Search Results - Muñoz‐Oreja, Mikel

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  1. 1
    2-Deoxy-D-glucose couples mitochondrial DNA replication with mitochondrial fitness and promotes the selection of wild-type over mutant mitochondrial DNA

    2-Deoxy-D-glucose couples mitochondrial DNA replication with mitochondrial fitness and promotes the selection of wild-type over mutant mitochondrial DNA by Pantic, Boris, Ives, Daniel, Mennuni, Mara, Perez-Rodriguez, Diego, Fernandez-Pelayo, Uxoa, Lopez de Arbina, Amaia, Muñoz-Oreja, Mikel, Villar-Fernandez, Marina, Dang, Thanh-mai Julie, Vergani, Lodovica, Johnston, Iain G., Pitceathly, Robert D. S., McFarland, Robert, Hanna, Michael G., Taylor, Robert W., Holt, Ian J., Spinazzola, Antonella

    Published in Nature communications
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  2. 2
    Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism

    Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism by De la Casa‐Fages, Beatriz, Fernández‐Eulate, Gorka, Gamez, Josep, Barahona‐Hernando, Raúl, Morís, Germán, García‐Barcina, María, Infante, Jon, Zulaica, Miren, Fernández‐Pelayo, Uxoa, Muñoz‐Oreja, Mikel, Urtasun, Miguel, Olaskoaga, Ander, Zelaya, Victoria, Jericó, Ivonne, Saez‐Villaverde, Raquel, Catalina, Irene, Sola, Emma, Martínez‐Sáez, Elena, Pujol, Aurora, Ruiz, Montserrat, Schlüter, Agatha, Spinazzola, Antonella, Muñoz‐Blanco, Jose Luis, Grandas, Francisco, Holt, Ian, Álvarez, Victoria, López de Munaín, Adolfo

    Published in Movement disorders
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  3. 3
    Reply to: “Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion”

    Reply to: “Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion” by De la Casa‐Fages, Beatriz, Fernández‐Eulate, Gorka, Gamez, Josep, Barahona‐Hernando, Raúl, Morís, Germán, García‐Barcina, María, Infante, Jon, Zulaica, Miren, Fernández‐Pelayo, Uxoa, Muñoz‐Oreja, Mikel, Urtasun, Miguel, Olaskoaga, Ander, Zelaya, Victoria, Jericó, Ivonne, Saez‐Villaverde, Raquel, Catalina, Irene, Sola, Emma, Martínez‐Sáez, Elena, Pujol, Aurora, Ruiz, Montserrat, Schlüter, Agatha, Spinazzola, Antonella, Muñoz‐Blanco, Jose Luis, Grandas, Francisco, Holt, Ian, Álvarez, Victoria, López de Munaín, Adolfo

    Published in Movement disorders
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  4. 4
    Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial Metabolism

    Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial Metabolism by Gunning, Adam C., Strucinska, Klaudia, Muñoz Oreja, Mikel, Parrish, Andrew, Caswell, Richard, Stals, Karen L., Durigon, Romina, Durlacher-Betzer, Karina, Cunningham, Mitchell H., Grochowski, Christopher M., Baptista, Julia, Tysoe, Carolyn, Baple, Emma, Lahiri, Nayana, Homfray, Tessa, Scurr, Ingrid, Armstrong, Catherine, Dean, John, Fernandez Pelayo, Uxoa, Jones, Aleck W.E., Taylor, Robert W., Misra, Vinod K., Yoon, Wan Hee, Wright, Caroline F., Lupski, James R., Spinazzola, Antonella, Harel, Tamar, Holt, Ian J., Ellard, Sian

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  5. 5
    Elevated cholesterol in ATAD3 mutants is a compensatory mechanism that leads to membrane cholesterol aggregation

    Elevated cholesterol in ATAD3 mutants is a compensatory mechanism that leads to membrane cholesterol aggregation by Muñoz-Oreja, Mikel, Sandoval, Abigail, Bruland, Ove, Perez-Rodriguez, Diego, Fernandez-Pelayo, Uxoa, de Arbina, Amaia Lopez, Villar-Fernandez, Marina, Hernández-Eguiazu, Haizea, Hernández, Ixiar, Park, Yohan, Goicoechea, Leire, Pascual-Frías, Nerea, Garcia-Ruiz, Carmen, Fernandez-Checa, Jose, Martí-Carrera, Itxaso, Gil-Bea, Francisco Javier, Hasan, Mazahir T, Gegg, Matthew E, Bredrup, Cecilie, Knappskog, Per-Morten, Gereñu-Lopetegui, Gorka, Varhaug, Kristin N, Bindoff, Laurence A, Spinazzola, Antonella, Yoon, Wan Hee, Holt, Ian J

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  6. 6
    Dysregulated FOXO1 activity drives skeletal muscle intrinsic dysfunction in amyotrophic lateral sclerosis

    Dysregulated FOXO1 activity drives skeletal muscle intrinsic dysfunction in amyotrophic lateral sclerosis by Zufiría, Mónica, Pikatza-Menoio, Oihane, Garciandia-Arcelus, Maddi, Bengoetxea, Xabier, Jiménez, Andrés, Elicegui, Amaia, Levchuk, María, Arnold-García, Olatz, Ondaro, Jon, Iruzubieta, Pablo, Rodríguez-Gómez, Laura, Fernández-Pelayo, Uxoa, Muñoz-Oreja, Mikel, Aiastui, Ana, García-Verdugo, José Manuel, Herranz-Pérez, Vicente, Zulaica, Miren, Poza, Juan José, Ruiz-Onandi, Rebeca, Fernández-Torrón, Roberto, Espinal, Juan Bautista, Bonilla, Mario, Lersundi, Ana, Fernández-Eulate, Gorka, Riancho, Javier, Vallejo-Illarramendi, Ainara, Holt, Ian James, Sáenz, Amets, Malfatti, Edoardo, Duguez, Stéphanie, Blázquez, Lorea, López de Munain, Adolfo, Gerenu, Gorka, Gil-Bea, Francisco, Alonso-Martín, Sonia

    Published in Acta neuropathologica
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  7. 7
    2-Deoxy-D-glucose couples mitochondrial DNA replication with mitochondrial fitness and promotes the selection of wild-type over mutant mitochondrial DNA

    2-Deoxy-D-glucose couples mitochondrial DNA replication with mitochondrial fitness and promotes the selection of wild-type over mutant mitochondrial DNA by Pantic, Boris, Ives, Daniel, Mennuni, Mara, Perez-Rodriguez, Diego, Fernandez-Pelayo, Uxoa, Lopez de Arbina, Amaia, Muñoz-Oreja, Mikel, Villar-Fernandez, Marina, Dang, Thanh-mai Julie, Vergani, Lodovica, Johnston, Iain George, Pitceathly, Robert D. S, McFarland, Robert, Hanna, Michael G, Taylor, Robert W, Holt, Ian J, Spinazzola, Antonella

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