Author

N. B. Wood

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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Biophysics· 1 Physiology· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

M. J. Previs· 2 shared A. Cario· 1 shared A. G. Hendricks· 1 shared A. Savastano· 1 shared C. A. Wolff· 1 shared C. Douglas· 1 shared C. L. Berger· 1 shared D. Hammers· 1 shared

Activity by Year

2021-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersBiophysics

M. J. Previs

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Author profile →

2 papers

Recent·Most cited

The Pathogenic R5L Mutation Disrupts Formation of Tau Complexes on the Microtubule by Altering Local N-Terminal Structure

A. Cario, A. Savastano, N. B. Wood, Z. Liu, M. J. Previs, A. G. Hendricks, M. Zweckstetter, C. L. Berger

This paper investigates the R5L mutation in Tau, showing it does not reduce microtubule-binding affinity but alters N-terminal structure, impairing Tau complex formation on microtubules.

bioRxiv · Oct 15, 2021Biophysics

The Skeletal Muscle Circadian Clock Regulates Titin Splicing Through RBM20

L. Riley, X. Zhang, C. Douglas, J. Mijares, D. Hammers, C. A. Wolff, N. B. Wood, H. Olafson, P. Du, S. Labeit, M. J. Previs, E. T. Wang, K. A. Esser

This study shows that the skeletal muscle circadian clock regulates titin splicing via RBM20, affecting sarcomere length and function.

bioRxiv · May 27, 2021Physiology