Accès ouvert
2026
article
OpenAlex
Marc Carceles‐Cordon, Eliza M. Brody, Masen L. Boucher, Michael D. Gallagher et autres
Glycoprotein nonmetastatic melanoma B (GPNMB) is critical to cellular uptake of pathological forms of alpha-synuclein (aSyn), the hallmark disease protein in Parkinson's disease (PD). Here, we demonstrate that the non-membrane-anchored, extracellular domain of GPNMB can function in a non-cell-autonomous manner. In the …
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Accès ouvert
2026
preprint
OpenAlex
Marc Carceles‐Cordon, Eliza M. Brody, Masen L. Boucher, Michael D. Gallagher et autres
ABSTRACT Glycoprotein nonmetastatic melanoma B (GPNMB), encoded by the target gene ( GPNMB ) of a Parkinson’s disease (PD) risk locus, acts as a secreted factor mediating inflammatory effects in the context of immunity and cancer. In a neurodegenerative disease context, GPNMB …
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2025
article
OpenAlex
George T. Kannarkat, R. Tyler Skrinak, Travis L. Unger, Rebecca Zack et autres
This study investigates the source and pathogenic potential of blood-based alpha-synuclein (aSyn) using conformation-selective antibodies.
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Accès ouvert
2023
article
OpenAlex
Maria E. Diaz‐Ortiz, Nimansha Jain, Michael D. Gallagher, Marijan Posavi et autres
allele-specific expression (ASE) in brain lysates from cognitively normal controls (NC) and Parkinson's disease (PD) individuals. • Builds on the ASE protocol of Mayba et al. (2014) and extends application from cells to human tissue. • Increased sensitivity by enrichment for desired …
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Accès ouvert
2022
article
OpenAlex
Maria E. Diaz‐Ortiz, Yunji Seo, Marijan Posavi, Marc Carceles Cordon et autres
Many risk loci for Parkinson’s disease (PD) have been identified by genome-wide association studies (GWASs), but target genes and mechanisms remain largely unknown. We linked the GWAS-derived chromosome 7 locus (sentinel single-nucleotide polymorphism rs199347) to GPNMB through colocalization analyses of expression quantitative …
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Accès ouvert
2022
article
OpenAlex
Junchao Shen, Noor Amari, Rebecca Zack, R. Tyler Skrinak et autres
OBJECTIVE: Using a multi-cohort, discovery-replication-validation design, we sought new plasma biomarkers that predict which individuals with Parkinson's disease (PD) will experience cognitive decline. METHODS: In 108 discovery cohort PD individuals and 83 replication cohort PD individuals, we measured 940 plasma proteins on …
us
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Accès ouvert
2022
preprint
OpenAlex
Junchao Shen, Noor Amari, Rebecca Zack, R. Tyler Skrinak et autres
ABSTRACT Objective Using a multi-cohort, Discovery-Replication-Validation design, we sought new plasma biomarkers that predict which PD individuals will experience cognitive decline. Methods In 108 Discovery Cohort PD individuals and 83 Replication Cohort PD individuals, we measured 940 plasma proteins on an aptamer-based …
us
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Accès ouvert
2021
article
OpenAlex
Fei Mao, John Robinson, Travis L. Unger, Marijan Posavi et autres
cn, us
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Accès ouvert
2021
preprint
OpenAlex
Fei Mao, John Robinson, Travis L. Unger, Marijan Posavi et autres
ABSTRACT The neurodegenerative diseases amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration with TAR DNA-binding protein-43 (TDP-43) inclusions (FTLD-TDP) share the neuropathological hallmark of aggregates of TDP-43. However, factors governing the severity and regional distribution of TDP-43 pathology, which may account for …
cn, us
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Accès ouvert
2021
preprint
OpenAlex
Elisia Clark, Rakshita A. Charan, Travis L. Unger, Johanna Busch et autres
us
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Accès ouvert
2019
erratum
OpenAlex
Chia-Yu Chung, Amit Berson, Jason R. Kennerdell, Ashley Sartoris et autres
The original version of this Article contained an error in the author affiliations. The affiliation of Alice Chen-Plotkin with the Department of Neurology, Perelman School of Medicine, Philadelphia, PA, 19104 USA was inadvertently omitted. This has now been corrected in both the …
us, kr
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Accès ouvert
2018
article
OpenAlex
Chia‐Yu Chung, Amit Berson, Jason R. Kennerdell, Ashley Sartoris et autres
TDP-43 is the major disease protein associated with amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration with ubiquitinated inclusions (FTLD-TDP). Here we identify the transcriptional elongation factor Ell-a shared component of little elongation complex (LEC) and super elongation complex (SEC)-as a strong …
us, kr
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