Accès ouvert
2025
preprint
OpenAlex
Fabio Lauria, Federica Maniscalco, Cecilia Perrucci, Marta Marchioretto et autres
Abstract The RNA-binding protein TDP-43 is a major contributor and a pathological hallmark of Amyotrophic Lateral Sclerosis (ALS), yet how TDP-43 dysregulation mechanistically alters protein synthesis across neuronal compartments and disease models remains unclear. Here, we dissected TDP-43–driven translational alterations in both …
it
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Accès ouvert
2023
article
OpenAlex
Valentina Laghezza Masci, Davide Stefanoni, Angelo D’Alessandro, Marta Zambelli et autres
Cancer therapies use different compounds of synthetic and natural origin. However, despite some positive results, relapses are common, as standard chemotherapy regimens are not fully capable of completely eradicating cancer stem cells. While vinblastine is a common chemotherapeutic agent in the treatment …
it, us
(code pays fourni par la source)
Accès ouvert
2021
article
OpenAlex
Nausicaa Valentina Licata, Riccardo Cristofani, Sally E. Salomonsson, Katherine Wilson et autres
Intronic GGGGCC (G4C2) hexanucleotide repeat expansion within the human C9orf72 gene represents the most common cause of familial forms of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) (C9ALS/FTD). Repeat‐associated non‐AUG (RAN) translation of repeat‐containing C9orf72 RNA results in the production of …
it, gb, us
(code pays fourni par la source)
Accès ouvert
2021
article
OpenAlex
Daniele Pollini, Rosa Loffredo, Federica Maniscalco, Marina Cardano et autres
Matrin3 (MATR3) is a nuclear RNA/DNA-binding protein that plays pleiotropic roles in gene expression regulation by directly stabilizing target RNAs and supporting the activity of transcription factors by modulating chromatin architecture. MATR3 is involved in the differentiation of neural cells, and, here, …
it
(code pays fourni par la source)
Accès ouvert
2020
preprint
OpenAlex
Daniele Pollini, Rosa Loffredo, Annalisa Rossi, Mariachiara Micaelli et autres
it
(code pays fourni par la source)
Accès ouvert
2018
article
OpenAlex
Daniele Pollini, Rosa Loffredo, Marina Cardano, Luciano Conti et autres
Fibroblasts isolated from an Amyotrophic Lateral Sclerosis (ALS)-patient carrying a mutation in Matrin-3 (p.Q66K -MATR3) gene were reprogrammed to the pluripotency stage by using non-integrating episomal plasmids. We generated the Q66K#44DRM induced pluripotent stem cell (iPSC) line that showed regular karyotype, expressed …
it
(code pays fourni par la source)