Author

J. D. Mueller

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cell Biology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:fluorescence / live-cell microscopy· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Organism:human· 1 Research Focus:synaptic & neural circuits· 1

Frequent Co-Authors

A. Schoenhoefen· 1 shared A. Varshney· 1 shared B. Huang· 1 shared C. A. Saunders· 1 shared C. M. Morris· 1 shared C. Modavi· 1 shared D. Coto Villa· 1 shared F. Farah· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCell Biology

A. Schoenhoefen

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2 papers

Recent·Most cited

The luminal AAA+ ATPase torsinA mediates distinct mechanisms of nuclear-cytoplasmic communication by adopting different functional assembly states.

K.-H. Hur, J. W. Hennen, C. A. Saunders, A. Schoenhoefen, P. T. Willey, C. M. Morris, R. H. Ibrahim, R. S. Maisuria, J. D. Mueller, G. W. G. Luxton

This study investigates how torsinA, a luminal AAA+ ATPase, mediates nuclear-cytoplasmic communication by adopting distinct functional assembly states during LINC complex and NPC biogenesis.

bioRxiv · Dec 9, 2021 · PreprintCell Biology

Bright split red fluorescent proteins with enhanced complementation efficiency for the tagging of endogenous proteins and visualization of synapses

S. Feng, A. Varshney, D. Coto Villa, C. Modavi, J. Kohler, F. Farah, N. Ali, J. D. Mueller, M. VanHoven, B. Huang

The paper improves split fluorescent proteins for better brightness and develops a new synaptic marker for visualizing synapses in living animals.

bioRxiv · Oct 25, 2018 · PreprintCell Biology