Drug-Induced Hepatotoxicity And Protection
85 researchers across 5 institutions
Researchers investigate the adverse effects of medications and other xenobiotics on liver function. This work involves identifying the molecular mechanisms by which drugs cause liver damage, including oxidative stress, inflammation, and cellular death pathways. Studies utilize various *in vitro* and *in vivo* models to assess drug metabolism, predict potential toxicities, and evaluate protective strategies. Areas of focus include the development of novel biomarkers for early detection of liver injury and the exploration of therapeutic interventions to mitigate or reverse drug-induced hepatotoxicity.
This research is pertinent to Arkansas’s public health landscape, particularly concerning the safe and effective use of pharmaceuticals within diverse patient populations. Understanding drug-induced liver injury is crucial for healthcare providers and pharmaceutical developers, impacting patient outcomes and the state’s healthcare system. Furthermore, investigations into environmental toxicants and their impact on liver health can inform public health initiatives and regulatory policies relevant to the state.
This field draws upon expertise in pharmacology, toxicology, molecular biology, and immunology. Engagement spans multiple Arkansas institutions, fostering collaboration across academic disciplines and contributing to a robust research ecosystem within the state.
Top Researchers
| Name | Institution | h-index | Citations | Career Stage | Badges |
|---|---|---|---|---|---|
| Daniel R. Doerge | NCTR | 76 | 19,620 | High Impact | |
| Laura P. James | UAMS | 52 | 10,574 | ||
| Lei Guo | NCTR | 52 | 18,086 | High Impact | |
| Jack Hinson | UAMS | 51 | 9,344 | High Impact | |
| Mitchell R. McGill | UAMS | 46 | 12,417 | Grant PI High Impact | |
| Baitang Ning | NCTR | 45 | 11,288 | ||
| Nan Mei | NCTR | 42 | 9,278 | High Impact | |
| Minjun Chen | NCTR | 42 | 5,690 | High Impact | |
| S. Michael Owens | UAMS | 36 | 3,541 | High Impact | |
| Qiang Shi | NCTR | 35 | 10,670 | High Impact | |
| Qingsu Xia | NCTR | 35 | 5,476 | High Impact | |
| Laura K. Schnackenberg | NCTR | 34 | 3,519 | ARA High Impact | |
| William B. Mattes | NCTR | 33 | 3,869 | High Impact | |
| Grover P. Miller | UAMS | 30 | 2,764 | Grant PI High Impact | |
| Erbin Dai | NCTR | 26 | 1,761 | High Impact | |
| Kelly E. Mercer | NCTR | 25 | 3,492 | High Impact | |
| Lijun Ren | NCTR | 24 | 1,846 | High Impact | |
| Qiangen Wu | NCTR | 21 | 1,145 | High Impact | |
| Dongying Li | NCTR | 20 | 1,222 | ||
| Bo‐Rong Pan | NCTR | 19 | 1,341 |
Related Research Areas
Strategic Outlook
Global signals from OpenAlex for this research area: where the field is growing, how concentrated leadership is, and where Arkansas sits relative to the world's top-100 institutions. Descriptive only — surfaced as input to the conversation about where to place bets, not a recommendation. Signal confidence: LOW
Top US institutions in this area
- 1 University of North Carolina at Chapel Hill 572
- 2 National Institutes of Health 532
- 3 University of Kansas Medical Center 498
- 4 University of Michigan 475
- 5 University of California, San Francisco 442
Cross-Institution Connections
Researchers at different institutions with overlapping expertise in Drug-Induced Hepatotoxicity And Protection.