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Jie Liu

Inorganic Carcinogenesis Section

Laboratory of Comparative Carcinogenesis

NCI at NIEHS

Research Triangle Park

USA

[email]@niehs.nih.gov

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Inorganic Carcinogenesis Section, Laboratory of Comparative Carcinogenesis, NCI at NIEHS, Research Triangle Park, USA. 2001 - 2009
  • University of Kansas Medical Center, Kansas City, USA. 1999

References

  1. Role of oxidative stress in cadmium toxicity and carcinogenesis. Liu, J., Qu, W., Kadiiska, M.B. Toxicol. Appl. Pharmacol. (2009) [Pubmed]
  2. Gene expression profiling for nitric oxide prodrug JS-K to kill HL-60 myeloid leukemia cells. Liu, J., Malavya, S., Wang, X., Saavedra, J.E., Keefer, L.K., Tokar, E., Qu, W., Waalkes, M.P., Shami, P.J. Genomics (2009) [Pubmed]
  3. Mineral arsenicals in traditional medicines: orpiment, realgar, and arsenolite. Liu, J., Lu, Y., Wu, Q., Goyer, R.A., Waalkes, M.P. J. Pharmacol. Exp. Ther. (2008) [Pubmed]
  4. Mercury in traditional medicines: is cinnabar toxicologically similar to common mercurials? Liu, J., Shi, J.Z., Yu, L.M., Goyer, R.A., Waalkes, M.P. Exp. Biol. Med. (Maywood) (2008) [Pubmed]
  5. Arsenic-induced aberrant gene expression in fetal mouse primary liver-cell cultures. Liu, J., Yu, L., Tokar, E.J., Bortner, C., Sifre, M.I., Sun, Y., Waalkes, M.P. Ann. N. Y. Acad. Sci. (2008) [Pubmed]
  6. Transplacental exposure to inorganic arsenic at a hepatocarcinogenic dose induces fetal gene expression changes in mice indicative of aberrant estrogen signaling and disrupted steroid metabolism. Liu, J., Xie, Y., Cooper, R., Ducharme, D.M., Tennant, R., Diwan, B.A., Waalkes, M.P. Toxicol. Appl. Pharmacol. (2007) [Pubmed]
  7. Transplacental arsenic plus postnatal 12-O-teradecanoyl phorbol-13-acetate exposures associated with hepatocarcinogenesis induce similar aberrant gene expression patterns in male and female mouse liver. Liu, J., Xie, Y., Merrick, B.A., Shen, J., Ducharme, D.M., Collins, J., Diwan, B.A., Logsdon, D., Waalkes, M.P. Toxicol. Appl. Pharmacol. (2006) [Pubmed]
  8. Further studies on aberrant gene expression associated with arsenic-induced malignant transformation in rat liver TRL1215 cells. Liu, J., Benbrahim-Tallaa, L., Qian, X., Yu, L., Xie, Y., Boos, J., Qu, W., Waalkes, M.P. Toxicol. Appl. Pharmacol. (2006) [Pubmed]
  9. Nitric oxide and chemically induced hepatotoxicity: beneficial effects of the liver-selective nitric oxide donor, V-PYRRO/NO. Liu, J., Waalkes, M.P. Toxicology (2005) [Pubmed]
  10. Focal adhesion kinase as a potential target in arsenic toxicity. Liu, J., Waalkes, M. Toxicol. Sci. (2005) [Pubmed]
  11. Limited protective role of V-PYRRO/NO against cholestasis produced by alpha-naphthylisothiocyanate in mice. Liu, J., He, Y.Y., Chignell, C.F., Clark, J., Myers, P., Saavedra, J.E., Waalkes, M.P. Biochem. Pharmacol. (2005) [Pubmed]
  12. Oleanolic acid and ursolic acid: research perspectives. Liu, J. J. Ethnopharmacol (2005) [Pubmed]
  13. Toxicogenomic analysis of aberrant gene expression in liver tumors and nontumorous livers of adult mice exposed in utero to inorganic arsenic. Liu, J., Xie, Y., Ward, J.M., Diwan, B.A., Waalkes, M.P. Toxicol. Sci. (2004) [Pubmed]
  14. Fas-mediated signaling pathway in ethanol-induced liver apoptosis: inhibition by zinc. Liu, J. Exp. Biol. Med. (Maywood) (2004) [Pubmed]
  15. Hybridization buffer systems impact the quality of filter array data. Liu, J., Walker, N., Waalkes, M.P. J. Pharmacol. Toxicol. Methods (2004) [Pubmed]
  16. The nitric oxide donor, V-PYRRO/NO, protects against acetaminophen-induced hepatotoxicity in mice. Liu, J., Li, C., Waalkes, M.P., Clark, J., Myers, P., Saavedra, J.E., Keefer, L.K. Hepatology (2003) [Pubmed]
  17. Multidrug-resistance mdr1a/1b double knockout mice are more sensitive than wild type mice to acute arsenic toxicity, with higher arsenic accumulation in tissues. Liu, J., Liu, Y., Powell, D.A., Waalkes, M.P., Klaassen, C.D. Toxicology (2002) [Pubmed]
  18. O(2)-Vinyl 1-(pyrrolidin-1-yl)diazen-1-ium-1,2-diolate protection against D-galactosamine/endotoxin-induced hepatotoxicity in mice: genomic analysis using microarrays. Liu, J., Saavedra, J.E., Lu, T., Song, J.G., Clark, J., Waalkes, M.P., Keefer, L.K. J. Pharmacol. Exp. Ther. (2002) [Pubmed]
  19. Chronic arsenic poisoning from burning high-arsenic-containing coal in Guizhou, China. Liu, J., Zheng, B., Aposhian, H.V., Zhou, Y., Chen, M.L., Zhang, A., Waalkes, M.P. Environ. Health Perspect. (2002) [Pubmed]
  20. Acute cadmium exposure induces stress-related gene expression in wild-type and metallothionein-I/II-null mice. Liu, J., Kadiiska, M.B., Corton, J.C., Qu, W., Waalkes, M.P., Mason, R.P., Liu, Y., Klaassen, C.D. Free Radic. Biol. Med. (2002) [Pubmed]
  21. Stress-related gene expression in mice treated with inorganic arsenicals. Liu, J., Kadiiska, M.B., Liu, Y., Lu, T., Qu, W., Waalkes, M.P. Toxicol. Sci. (2001) [Pubmed]
  22. Metallothionein-I/II knockout mice are sensitive to acetaminophen-induced hepatotoxicity. Liu, J., Liu, Y., Hartley, D., Klaassen, C.D., Shehin-Johnson, S.E., Lucas, A., Cohen, S.D. J. Pharmacol. Exp. Ther. (1999) [Pubmed]
 
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