Dermic-derived fibroblasts for the study of amyotrophic lateral sclerosis

le Riancho, Javier, Arozamena, Sara, López de Munaín, Adolfo
Foilsithe in Neural Regen Res (2020)

Editorial: Role of Stem Cells in Skeletal Muscle Development, Regeneration, Repair, Aging, and Disease

le Muñoz-Cánoves, Pura, Carvajal, Jaime J., Lopez de Munain, Adolfo, Izeta, Ander
Foilsithe in Front Aging Neurosci (2016)

Age‐related cognitive decline in myotonic dystrophy type 1: An 11‐year longitudinal follow‐up study

le Labayru, Garazi, Aliri, Jone, Zulaica, Miren, López de Munain, Adolfo, Sistiaga, Andone
Foilsithe in J Neuropsychol (2019)

Epitope Mapping of Antibodies to Alpha-Synuclein in LRRK2 Mutation Carriers, Idiopathic Parkinson Disease Patients, and Healthy Controls

le Alvarez-Castelao, Beatriz, Gorostidi, Ana, Ruíz-Martínez, Javier, López de Munain, Adolfo, Castaño, José G.
Foilsithe 2014

Social cognition in myotonic dystrophy type 1: Specific or secondary impairment?

le Labayru, Garazi, Arenzana, Irati, Aliri, Jone, Zulaica, Miren, López de Munain, Adolfo, Sistiaga A., Andone
Foilsithe in PLoS One (2018)

High prevalence of mutations affecting the splicing process in a Spanish cohort with autosomal dominant retinitis pigmentosa

le Ezquerra-Inchausti, Maitane, Barandika, Olatz, Anasagasti, Ander, Irigoyen, Cristina, López de Munain, Adolfo, Ruiz-Ederra, Javier
Foilsithe in Sci Rep (2017)

Increased Muscleblind levels by chloroquine treatment improve myotonic dystrophy type 1 phenotypes in in vitro and in vivo models

le Bargiela, Ariadna, Sabater-Arcis, Maria, Espinosa-Espinosa, Jorge, Zulaica, Miren, Lopez de Munain, Adolfo, Artero, Ruben
Foilsithe in Proc Natl Acad Sci U S A (2019)

Genealogy of the neurodegenerative diseases based on a meta-analysis of age-stratified incidence data

le Gerovska, Daniela, Irizar, Haritz, Otaegi, David, Ferrer, Isidre, López de Munain, Adolfo, Araúzo-Bravo, Marcos J.
Foilsithe in Sci Rep (2020)

Inactivation of CDK/pRb Pathway Normalizes Survival Pattern of Lymphoblasts Expressing the FTLD-Progranulin Mutation c.709-1G>A

le Alquezar, Carolina, Esteras, Noemí, Alzualde, Ainhoa, Moreno, Fermín, Ayuso, Matilde S., López de Munain, Adolfo, Martín-Requero, Ángeles
Foilsithe 2012

The panniculus carnosus muscle: an evolutionary enigma at the intersection of distinct research fields

le Naldaiz‐Gastesi, Neia, Bahri, Ola A., López de Munain, Adolfo, McCullagh, Karl J. A., Izeta, Ander
Foilsithe in J Anat (2018)

Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations

le Lasa-Elgarresta, Jaione, Mosqueira-Martín, Laura, Naldaiz-Gastesi, Neia, Sáenz, Amets, López de Munain, Adolfo, Vallejo-Illarramendi, Ainara
Foilsithe in Int J Mol Sci (2019)

Regional brain atrophy in gray and white matter is associated with cognitive impairment in Myotonic Dystrophy type 1

le Labayru, Garazi, Diez, Ibai, Sepulcre, Jorge, Fernández, Esther, Zulaica, Miren, Cortés, Jesús M., López de Munain, Adolfo, Sistiaga, Andone
Foilsithe in Neuroimage Clin (2019)

Modeling neural differentiation on micropatterned substrates coated with neural matrix components

le García-Parra, Patricia, Cavaliere, Fabio, Maroto, Marcos, Bilbao, Leire, Obieta, Isabel, López de Munain, Adolfo, Álava, José Iñaki, Izeta, Ander
Foilsithe 2012

Muscle wasting in myotonic dystrophies: a model of premature aging

le Mateos-Aierdi, Alba Judith, Goicoechea, Maria, Aiastui, Ana, Fernández-Torrón, Roberto, Garcia-Puga, Mikel, Matheu, Ander, López de Munain, Adolfo
Foilsithe in Front Aging Neurosci (2015)

Calpain 3 deficiency affects SERCA expression and function in the skeletal muscle

le Toral-Ojeda, Ivan, Aldanondo, Garazi, Lasa-Elgarresta, Jaione, Lasa-Fernández, Haizpea, Fernández-Torrón, Roberto, López de Munain, Adolfo, Vallejo-Illarramendi, Ainara
Foilsithe in Expert Rev Mol Med (2016)

A new approach based on targeted pooled DNA sequencing identifies novel mutations in patients with Inherited Retinal Dystrophies

le Ezquerra-Inchausti, Maitane, Anasagasti, Ander, Barandika, Olatz, Garay-Aramburu, Gonzaga, Galdós, Marta, López de Munain, Adolfo, Irigoyen, Cristina, Ruiz-Ederra, Javier
Foilsithe in Sci Rep (2018)

Author Correction: A new approach based on targeted pooled DNA sequencing identifies novel mutations in patients with Inherited Retinal Dystrophies

le Ezquerra-Inchausti, Maitane, Anasagasti, Ander, Barandika, Olatz, Garay-Aramburu, Gonzaga, Galdós, Marta, López de Munain, Adolfo, Irigoyen, Cristina, Ruiz-Ederra, Javier
Foilsithe in Sci Rep (2019)

Allosteric Modulation of GSK-3β as a New Therapeutic Approach in Limb Girdle Muscular Dystrophy R1 Calpain 3-Related

le Rico, Anabel, Guembelzu, Garazi, Palomo, Valle, Martínez, Ana, Aiastui, Ana, Casas-Fraile, Leire, Valls, Andrea, López de Munain, Adolfo, Sáenz, Amets
Foilsithe in Int J Mol Sci (2021)

A neural extracellular matrix-based method for in vitro hippocampal neuron culture and dopaminergic differentiation of neural stem cells

le García-Parra, Patricia, Maroto, Marcos, Cavaliere, Fabio, Naldaiz-Gastesi, Neia, Álava, José Iñaki, García, Antonio G, López de Munain, Adolfo, Izeta, Ander
Foilsithe 2013

Expression Profiling Analysis Reveals Key MicroRNA–mRNA Interactions in Early Retinal Degeneration in Retinitis Pigmentosa

le Anasagasti, Ander, Ezquerra-Inchausti, Maitane, Barandika, Olatz, Muñoz-Culla, Maider, Caffarel, María M., Otaegui, David, López de Munain, Adolfo, Ruiz-Ederra, Javier
Foilsithe in Invest Ophthalmol Vis Sci (2018)