Results 251 to 260 of about 67,783 (305)

A Cross‐Disease Microglial Transcriptional Program Characterizes Neurodegeneration and Highlights SPP1 as a Biomarker

Glia, Volume 74, Issue 6, June 2026.
Distinct microglial subpopulations are depicted, highlighting variations in gene expression and functional roles in response to specific disease conditions and the complexity of microglial activation and differentiation in neurodegeneration. ABSTRACT Microglial cells are key players in maintaining brain homeostasis and responding to pathological ...
Alessandro Palma, Roberta Stefanelli, Francesco Trenta, Chiara Projetti, Greta Massa, Sonia Canterini, Maria Teresa Fiorenza   +6 more
wiley   +1 more source

Elevated plasma levels of alpha-synuclein are dispensable for Parkinson's disease pathology. [PDF]

NPJ Parkinsons Dis
Jeong JY, Kim N, Li Y, Kim DJ, Kim HK, Oh WJ.   +5 more
europepmc   +1 more source

Alpha-synuclein interacts with regulators of ATP homeostasis in mitochondria. [PDF]

Nat Commun
Serdiuk T, Fleischmann Y, Ghosh D, Delparente A, Reber V, Frey L, Rhyner D, Gerez J, Volkmar N, Kralickova L, Mas G, Dörig C, Hiller S, Schibli R, Mu L, Picotti P, Riek R.   +16 more
europepmc   +1 more source

Alpha-Synuclein Lesions in the Peripheral Nervous System of the Larynx in Parkinson's Disease. [PDF]

Dysphagia
Mu L, Chen J, Nyirenda T, Li J, Hegland KW, Adler CH, Caviness JN, Shill HA, Serrano GE, Beach TG, Arizona Parkinson’s Disease Consortium.   +10 more
europepmc   +1 more source

Imaging alpha-synuclein pathology in Parkinson's disease. [PDF]

Neural Regen Res
Ni R.
europepmc   +1 more source

Expression of human A53T alpha-synuclein without endogenous rat alpha-synuclein fails to elicit Parkinson's disease-related phenotypes in a novel humanized rat model. [PDF]

PLoS One
Polinski NK, Puoliväli J, Rauhala L, Stenius TK, Bragge T, Parkkari T, Penttinen AM, Chen Y, Mabrouk OS, Glajch KE, Hirst WD, Perkinton M, Martinez TN, Frasier MA.   +13 more
europepmc   +1 more source

Interaction between alpha-synuclein and tau pathologies in a mouse model of Lewy body dementia [PDF]

Jiang, Hong
core  

WWOX Mutation as a Rare Cause of Neonatal‐Infantile Parkinsonism Mimicking a Neurotransmitter Disorder: A Case Report

Journal of Paediatrics and Child Health, EarlyView.
Ozge Serce Pehlevan, Gizem Gider Yaman, Anıl Gok, Leman Tekin Orgun   +3 more
wiley   +1 more source