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Ruben Artero
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Journal Articles

Taurine activates the AKT–mTOR axis to restore muscle mass and contractile strength in human 3D in vitro models of steroid myopathy

In collection:
Advanced in vitro models
Sheeza Mughal, Maria Sabater-Arcis, Ruben Artero, Javier Ramón-Azcón, Juan M. Fernández-Costa
Journal: Disease Models & Mechanisms
Dis Model Mech (2024) 17 (4): dmm050540.
https://doi.org/10.1242/dmm.050540
Published: 24 April 2024
View article titled, Taurine activates the AKT–mTOR axis to restore muscle mass and contractile strength in human 3D in vitro models of steroid myopathy
Open the PDF for Taurine activates the AKT–mTOR axis to restore muscle mass and contractile strength in human 3D in vitro models of steroid myopathy in another window
Includes: Supplementary data
Journal Articles

Rabphilin involvement in filtration and molecular uptake in Drosophila nephrocytes suggests a similar role in human podocytes

In collection:
Drosophila as a Disease Model
Estela Selma-Soriano, Beatriz Llamusi, Juan Manuel Fernández-Costa, Lauren Louise Ozimski, Rubén Artero, Josep Redón
Journal: Disease Models & Mechanisms
Dis Model Mech (2020) 13 (9): dmm041509.
https://doi.org/10.1242/dmm.041509
Published: 21 September 2020
View article titled, Rabphilin involvement in filtration and molecular uptake in Drosophila nephrocytes suggests a similar role in human podocytes
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Includes: Supplementary data
Journal Articles

Daunorubicin reduces MBNL1 sequestration caused by CUG-repeat expansion and rescues cardiac dysfunctions in a Drosophila model of myotonic dystrophy

Mouli Chakraborty, Chantal Sellier, Michel Ney, Villa Pascal, Nicolas Charlet-Berguerand, Ruben Artero, Beatriz Llamusi
Journal: Disease Models & Mechanisms
Dis Model Mech (2018) 11 (4): dmm032557.
https://doi.org/10.1242/dmm.032557
Published: 23 April 2018
View article titled, Daunorubicin reduces MBNL1 sequestration caused by CUG-repeat expansion and rescues cardiac dysfunctions in a Drosophila model of myotonic dystrophy
Open the PDF for Daunorubicin reduces MBNL1 sequestration caused by CUG-repeat expansion and rescues cardiac dysfunctions in a Drosophila model of myotonic dystrophy in another window
Includes: Supplementary data
Journal Articles

The Drosophila junctophilin gene is functionally equivalent to its four mammalian counterparts and is a modifier of a Huntingtin poly-Q expansion and the Notch pathway

In collection:
Drosophila as a Disease Model
Eduardo Calpena, Víctor López del Amo, Mouli Chakraborty, Beatriz Llamusí, Rubén Artero, Carmen Espinós, Máximo I. Galindo
Journal: Disease Models & Mechanisms
Dis Model Mech (2018) 11 (1): dmm029082.
https://doi.org/10.1242/dmm.029082
Published: 17 January 2018
View article titled, The Drosophila junctophilin gene is functionally equivalent to its four mammalian counterparts and is a modifier of a Huntingtin poly-Q expansion and the Notch pathway
Open the PDF for The Drosophila junctophilin gene is functionally equivalent to its four mammalian counterparts and is a modifier of a Huntingtin poly-Q expansion and the Notch pathway in another window
Includes: Supplementary data
Journal Articles

Pentamidine rescues contractility and rhythmicity in a Drosophila model of myotonic dystrophy heart dysfunction

Mouli Chakraborty, Estela Selma-Soriano, Emile Magny, Juan Pablo Couso, Manuel Pérez-Alonso, Nicolas Charlet-Berguerand, Ruben Artero, Beatriz Llamusi
Journal: Disease Models & Mechanisms
Dis Model Mech (2015) 8 (12): 1569–1578.
https://doi.org/10.1242/dmm.021428
Published: 1 December 2015
View article titled, Pentamidine rescues contractility and rhythmicity in a Drosophila model of myotonic dystrophy heart dysfunction
Open the PDF for Pentamidine rescues contractility and rhythmicity in a Drosophila model of myotonic dystrophy heart dysfunction in another window
Includes: Supplementary data
Journal Articles

Increased autophagy and apoptosis contribute to muscle atrophy in a myotonic dystrophy type 1 Drosophila model

Ariadna Bargiela, Estefanía Cerro-Herreros, Juan M. Fernandez-Costa, Juan J. Vilchez, Beatriz Llamusi, Ruben Artero
Journal: Disease Models & Mechanisms
Dis Model Mech (2015) 8 (7): 679–690.
https://doi.org/10.1242/dmm.018127
Published: 1 July 2015
View article titled, Increased autophagy and apoptosis contribute to muscle atrophy in a myotonic dystrophy type 1 Drosophila model
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Includes: Supplementary data
Journal Articles

Development of a Drosophila melanogaster spliceosensor system for in vivo high-throughput screening in myotonic dystrophy type 1

Irma García-Alcover, Jordi Colonques-Bellmunt, Raquel Garijo, José R. Tormo, Rubén Artero, Mari Carmen Álvarez-Abril, Arturo López Castel, Manuel Pérez-Alonso
Journal: Disease Models & Mechanisms
Dis Model Mech (2014) 7 (11): 1297–1306.
https://doi.org/10.1242/dmm.016592
Published: 1 November 2014
View article titled, Development of a Drosophila melanogaster spliceosensor system for in vivo high-throughput screening in myotonic dystrophy type 1
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Includes: Supplementary data
Journal Articles

Muscleblind, BSF and TBPH are mislocalized in the muscle sarcomere of a Drosophila myotonic dystrophy model

Beatriz Llamusi, Ariadna Bargiela, Juan M. Fernandez-Costa, Amparo Garcia-Lopez, Raffaella Klima, Fabian Feiguin, Ruben Artero
Journal: Disease Models & Mechanisms
Dis Model Mech (2013) 6 (1): 184–196.
https://doi.org/10.1242/dmm.009563
Published: 1 January 2013
View article titled, Muscleblind, BSF and TBPH are mislocalized in the muscle sarcomere of a Drosophila myotonic dystrophy model
Open the PDF for Muscleblind, BSF and TBPH are mislocalized in the muscle sarcomere of a Drosophila myotonic dystrophy model in another window
Includes: Supplementary data