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1. FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium.

2. Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk

3. The IARC Perspective on Cervical Cancer Screening

6. The functional ALDH2 polymorphism is associated with breast cancer risk: A pooled analysis from the Breast Cancer Association Consortium

7. Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (vol 5, 4999, 2014)

8. Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.

9. Global surveillance of trends in cancer survival 2000–14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries

10. rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk

11. Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation

12. Evidence that the 5p12 variant rs10941679 confers susceptibility to estrogen receptor positive breast cancer through FGF10 and MRPS30 regulation

13. Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer

14. Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

15. No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing

16. DNA adducts and combinations of multiple lung cancer at-risk alleles in environmentally exposed and smoking subjects

17. Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2

18. Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

19. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

20. Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation

21. Fine-mapping of the 1p11.2 breast cancer susceptibility locus

22. Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

23. Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)

24. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

25. Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

26. Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer

27. No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing

28. Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus

29. rs2735383, located at a microRNA binding site in the 3 ' UTR of NBS1, is not associated with breast cancer risk

30. Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

31. Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

32. Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1

33. Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression

34. Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

35. Fine-scale mapping of the 4q24 locus identifies & pr two Independent loci associated with breast cancer risk

36. Fine-Scale Mapping of the 4q24 Locus Identifies Two Independent Loci Associated with Breast Cancer Risk

37. Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

38. Fine-Scale Mapping of the 5q11.2 Breast Cancer Locus Reveals at Least Three Independent Risk Variants Regulating MAP3K1

39. Large-scale genotyping identifies 41 new loci associated with breast cancer risk

40. Comparison of 6q25 Breast Cancer Hits from Asian and\ud European Genome Wide Association Studies in the\ud Breast Cancer Association Consortium (BCAC)

41. Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

42. Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

43. Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

44. Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

45. Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

46. Comparison of 6q25 breast cancer hits from Asian and European genome wide association studies in the Breast Cancer Association consortium (BCAC)

47. Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

48. Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

49. Confirmation of 5p12 as a susceptibility locus for progesterone-receptor- positive, lower grade breast cancer

50. Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk

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