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Autophagy|December 15, 2024
Endogenous interactomes of MFN1 and MFN2 provide novel insights into interorganelle communication and autophagyIsabel Gordaliza-Alaguero, Paula Sànchez-Fernàndez-de-Landa, Dragana Radivojevikj, et al.
Acta Oto-Laryngologica|July 7, 2015
Development and evaluation of an audiology app for iPhone/iPad mobile devicesFrancisco Larrosa, Julio Rama-Lopez, Jesus Benitez, et al.
Journal of Neuromuscular Diseases|August 29, 2022
Real-world Adherence to Nusinersen in Adults with Spinal Muscular Atrophy in the US: A Multi-site Chart Review StudyLauren Elman, Bora Youn, Crystal M Proud, et al.
Analytical Chemistry|July 24, 2024
Evaluation of a Liquid Chromatography-Tandem Mass Spectrometry Method for the Analysis of Glucosylceramide and Galactosylceramide Isoforms in Cerebrospinal Fluid of Parkinson's Disease PatientsLaura Castillo-Ribelles, Jose Antonio Arranz-Amo, Jorge Hernández-Vara, et al.
Nature Communications|March 9, 2019
Brain tyrosinase overexpression implicates age-dependent neuromelanin production in Parkinson's disease pathogenesisIria Carballo-Carbajal, Ariadna Laguna, Jordi Romero-Giménez, et al.
Cell|June 15, 2010
Lysosomal proteolysis and autophagy require presenilin 1 and are disrupted by Alzheimer-related PS1 mutationsJu-Hyun Lee, W Haung Yu, Asok Kumar, et al.
The Journal of Clinical Investigation|January 4, 2008
Dopamine-modified alpha-synuclein blocks chaperone-mediated autophagyMarta Martinez-Vicente, Zsolt Talloczy, Susmita Kaushik, et al.
JCI Insight|November 9, 2023
FGF23 directly inhibits osteoprogenitor differentiation in Dmp1-knockout miceGuillaume Courbon, Dominik Kentrup, Jane Joy Thomas, et al.
Antimicrobial Agents and Chemotherapy|May 17, 2023
Antimicrobial Activity of Cefiderocol against the Carbapenemase-Producing Enterobacter cloacae Complex and Characterization of Reduced Susceptibility Associated with Metallo-β-Lactamase VIM-1Cristina Lasarte-Monterrubio, Paula Guijarro-Sánchez, Juan Carlos Vázquez-Ucha, et al.
NPJ Parkinson'S Disease|October 6, 2022
Lysosomal lipid alterations caused by glucocerebrosidase deficiency promote lysosomal dysfunction, chaperone-mediated-autophagy deficiency, and alpha-synuclein pathologyAlba Navarro-Romero, Irene Fernandez-Gonzalez, Jordi Riera, et al.
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