Glial α‐synuclein promotes neurodegeneration characterized by a distinct transcriptional program in vivo

AL Olsen, MB Feany - Glia, 2019 - Wiley Online Library
Abstract α‐Synucleinopathies are neurodegenerative diseases that are characterized
pathologically by α‐synuclein inclusions in neurons and glia. The pathologic contribution of …

Prenatal bisphenol A exposure in mice induces multitissue multiomics disruptions linking to cardiometabolic disorders

L Shu, Q Meng, G Diamante, B Tsai, YW Chen… - …, 2019 - academic.oup.com
The health impacts of endocrine-disrupting chemicals (EDCs) remain debated, and their
tissue and molecular targets are poorly understood. In this study, we leveraged systems …

[HTML][HTML] Can targeted metabolomics predict depression recovery? Results from the CO-MED trial

AH Czysz, C South, BS Gadad, E Arning… - Translational …, 2019 - nature.com
Metabolomics is a developing and promising tool for exploring molecular pathways
underlying symptoms of depression and predicting depression recovery. The Absolute …

[HTML][HTML] Gene co-expression networks shed light into diseases of brain iron accumulation

C Bettencourt, P Forabosco, S Wiethoff, M Heidari… - Neurobiology of …, 2016 - Elsevier
Aberrant brain iron deposition is observed in both common and rare neurodegenerative
disorders, including those categorized as Neurodegeneration with Brain Iron Accumulation …

[HTML][HTML] Identification and characterization of noncoding RNAs-associated competing endogenous RNA networks in major depressive disorder

ZL Zou, Y Ye, B Zhou, Y Zhang - World Journal of Psychiatry, 2023 - ncbi.nlm.nih.gov
BACKGROUND Major depressive disorder (MDD) is a common and serious mental illness.
Many novel genes in MDD have been characterized by high-throughput methods such as …

Identification of key genes and signaling pathway in the pathogenesis of Huntington's disease via bioinformatics and next generation sequencing data analysis

BM Vastrad, CM Vastrad - bioRxiv, 2024 - biorxiv.org
Huntington's disease (HD) is the primary cause of progressive motor deficits, psychiatric
symptoms, and cognitive impairment. The exact molecular mechanisms of HD pathogenesis …

Next generation sequencing for rapid diagnosis of a rare early onset spastic paraplegia: a novel pathological variant in FA2H gene

MC González-González, M Gutierrez… - Revista del Laboratorio …, 2018 - Elsevier
Introduction Hereditary spastic paraplegia is a group of inherited neurological disorders with
predominant manifestations of lower extremity weakness and severe spasticity. This is a …

[PDF][PDF] Unravel the role of fatty acid hydroxylase FAXDC2

PMM Pereira - 2019 - repositorio-aberto.up.pt
In mammalian cells, lipids are the second major component of cellular mass and serve as
structural components and building blocks of cellular membranes. However, lipids are also …

Prenatal Bisphenol A Exposure in Mice Induces Multitissue Multiomics Disruptions Linking to Cardiometabolic Disorders

A Mikhail, H Luk, B Ritz, P Allard, X Yang - 2019 - academic.oup.com
The health impacts of endocrine-disrupting chemicals (EDCs) remain debated, and their
tissue and molecular targets are poorly understood. In this study, we leveraged systems …

The functional analysis of rare genetic variants in a familial neurodegenerative spectrum disorder

S Faergeman - 2018 - ora.ox.ac.uk
Whole genome sequencing can enable an unbiased approach to the diagnosis and to the
understanding of genetic aetiology of neurodegenerative diseases, which are a clinically …