CYP4F2 genetic variant alters required warfarin dose von Caldwell, Michael D., Awad, Tarif, Johnson, Julie A., Gage, Brian F., Falkowski, Mat, Gardina, Paul, Hubbard, Jason, Turpaz, Yaron, Langaee, Taimour Y., Eby, Charles, King, Cristi R., Brower, Amy, Schmelzer, John R., Glurich, Ingrid, Vidaillet, Humberto J., Yale, Steven H., Qi Zhang, Kai, Berg, Richard L., Burmester, James K.

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Two CES1 Gene Mutations Lead to Dysfunctional Carboxylesterase 1 Activity in Man: Clinical Significance and Molecular Basis von Zhu, Hao-Jie, Patrick, Kennerly S., Yuan, Hong-Jie, Wang, Jun-Sheng, Donovan, Jennifer L., DeVane, C. Lindsay, Malcolm, Robert, Johnson, Julie A., Youngblood, Geri L., Sweet, Douglas H., Langaee, Taimour Y., Markowitz, John S.

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Implementing Personalized Medicine: Development of a Cost-Effective Customized Pharmacogenetics Genotyping Array von Johnson, J A, Burkley, B M, Langaee, T Y, Clare-Salzler, M J, Klein, T E, Altman, R B

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SIRT1/HERC4 Locus Associated With Bisphosphonate‐Induced Osteonecrosis of the Jaw: An Exome‐Wide Association Analysis von Yang, Guang, Hamadeh, Issam S, Katz, Joseph, Riva, Alberto, Lakatos, Peter, Balla, Bernadett, Kosa, Janos, Vaszilko, Mihaly, Pelliccioni, Gian Andrea, Davis, Noa, Langaee, Taimour Y, Moreb, Jan S, Gong, Yan

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β-Adrenergic Receptor Gene Polymorphisms and β-Blocker Treatment Outcomes in Hypertension von Pacanowski, MA, Gong, Y, Cooper‐DeHoff, RM, Schork, NJ, Shriver, MD, Langaee, TY, Pepine, CJ, Johnson, JA

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Promoter Polymorphisms in ACE (Angiotensin I-Converting Enzyme) Associated With Clinical Outcomes in Hypertension von Johnson, AD, Gong, Y, Wang, D, Langaee, TY, Shin, J, Cooper‐DeHoff, RM, Schork, NJ, Binkley, P, Pepine, CJ, Johnson, JA, Sadee, W

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Association of KCNJ1 variation with change in fasting glucose and new onset diabetes during HCTZ treatment von Karnes, J H, McDonough, C W, Gong, Y, Vo, T T, Langaee, T Y, Chapman, A B, Gums, J G, Beitelshees, A L, Bailey, K R, Del-Aguila, J L, Boerwinkle, E A, Pepine, C J, Turner, S T, Johnson, J A, Cooper-DeHoff, R M

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Melatonin Pathway and Atenolol‐Related Glucose Dysregulation: Is There a Correlation? von Chang, SW, Gong, Y, McDonough, CW, Langaee, TY, Nasiri Kenari, N, Beitelshees, AL, Gums, JG, Chapman, AB, Turner, ST, Johnson, JA, Cooper‐DeHoff, RM

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Impact of GGCX, STX1B and FPGS Polymorphisms on Warfarin Dose Requirements in European‐Americans and Egyptians von Hamadeh, IS, Shahin, MH, Lima, SM, Oliveira, F, Wilson, L, Khalifa, SI, Langaee, TY, Cooper‐DeHoff, RM, Cavallari, LH, Johnson, JA

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Inactivation of the ampD gene in Pseudomonas aeruginosa leads to moderate-basal-level and hyperinducible AmpC β-lactamase expression von LANGAEE, T. Y, GAGNON, L, HULETSKY, A

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The effect of trimethoprim on CYP2C8 mediated rosiglitazone metabolism in human liver microsomes and healthy subjects von Hruska, M. W., Amico, J. A., Langaee, T. Y., Ferrell, R. E., Fitzgerald, S. M., Frye, R. F.

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Persistence of restricted CD4 T cell expansions in SIV-infected macaques resistant to SHIV89.6P superinfection von Salha, M.-D, Cheynier, R, Halwani, R, McGrath, H, Langaee, T.Y, Yassine Diab, B, Fournier, J, Parenteau, M, Edgar, J, Ko, D, Sherring, A, Bogdanovic, D, Sekaly, R.-P, Rud, E.W

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CXCL5 gene polymorphisms are related to systemic concentrations and leukocyte production of epithelial neutrophil-activating peptide (ENA-78) von Zineh, Issam, Aquilante, Christina L., Langaee, Taimour Y., Beitelshees, Amber L., Arant, Christopher B., Wessel, Timothy R., Schofield, Richard S.

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Genotyping the GGGCGG tandem repeat promoter polymorphism in the 5-lipoxygenase enzyme gene (ALOX5) by pyrosequencing assay von Schentrup, Anzeela M, Allayee, Hooman, Lima, John J, Johnson, Julie A, Langaee, Taimour Y

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An ampD Gene in Pseudomonas aeruginosa Encodes a Negative Regulator of AmpC β-Lactamase Expression von Langaee, T Y, Dargis, M, Huletsky, A

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