David Bourdon

University of North Carolina at Chapel Hill

Papers

1

Total Citations

25

H-Index

1

About

David Bourdon’s research centers on the intricate signaling networks of small GTPases and phospholipase C (PLC) enzymes, with a focus on how these molecular switches orchestrate cellular responses. His most-cited work, a 2006 study, provided a critical methodological advance by developing an intact cell assay system to quantify isozyme-specific activation of PLC-β2 by Rac GTPases and PLC-ɛ by Rho GTPases. This contribution clarified the selective coupling between GTPase families and PLC isoforms, offering a more physiologically relevant framework for understanding signal transduction in processes like cell migration and growth. Though his citation count (25 for this key paper) reflects a focused, specialized impact, Bourdon’s work has been instrumental for researchers dissecting the specificity of G protein–effector interactions. His findings have implications for cancer biology and inflammatory diseases, where aberrant GTPase-PLC signaling is implicated. Bourdon’s dedication to precise, quantitative assays underscores his role as a meticulous experimentalist, advancing our grasp of how cells decode complex environmental cues through discrete molecular partnerships.

Research Focus

Key Achievements

1
H-Index
1
Papers
25
Total Citations
25
Avg Citations/Paper
🏆 Most Cited Paper
Quantification of Isozyme‐Specific Activation of Phospholipase C‐β2 by Rac GTPases and Phospholipase C‐ɛ by Rho GTPases in an Intact Cell Assay System
25 citations · 2006
📈 Most Prolific Year: 2006 (1 Papers)
🤝 Key Collaborators: 4
🏛 Institutions: University of North Carolina at Chapel Hill

Top Papers

  1. 1

Key Collaborators

Contact & Links

Available for collaboration
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