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EMBO Reports|July 12, 2015
(Patho-)physiological relevance of PINK1-dependent ubiquitin phosphorylationFabienne C Fiesel, Maya Ando, Roman Hudec, et al.
BMC Genomics|February 4, 2014
Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathiesSusana Graciela Kalko, Sonia Paco, Cristina Jou, et al.
Human Molecular Genetics|September 17, 2018
Nuclear localization and phosphorylation modulate pathological effects of alpha-synucleinRaquel Pinho, Isabel Paiva, Kristina Gotovac Jercic, et al.
Acta Neuropathologica Communications|August 17, 2022
Sporadic Creutzfeldt-Jakob disease VM1: phenotypic and molecular characterization of a novel subtype of human prion diseaseEllen Gelpi, Simone Baiardi, Carlos Nos, et al.
Autophagy|June 28, 2018
Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body diseaseXu Hou, Fabienne C Fiesel, Dominika Truban, et al.
Acta Neuropathologica|April 21, 2021
TREM2 expression in the brain and biological fluids in prion diseasesDaniela Diaz-Lucena, Niels Kruse, Katrin Thüne, et al.
Genome Research|May 27, 2011
A DNA methylation fingerprint of 1628 human samplesAgustin F Fernandez, Yassen Assenov, Jose Ignacio Martin-Subero, et al.
JAMA Neurology|November 18, 2014
Clinical correlations with Lewy body pathology in LRRK2-related Parkinson diseaseLorraine V Kalia, Anthony E Lang, Lili-Naz Hazrati, et al.
Nature Communications|March 29, 2019
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusionsMontse Olivé, Martin Engvall, Gianina Ravenscroft, et al.
Brain : a Journal of Neurology|August 24, 2018
The human brainome: network analysis identifies HSPA2 as a novel Alzheimer’s disease targetVladislav A Petyuk, Rui Chang, Manuel Ramirez-Restrepo, et al.
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