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Volumn 13, Issue 5, 2012, Pages 525-528

Conference Scene: Golden Helix Pharmacogenomics Days: Educational activities on pharmacogenomics and personalized medicine

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL MARKER; CARBAMAZEPINE; DASATINIB; HEMOGLOBIN; HLA A ANTIGEN; IMATINIB; LITHIUM; NILOTINIB; VASCULOTROPIN;

EID: 84859229190     PISSN: 14622416     EISSN: 17448042     Source Type: Journal    
DOI: 10.2217/pgs.12.22     Document Type: Conference Paper
Times cited : (10)

References (8)
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    • Golden Helix Institute of Biomedical Research: Interdisciplinary research and educational activities in pharmacogenomics and personalized medicine
    • Mitropoulos K, Innocenti F, van Schaik RH et al. Golden Helix Institute of Biomedical Research: interdisciplinary research and educational activities in pharmacogenomics and personalized medicine. Pharmacogenomics 13(4), 387-392 (2012).
    • (2012) Pharmacogenomics , vol.13 , Issue.4 , pp. 387-392
    • Mitropoulos, K.1    Innocenti, F.2    Van Schaik, R.H.3
  • 3
    • 80051705165 scopus 로고    scopus 로고
    • Novel functional germline variants in the VEGF receptor 2 gene and their effect on gene expression and microvessel density in lung cancer
    • Glubb DM, Cerri E, Giese A et al. Novel functional germline variants in the VEGF receptor 2 gene and their effect on gene expression and microvessel density in lung cancer. Clin. Cancer Res. 17(16), 5257-5267 (2011).
    • (2011) Clin. Cancer Res. , vol.17 , Issue.16 , pp. 5257-5267
    • Glubb, D.M.1    Cerri, E.2    Giese, A.3
  • 4
    • 79955738088 scopus 로고    scopus 로고
    • Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin
    • Satta S, Perseu L, Moi P et al. Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin. Haematologica 96(5), 767-770 (2011).
    • (2011) Haematologica , vol.96 , Issue.5 , pp. 767-770
    • Satta, S.1    Perseu, L.2    Moi, P.3
  • 5
    • 80455126100 scopus 로고    scopus 로고
    • Evidence for association of an ACCN1 gene variant with response to lithium treatment in Sardinian patients with bipolar disorder
    • Squassina A, Manchia M, Borg J et al. Evidence for association of an ACCN1 gene variant with response to lithium treatment in Sardinian patients with bipolar disorder. Pharmacogenomics 12(11), 1559-1569 (2011).
    • (2011) Pharmacogenomics , vol.12 , Issue.11 , pp. 1559-1569
    • Squassina, A.1    Manchia, M.2    Borg, J.3
  • 6
    • 53449102851 scopus 로고    scopus 로고
    • Igbp1 is part of a positive feed-back loop in SCF-dependent, selective mRNA translation initiation inhibiting erythroid differentiation
    • Grech G, Blazquez-Domingo M, Kolbus A et al. Igbp1 is part of a positive feed-back loop in SCF-dependent, selective mRNA translation initiation inhibiting erythroid differentiation. Blood 112(7), 2750-2760 (2008).
    • (2008) Blood , vol.112 , Issue.7 , pp. 2750-2760
    • Grech, G.1    Blazquez-Domingo, M.2    Kolbus, A.3
  • 7
    • 79957585507 scopus 로고    scopus 로고
    • Targeting the Akt/mTOR pathway in Brca1-deficient cancers
    • Xiang T, Jia Y, Sherris D et al. Targeting the Akt/mTOR pathway in Brca1-deficient cancers. Oncogene 30(21), 2443-2450 (2011).
    • (2011) Oncogene , vol.30 , Issue.21 , pp. 2443-2450
    • Xiang, T.1    Jia, Y.2    Sherris, D.3
  • 8
    • 77956622584 scopus 로고    scopus 로고
    • Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin
    • Borg J, Papadopoulos P, Georgitsi M et al. Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin. Nat. Genet. 42(9), 801-805 (2010).
    • (2010) Nat. Genet. , vol.42 , Issue.9 , pp. 801-805
    • Borg, J.1    Papadopoulos, P.2    Georgitsi, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.