Author

R. W. Ludwig

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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Physiology· 2 Cell Biology· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

E. Lau· 3 shared M. P. Y. Lam· 2 shared C. Franco· 1 shared C. Lai· 1 shared D. E. Hammond· 1 shared D. M. Simpson· 1 shared J. Currie· 1 shared J. L. Hurst· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 23 mutual co-author links

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3 shared papersPhysiology

E. Lau

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Author profile →

3 papers

Recent·Most cited

Simultaneous proteome localization and turnover analysis reveals spatiotemporal dynamics of unfolded protein responses

J. Currie, V. Manda, S. K. Robinson, C. Lai, V. Agnihotri, V. Hidalgo, R. W. Ludwig, K. Zhang, Z. V. Wang, J.-W. Rhee, M. P. Y. Lam, E. Lau

This study introduces SPLAT, a proteomics method to analyze protein turnover and localization simultaneously, revealing spatiotemporal changes in the unfolded protein response in human cells.

bioRxiv · Jan 4, 2023Cell Biology

Proteogenomic characterization of age and sex interactions in cardiac gene expression

Y. Han, S. A. Wennersten, J. Wright, R. W. Ludwig, E. Lau, M. P. Y. Lam

This study uses proteogenomics to identify age and sex-dependent gene expression and splicing changes in mouse hearts, revealing sexual dimorphism in cardiac aging and regulatory networks.

bioRxiv · May 11, 2022Physiology

Harmonizing labeling and analytical strategies to obtain protein turnover rates in intact adult animals.

D. E. Hammond, D. M. Simpson, C. Franco, M. W. Muelas, J. Waters, R. W. Ludwig, M. C. Prescott, J. L. Hurst, R. J. Beynon, E. Lau

This study compares protein turnover rates in mouse tissues using two labeling methods, showing they yield similar results for long-lived proteins but require adjustments for short-lived proteins.

bioRxiv · Dec 13, 2021Physiology