Amyotrophic lateral sclerosis (ALS) is adevastating adult-onset disease characterized by gradual degeneration of upperand lower motor neurons (MN) which leads to progressive muscle weakness andparalysis. Non-cell autonomous mechanisms are nowadays considered to play acrucial role in its onset and progression. Thus, the skeletal muscle ishypothesized to actively contribute to ALS
20/06/25
Mecanismos celulares no neuronales de patología TDP-43 y su propagación en la ELA: nuevas perspectivas a partir de modelos de Drosophila melanogaster
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16/06/25
RNA Misprocessing in Neurodegeneration: Investigation of Novel RNA Targeting and Sequencing Approaches in Frontotemporal Dementia and Huntington’s Disease
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27/05/25
Modeling bone metastatic cancer microenvironments: In vitro, ex vivo, and humanized tissue-engineered approaches
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23/05/25
Evaluación del Riesgo Cardiovascular en Mujeres con Menopausia mediante el Análisis Multimodal de Datos que Permite Estrategias de Prevención Personalizadas. / An iPSC-derived motor neuron platform to study non-cell-autonomous ALS pathogenesis
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15/04/25
Uncovering biomarkers of response to neoadjuvant endocrine therapy in oestrogen receptor-positive breast cancer
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