Author

U. Patel

Boston College

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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Biochemistry· 1 Biophysics· 1 Cancer Biology· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell signaling & trafficking· 2 Research Focus:cell type annotation· 2 Organism:human· 2 Approach:statistical model· 2 Approach:biophysical modeling· 1 Organism:C. elegans· 1 Research Focus:development & morphogenesis· 1

Frequent Co-Authors

J. Roche· 2 shared Ashlei R. Williams· 1 shared B. Chen· 1 shared B. J. Nolen· 1 shared Bethany F. CampbelliD· 1 shared D. A. Kramer· 1 shared D. Potoyan· 1 shared Dhanya KalathiliD· 1 shared

Activity by Year

2022-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersBiophysics

J. Roche

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Author profile →

4 papers

Recent·Most cited

Endocytic Patch Dynamics are Differentially Regulated at Distinct Cell Sites in Fission Yeast

Bethany F. Campbell, Dhanya Kalathil, U. Patel, Ashlei R. Williams, Maitreyi E. Das

The paper shows that endocytic patch dynamics in fission yeast are differentially regulated at cell ends, division site, and cell sides by Cdc42 and Pak1 kinase.

Journal of Cell Science · Aug 29, 2025Peer-reviewedCell Biology

Conformational landscape of the transcription factor ATF4 is dominated by disordered-mediated inter-domain coupling

U. Patel, S. Siang, D. Potoyan, J. Roche

This study investigates the structural basis of inter-domain interactions in ATF4, revealing that disorder-mediated coupling between transactivation and bZip domains shapes its conformational landscape.

bioRxiv · May 12, 2023 · PreprintBiophysics

Podocyte lineage marker expression is preserved across Wilms tumor subtypes and enhanced in tumors harboring the SIX1/2 p.Q177R mutation

M. J. Stevenson, S. K. Phanor, U. Patel, S. S. Gisselbrecht, M. L. Bulyk, L. L. O'Brien

bioRxiv · Nov 2, 2022 · PreprintCancer Biology

The intrinsically disordered cytoplasmic tail of a dendrite branching receptor uses two distinct mechanisms to regulate the actin cytoskeleton

D. A. Kramer, H. Y. Narvaez-Ortiz, U. Patel, R. Shi, K. Shen, B. J. Nolen, J. Roche, B. Chen

This study identifies two distinct mechanisms by which the intrinsically disordered cytoplasmic tail of HPO-30 regulates actin dynamics during dendrite branching in C. elegans.

bioRxiv · May 13, 2022Biochemistry