Prion strains viewed through the lens of cryo-EM
SW Manka, A Wenborn, J Collinge… - Cell and Tissue …, 2023 - Springer
Mammalian prions are lethal transmissible pathogens that cause fatal neurodegenerative
diseases in humans and animals. They consist of fibrils of misfolded, host-encoded prion …
diseases in humans and animals. They consist of fibrils of misfolded, host-encoded prion …
New insight into brain disease therapy: nanomedicines-crossing blood–brain barrier and extracellular space for drug delivery
Z Gu, H Chen, H Zhao, W Yang, Y Song… - Expert Opinion on …, 2022 - Taylor & Francis
Introduction Brain diseases including brain tumor, Alzheimer's disease, Parkinson's disease,
etc. are difficult to treat. The blood–brain barrier (BBB) is a major obstacle for drug delivery …
etc. are difficult to treat. The blood–brain barrier (BBB) is a major obstacle for drug delivery …
Effect of electric field on α-synuclein fibrils: Revealed by molecular dynamics simulations
The self-association of amylogenic proteins to the fibril form is considered a pivotal factor in
the pathogenesis of neurodegenerative diseases, including Parkinson's disease (PD). PD …
the pathogenesis of neurodegenerative diseases, including Parkinson's disease (PD). PD …
Tau truncation in the pathogenesis of Alzheimer's disease: a narrative review
D Chu, X Yang, J Wang, Y Zhou, JH Gu… - Neural Regeneration …, 2024 - journals.lww.com
Alzheimer's disease is characterized by two major neuropathological hallmarks—the
extracellular β-amyloid plaques and intracellular neurofibrillary tangles consisting of …
extracellular β-amyloid plaques and intracellular neurofibrillary tangles consisting of …
[HTML][HTML] C9orf72 poly-GA proteins impair neuromuscular transmission
WY Tu, W Xu, J Zhang, S Qi, L Bai, C Shen… - Zoological …, 2023 - ncbi.nlm.nih.gov
Amyotrophic lateral sclerosis (ALS) is a devastating motoneuron disease, in which lower
motoneurons lose control of skeletal muscles. Degeneration of neuromuscular junctions …
motoneurons lose control of skeletal muscles. Degeneration of neuromuscular junctions …
Upregulation of the ESCRT pathway and multivesicular bodies accelerates degradation of proteins associated with neurodegeneration
R Benyair, SS Panapakkam Giridharan… - Autophagy …, 2023 - Taylor & Francis
Many neurodegenerative diseases, including Huntington's disease (HD) and Alzheimer's
disease (AD), occur due to an accumulation of aggregation-prone proteins, which results in …
disease (AD), occur due to an accumulation of aggregation-prone proteins, which results in …
[HTML][HTML] Large-scale network analysis of the cerebrospinal fluid proteome identifies molecular signatures of frontotemporal lobar degeneration
The pathophysiological mechanisms driving disease progression of frontotemporal lobar
degeneration (FTLD) and corresponding biomarkers are not fully understood. We leveraged …
degeneration (FTLD) and corresponding biomarkers are not fully understood. We leveraged …
Parkinson's disease-related Miro1 mutation induces mitochondrial dysfunction and loss of dopaminergic neurons in vitro and in vivo
A Chemla, G Arena, G Sacripanti, K Barmpa, A Zagare… - bioRxiv, 2023 - biorxiv.org
The complex and heterogeneous nature of Parkinson disease (PD) is still not fully
understood, however, increasing evidence supports mitochondrial impairments as a major …
understood, however, increasing evidence supports mitochondrial impairments as a major …
tau 截短体与阿尔茨海默病的发病机制
D Chu, X Yang, J Wang, Y Zhou, JH Gu… - 中国神经再生研究 …, 2024 - sjzsyj.com.cn
阿尔茨海默病存在2 个主要的神经病理学特征: 细胞外β 淀粉样蛋白斑块和细胞内过度磷酸化tau
蛋白聚集成的神经纤维缠结. 最近有研究发现微管相关蛋白tau 的失调, 特别是特异性蛋白水解 …
蛋白聚集成的神经纤维缠结. 最近有研究发现微管相关蛋白tau 的失调, 特别是特异性蛋白水解 …
Retinal Ganglion Cell Excitability and Adaptations to Ionic Stress in Glaucomatous Optic Neuropathy
A Boal - 2023 - ir.vanderbilt.edu
Neurodegenerative diseases are complex disorders that affect various regions and cells in
the central nervous system, sharing common hallmark features of progression. Intrinsic and …
the central nervous system, sharing common hallmark features of progression. Intrinsic and …