DI BIOSCIENZE , BIOTECNOLOGIE E AMBIENTE  

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Risultati 1 - 20 di 117 (tempo di esecuzione: 0.048 secondi).
Titolo Data di pubblicazione Autore(i) File
A new Caucasian case of neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD): A clinical, molecular, and functional study 1-gen-2011 Fiermonte, Giuseppe; Parisi, G; Martinelli, D; DE LEONARDIS, F; Torre, G; Pierri, CIRO LEONARDO; Saccari, A; Lasorsa, Fm; Vozza, Angelo; Palmieri, F; DIONISI VICI, C.
A novel member of solute carrier family 25 (SLC25A42) is a transporter of coenzyme A and adenosine 3',5'-diphosphate in human mitochondria 1-gen-2009 Fiermonte, Giuseppe; Paradies, E; Todisco, Simona; Marobbio, CARLO MARYA; Palmieri, F.
A Picrocrocin-Enriched Fraction from a Saffron Extract Affects Lipid Homeostasis in HepG2 Cells through a Non-Statin-like Mode 1-gen-2023 Frattaruolo, L.; Marra, F.; Lauria, G.; Siciliano, C.; Curcio, R.; Muto, L.; Brindisi, M.; Aiello, D.; Napoli, A.; Fiermonte, G.; Cappello, A. R.; Fiorillo, M.; Ahmed, A.; Dolce, V.
Abundant bacterial expression and reconstitution of an intrinsic membrane-transport protein from bovine mitochondria 1-gen-1993 Fiermonte, Giuseppe; Walker, J. E. AND PALMIERI F.
AGC1 and AGC2 are novel Ca2+-sensitive regulators of mitochondrial metabolism 1-gen-2003 Lasorsa, Fm; Pinton, P; Palmieri, L; Fiermonte, Giuseppe; Rizzuto, R; Palmieri, F.
Amish microcephaly is caused by mutation in the deoxynucleotide carrier DNC 1-gen-2002 Rosenberg, Mj; Agarwala, R; Bouffard, G; Davis, J; Fiermonte, Giuseppe; Hilliard, Ms; Koch, T; Kalikin, Lm; Makalowska, I; Morton, Dh; Petty, Em; Weber, Jl; Palmieri, F; Kelley, Ri; Schaffer, Aa; Biesecker, Lg
An Adult with Type 2 Citrullinemia Presenting in Europe 1-gen-2008 Fiermonte, Giuseppe; Soon, D; Paradies, E; LEE P., J; Krywawych, S; Palmieri, F; Lachmann, R. H.
An overview of mitochondrial protein defects in neuromuscular diseases 1-gen-2021 Marra, F.; Lunetti, P.; Curcio, R.; Lasorsa, F. M.; Capobianco, L.; Porcelli, V.; Dolce, V.; Fiermonte, G.; Scarcia, P.
Assignment of the human dicarboxylate carrier gene (DIC) to chromosome 17 band 17q25.3 1-gen-1998 Pannone, E; Fiermonte, Giuseppe; Dolce, V; Rocchi, Mariano; Palmieri, F.
Biochemical characterization of a new mitochondrial transporter of dephosphocoenzyme A in Drosophila melanogaster 1-gen-2016 Vozza, Angelo; DE LEONARDIS, Francesco; Paradies, Eleonora; DE GRASSI, Anna; Pierri, CIRO LEONARDO; Parisi, Giovanni; Marobbio, CARLO MARYA; Lasorsa, Francesco Massimo; Muto, Luigina; Capobianco, Loredana; Dolce, Vincenza; Raho, Susanna; Fiermonte, Giuseppe
Citrin deficiency, a perplexing global disorder 1-gen-2009 Dimmock, D; Maranda, B; DIONISI VICI, C; Wang, J; Kleppe, S; Fiermonte, Giuseppe; Bai, R; Hainline, B; Hamosh, A; O'Brien, W. E.; Scaglia, F; Wong, L. J.
Clonaggio e sequenza del cDNA codificante la proteina di trasporto per il fosfato nei mitocondri di cuore umano 1-gen-1991 Dolce, V; Fiermonte, Giuseppe; Palmieri, F.
Cloning, Purification, and Characterization of the Catalytic C-Terminal Domain of the Human 3-Hydroxy-3-methyl glutaryl-CoA Reductase: An Effective, Fast, and Easy Method for Testing Hypocholesterolemic Compounds 1-gen-2020 Curcio, Rosita; Aiello, Donatella; Vozza, Angelo; Muto, Luigina; Martello, Emanuela; Cappello, Anna Rita; Capobianco, Loredana; Fiermonte, Giuseppe; Siciliano, Carlo; Napoli, Anna; Dolce, Vincenza
Coding region mutations associated with aberrant mRNA splicing in patients with carnitine/acylcarnitine translocase (CACT) deficiency 1-gen-2001 Iacobazzi, Vito; Hsu, B. Y. L.; Fiermonte, Giuseppe; Stanley, C. A.; Palmieri, F.
Corrigendum for: Novel hypoglycemia phenotype in congenital hyperinsulinism due to dominant mutations of uncoupling protein 2 (Journal of Clinical Endocrinology and Metabolism (2017) 102:3 (942-949) DOI: 10.1210/jc.2016-3164) 1-gen-2017 Ferrara, C. T.; Boodhansingh, K. E.; Paradies, E.; Fiermonte, G.; Steinkrauss, L. J.; Swartz Topor, L.; Quintos, J. B.; Ganguly, A.; De Leon, D. D.; Palmieri, F.; Stanley, C. A.
CUGC for hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome 1-gen-2020 Martinelli, D.; Fiermonte, G.; Haberle, J.; Boenzi, S.; Goffredo, B. M.; Travaglini, L.; Agolini, E.; Porcelli, V.; Dionisi-Vici, C.
Determination of the primary structure of the rat and human mitochondrial dicarboxylate transporter via distant homologs in yeast and Caenorhabditis elegans 1-gen-1999 Dolce, V; Fiermonte, Giuseppe; Palmieri, L; Palmieri, F; Walker, Je
Determination of the primary structure of the rat mitochondrial dicarboxylate transporter via distant homologues in yeast and Caenorhabditis elegans 1-gen-1998 Fiermonte, Giuseppe; Palmieri, L; Dolce, V; Lasorsa, Fm; Palmieri, F.
Dimostrazione dell'esistenza di due isoforme del trasportatore mitocondriale per il fosfato e loro espressione in E. coli 1-gen-1996 Fiermonte, Giuseppe; Dolce, V; Palmieri, F.
Distribuzione tissutale, espressione in E. coli ed analisi funzionale delle due isoforme del carrier del fosfato di mitocondri di bue 1-gen-1997 Dolce, V; Fiermonte, Giuseppe; Palmieri, F.