Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches

מאת García-López, Marta, Arenas, Joaquín, Gallardo, M. Esther
הוצא לאור ב Genes (Basel) (2021)

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

מאת Kirino, Yohei, Goto, Yu-ichi, Campos, Yolanda, Arenas, Joaquin, Suzuki, Tsutomu
יצא לאור 2005

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

מאת de Andrés, María C, Maneiro, Emilia, Martín, Miguel A, Arenas, Joaquín, Blanco, Francisco J
יצא לאור 2013

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

מאת Nogales‐Gadea, Gisela, Santalla, Alfredo, Arenas, Joaquín, Martín, Miguel A., Morán, María, Lucia, Alejandro
הוצא לאור ב J Physiol (2017)

Effect of nitric oxide on mitochondrial activity of human synovial cells

מאת Arenas Joaquín, López-Armada María J, Martin Miguel A, Cillero-Pastor Berta, Blanco Francisco J
יצא לאור 2011-02-01

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

מאת Rocha, Hugo, Flores, Carlos, Campos, Yolanda, Arenas, Joaquín, Vilarinho, Laura, Santorelli, Filippo M., Torroni, Antonio
יצא לאור 1999

Effect of nitric oxide on mitochondrial activity of human synovial cells

מאת Cillero-Pastor, Berta, Martin, Miguel A, Arenas, Joaquín, López-Armada, María J, Blanco, Francisco J
יצא לאור 2011

Mitochondrial Complex I plays an Essential Role in Human Respirasome Assembly

מאת Moreno-Lastres, David, Fontanesi, Flavia, García-Consuegra, Inés, Martín, Miguel A., Arenas, Joaquín, Barrientos, Antoni, Ugalde, Cristina
יצא לאור 2012

Small GTPases of the Ras superfamily and glycogen phosphorylase regulation in T cells

מאת Llavero, Francisco, Arrazola Sastre, Alazne, Luque Montoro, Miriam, Martín, Miguel A., Arenas, Joaquín, Lucia, Alejandro, Zugaza, José L.
הוצא לאור ב Small GTPases (2019)

C34T mutation of the AMPD1 gene in an elite white runner

מאת Lucia, Alejandro, Martin, Miguel A, Esteve-Lanao, Jonathan, Juan, Alejandro F San, Rubio, Juan C, Oliván, Jesús, Arenas, Joaquín
יצא לאור 2009

Plasma LDH: A specific biomarker for lung affectation in COVID-19?

מאת Serrano-Lorenzo, Pablo, Coya, Olga N., López-Jimenez, Ana, Blázquez, Alberto, Delmiro, Aitor, Lucia, Alejandro, Arenas, Joaquín, Martín, Miguel A.
הוצא לאור ב Pract Lab Med (2021)

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

מאת Torroni, Antonio, Campos, Yolanda, Rengo, Chiara, Sellitto, Daniele, Achilli, Alessandro, Magri, Chiara, Semino, Ornella, García, Alberto, Jara, Pilar, Arenas, Joaquín, Scozzari, Rosaria
יצא לאור 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...

מאת de Luna, Noemí, Brull, Astrid, Guiu, Josep Maria, Lucia, Alejandro, Martin, Miguel Angel, Arenas, Joaquin, Martí, Ramon, Andreu, Antoni L., Pinós, Tomàs
הוצא לאור ב Dis Model Mech (2015)

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

מאת Brull, Astrid, de Luna, Noemí, Blanco-Grau, Albert, Lucia, Alejandro, Martin, Miguel Angel, Arenas, Joaquin, Martí, Ramon, Andreu, Antoni L, Pinós, Tomàs
הוצא לאור ב J Physiol (2015)

Respiratory chain enzyme deficiency induces mitochondrial location of actin-binding gelsolin to modulate the oligomerization of VDAC complexes and cell survival

מאת García-Bartolomé, Alberto, Peñas, Ana, Marín-Buera, Lorena, Lobo-Jarne, Teresa, Pérez-Pérez, Rafael, Morán, María, Arenas, Joaquín, Martín, Miguel A., Ugalde, Cristina
הוצא לאור ב Hum Mol Genet (2017)

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

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

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

מאת 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
יצא לאור 2010-10-01

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

מאת 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
הוצא לאור ב J Proteomics (2014)

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

מאת 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
הוצא לאור ב Biol Open (2014)

A Novel Missense Variant Associated with A Splicing Defect in A Myopathic Form of PGK1 Deficiency in The Spanish Population

מאת Garcia-Solaesa, Virginia, Serrano-Lorenzo, Pablo, Ramos-Arroyo, Maria Antonia, Blázquez, Alberto, Pagola-Lorz, Inmaculada, Artigas-López, Mercè, Arenas, Joaquín, Martín, Miguel A., Jericó-Pascual, Ivonne
הוצא לאור ב Genes (Basel) (2019)