Author

Gregory R. Gipson

Harvard UniversityORCID 0000-0002-3698-4182Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Benjamin P. KeithiD· 1 shared Bianca PlouffeiD· 1 shared Carole A. Daly· 1 shared Connor Brown· 1 shared Derek P. BraziliD· 1 shared Dessislava MalinovaiD· 1 shared Dimitri G. TrembathiD· 1 shared Elisabeth A. Wolber· 1 shared

Activity by Year

2018-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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1 shared paperGenomics

Benjamin P. KeithORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

BMP9-mediated regulation of endothelin-1 requires integrated SMAD1/5 and SMAD2/3 signaling

Jana Bagarova, Shreya Sangam, Luca Troncone, Ying Zhong, Lillian R. Worst, Gregory R. Gipson, Ivana Nikolić, Samuel D Paskin-Flerlage, S. Paul Oh, Fernando Rodríguez‐Pascual, Paul B. Yu

This study shows BMP9 regulates ET-1 through coordinated SMAD1/5 and SMAD2/3 signaling in endothelial cells, revealing a non-canonical mechanism relevant to pulmonary arterial hypertension.

bioRxiv · Dec 26, 2025 · PreprintCell Biology

Identification of a novel GREMLIN1 uptake pathway in epithelial cells that requires BMP binding

Zhichun Gao, Yuhan Gao, Louise R. Dutton, Melibea Berzosa, Grace Todd, Gregory R. Gipson, Connor Brown, Emma M. Kerr, Carole A. Daly, Bianca Plouffe, Philip D. Dunne, Dessislava Malinova, Derek P. Brazil

The paper identifies a BMP-dependent endocytosis pathway for GREM1 in epithelial cells, showing BMP binding is required for GREM1 uptake and antagonism of BMP signaling.

Journal of Biological Chemistry · Sep 30, 2025Peer-reviewedCell Biology

Colonic Epithelial miR-31 Associates with the Development of Crohn’s Phenotypes

Benjamin P. Keith, Jasmine Barrow, Takahiko Toyonaga, Nevzat Kazgan, Michelle Hoffner, Neil Shah, Matthew S. Schaner, Elisabeth A. Wolber, Omar K. Trad, Gregory R. Gipson, Wendy A. Pitman, Matthew Kanke, Shruti Saxena, Nicole Chaumont, Timothy S. Sadiq, , Shehzad Z. Sheikh

This study identifies miR-31 as a marker that stratifies Crohn’s disease patients into two subtypes with distinct clinical outcomes.

JCI Insight · Oct 3, 2018Peer-reviewedGenomics