Maria Sabater-Arcis
Overview
Explore the profile of Maria Sabater-Arcis including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
12
Citations
1310
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Moreno N, Sabater-Arcis M, Sevilla T, Alonso M, Ohana J, Bargiela A, et al.
Biol Res
. 2024 May;
57(1):29.
PMID: 38760841
Background: We recently reported that upregulation of Musashi 2 (MSI2) protein in the rare neuromuscular disease myotonic dystrophy type 1 contributes to the hyperactivation of the muscle catabolic processes autophagy...
2.
Mughal S, Sabater-Arcis M, Artero R, Ramon-Azcon J, Fernandez-Costa J
Dis Model Mech
. 2024 Apr;
17(4).
PMID: 38655653
Steroid myopathy is a clinically challenging condition exacerbated by prolonged corticosteroid use or adrenal tumors. In this study, we engineered a functional three-dimensional (3D) in vitro skeletal muscle model to...
3.
Sabater-Arcis M, Moreno N, Sevilla T, Alonso M, Bargiela A, Artero R
Biomed J
. 2023 Oct;
47(4):100667.
PMID: 37797921
Background: Myotonic dystrophy type 1 (DM1) is a rare neuromuscular disease caused by a CTG repeat expansion in the 3' untranslated region of the DM1 protein kinase gene. Characteristic degenerative...
4.
Pont I, Galiana-Rosello C, Sabater-Arcis M, Bargiela A, Frias J, Albelda M, et al.
Org Biomol Chem
. 2022 Dec;
21(5):1000-1007.
PMID: 36541358
Two new ligands (TPB3P and TPB3Py) showing a strong stabilisation effect and good selectivity for G4 over duplex DNAs have been synthesised. The ligands hold three analogous polyamine pendant arms...
5.
Sabater-Arcis M, Bargiela A, Moreno N, Poyatos-Garcia J, Vilchez J, Artero R
Mol Ther Nucleic Acids
. 2021 Sep;
25:652-667.
PMID: 34589284
Skeletal muscle symptoms strongly contribute to mortality of myotonic dystrophy type 1 (DM1) patients. DM1 is a neuromuscular genetic disease caused by CTG repeat expansions that, upon transcription, sequester the...
6.
Martinez-Chacon G, Paredes-Barquero M, Yakhine-Diop S, Uribe-Carretero E, Bargiela A, Sabater-Arcis M, et al.
Cell Biol Toxicol
. 2021 Aug;
39(3):751-770.
PMID: 34448959
Autophagy is a conserved intracellular catabolic pathway that removes cytoplasmic components to contribute to neuronal homeostasis. Accumulating evidence has increasingly shown that the induction of autophagy improves neuronal health and...
7.
Klionsky D, Abdel-Aziz A, Abdelfatah S, Abdellatif M, Abdoli A, Abel S, et al.
Autophagy
. 2021 Feb;
17(1):1-382.
PMID: 33634751
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our...
8.
Ozimski L, Sabater-Arcis M, Bargiela A, Artero R
Biol Rev Camb Philos Soc
. 2020 Dec;
96(2):716-730.
PMID: 33269537
Myotonic dystrophy type 1 (DM1) is the most prevalent form of muscular dystrophy in adults and yet there are currently no treatment options. Although this disease causes multisystemic symptoms, it...
9.
Sabater-Arcis M, Bargiela A, Furling D, Artero R
Mol Ther Nucleic Acids
. 2019 Dec;
19:278-292.
PMID: 31855836
Unstable CTG expansions in the 3' UTR of the DMPK gene are responsible for myotonic dystrophy type 1 (DM1) condition. Muscle dysfunction is one of the main contributors to DM1...
10.
Bargiela A, Sabater-Arcis M, Espinosa-Espinosa J, Zulaica M, de Munain A, Artero R
Proc Natl Acad Sci U S A
. 2019 Nov;
116(50):25203-25213.
PMID: 31754023
Myotonic dystrophy type 1 (DM1) is a life-threatening and chronically debilitating neuromuscular disease caused by the expansion of a CTG trinucleotide repeat in the 3' UTR of the gene. The...