Author

J. A. Whitsett

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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Cancer Biology· 2 Pathology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Approach:experimental assay· 3 Research Focus:differential expression· 2 Organism:human· 2 Assay:scRNA-seq· 2 Assay:bulk RNA-seq· 1 Organism:mouse· 1 Assay:proteomics· 1

Frequent Co-Authors

A. Potter· 2 shared E. J. Kopras· 2 shared E. Y. Zhang· 2 shared F. X. McCormack· 2 shared J. J. Yu· 2 shared M. Guo· 2 shared Y. Xu· 2 shared A. A. Astrinidis· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersPathology

A. Potter

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Author profile →

3 papers

Recent·Most cited

Integrative Single Cell Multiomic Profiling Analysis Reveals HOX-PBX Gene Regulatory Network Contributing to the Survival of mTOR Hyperactive Cells

T. F. Olatoke, A. Wagner, A. A. Astrinidis, M. Guo, E. Y. Zhang, A. A. Zhang, U. Mattam, K. Chilton, E. J. Kopras, N. Gupta, E. P. Smith, M. Karbowniczek, M. M. Markiewski, K. Wikenheiser-Brokamp, J. A. Whitsett, , J. J. Yu

This study identifies PBX1 as a critical regulator of LAM progression by analyzing scRNA-seq data and validating its role in LAM cell survival and lung colonization.

bioRxiv · Sep 27, 2022 · PreprintCancer Biology

Short-term exposure to intermittent hypoxia leads to changes in gene expression seen in chronic pulmonary disease

G. Wu, Y. Y. Lee, E. M. Gulla, A. Potter, J. Kitzmiller, M. D. Ruben, N. Salomonis, J. A. Whitsett, L. J. Francey, J. B. Hogenesch, D. F. Smith

This study shows that intermittent hypoxia in mice alters gene expression in lung cells, particularly in endothelial cells, linking it to pulmonary fibrosis and hypertension pathways.

bioRxiv · Mar 6, 2020Pathology

Identification of the lymphangioleiomyomatosis cell and its uterine origin

M. Guo, J. J. Yu, A. K. Perl, K. A. Wikenheiser-Brokamp, M. Riccetti, E. Y. Zhang, P. Sudha, M. Adam, A. Potter, E. J. Kopras, K. Giannikou, S. S. Potter, S. Sherman, S. R. Hammes, D. J. Kwiatkowski, , Y. Xu

This study identifies LAMCORE cells as the source of lymphangioleiomyomatosis, showing their uterine neural crest origin and identifying potential biomarkers and therapeutic targets.

bioRxiv · Oct 8, 2019 · PreprintCancer Biology