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Probing Neuronal Nuclear Pore Complexes Using Single Molecule Localization Microscopy

Published online by Cambridge University Press:  30 July 2020

Sumin Kim
Affiliation:
University of Michigan, Ann Arbor, Michigan, United States
Sami Barmada
Affiliation:
University of Michigan Medical School, Ann Arbor, Michigan, United States
William Dauer
Affiliation:
UT Southwestern Medical Center, Dallas, Texas, United States
Sarah Veatch
Affiliation:
University of Michigan, Ann Arbor, Michigan, United States

Abstract

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Type
Methods and Applications in Localization-based Super-resolution Microscopy
Copyright
Copyright © Microscopy Society of America 2020

References

Kim, SJ, Fernandez-Martinez, J, Nudelman, I, et al. Integrative structure and functional anatomy of a nuclear pore complex. Nature. 2018. doi:10.1038/nature26003CrossRefGoogle ScholarPubMed
Knockenhauer, KE, Schwartz, TU. The Nuclear Pore Complex as a Flexible and Dynamic Gate. Cell. 2016;164(6):11621171. doi:10.1016/j.cell.2016.01.034CrossRefGoogle ScholarPubMed
Grima, JC, Daigle, JG, Arbez, N, et al. Mutant Huntingtin Disrupts the Nuclear Pore Complex. Neuron. 2017. doi:10.1016/j.neuron.2017.03.023CrossRefGoogle ScholarPubMed
Chou, C-C, Zhang, Y, Umoh, ME, et al. TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTD. Nat Neurosci. 2018. doi:10.1038/s41593-017-0047-3CrossRefGoogle ScholarPubMed
Eftekharzadeh, B, Daigle, JG, Kapinos, LE, et al. Tau Protein Disrupts Nucleocytoplasmic Transport in Alzheimer's Disease. Neuron. 2018. doi:10.1016/j.neuron.2018.07.039CrossRefGoogle ScholarPubMed
Pappas, SS, Liang, CC, Kim, S, Rivera, CAO, Dauer, WT. TorsinA dysfunction causes persistent neuronal nuclear pore defects. Hum Mol Genet. 2018;27(3):407420. doi:10.1093/hmg/ddx405CrossRefGoogle ScholarPubMed
Ozelius, LJ, Hewett, J, Kramer, P, et al. Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium. Genome Res. 1997;7(5):483494. doi:10.1101/gr.7.5.483CrossRefGoogle ScholarPubMed
Goodchild, RE, Kim, CE, Dauer, WT. Loss of the dystonia-associated protein torsinA selectively disrupts the neuronal nuclear envelope. Neuron. 2005;48(6):923932. doi:10.1016/j.neuron.2005.11.010CrossRefGoogle ScholarPubMed