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  • Search Condition : Filter (MeSH = Neurodegenerative Diseases / genetics*)
Species Resource Title
Human and Animal Cells ASF-4-3L(RCB3580) A sublethal ATP11A mutation associated with neurological deterioration causes aberrant phosphatidylcholine flipping in plasma membranes.
C.elegans tm6026 Increased mitochondrial calcium uptake and concomitant mitochondrial activity by presenilin loss promotes mTORC1 signaling to drive neurodegeneration.
C.elegans tm781 Tyrosine phosphorylation regulates hnRNPA2 granule protein partitioning and reduces neurodegeneration.
C.elegans tm985 , tm1978 , tm4450 Age- and stress-associated C. elegans granulins impair lysosomal function and induce a compensatory HLH-30/TFEB transcriptional response.
Drosophila RNP-Granule Assembly via Ataxin-2 Disordered Domains Is Required for Long-Term Memory and Neurodegeneration.
Drosophila A Neuron-Glial Trans-Signaling Cascade Mediates LRRK2-Induced Neurodegeneration.
Drosophila 4322R-2 Glial expression of disease-associated poly-glutamine proteins impairs the blood-brain barrier in Drosophila.
C.elegans tm985 A neurodegenerative disease mutation that accelerates the clearance of apoptotic cells.
Drosophila Drosophila as a screening tool to study human neurodegenerative diseases.
Drosophila DGRC#200507 Isolation of gene sets affected specifically by polyglutamine expression: implication of the TOR signaling pathway in neurodegeneration.