Author

J. D. Shepherd

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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Research Focus:cell type annotation· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Assay:proteomics· 1

Frequent Co-Authors

A. D. Echard· 1 shared A. Jambhekar· 1 shared A. Presle· 1 shared A. R. Skop· 1 shared C. Moravec· 1 shared D. Bae· 1 shared E. Kurt· 1 shared J. Hollien· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperCell Biology

A. D. Echard

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Author profile →

2 papers

Recent·Most cited

The midbody and midbody remnant are assembly sites for RNA and active translation

S. Park, R. D. Dahn, E. Kurt, A. Presle, K. VandenHeuvel, C. Moravec, A. Jambhekar, O. K. Olukoga, J. D. Shepherd, A. D. Echard, M. D. Blower, A. R. Skop

This paper identifies the midbody and its remnants as sites of RNA assembly and active translation, proposing them as novel RNA-based organelles involved in intercellular communication.

bioRxiv · Nov 1, 2022 · PreprintCell Biology

Regulation of Blos1 by IRE1 prevents the accumulation of Huntingtin protein aggregates

D. Bae, R. E. Jones, K. M. Piscopo, M. Tyagi, J. D. Shepherd, J. Hollien

The paper shows that IRE1-mediated degradation of Blos1 prevents mHTT aggregation by promoting endosomal microautophagy, protecting cells from toxic mHTT forms.

bioRxiv · Sep 28, 2021Cell Biology