検索結果 - Sabrina Dusi
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Mitochondrial iron and energetic dysfunction distinguish fibroblasts and induced neurons from pantothenate kinase-associated neurodegeneration patients 著者: Paolo Santambrogio, Sabrina Dusi, Michela Guaraldo, Luisa Ida Rotundo, Vania Broccoli, Barbara Garavaglia, Valeria Tiranti, Sonia Levi
出版事項 2015Artigo -
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Gene-specific mitochondria dysfunctions in human TARDBP and C9ORF72 fibroblasts 著者: Elisa Onesto, Claudia Colombrita, Valentina Gumina, María Orietta Borghi, Sabrina Dusi, Alberto Doretti, Gigliola Fagiolari, Federica Invernizzi, Maurizio Moggio, Valeria Tiranti, Vincenzo Silani, Antonia Ratti
出版事項 2016Artigo -
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Pantethine treatment is effective in recovering the disease phenotype induced by ketogenic diet in a pantothenate kinase-associated neurodegeneration mouse model 著者: Dario Brunetti, Sabrina Dusi, Carla Giordano, Costanza Lamperti, Michela Morbin, Valeria Fugnanesi, Silvia Marchet, Gigliola Fagiolari, Ody C.M. Sibon, Maurizio Moggio, Giulia d’Amati, Valeria Tiranti
出版事項 2013Artigo -
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Pantothenate kinase-associated neurodegeneration: altered mitochondria membrane potential and defective respiration in Pank2 knock-out mouse model 著者: Dario Brunetti, Sabrina Dusi, Michela Morbin, Andrea Uggetti, Fabio Moda, Ilaria D’Amato, Carla Giordano, Giulia d’Amati, Anna Cozzi, Sonia Levi, Susan J. Hayflick, Valeria Tiranti
出版事項 2012Artigo -
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Coenzyme A corrects pathological defects in human neurons of <scp>PANK</scp> 2‐associated neurodegeneration 著者: Daniel Orellana, Paolo Santambrogio, Alicia Rubio, Latefa Yekhlef, Cinzia Cancellieri, Sabrina Dusi, Serena Giannelli, Paola Venco, Pietro Giuseppe Mazzara, Anna Cozzi, Maurizio Ferrari, Barbara Garavaglia, Stefano Taverna, Valeria Tiranti, Vania Broccoli, Sonia Levi
出版事項 2016Artigo -
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Metabolic consequences of mitochondrial coenzyme A deficiency in patients with PANK2 mutations 著者: Valerio Leoni, Laura Strittmatter, Giovanna Zorzi, Federica Zibordi, Sabrina Dusi, Barbara Garavaglia, Paola Venco, Claudio Caccia, Amanda L. Souza, Amy Deik, Clary B. Clish, Marco Rimoldi, Emilio Ciusani, Enrico Bertini, Nardo Nardocci, Vamsi K. Mootha, Valeria Tiranti
出版事項 2011Artigo -
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Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation 著者: Monika Hartig, Arcangela Iuso, Tobias B. Haack, Tomasz Kmieć, Elżbieta Jurkiewicz, Katharina Heim, Sigrun Roeber, Victoria Tarabin, Sabrina Dusi, Małgorzata Krajewska‐Walasek, Sergiusz Jóźwiak, Maja Hempel, Juliane Winkelmann, Matthias Elstner, Konrad Oexle, Thomas Klopstock, Wolfgang Mueller‐Felber, Thomas Gasser, Claudia Trenkwalder, Valeria Tiranti, Hans A. Kretzschmar, Gerd Schmitz, Tim M. Strom, Thomas Meitinger, Holger Prokisch
出版事項 2011Artigo -
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Exome Sequence Reveals Mutations in CoA Synthase as a Cause of Neurodegeneration with Brain Iron Accumulation 著者: Sabrina Dusi, Lorella Valletta, Tobias B. Haack, Yugo Tsuchiya, Paola Venco, Sebastiano Pasqualato, P Goffrini, Marco Tigano, Nikita Demchenko, Thomas Wieland, Thomas Schwarzmayr, Tim M. Strom, Federica Invernizzi, Barbara Garavaglia, Allison Gregory, Lynn Sanford, Jeffrey Hamada, Conceição Bettencourt, Henry Houlden, Luisa Chiapparini, Giovanna Zorzi, Manju A. Kurian, Nardo Nardocci, Holger Prokisch, Susan J. Hayflick, Ivan Gout, Valeria Tiranti
出版事項 2013Artigo -
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COQ4 Mutations Cause a Broad Spectrum of Mitochondrial Disorders Associated with CoQ10 Deficiency 著者: Gloria Brea‐Calvo, Tobias B. Haack, Daniela Karall, Akira Ohtake, Federica Invernizzi, Rosalba Carrozzo, Laura S. Kremer, Sabrina Dusi, Christine Fauth, Sabine Scholl‐Bürgi, Elisabeth Graf, Uwe Ahting, Nicoletta Resta, Nicola Laforgia, Daniela Verrigni, Yasushi Okazaki, Masakazu Kohda, Diego Martinelli, Peter Freisinger, Tim M. Strom, Thomas Meitinger, Costanza Lamperti, Atilano Lacson, Plácido Navas, Johannes A. Mayr, Enrico Bertini, Kei Murayama, Massimo Zeviani, Holger Prokisch, Daniele Ghezzi
出版事項 2015Artigo
関連主題
Biology
Gene
Medicine
Disease
Genetics
Neurodegeneration
Mitochondrion
Biochemistry
Cell biology
Internal medicine
Mitochondrial DNA
Pathology
Mitochondrial disease
Mutation
Neuroscience
Retinal degeneration
Bioinformatics
Computer science
Endocrinology
Exome sequencing
ATP synthase
Aconitase
Allele
Amyotrophic lateral sclerosis
Apoptosis
Atrophy
Autophagy
C9orf72
Cerebellar hypoplasia (non-human)
Cerebellum