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Metabolic profiling of the human response to a glucose challenge reveals distinct axes of insulin sensitivity. Molecular systems biology, 2012/01/09, Volume 4, p.214, (2012)
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Disease gene discovery through integrative genomics. Annual review of genomics and human genetics, 2011/12/08, Volume 6, p.381-406, (2011)
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Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation. Cell metabolism, 2011/09/07, Volume 14, Issue 3, p.428-34, (2011)
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Metabolite profiles and the risk of developing diabetes. Nature medicine, 2011/04/01, Volume 17, Issue 4, p.448-53, (2011)
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The mitochondrial proteome and human disease. Annual review of genomics and human genetics, 2010/09/22, Volume 11, p.25-44, (2010)
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Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits. PLoS genetics, 2010/08/12, Volume 6, Issue 8, (2010)
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Nutrient-sensitized screening for drugs that shift energy metabolism from mitochondrial respiration to glycolysis. Nature biotechnology, 2010/03/01, Volume 28, Issue 3, p.249-55, (2010)
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A plasma signature of human mitochondrial disease revealed through metabolic profiling of spent media from cultured muscle cells. Proceedings of the National Academy of Sciences of the United States of America, 2010/01/26, Volume 107, Issue 4, p.1571-5, (2010)
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Upstream open reading frames cause widespread reduction of protein expression and are polymorphic among humans. Proceedings of the National Academy of Sciences of the United States of America, 2009/05/05, Volume 106, Issue 18, p.7507-12, (2009)
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Metabolite profiling of blood from individuals undergoing planned myocardial infarction reveals early markers of myocardial injury. The Journal of clinical investigation, 2008/10/01, Volume 118, Issue 10, p.3503-12, (2008)
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A mitochondrial protein compendium elucidates complex I disease biology Cell, 2008/07/11/, Volume 134, Issue 1, p.112 - 23, (2008)
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A mitochondrial protein compendium elucidates complex I disease biology. Cell, 2008/07/11, Volume 134, Issue 1, p.112-23, (2008)
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Large-scale chemical dissection of mitochondrial function. Nature biotechnology, 2008/03/01, Volume 26, Issue 3, p.343-51, (2008)
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Systematic identification of human mitochondrial disease genes through integrative genomics. Nature genetics, 2006/05/01, Volume 38, Issue 5, p.576-82, (2006)
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Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles Proceedings of the National Academy of Sciences of the United States of America, 2005/10/25/, Volume 102, Issue 43, p.15545 - 50, (2005)
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Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proceedings of the National Academy of Sciences of the United States of America, 2005/10/25, Volume 102, Issue 43, p.15545-50, (2005)
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Systematic discovery of regulatory motifs in human promoters and 3' UTRs by comparison of several mammals Nature, 2005/03/17/, Volume 434, Issue 7031, p.338 - 45, (2005)
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Systematic discovery of regulatory motifs in human promoters and 3' UTRs by comparison of several mammals. Nature, 2005/03/17, Volume 434, Issue 7031, p.338-45, (2005)
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Erralpha and Gabpa/b specify PGC-1alpha-dependent oxidative phosphorylation gene expression that is altered in diabetic muscle Proceedings of the National Academy of Sciences of the United States of America, 2004/04/27/, Volume 101, Issue 17, p.6570 - 5, (2004)
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Erralpha and Gabpa/b specify PGC-1alpha-dependent oxidative phosphorylation gene expression that is altered in diabetic muscle. Proceedings of the National Academy of Sciences of the United States of America, 2004/04/27, Volume 101, Issue 17, p.6570-5, (2004)
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Integrated analysis of protein composition, tissue diversity, and gene regulation in mouse mitochondria Cell, 2003/11/26/, Volume 115, Issue 5, p.629 - 40, (2003)
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PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes Nature Genetics, 2003/07//, Volume 34, Issue 3, p.267 - 73, (2003)
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Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics Proceedings of the National Academy of Sciences of the United States of America, 2003/01/21/, Volume 100, Issue 2, p.605 - 10, (2003)
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