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Nucleic Acids Research|August 22, 2003
An enhanced U6 promoter for synthesis of short hairpin RNAXu Gang Xia, Hongxia Zhou, Hongliu Ding, et al.
The Journal of Biological Chemistry|March 9, 2005
Inhibition of chaperone activity is a shared property of several Cu,Zn-superoxide dismutase mutants that cause amyotrophic lateral sclerosisHemachand Tummala, Cheolwha Jung, Ashutosh Tiwari, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2026
PAD2 knockout reduces myelin protein aggregates, modulates neuroinflammation and protects motor neurons, axons and neuromuscular junction in a SOD1-ALS mouse modelIssa O Yusuf, Rogerio L A Silva, George G Amoako, et al.
International Journal of Biological Sciences|March 29, 2007
Silencing of the Pink1 gene expression by conditional RNAi does not induce dopaminergic neuron death in miceHongxia Zhou, Björn H Falkenburger, Jörg B Schulz, et al.
Acta Neuropathologica Communications|November 22, 2022
The enhanced association between mutant CHMP2B and spastin is a novel pathological link between frontotemporal dementia and hereditary spastic paraplegiasYongping Chen, Gopinath Krishnan, Sepideh Parsi, et al.
Neurobiology of Aging|December 16, 2011
Deficits in the mitochondrial enzyme α-ketoglutarate dehydrogenase lead to Alzheimer's disease-like calcium dysregulationGary E Gibson, Huan-Lian Chen, Hui Xu, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 30, 2016
Mutant PFN1 causes ALS phenotypes and progressive motor neuron degeneration in mice by a gain of toxicityChunxing Yang, Eric W Danielson, Tao Qiao, et al.
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