Henry, Anastasia G.
Denali Therapeutics (United States)
3 papers on CoChatORCID 0000-0002-8124-5477
Most cited papers
- Verified
Pathogenic LRRK2 mutations, through increased kinase activity, produce enlarged lysosomes with reduced degradative capacity and increase ATP13A2 expression
Henry, A. G., Aghamohammadzadeh, S., Samaroo, H., Chen, Y., Mou, K., Needle, E., & Hirst, W. D. (2015) · Human Molecular Genetics
Parkinson's Disease Mechanisms and TreatmentsAutophagy in Disease and Therapy
Cited by 235
- Verified
Rescue of a lysosomal storage disorder caused by Grn loss of function with a brain penetrant progranulin biologic
Logan, T., Simon, M. J., Rana, A., Cherf, G. M., Srivastava, A., Davis, S. S., Low, R. L. Y., Chiu, C.-L., Fang, M., Huang, F., et al. (2021) · Cell
Lysosomal Storage Disorders ResearchAmyotrophic Lateral Sclerosis Research
Cited by 233
- Verified
Brain delivery and activity of a lysosomal enzyme using a blood–brain barrier transport vehicle in mice
Ullman, J. C., Arguello, A., Getz, J. A., Bhalla, A., Mahon, C. S., Wang, J., Giese, T., Bedard, C., Kim, D. J., Blumenfeld, J. R., et al. (2020) · Science Translational Medicine
Lysosomal Storage Disorders ResearchBarrier Structure and Function Studies
Cited by 205
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