Search Results - Grant A. Mitchell
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Disorders of mitochondrial function by François‐Guillaume Debray, Marie Lambert, Grant A. Mitchell
Published 2008Revisão -
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The role of the <i>LRPPRC</i> (leucine-rich pentatricopeptide repeat cassette) gene in cytochrome oxidase assembly: mutation causes lowered levels of COX (cytochrome <i>c</i> oxida... by Fenghao Xu, Charles Morin, Grant A. Mitchell, Cameron Ackerley, Brian H. Robinson
Published 2004Artigo -
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Enzymes of Ketone Body Utilization in Human Tissues: Protein and Messenger RNA Levels of Succinyl-Coenzyme A (CoA):3-Ketoacid CoA Transferase and Mitochondrial and Cytosolic Acetoa... by Toshiyuki Fukao, Xiang‐Qian Song, Grant A. Mitchell, Seiji Yamaguchi, Kazuko Sukegawa, Tadao Or, Naomi Kondo
Published 1997Artigo -
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Adipocyte death defines macrophage localization and function in adipose tissue of obese mice and humans by Saverio Cinti, Grant A. Mitchell, Giorgio Barbatelli, Incoronata Murano, E Ceresi, Emanuela Faloia, Shupei Wang, Mélanie Fortier, Andrew S. Greenberg, Martin S. Obin
Published 2005Artigo -
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Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation. by Grant A. Mitchell, Damian Labuda, G Fontaine, Jean Marie Saudubray, Jean‐Paul Bonnefont, Stanislas Lyonnet, Lawrence C. Brody, Gary Steel, Cassandra Obie, David Valle
Published 1991Artigo -
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Hormone-Sensitive Lipase Has a Role in Lipid Signaling for Insulin Secretion but Is Nonessential for the Incretin Action of Glucagon-Like Peptide 1 by Marie‐Line Peyot, Christopher J. Nolan, Krishnakant G. Soni, Érik Joly, Roxane Lussier, Barbara E. Corkey, Shu Pei Wang, Grant A. Mitchell, Marc Prentki
Published 2004Artigo -
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Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences. by Larry Brody, Grant A. Mitchell, Cassandra Obie, Jacques L. Michaud, Gary Steel, G Fontaine, M.F. Robert, Ilkka Sipilä, Muriel I. Kaiser‐Kupfer, David Valle
Published 1992Artigo
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