C. J. Wang
Indiana University
4 Papers
C. J. Wang is an academic researcher from Indiana University. The author has contributed to research in topics: DNA-binding domain & Computer science. The author has an hindex of 2, co-authored 2 publications.
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Papers
A Testing and Quarantine Algorithm for Individual International Travelers Using Published Data on WHO-Approved Vaccines and Bayes’ Theorem
TL;DR: A negative preboarding test and a negative arrival test can ensure that a traveler has a lower expected transmission than an unvaccinated person who is quarantined for 14 days.
Effective approaches to disaster evacuation during a COVID-like pandemic
Yi-Lin Tsai,Dymasius Y. Sitepu,Karyn E. Chappell,Rishi P. Mediratta,C. J. Wang,Peter K. Kitanidis,Christopher B. Field Department of Civil,Environmental Engineering,Stanford University,Stanford,Ca,Usa,National University of Singapore,Singapore,Department of Electrical Engineering,I. -. London,London,Uk,Department of Pediatrics,Stanford School of Medicine,Department of Health Policy,Woods Institute for the Environment,Bio-X,Institute for Computational,Department of Biology,Department of Materials Science,Interdisciplinary Environmental Studies Program +26 more
TL;DR: An age-structured epidemiological model is applied, known as the Susceptible-Exposed-Infectious-Recovered (SEIR) model, to investigate to what extent vaccine uptake levels and the Diversion protocol implemented in Taiwan decrease infections and delay pandemic peak occurrences.
Erratum: Small-molecule inhibitors targeting the DNA-binding domain of STAT3 suppress tumor growth, metastasis and STAT3 target gene expression in vivo (Oncogene (2016) 35 (783-792) DOI:10.1038/onc.2015.215)
Small-molecule inhibitors targeting the DNA-binding domain of STAT3 suppress tumor growth, metastasis and STAT3 target gene expression in vivo.
W. Huang,Zizheng Dong,Yan(陈雁) Chen,Fang Wang,C. J. Wang,Hui Peng,Y. He,G. Hangoc,Karen E. Pollok,George E. Sandusky,Xin-Yuan Fu,Hal E. Broxmeyer,Zhong Yin Zhang,Jing-Yuan Liu,Jing-Yuan Liu,Jian Ting Zhang +15 more
TL;DR: InS3-54A18 is completely soluble in an oral formulation and effectively inhibits lung xenograft tumor growth and metastasis with little adverse effect on animals and may serve as a potential candidate for further development as anticancer therapeutics targeting the DBD of human STAT3 and D BD of transcription factors may not be ‘undruggable‘ as previously thought.