Search Results - LOMMARINI, Luisa

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  1. 1
    Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy

    Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy by GIORDANO, Carla, LOMMARINI, Luisa, FANELLI, Francesca, FRACASSO, Flavio, ROSS-CISNEROS, Fred N, D'ADAMO, Pio, HUDSON, Gavin, PYLE, Angela, YU-WAI-MAN, Patrick, CHINNERY, Patrick F, ZEVIANI, Massimo, SALOMAO, Solange R, GIORDANO, Luca, BEREZOVSKY, Adriana, BELFORT, Rubens, VENTURA, Dora Fix, MORAES, Milton, BARBONI, Piero, SADUN, Federico, DE NEGRI, Annamaria, SADUN, Alfredo A, TANCREDI, Andrea, MARESCA, Alessandra, MANCINI, Massimiliano, D'AMATI, Giulia, POLOSA, Paola Loguercio, CANTATORE, Palmiro, CARELLI, Valerio, PISANO, Annalinda, VALENTINO, Maria Lucia, CAPORALI, Leonardo, LIGUORI, Rocco, DECEGLIE, Stefania, ROBERTI, Marina

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  2. 2
    A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function

    A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function by GASPARRE, Giuseppe, KURELAC, Ivana, BETTS, Christine M, CARELLI, Valerio, LUIGI LOLLINI, Pier, ROMEO, Giovanni, RUGOLO, Michela, PORCELLI, Anna Maria, CAPRISTO, Mariantonietta, LOMMARINI, Luisa, GHELLI, Anna, CECCARELLI, Claudio, NICOLETTI, Giordano, NANNI, Patrizia, DE GIOVANNI, Carla, SCOTLANDI, Katia

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  3. 3
    A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16

    A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16 by CARELLI, Valerio, SCHIMPF, Simone, BARBONI, Piero, LONGANESI, Lora, RUGOLO, Michela, GHELLI, Anna, ALAVI, Marcel V, YOULE, Richard J, BUCCHI, Laura, CARROCCIA, Rosanna, PIA GIANNOCCARO, Maria, TONON, Caterina, FUHRMANN, Nico, LODI, Raffaele, CENACCHI, Giovanna, MONTAGNA, Pasquale, LIGUORI, Rocco, WISSINGER, Bernd, VALENTINO, Maria Lucia, ZANNA, Claudia, LOMMARINI, Luisa, PAPKE, Monika, SCHAICH, Simone, TIPPMANN, Sabine, BAUMANN, Britta

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  4. 4
    OPAI mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes. Commentary

    OPAI mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes. Commentary by ZEVIANI, Massimo, AMATI-BONNEAU, Patrizia, CARROCCIA, Rosanna, LOMMARINI, Luisa, LABAUGE, Pierre, FIGARELLA-BRANGER, Dominique, MARCORELLES, Pascale, FURBY, Alain, BEAUVAIS, Katell, LETOURNEL, Franck, LIGUORI, Rocco, LA MORGIA, Chiara, VALENTINO, Maria Lucia, MONTAGNA, Pasquale, LIGUORI, Maria, ZANNA, Claudia, RUGOLO, Michela, COSSARIZZA, Andrea, WISSINGER, Bernd, VERNY, Christophe, SCHWARZENBACHER, Robert, MARTIA, Miguel Ngel, ARENAS, Joaquin, REYNIER, Pascal, AYUSO, Carmen, GARESSE, Rafael, LENAERS, Guy, BONNEAU, Dominique, CARELLI, Valerio, GALLARDO, Maria Esther, BORNSTEIN, Belén, BOISSIERE, Anne, CAMPOS, Yolanda, RIVERA, Henry, DE LA ALEJA, Jesus Gonzalez

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