Biography and Research Information
OverviewAI-generated summary
Chengzhong Cai's research program investigates molecular mechanisms underlying disease and explores novel diagnostic and therapeutic strategies. His work has focused on identifying key proteins involved in cell proliferation, such as the importin beta superfamily member RanBP17, and its association with patient survival in HPV+ head and neck squamous cell carcinoma. Cai has also contributed to the development of predictive models for drug-induced cardiotoxicity, utilizing induced pluripotent stem cell-derived cardiomyocytes. Furthermore, his research extends to the application of mass spectrometry for early cancer screening, including a model for accurate prostate cancer detection through urine protein enrichment. His scholarship metrics include an h-index of 11, with 26 total publications and 404 citations. Cai has collaborated with several researchers at the National Center for Toxicological Research, including Vikrant Vijay, William B. Mattes, Katy S Papineau, and Lijun Ren.
Metrics
- h-index: 11
- Publications: 26
- Citations: 406
Selected Publications
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Predicting oncology drug-induced cardiotoxicity with donor-specific iPSC-CMs—a proof-of-concept study with doxorubicin (2024)
Collaboration Network
Top Collaborators
- The importin beta superfamily member RanBP17 exhibits a role in cell proliferation and is associated with improved survival of patients with HPV+ HNSCC
- The importin beta superfamily member RanBP17 exhibits a role in cell proliferation and is associated with improved survival of patients with HPV+ HNSCC
- The importin beta superfamily member RanBP17 exhibits a role in cell proliferation and is associated with improved survival of patients with HPV+ HNSCC
- The importin beta superfamily member RanBP17 exhibits a role in cell proliferation and is associated with improved survival of patients with HPV+ HNSCC
- The importin beta superfamily member RanBP17 exhibits a role in cell proliferation and is associated with improved survival of patients with HPV+ HNSCC
- The importin beta superfamily member RanBP17 exhibits a role in cell proliferation and is associated with improved survival of patients with HPV+ HNSCC
- The importin beta superfamily member RanBP17 exhibits a role in cell proliferation and is associated with improved survival of patients with HPV+ HNSCC
- The importin beta superfamily member RanBP17 exhibits a role in cell proliferation and is associated with improved survival of patients with HPV+ HNSCC
- The importin beta superfamily member RanBP17 exhibits a role in cell proliferation and is associated with improved survival of patients with HPV+ HNSCC
- The importin beta superfamily member RanBP17 exhibits a role in cell proliferation and is associated with improved survival of patients with HPV+ HNSCC
- The importin beta superfamily member RanBP17 exhibits a role in cell proliferation and is associated with improved survival of patients with HPV+ HNSCC
- The importin beta superfamily member RanBP17 exhibits a role in cell proliferation and is associated with improved survival of patients with HPV+ HNSCC
- Predicting oncology drug-induced cardiotoxicity with donor-specific iPSC-CMs—a proof-of-concept study with doxorubicin
- Predicting oncology drug-induced cardiotoxicity with donor-specific iPSC-CMs—a proof-of-concept study with doxorubicin
- Predicting oncology drug-induced cardiotoxicity with donor-specific iPSC-CMs—a proof-of-concept study with doxorubicin
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