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  1. A NOVEL COLORECTAL CANCER SUSCEPTIBILITY SNP IN THE EIF3H PROMOTER INFLUENCES PATIENT...

    http://iris.ucl.ac.uk/iris/publication/1171404/3

  2. Allelic variation at the 8q23.3 colorectal cancer risk locus functions as a cis-acting...

    Common genetic variation at human 8q23.3 is significantly associated with colorectal cancer (CRC) risk. To elucidate the basis of this association we compared the frequency of common variants at 8q23.3 in 1,964 CRC cases and 2,081 healthy controls.

    http://iris.ucl.ac.uk/iris/publication/428709/2

  3. Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11:...

    We have previously identified several colorectal cancer (CRC)-associated polymorphisms using genome-wide association (GWA) analysis. We sought to fine-map the location of the functional variants for three of these regions at 8q23.3 (EIF3H), 16q22.1

    http://iris.ucl.ac.uk/iris/publication/428718/7

  4. A genome-wide association study identifies colorectal cancer susceptibility loci on...

    To identify colorectal cancer (CRC) susceptibility alleles, we conducted a genome-wide association study. In phase 1, we genotyped 550,163 tagSNPs in 940 familial colorectal tumor cases (627 CRC, 313 high-risk adenoma) and 965 controls. In phase 2,

    http://iris.ucl.ac.uk/iris/publication/428724/7

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