Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease

Por Kirino, Yohei, Goto, Yu-ichi, Campos, Yolanda, Arenas, Joaquin, Suzuki, Tsutomu
Publicado em 2005

Nitric oxide compounds have different effects profiles on human articular chondrocyte metabolism

Por de Andrés, María C, Maneiro, Emilia, Martín, Miguel A, Arenas, Joaquín, Blanco, Francisco J
Publicado em 2013

Low versus high carbohydrates in the diet of the world‐class athlete: insights from McArdle's disease

Por Nogales‐Gadea, Gisela, Santalla, Alfredo, Arenas, Joaquín, Martín, Miguel A., Morán, María, Lucia, Alejandro
Publicado no J Physiol (2017)

Effect of nitric oxide on mitochondrial activity of human synovial cells

Por Arenas Joaquín, López-Armada María J, Martin Miguel A, Cillero-Pastor Berta, Blanco Francisco J
Publicado em 2011-02-01

About the “Pathological” Role of the mtDNA T3308C Mutation…

Por Rocha, Hugo, Flores, Carlos, Campos, Yolanda, Arenas, Joaquín, Vilarinho, Laura, Santorelli, Filippo M., Torroni, Antonio
Publicado em 1999

Effect of nitric oxide on mitochondrial activity of human synovial cells

Por Cillero-Pastor, Berta, Martin, Miguel A, Arenas, Joaquín, López-Armada, María J, Blanco, Francisco J
Publicado em 2011

Mitochondrial Complex I plays an Essential Role in Human Respirasome Assembly

Por Moreno-Lastres, David, Fontanesi, Flavia, García-Consuegra, Inés, Martín, Miguel A., Arenas, Joaquín, Barrientos, Antoni, Ugalde, Cristina
Publicado em 2012

C34T mutation of the AMPD1 gene in an elite white runner

Por Lucia, Alejandro, Martin, Miguel A, Esteve-Lanao, Jonathan, Juan, Alejandro F San, Rubio, Juan C, Oliván, Jesús, Arenas, Joaquín
Publicado em 2009

Mitochondrial DNA Haplogroups Do Not Play a Role in the Variable Phenotypic Presentation of the A3243G Mutation

Por Torroni, Antonio, Campos, Yolanda, Rengo, Chiara, Sellitto, Daniele, Achilli, Alessandro, Magri, Chiara, Semino, Ornella, García, Alberto, Jara, Pilar, Arenas, Joaquín, Scozzari, Rosaria
Publicado em 2003

Sodium valproate increases the brain isoform of glycogen phosphorylase: looking for a compensation mechanism in McArdle disease using a mouse primary skeletal-muscle culture in vit...

Por de Luna, Noemí, Brull, Astrid, Guiu, Josep Maria, Lucia, Alejandro, Martin, Miguel Angel, Arenas, Joaquin, Martí, Ramon, Andreu, Antoni L., Pinós, Tomàs
Publicado no Dis Model Mech (2015)

Phenotype consequences of myophosphorylase dysfunction: insights from the McArdle mouse model

Por Brull, Astrid, de Luna, Noemí, Blanco-Grau, Albert, Lucia, Alejandro, Martin, Miguel Angel, Arenas, Joaquin, Martí, Ramon, Andreu, Antoni L, Pinós, Tomàs
Publicado no J Physiol (2015)

A new mutation in the gene encoding mitochondrial seryl-tRNA synthetase as a cause of HUPRA syndrome

Por Rivera, Henry, Martín-Hernández, Elena, Delmiro, Aitor, García-Silva, María Teresa, Quijada-Fraile, Pilar, Muley, Rafael, Arenas, Joaquín, Martín, Miguel A, Martínez-Azorín, Francisco
Publicado em 2013

Oxidative stress in skin fibroblasts cultures from patients with Parkinson's disease

Por Arenas Joaquín, Caballero Luis, Alonso-Navarro Hortensia, Sayed Youssef, Molina José, de Bustos Fernando, García-Redondo Alberto, del Hoyo Pilar, Agúndez José AG, Jiménez-Jiménez Félix
Publicado em 2010-10-01

Differential proteomic profiling unveils new molecular mechanisms associated with mitochondrial complex III deficiency

Por Marín-Buera, Lorena, García-Bartolomé, Alberto, Morán, María, López-Bernardo, Elia, Cadenas, Susana, Hidalgo, Beatriz, Sánchez, Ricardo, Seneca, Sara, Arenas, Joaquín, Martín, Miguel A., Ugalde, Cristina
Publicado no J Proteomics (2014)

McArdle disease does not affect skeletal muscle fibre type profiles in humans

Por Kohn, Tertius Abraham, Noakes, Timothy David, Rae, Dale Elizabeth, Rubio, Juan Carlos, Santalla, Alfredo, Nogales-Gadea, Gisela, Pinós, Tomas, Martín, Miguel A., Arenas, Joaquin, Lucia, Alejandro
Publicado no Biol Open (2014)

Oxidative stress in skin fibroblasts cultures from patients with Parkinson's disease

Por del Hoyo, Pilar, García-Redondo, Alberto, de Bustos, Fernando, Molina, José Antonio, Sayed, Youssef, Alonso-Navarro, Hortensia, Caballero, Luis, Arenas, Joaquín, Agúndez, José AG, Jiménez-Jiménez, Félix Javier
Publicado em 2010

Expression of Glycogen Phosphorylase Isoforms in Cultured Muscle from Patients with McArdle's Disease Carrying the p.R771PfsX33 PYGM Mutation

Por Nogales-Gadea, Gisela, Mormeneo, Emma, García-Consuegra, Inés, Rubio, Juan C., Orozco, Anna, Arenas, Joaquin, Martín, Miguel A., Lucia, Alejandro, Gómez-Foix, Anna M., Martí, Ramon, Andreu, Antoni L.
Publicado em 2010

Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene

Por Bornstein, Belén, Mas, José Antonio, Patrono, Clarice, Fernández-Moreno, Miguel Angel, González-Vioque, Emiliano, Campos, Yolanda, Carrozzo, Rosalba, Martín, Miguel Angel, Hoyo, Pilar del, Santorelli, Filippo M., Arenas, Joaquín, Garesse, Rafael
Publicado em 2005

Impact of the Mitochondrial Genetic Background in Complex III Deficiency

Por Gil Borlado, Mari Carmen, Moreno Lastres, David, Gonzalez Hoyuela, Maritza, Moran, Maria, Blazquez, Alberto, Pello, Rosa, Marin Buera, Lorena, Gabaldon, Toni, Garcia Peñas, Juan Jose, Martín, Miguel A., Arenas, Joaquin, Ugalde, Cristina
Publicado em 2010

A Transcriptomic Approach to Search for Novel Phenotypic Regulators in McArdle Disease

Por Nogales-Gadea, Gisela, Consuegra-García, Inés, Rubio, Juan C., Arenas, Joaquin, Cuadros, Marc, Camara, Yolanda, Torres-Torronteras, Javier, Fiuza-Luces, Carmen, Lucia, Alejandro, Martín, Miguel A., García-Arumí, Elena, Andreu, Antoni L.
Publicado em 2012