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

Click to filter author papers

Cancer Biology· 1 Pathology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperCancer Biology

A. K. Perl

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Cancer BiologybioRxivPreprintOct 8, 2019

Identification of the lymphangioleiomyomatosis cell and its uterine origin

M. Guo, J. J. Yu, A. K. Perl…·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.

DOI 10.1101/784199

humanscRNA-seq

𝕏 PostBluesky

PathologybioRxivApr 18, 2019

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.

DOI 10.1371/journal.pone.0216261

mousebulk RNA-seq

𝕏 PostBluesky