Resultados de procura - Goffrini, Paola

Respiration-Dependent Utilization of Sugars in Yeasts: a Determinant Role for Sugar Transporters por Goffrini, Paola, Ferrero, Iliana, Donnini, Claudia

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Three Target Genes for the Transcriptional Activator Cat8p of Kluyveromyces lactis: Acetyl Coenzyme A Synthetase Genes KlACS1 and KlACS2 and Lactate Permease Gene KlJEN1 por Lodi, Tiziana, Saliola, Michele, Donnini, Claudia, Goffrini, Paola

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Extension of Chronological Lifespan by Hexokinase Mutation in Kluyveromyces lactis Involves Increased Level of the Mitochondrial Chaperonin Hsp60 por Rizzetto, Lisa, Zanni, Elena, Uccelletti, Daniela, Ferrero, Ileana, Goffrini, Paola

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DNA polymerase γ and disease: what we have learned from yeast por Lodi, Tiziana, Dallabona, Cristina, Nolli, Cecilia, Goffrini, Paola, Donnini, Claudia, Baruffini, Enrico

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Exploring Yeast as a Study Model of Pantothenate Kinase-Associated Neurodegeneration and for the Identification of Therapeutic Compounds por Ceccatelli Berti, Camilla, Gilea, Alexandru Ionut, De Gregorio, Marco Armando, Goffrini, Paola

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Mitochondrial Aminoacyl-tRNA Synthetase and Disease: The Yeast Contribution for Functional Analysis of Novel Variants por Figuccia, Sonia, Degiorgi, Andrea, Ceccatelli Berti, Camilla, Baruffini, Enrico, Dallabona, Cristina, Goffrini, Paola

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Improved Production of Heterologous Proteins by a Glucose Repression-Defective Mutant of Kluyveromyces lactis por Donnini, Claudia, Farina, Francesca, Neglia, Barbara, Compagno, Maria Concetta, Uccelletti, Daniela, Goffrini, Paola, Palleschi, Claudio

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Modeling human Coenzyme A synthase mutation in yeast reveals altered mitochondrial function, lipid content and iron metabolism por Ceccatelli Berti, Camilla, Dallabona, Cristina, Lazzaretti, Mirca, Dusi, Sabrina, Tosi, Elena, Tiranti, Valeria, Goffrini, Paola

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The Golgi Ca(2+)-ATPase KlPmr1p Function Is Required for Oxidative Stress Response by Controlling the Expression of the Heat-Shock Element HSP60 in Kluyveromyces lactis por Uccelletti, Daniela, Farina, Francesca, Pinton, Paolo, Goffrini, Paola, Mancini, Patrizia, Talora, Claudio, Rizzuto, Rosario, Palleschi, Claudio

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Biallelic Mutations in DNM1L are Associated with a Slowly Progressive Infantile Encephalopathy por Nasca, Alessia, Legati, Andrea, Baruffini, Enrico, Nolli, Cecilia, Moroni, Isabella, Ardissone, Anna, Goffrini, Paola, Ghezzi, Daniele

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The Power of Yeast in Modelling Human Nuclear Mutations Associated with Mitochondrial Diseases por Ceccatelli Berti, Camilla, di Punzio, Giulia, Dallabona, Cristina, Baruffini, Enrico, Goffrini, Paola, Lodi, Tiziana, Donnini, Claudia

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Saccharomyces cerevisiae as a Tool for Studying Mutations in Nuclear Genes Involved in Diseases Caused by Mitochondrial DNA Instability por Gilea, Alexandru Ionut, Ceccatelli Berti, Camilla, Magistrati, Martina, di Punzio, Giulia, Goffrini, Paola, Baruffini, Enrico, Dallabona, Cristina

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Severe Infantile Encephalomyopathy Caused by a Mutation in COX6B1, a Nucleus-Encoded Subunit of Cytochrome C Oxidase por Massa, Valeria, Fernandez-Vizarra, Erika, Alshahwan, Saad, Bakhsh, Eman, Goffrini, Paola, Ferrero, Ileana, Mereghetti, Paolo, D'Adamo, Pio, Gasparini, Paolo, Zeviani, Massimo

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The impairment of HCCS leads to MLS syndrome by activating a non-canonical cell death pathway in the brain and eyes por Indrieri, Alessia, Conte, Ivan, Chesi, Giancarlo, Romano, Alessia, Quartararo, Jade, Tatè, Rosarita, Ghezzi, Daniele, Zeviani, Massimo, Goffrini, Paola, Ferrero, Ileana, Bovolenta, Paola, Franco, Brunella

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The impairment of HCCS leads to MLS syndrome by activating a non-canonical cell death pathway in the brain and eyes por Indrieri, Alessia, Conte, Ivan, Chesi, Giancarlo, Romano, Alessia, Quartararo, Jade, Tatè, Rosarita, Ghezzi, Daniele, Zeviani, Massimo, Goffrini, Paola, Ferrero, Ileana, Bovolenta, Paola, Franco, Brunella

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Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations por Aleo, Serena J, Del Dotto, Valentina, Fogazza, Mario, Maresca, Alessandra, Lodi, Tiziana, Goffrini, Paola, Ghelli, Anna, Rugolo, Michela, Carelli, Valerio, Baruffini, Enrico, Zanna, Claudia

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A novel de novo dominant mutation in ISCU associated with mitochondrial myopathy por Legati, Andrea, Reyes, Aurelio, Ceccatelli Berti, Camilla, Stehling, Oliver, Marchet, Silvia, Lamperti, Costanza, Ferrari, Alberto, Robinson, Alan J, Mühlenhoff, Ulrich, Lill, Roland, Zeviani, Massimo, Goffrini, Paola, Ghezzi, Daniele

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Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease por Oláhová, Monika, Berti, Camilla Ceccatelli, Collier, Jack J, Alston, Charlotte L, Jameson, Elisabeth, Jones, Simon A, Edwards, Noel, He, Langping, Chinnery, Patrick F, Horvath, Rita, Goffrini, Paola, Taylor, Robert W, Sayer, John A

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Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency por Alston, Charlotte L, Davison, James E, Meloni, Francesca, van der Westhuizen, Francois H, He, Langping, Hornig-Do, Hue-Tran, Peet, Andrew C, Gissen, Paul, Goffrini, Paola, Ferrero, Ileana, Wassmer, Evangeline, McFarland, Robert, Taylor, Robert W

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A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency por Alston, Charlotte L., Ceccatelli Berti, Camilla, Blakely, Emma L., Oláhová, Monika, He, Langping, McMahon, Colin J., Olpin, Simon E., Hargreaves, Iain P., Nolli, Cecilia, McFarland, Robert, Goffrini, Paola, O’Sullivan, Maureen J., Taylor, Robert W.

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