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Biomedicines|May 28, 2022
Lipid Metabolic Alterations in the ALS-FTD Spectrum of DisordersJuan Miguel Godoy-Corchuelo, Luis C Fernández-Beltrán, Zeinab Ali, et al.
Human Molecular Genetics|June 28, 2013
IGF-1 receptor antagonism inhibits autophagyMaurizio Renna, Carla F Bento, Angeleen Fleming, et al.
Human Molecular Genetics|March 7, 2018
A genetic modifier suggests that endurance exercise exacerbates Huntington's diseaseSilvia Corrochano, Gonzalo Blanco, Debbie Williams, et al.
Scientific Reports|February 1, 2024
Leptin haploinsufficiency exerts sex-dependent partial protection in SOD1<sup>G93A</sup> mice by reducing inflammatory pathways in the adipose tissueLuis C Fernández-Beltrán, Zeinab Ali, Angélica Larrad-Sanz, et al.
Acta Neuropathologica|September 4, 2025
TDP-43 dysregulation impairs cholesterol metabolism linked with myelination defectsIrene García-Toledo, Juan M Godoy-Corchuelo, Luis C Fernández-Beltrán, et al.
Disease Models & Mechanisms|September 29, 2023
Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterationsZeinab Ali, Juan M Godoy-Corchuelo, Aurea B Martins-Bach, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 2018
ZNRF3 functions in mammalian sex determination by inhibiting canonical WNT signalingAbigail Harris, Pam Siggers, Silvia Corrochano, et al.
Human Molecular Genetics|December 4, 2014
A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicityPeter I Joyce, Philip Mcgoldrick, Rachele A Saccon, et al.
Brain : a Journal of Neurology|October 29, 2014
Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysisSilvia Corrochano, Roope Männikkö, Peter I Joyce, et al.
Neurobiology of Disease|February 17, 2024
TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43Juan M Godoy-Corchuelo, Zeinab Ali, Jose M Brito Armas, et al.
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