PubMed · 12127882
Using genetic variation to study immunomodulation.
Abstract
The generation of a draft sequence of a human genome has led to the identification of millions of common variants, known as single nucleotide polymorphisms, which constitute a resource for studying complex diseases. Currently, high-density maps of variants in candidate genes, chromosomal regions or the entire genome should encourage investigation of determinants of human immune response, using quantitative analysis. Ultimately, this approach should identify novel targets for therapeutic intervention.
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Stephen Chanock, James G Taylor. 2002. Using genetic variation to study immunomodulation.. https://doi.org/10.1016/s1471-4892(02)00186-8
Cite the original work for its findings. Save a collection to share your selection of sources.