Personalized Medicine in Vascular Medicine

Toshihisa Ishikawa, Yoshihide Hayashizaki, Clinical SNP Detection by the SmartAmp Method Methods of Molecular Biology. ,vol. 1015, pp. 55- 69 ,(2013) , 10.1007/978-1-62703-435-7_3

Marianne K DeGorter, Richard B Kim, Liangfu Chen, Joseph W Polli, Lei Zhang, Gilbert J Burckart, Lawrence J Lesko, Shiew-Mei Huang, Sook Wah Yee, Deanna L Kroetz, Kathleen M Giacomini, Toshihisa Ishikawa, Yoshihide Hayashizaki, Rommel G Tirona, Jörg König, Martin F Fromm, Sophie L Stocker, Arian Emami Riedmaier, Matthias Schwab, MATE SLC47 Family, Atsushi Yonezawa, Ken-ichi Inui, PEPT SLC15A Family, Tomoko Sugiura, Saki Umeda, Akira Tsuji, Yukio Kato, Míriam Molina-Arcas, Marçal Pastor-Anglada, Ingolf Cascorbi, Bruno Stieger, Gerd A Kullak-Ublick, Agnes Basseville, Susan E Bates, William D Figg, Alex Sparreboom, Anne T Nies, Satish B Cheepala, Mugdha Sukthankar, John D Schuetz, Yu Toyoda, Joseph Ware, Pharmacogenomics of Human Drug Transporters: Clinical Impacts ,(2013)

Richard M. Weinshilboum, Susan L. Sladek, Mercaptopurine pharmacogenetics: monogenic inheritance of erythrocyte thiopurine methyltransferase activity. American Journal of Human Genetics. ,vol. 32, pp. 651- 662 ,(1980)

Victor Lyamichev, Andrea L. Mast, Jeff G. Hall, James R. Prudent, Michael W. Kaiser, Tsetska Takova, Robert W. Kwiatkowski, Tamara J. Sander, Monika de Arruda, David A. Arco, Bruce P. Neri, Mary Ann D. Brow, Polymorphism identification and quantitative detection of genomic DNA by invasive cleavage of oligonucleotide probes. Nature Biotechnology. ,vol. 17, pp. 292- 296 ,(1999) , 10.1038/7044

Liangfu Chen, Joseph W. Polli, ADME Pharmacogenomics in Drug Development John Wiley & Sons, Inc.. pp. 13- 37 ,(2013) , 10.1002/9781118353240.CH2

Philip Ross, Laura Hall, Igor Smirnov, Larry Haff, High level multiplex genotyping by MALDI-TOF mass spectrometry Nature Biotechnology. ,vol. 16, pp. 1347- 1351 ,(1998) , 10.1038/4328

U A Meyer, M Blum, R Gaedigk, A Gaedigk, M Eichelbaum, Deletion of the entire cytochrome P450 CYP2D6 gene as a cause of impaired drug metabolism in poor metabolizers of the debrisoquine/sparteine polymorphism. American Journal of Human Genetics. ,vol. 48, pp. 943- 950 ,(1991)

J D Kirby, L Lennard, A Anstey, S C Mayou, Pancytopenia related to azathioprine--an enzyme deficiency caused by a common genetic polymorphism: a review. Journal of the Royal Society of Medicine. ,vol. 85, pp. 752- 756 ,(1992) , 10.1177/014107689208501213

Takashi Chishima, Alexander Lezhava, Koh-Ichiro Yoshiura, Itaru Endo, Y. U. Toyoda, Takefumi Ishidao, Ikuko Ota, Yoshihide Hayashizaki, Hiroshi Shimada, Yuki Kawai, Takeshi Sasaki, Satoshi Morita, Toshihisa Ishikawa, Aki Sakurai, Takashi Ishikawa, Shinji Togo, Minoru Yamakado, Association between breast cancer risk and the wild-type allele of human ABC transporter ABCC11. Anticancer Research. ,vol. 30, pp. 5189- 5194 ,(2010)

Hong-Guang Xie, Harish C Prasad, Richard B Kim, C.Michael Stein, CYP2C9 allelic variants: ethnic distribution and functional significance Advanced Drug Delivery Reviews. ,vol. 54, pp. 1257- 1270 ,(2002) , 10.1016/S0169-409X(02)00076-5