Leiyang Li, Jinpeng Zhou, Liying Han, Xun Wu, Yingwu Shi, Wenxing Cui, Shenghao Zhang, Qing Hu, Jin Wang, Hao Bai, Haixiao Liu, Wei Guo, Dayun Feng, Yan Qu. Front Cell Neurosci 2022
Times Cited: 5
Times Cited: 5
Times Cited
Times Co-cited
Similarity
Astrocyte Crosstalk in CNS Inflammation.
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Neurotoxic reactive astrocytes are induced by activated microglia.
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Activation of endothelial Wnt/β-catenin signaling by protective astrocytes repairs BBB damage in ischemic stroke.
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A paravascular pathway facilitates CSF flow through the brain parenchyma and the clearance of interstitial solutes, including amyloid β.
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Mitochondria and quality control defects in a mouse model of Gaucher disease--links to Parkinson's disease.
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Poly(GR) impairs protein translation and stress granule dynamics in C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis.
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Low levels of astroglial markers in Parkinson's disease: relationship to α-synuclein accumulation.
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Astrocyte reactivity with late-onset cognitive impairment assessed in vivo using 11C-BU99008 PET and its relationship with amyloid load.
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Autophagy lysosomal pathway dysfunction in Parkinson's disease; evidence from human genetics.
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Enhanced SIRT6 activity abrogates the neurotoxic phenotype of astrocytes expressing ALS-linked mutant SOD1.
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Reduced astrocytic reactivity in human brains and midbrain organoids with PRKN mutations.
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Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity.
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A characterization of Gaucher iPS-derived astrocytes: Potential implications for Parkinson's disease.
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Astrocytes expressing mutant SOD1 and TDP43 trigger motoneuron death that is mediated via sodium channels and nitroxidative stress.
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APOE4 Causes Widespread Molecular and Cellular Alterations Associated with Alzheimer's Disease Phenotypes in Human iPSC-Derived Brain Cell Types.
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An autopsy case report of neuronal intermediate filament inclusion disease presenting with predominantly upper motor neuron features.
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Excess glutamate secreted from astrocytes drives upregulation of P-glycoprotein in endothelial cells in amyotrophic lateral sclerosis.
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Astrocyte dysfunction triggers neurodegeneration in a lysosomal storage disorder.
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Parkinson's Disease Phenotypes in Patient Neuronal Cultures and Brain Organoids Improved by 2-Hydroxypropyl-β-Cyclodextrin Treatment.
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SOD1 mutations associated with amyotrophic lateral sclerosis analysis of variant severity.
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Genetic mutations and functions of PINK1.
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Reactive astrocytes secrete lcn2 to promote neuron death.
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Loss of TDP-43 function underlies hippocampal and cortical synaptic deficits in TDP-43 proteinopathies.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.