ADOLFO JOSE
LOPEZ DE MUNAIN ARREGUI
PROFESORADO ASOCIADO
![Foto de Ana](/img/nophoto.png)
Ana
Aiastui Pujana
Publicaciones en las que colabora con Ana Aiastui Pujana (21)
2023
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Altered expression of proteins involved in metabolism in LGMDR1 muscle is lost in cell culture conditions
Orphanet Journal of Rare Diseases, Vol. 18, Núm. 1
2022
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Delay of EGF-Stimulated EGFR Degradation in Myotonic Dystrophy Type 1 (DM1)
Cells, Vol. 11, Núm. 19
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Pathogenic LRRK2 regulates centrosome cohesion via Rab10/RILPL1-mediated CDK5RAP2 displacement
iScience, Vol. 25, Núm. 6
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The parkinsonian LRRK2 R1441G mutation shows macroautophagy-mitophagy dysregulation concomitant with endoplasmic reticulum stress
Cell Biology and Toxicology, Vol. 38, Núm. 5, pp. 889-911
2021
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Allosteric modulation of GSK‐3β as a new therapeutic approach in limb girdle muscular dystrophy R1 Calpain 3‐related
International Journal of Molecular Sciences, Vol. 22, Núm. 14
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Patient-specific iPSC-derived cellular models of LGMDR1
Stem Cell Research, Vol. 53
2020
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Metabolic alterations in plasma from patients with familial and idiopathic Parkinson's disease
Aging, Vol. 12, Núm. 17, pp. 16690-16708
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Toxicity of necrostatin-1 in Parkinson’s disease models
Antioxidants, Vol. 9, Núm. 6, pp. 1-13
2019
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Impaired Mitophagy and Protein Acetylation Levels in Fibroblasts from Parkinson’s Disease Patients
Molecular Neurobiology, Vol. 56, Núm. 4, pp. 2466-2481
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RAB8, RAB10 and RILPL1 contribute to both LRRK2 kinase-mediated centrosomal cohesion and ciliogenesis deficits
Human Molecular Genetics, Vol. 28, Núm. 21, pp. 3552-3568
2018
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Acetylome in human fibroblasts from Parkinson’s disease patients
Frontiers in Cellular Neuroscience, Vol. 12
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Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
Molecular Neurodegeneration, Vol. 13, Núm. 1
2017
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FRZB and melusin, overexpressed in LGMD2A, regulate integrin β1D isoform replacement altering myoblast fusion and the integrin-signalling pathway
Expert Reviews in Molecular Medicine, Vol. 19
2016
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Identification and Characterization of the Dermal Panniculus Carnosus Muscle Stem Cells
Stem Cell Reports, Vol. 7, Núm. 3, pp. 411-424
2015
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Muscle wasting in myotonic dystrophies: A model of premature aging
Frontiers in Aging Neuroscience, Vol. 7, Núm. JUN
2014
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G2019S LRRK2 mutant fibroblasts from Parkinson's disease patients show increased sensitivity to neurotoxin 1-methyl-4-phenylpyridinium dependent of autophagy
Toxicology, Vol. 324, pp. 1-9
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LRRK2 delays degradative receptor trafficking by impeding late endosomal budding through decreasing Rab7 activity
Human Molecular Genetics, Vol. 23, Núm. 25, pp. 1-18
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Leucine-rich repeat kinase 2 modulates cyclooxygenase 2 and the inflammatory response in idiopathic and genetic Parkinson's disease
Neurobiology of Aging, Vol. 35, Núm. 5, pp. 1116-1124
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Murine muscle engineered from dermal precursors: An in vitro model for skeletal muscle generation, degeneration, and fatty infiltration
Tissue Engineering - Part C: Methods, Vol. 20, Núm. 1, pp. 28-41
2013
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Expanded CTG repeats trigger miRNA alterations in Drosophila that are conserved in myotonic dystrophy type 1 patients
Human Molecular Genetics, Vol. 22, Núm. 4, pp. 704-716