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1. Germline genetic regulation of the colorectal tumor immune microenvironment

2. Differences in tumor-associated T-cell receptor repertoires between early-onset and average-onset colorectal cancer.

3. Common variants at 19p13 are associated with susceptibility to ovarian cancer (vol 42, pg 880, 2010)

4. Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer.

5. Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk

6. Heterozygote advantage at HLA class I and II loci and reduced risk of colorectal cancer

7. GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.

8. Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31

9. Polymorphisms in Stromal Genes and Susceptibility to Serous Epithelial Ovarian Cancer: A Report from the Ovarian Cancer Association Consortium

10. Common variants at 19p13 are associated with susceptibility to ovarian cancer.

11. Data from Safety and Chemopreventive Effect of Polyphenon E in Preventing Early and Metastatic Progression of Prostate Cancer in TRAMP Mice

12. Supplementary Figures 1 - 2 from Safety and Chemopreventive Effect of Polyphenon E in Preventing Early and Metastatic Progression of Prostate Cancer in TRAMP Mice

13. Supplementary Figure Legends from Safety and Chemopreventive Effect of Polyphenon E in Preventing Early and Metastatic Progression of Prostate Cancer in TRAMP Mice

14. Supplementary Table 1 from Gene Set Analysis of Survival Following Ovarian Cancer Implicates Macrolide Binding and Intracellular Signaling Genes

15. Data from Inherited Variants in Mitochondrial Biogenesis Genes May Influence Epithelial Ovarian Cancer Risk

16. Data from Assessment of Hepatocyte Growth Factor in Ovarian Cancer Mortality

17. Data from Network-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer Risk

18. Supplementary Table 1 from Inherited Variants in Mitochondrial Biogenesis Genes May Influence Epithelial Ovarian Cancer Risk

19. Supplementary Tables S1-6, Figures S1-2 from Network-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer Risk

20. Supplementary Tables 1-7 from Common Variation in Nemo-Like Kinase Is Associated with Risk of Ovarian Cancer

21. Supplementary Table 2 from Gene Set Analysis of Survival Following Ovarian Cancer Implicates Macrolide Binding and Intracellular Signaling Genes

22. Supplementary Figure Legend 1 from Common Variation in Nemo-Like Kinase Is Associated with Risk of Ovarian Cancer

23. Supplementary Figure 1 from Inherited Variants in Mitochondrial Biogenesis Genes May Influence Epithelial Ovarian Cancer Risk

24. Supplementary Table 2 from Inherited Variants in Mitochondrial Biogenesis Genes May Influence Epithelial Ovarian Cancer Risk

25. Supplementary Tables 1-7 from Assessment of Hepatocyte Growth Factor in Ovarian Cancer Mortality

26. Supplementary Figures 1-4 from Assessment of Hepatocyte Growth Factor in Ovarian Cancer Mortality

27. Supplementary Figure 1 from Common Variation in Nemo-Like Kinase Is Associated with Risk of Ovarian Cancer

28. Supplementary Table 3 from Gene Set Analysis of Survival Following Ovarian Cancer Implicates Macrolide Binding and Intracellular Signaling Genes

29. Supplementary Table S2 from LIN28B Polymorphisms Influence Susceptibility to Epithelial Ovarian Cancer

30. Data from LIN28B Polymorphisms Influence Susceptibility to Epithelial Ovarian Cancer

31. Supplementary Figure S1 from LIN28B Polymorphisms Influence Susceptibility to Epithelial Ovarian Cancer

32. Differences in tumor-associated T cell receptor repertoires between young-onset and average-onset colorectal cancer.

33. ABO blood group and risk of epithelial ovarian cancer within the Ovarian Cancer Association Consortium

34. Variation at 8q24 and 9p24 and Risk of Epithelial Ovarian Cancer

36. Cell-type-specific enrichment of risk-associated regulatory elements at ovarian cancer susceptibility loci

37. Abstract 2737: Clinical and epidemiologic predictors of clonal immune responses in colorectal cancer

38. Abstract 835: T-cell abundance, clonality and disease specific survival in colorectal cancer

39. Abstract 824: Germline genetic regulation of the adaptive immune response in colorectal cancer

43. Meta-analysis of 8q24 for seven cancers reveals a locus between NOV and ENPP2 associated with cancer development

44. Nonsurgical Correction of Skeletal Class III Malocclusion by Multibends Edgewise Archwire Technique in an Adult

45. Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer

46. PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

47. Common variants at 19p13 are associated with susceptibility to ovarian cancer (vol 42, pg 880, 2010)

48. Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer

50. Identification of six new susceptibility loci for invasive epithelial ovarian cancer

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