Page 120 - Hematology_ Basic Principles and Practice ( PDFDrive )
P. 120

Chapter 8  Pharmacogenomics and Hematologic Diseases  91


            17.  Ramsey LB, Panetta JC, Smith C, et al: Genome-wide study of metho-  24.  Mullighan CG, Su X, Zhang J, et al: Deletion of IKZF1 and prognosis
               trexate clearance replicates SLCO1B1. Blood 121(6):898–904, 2013.  in acute lymphoblastic leukemia. New Engl J Med 360:470–480, 2009.
            18.  Ramsey LB, Bruun GH, Yang W, et al: Rare versus common variants in   25.  Andersson AK, Ma J, Wang J, et al: The landscape of somatic mutations
               pharmacogenetics:  SLCO1B1  variation  and  methotrexate  disposition.   in  infant  MLL-rearranged  acute  lymphoblastic  leukemias.  Nat  Genet
               Genome Res 22:1–8, 2012.                              47(4):330–337, 2015.
            19.  Zabriskie MS, Eide CA, Tantravahi SK, et al: BCR–ABL1 compound   26.  Neff T, Armstrong SA: Recent progress toward epigenetic therapies: the
               mutations combining key domain positions confer clinical resistance to   example of mixed lineage leukemia. Blood 121(24):4847–4853, 2013.
               ponatinib in Ph chromosome-positive leukemia. Cancer Cell 26:428–442,   27.  Annesley CE, Brown P: The biology and targeting of FLT3 in pediatric
               2014.                                                 leukemia.  Front  Oncol  4:263,  2014.  doi:  10.3389/fonc.2014.00263.
            20.  Luzzatto L, Seneca E: G6PD deficiency: a classic example of pharmacoge-  eCollection 2014.
               nomics with on-going clinical implications. Br J Haematol 164:469–480,   28.  Roberts  KG,  Li Y,  Payne-Turner  D,  et al: Targetable  kinase-activating
               2014.                                                 lesions  in  Ph-like  acute  lymphoblastic  leukemia.  N  Engl  J  Med
            21.  Relling MV, McDonagh EM, Chang T, et al: Clinical pharmacogenetics   371:1005–1015, 2014.
               implementation consortium (CPIC) guidelines for rasburicase therapy   29.  Hoffman JM, Haidar CE, Wilkinson MR, et al: PG4KDS: a model for
               in  the  context  of  G6PD  deficiency  genotype.  Clin  Pharmacol  Ther   the pre-emptive implementation of pharmacogenetics. Am J Med Genet
               96(2):169–174, 2014.                                  C Semin Med Genet 166C:45–55, 2014.
            22.  Makarona K, Caputo VS, Costa JR, et al: Transcriptional and epigenetic   30.  Ritchie  MD,  Holzinger  ER,  Li  R,  et al:  Methods  of  integrating  data
               basis  for  restoration  of  G6PD  enzymatic  activity  in  human  G6PD-  to uncover genotype-phenotype interactions. Nat Rev Genet 16:85–97,
               deficient cells. Blood 124(1):134–141, 2014.          2015.
            23.  Den Boer ML, van Slegtenhorst M, De Menezes RX, et al: A subtype of   31.  Relling  MV,  Evans  WE:  Pharmacogenomics  in  the  clinic.  Nature
               childhood acute lymphoblastic leukemia with poor treatment outcome:   526:343–350, 2015.
               a genome-wide classification study. Lancet Oncol 10:125–134, 2009.
   115   116   117   118   119   120   121   122   123   124   125