Results 211 to 220 of about 3,985,879 (249)
Presynaptic accumulation of APP-CTFβ may contribute to synaptic dysfunction in Alzheimer's disease. [PDF]
Kapadia A +10 more
europepmc +1 more source
Objective Amyotrophic lateral sclerosis (ALS) has a markedly distinctive clinical and neuroradiological signature, with the preferential involvement of specific brain networks and the apparent sparing of others. The molecular underpinnings of the strikingly selective anatomical vulnerability have not been fully elucidated to date despite the potential ...
Marlene Tahedl +10 more
wiley +1 more source
Synaptic vesicle architecture modulates α-synuclein conformation and pathogenic transitions in Parkinson's disease. [PDF]
Ranjan P.
europepmc +1 more source
In sepsis‐associated encephalopathy (SAE), enhanced micro‐ER‐phagy mediated by Sec62 facilitates the delivery of STING to lysosomes for degradation in hippocampal neurons. This process relieves STING‐mediated inhibition of PKM2 activity, which further modulates cellular energy metabolism indicators including the ATP/ADP and NAD+/NADH ratios ...
Xiaofeng Guo +9 more
wiley +1 more source
STX1B variant-specific synaptic dysfunction is associated with network hyperexcitability in human iPSC-derived neurons. [PDF]
Haag C +15 more
europepmc +1 more source
ABSTRACT Epilepsy is the most disabling neurological disease that affects all economic classes, age groups, regions, and races. Although many antiseizure drugs are approved for epilepsy treatment, they fail to work in about 30%–40% of patients. Thus, there is a great need to identify better pharmacological agents to treat epilepsy.
Janakiraman Pillai Udaiyappan +3 more
wiley +1 more source
Decoding Synaptic Diversity: Molecular Architectures, Phase Transitions, and Shared Postsynaptic Failure in Alzheimer's and Parkinson's Disease. [PDF]
Cipriano GL +7 more
europepmc +1 more source
Tau A152T risk variant drives distinct cell type transcriptional signatures in AD and PSP. [PDF]
Lilley MT +10 more
europepmc +1 more source
Pathogenic variants alter hepaCAM protein distribution. Astrocyte‐specific hepaCAM TurboID reveals KCNQ2 as a new interaction partner. Pathogenic variants alter hepaCAM association with key transmembrane proteins. ABSTRACT Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is a rare leukodystrophy characterized by early‐onset macrocephaly,
Robert W. Lewis +10 more
wiley +1 more source
NLGN3 autism variants have distinct functional impact on synapses and sleep behavior in Drosophila. [PDF]
Townsley RE +8 more
europepmc +1 more source

