Author

S. S. Potter

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· 1 Pathology· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

A. K. Perl· 1 shared A. Potter· 1 shared A. S. Potter· 1 shared D. J. Kwiatkowski· 1 shared E. J. Kopras· 1 shared E. W. Brunskill· 1 shared E. Y. Zhang· 1 shared F. X. McCormack· 1 shared

Activity by Year

2019-2019 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperCancer Biology

A. K. Perl

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Author profile →

2 papers

Recent·Most cited

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

A Bigenic mouse model of FSGS reveals perturbed pathways in podocytes, mesangial cells and endothelial cells

A. S. Potter, K. Drake, E. W. Brunskill, S. S. Potter

This study uses RNA-seq to analyze gene expression in podocytes, mesangial cells, and endothelial cells of a bigenic FSGS mouse model, identifying upregulated pathways and genes associated with fibrosis and disease progression.

bioRxiv · Apr 18, 2019Pathology