SGC in the News

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Pfizer and SGC Oxford receive the first Wellcome Trust Pathfinder Award for Rare Diseases

The Pfizer-SGC project aims to tackle a rare, hereditary metabolic disorder called homocystinuria, which leaves patients unable to metabolise the amino acid methionine. A team of researchers at Pfizer Rare Disease unit will work with Dr Wyatt Yue at the Structural Genomics Consortium at the…

An epigenetic mechanism to inhibit inflammation

Researchers from Oxford University, GlaxoSmithKline and Cellzome, as well as Memorial Sloan Kettering Hospital have developed and characterised the first selective inhibitor for a specific class of histone demethylases and demonstrated its utility in inhibiting proinflammatory cytokine…

SGC and collaborators release renewable recombinant antibodies for 12 high-impact epigenetics targets

Antibodies are first released in massive collaboration to create ‘master set’ of high-quality renewable epigenetics antibodies

TORONTO, June 4, 2012 – The Structural Genomics Consortium (SGC), a group of expert researchers in recombinant antibody technology from the…

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