Resultats de la cerca - Eleonora Paradies

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  1. 1
    A Novel Member of Solute Carrier Family 25 (SLC25A42) Is a Transporter of Coenzyme A and Adenosine 3′,5′-Diphosphate in Human Mitochondria

    A Novel Member of Solute Carrier Family 25 (SLC25A42) Is a Transporter of Coenzyme A and Adenosine 3′,5′-Diphosphate in Human Mitochondria per Giuseppe Fiermonte, Eleonora Paradies, Simona Todisco, C Marobbio, Ferdinando Palmieri

    Publicat 2009
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  2. 2
    α-Isopropylmalate, a Leucine Biosynthesis Intermediate in Yeast, Is Transported by the Mitochondrial Oxalacetate Carrier

    α-Isopropylmalate, a Leucine Biosynthesis Intermediate in Yeast, Is Transported by the Mitochondrial Oxalacetate Carrier per C Marobbio, Giulia Giannuzzi, Eleonora Paradies, Ciro Leonardo Pierri, Ferdinando Palmieri

    Publicat 2008
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  3. 3
    The ARL2 GTPase Is Required for Mitochondrial Morphology, Motility, and Maintenance of ATP Levels

    The ARL2 GTPase Is Required for Mitochondrial Morphology, Motility, and Maintenance of ATP Levels per Laura Newman, Chengjing Zhou, Samatha Mudigonda, Alexa L. Mattheyses, Eleonora Paradies, C Marobbio, Richard Kahn

    Publicat 2014
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  4. 4
    Characterization of Human and Yeast Mitochondrial Glycine Carriers with Implications for Heme Biosynthesis and Anemia

    Characterization of Human and Yeast Mitochondrial Glycine Carriers with Implications for Heme Biosynthesis and Anemia per Paola Lunetti, Fabrizio Damiano, Giuseppe Egidio De Benedetto, Luisa Siculella, Antonio Pennetta, Luigina Muto, Eleonora Paradies, C Marobbio, Vincenza Dolce, Loredana Capobianco

    Publicat 2016
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  5. 5
    Novel Hypoglycemia Phenotype in Congenital Hyperinsulinism Due to Dominant Mutations of Uncoupling Protein 2

    Novel Hypoglycemia Phenotype in Congenital Hyperinsulinism Due to Dominant Mutations of Uncoupling Protein 2 per Christine T. Ferrara, Kara E. Boodhansingh, Eleonora Paradies, Giuseppe Fiermonte, Linda Steinkrauss, Lisa Swartz Topor, Jose Bernardo Quintos, Arupa Ganguly, Diva D. De León, Ferdinando Palmieri, Charles A. Stanley

    Publicat 2016
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  6. 6
    Biochemical characterization of a new mitochondrial transporter of dephosphocoenzyme A in Drosophila melanogaster

    Biochemical characterization of a new mitochondrial transporter of dephosphocoenzyme A in Drosophila melanogaster per Angelo Vozza, Francesco De Leonardis, Eleonora Paradies, Anna Grassi, Ciro Leonardo Pierri, Giovanni Parisi, C Marobbio, Francesco M. Lasorsa, Luigina Muto, Loredana Capobianco, Vincenza Dolce, Susanna Raho, Giuseppe Fiermonte

    Publicat 2016
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  7. 7
    Molecular Identification and Functional Characterization of Arabidopsis thaliana Mitochondrial and Chloroplastic NAD+ Carrier Proteins

    Molecular Identification and Functional Characterization of Arabidopsis thaliana Mitochondrial and Chloroplastic NAD+ Carrier Proteins per Ferdinando Palmieri, Benjamin Rieder, Angela Ventrella, Emanuela Blanco, Phuc Thi, Adriano Nunes‐Nesi, A.Ulrike Trauth, Giuseppe Fiermonte, Joachim Tjaden, Gennaro Agrimi, Simon Kirchberger, Eleonora Paradies, Alisdair R. Fernie, H. Ekkehard Neuhaus

    Publicat 2009
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  8. 8
    UCP2 transports C4 metabolites out of mitochondria, regulating glucose and glutamine oxidation

    UCP2 transports C4 metabolites out of mitochondria, regulating glucose and glutamine oxidation per Angelo Vozza, Giovanni Parisi, Francesco De Leonardis, Francesco M. Lasorsa, Alessandra Castegna, Daniela Amorese, Raffaele Marmo, Valeria M. Calcagnile, Luigi Palmieri, Daniel Ricquier, Eleonora Paradies, Pasquale Scarcia, Ferdinando Palmieri, Frédéric Bouillaud, Giuseppe Fiermonte

    Publicat 2014
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  9. 9
    SLC25A10 biallelic mutations in intractable epileptic encephalopathy with complex I deficiency

    SLC25A10 biallelic mutations in intractable epileptic encephalopathy with complex I deficiency per Giuseppe Punzi, Vito Porcelli, Matteo Ruggiu, Md. Faruk Hossain, Alessio Menga, Pasquale Scarcia, Alessandra Castegna, Ruggiero Gorgoglione, Ciro Leonardo Pierri, Luna Laera, Francesco M. Lasorsa, Eleonora Paradies, Isabella Pisano, C Marobbio, Eleonora Lamantea, Daniele Ghezzi, Valeria Tiranti, Sergio Giannattasio, Maria Alice Donati, Renzo Guerrini, Luigi Palmieri, Ferdinando Palmieri, Anna Grassi

    Publicat 2017
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  10. 10
    Identification of novel mutations in the<i>SLC25A15</i>gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: A clinical, molecular, and functional study

    Identification of novel mutations in the<i>SLC25A15</i>gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: A clinical, molecular, and functional study per Alessandra Tessa, Giuseppe Fiermonte, Carlo Dionisi‐Vici, Eleonora Paradies, Matthias R. Baumgartner, Yin‐Hsiu Chien, C. Loguercio, Hélène Ogier de Baulny, Marie‐Cécile Nassogne, Manuel Schiff, Federica Deodato, Giancarlo Parenti, S. Lane Rutledge, Marta Vilaseca, Mariarosa Anna Beatrice Melone, Gioacchino Scarano, Luiz Aldamiz-Echevarría, G. T. N. Besley, John H. Walter, Eugenia Martínez‐Hernández, José Manuel Hernández, Ciro Leonardo Pierri, Ferdinando Palmieri, Filippo M. Santorelli

    Publicat 2009
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