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Volumn 54, Issue 8, 2015, Pages 1227-1229

RWDD3 and TECTA variants not linked to paclitaxel induced peripheral neuropathy in North American trial Alliance N08C1

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; PACLITAXEL; ANTINEOPLASTIC AGENT; GLYCOSYLPHOSPHATIDYLINOSITOL ANCHORED PROTEIN; RSUME PROTEIN, HUMAN; SCLEROPROTEIN; TECTA PROTEIN, HUMAN; TRANSCRIPTION FACTOR;

EID: 84940509229     PISSN: 0284186X     EISSN: 1651226X     Source Type: Journal    
DOI: 10.3109/0284186X.2014.985388     Document Type: Letter
Times cited : (10)

References (9)
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    • Cavaletti, G.1    Alberti, P.2    Marmiroli, P.3
  • 4
    • 84870784543 scopus 로고    scopus 로고
    • GWAS-based association between RWDD3 and TECTA variants and paclitaxel induced neuropathy could not be confirmed in Scandinavian ovarian cancer patients
    • Bergmann TK, Vach W, Feddersen S, Eckhoff L, Green H, Herrstedt J, et al. GWAS-based association between RWDD3 and TECTA variants and paclitaxel induced neuropathy could not be confirmed in Scandinavian ovarian cancer patients. Acta Oncol 2012;52:871.
    • (2012) Acta Oncol , vol.52 , pp. 871
    • Bergmann, T.K.1    Vach, W.2    Feddersen, S.3    Eckhoff, L.4    Green, H.5    Herrstedt, J.6
  • 5
    • 21144457498 scopus 로고    scopus 로고
    • The development of an EORTC quality of life questionnaire to assess chemotherapy-induced peripheral neuropathy: The QLQ-CIPN20
    • Postma TJ, Aaronson NK, Heimans JJ, Muller MJ, Hildebrand JG, Delattre JY, et al. The development of an EORTC quality of life questionnaire to assess chemotherapy-induced peripheral neuropathy: The QLQ-CIPN20. Eur J Cancer 2005;41:1135-9.
    • (2005) Eur J Cancer , vol.41 , pp. 1135-1139
    • Postma, T.J.1    Aaronson, N.K.2    Heimans, J.J.3    Muller, M.J.4    Hildebrand, J.G.5    Delattre, J.Y.6
  • 7
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    • Barnett, I.J.1    Lee, S.2    Lin, X.3
  • 8
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    • Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies
    • Li D, Lewinger JP, Gauderman WJ, Murcray CE, Conti D. Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies. Genet Epidemiol 2011;35:790-9.
    • (2011) Genet Epidemiol , vol.35 , pp. 790-799
    • Li, D.1    Lewinger, J.P.2    Gauderman, W.J.3    Murcray, C.E.4    Conti, D.5
  • 9
    • 33846563409 scopus 로고    scopus 로고
    • Why most published research findings are false
    • Ioannidis JP. Why most published research findings are false. PLoS Med 2005;2:e124.
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    • Ioannidis, J.P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.