M. Goicoechea

发表

Muscle wasting in myotonic dystrophies: a model of premature aging

A. Matheu, A. Aiastui, A. López de Munain, 2015, Front. Aging Neurosci..

Isolation and characterization of myogenic precursor cells from human cremaster muscle

Pedro M. Baptista, A. Izeta, A. López de Munain, 2019, Scientific Reports.

CAPN3 mutations in patients with idiopathic eosinophilic myositis

N. Romero, N. Lévy, F. Leturcq, 2006 .

Identification and Characterization of the Dermal Panniculus Carnosus Muscle Stem Cells

M. Araúzo-Bravo, J. García-Verdugo, A. Bernad, 2016, Stem cell reports.

Advances in gene therapies for limb-girdle muscular dystrophies

A. Aiastui, A. L. de Munain, A. J. Mateos-Aierdi, 2014 .

Molecular Characterization of Putative Modulatory Factors in Two Spanish Families with A1555G Deafness

A. López de Munain, J. Pérez-Tur, D. Otaegui, 2008, Audiology and Neurotology.

Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy?

K. Bushby, N. Lévy, F. Leturcq, 2011, Clinical genetics.

Characterization of novel CAPN3 isoforms in white blood cells: an alternative approach for limb-girdle muscular dystrophy 2A diagnosis

A. López de Munain, I. Illa, X. Ferrer, 2008, neurogenetics.

Patient-specific iPSC-derived cellular models of LGMDR1.

Á. Raya, A. Aiastui, A. López de Munain, 2021, Stem cell research.

Minimizing creatine kinase variability in rats for neuromuscular research purposes

J. Emparanza, A. L. de Munain, D. Otaegui, 2008, Laboratory animals.

Negative evidence for stachydrine or Galeopsis ladanum L. seeds as the causal agents of coturnism after quail meat ingestion.

A. López de Munain, A. López de Cerain, A. Gil, 2009, Journal of agricultural and food chemistry.

LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene.

J. Emparanza, D. Figarella-Branger, C. Bönnemann, 2005, Brain : a journal of neurology.

Isolation and characterization of myogenic precursor cells from human cremaster muscle

Pedro M. Baptista, A. Izeta, A. López de Munain, 2019, Scientific Reports.

Murine muscle engineered from dermal precursors: an in vitro model for skeletal muscle generation, degeneration, and fatty infiltration.

J. García-Verdugo, A. Izeta, A. Aiastui, 2014, Tissue engineering. Part C, Methods.

CD24 V/V is an allele associated with the risk of developing multiple sclerosis in the Spanish population

J. Ruiz‐Martinez, A. L. de Munain, D. Otaegui, 2006, Multiple sclerosis.

Mis-splicing of Tau exon 10 in myotonic dystrophy type 1 is reproduced by overexpression of CELF2 but not by MBNL1 silencing.

L. Buée, V. Deramecourt, N. Sergeant, 2011, Biochimica et biophysica acta.

In Vitro Correction of a Pseudoexon‐Generating Deep Intronic Mutation in LGMD2A by Antisense Oligonucleotides and Modified Small Nuclear RNAs

J. Valcárcel, L. García, P. Fortes, 2013, Human mutation.

Gynecologic cancer screening in women at high risk of Lynch syndrome.

A. Carrato, D. Salas, C. Guillén-Ponce, 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Late-Stage Metastatic Melanoma Emerges through a Diversity of Evolutionary Pathways

G. Stamp, L. Pickering, K. Edmonds, 2023, Cancer discovery.

Does the severity of the LGMD2A phenotype in compound heterozygotes depend on the combination of mutations?

F. Leturcq, J. Kaplan, H. Sorimachi, 2011, Muscle & nerve.

G.P.4.15 CAPN3 mutations in patients with idiopathic eosinophilic myositis: A predystrophic stage of LGMD2A?

K. Bushby, F. Leturcq, F. Hanisch, 2007, Neuromuscular Disorders.