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coactivation fatty acid genes ( Lin et al . 2005 , Nagai et al . 2009 ). Furthermore, previous studies have reported that SIRT1 can deacetylate PGC1β in skeletal muscle, inducing the expression of PGC1β gene targets. We provide evidence that a similar
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gene targeting . Journal of Steroid Biochemistry and Molecular Biology 65 111 – 115 doi:10.1016/S0960-0760(97)00181-7 . Rudy J 2008 Is there a baby in the bathwater? Maybe: some methodological issues for the de novo protein synthesis
School of Medicine, Conjoint Endocrine Laboratory, Disciplines of Medicine, Royal Brisbane and Women's Hospital, The University of Queensland, Herston, Brisbane, Queensland 4029, Australia
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School of Medicine, Conjoint Endocrine Laboratory, Disciplines of Medicine, Royal Brisbane and Women's Hospital, The University of Queensland, Herston, Brisbane, Queensland 4029, Australia
School of Medicine, Conjoint Endocrine Laboratory, Disciplines of Medicine, Royal Brisbane and Women's Hospital, The University of Queensland, Herston, Brisbane, Queensland 4029, Australia
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School of Medicine, Conjoint Endocrine Laboratory, Disciplines of Medicine, Royal Brisbane and Women's Hospital, The University of Queensland, Herston, Brisbane, Queensland 4029, Australia
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2006 ). It is also interesting to note that both C/EBP and AP-1 are up-regulated under hypoxic conditions and closely interact with HIF-1α, leading to the transcription of specific gene targets ( Cummins & Taylor 2005 , Janardhan 2008 ). In this study
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usually start in mouse models and other species. The prerequisite in this direction is to describe an expression pattern of a molecule followed by more mechanistic approaches such as gene targeting to correct the abnormality. Previous studies have
Department of Physiology, Michigan State University, East Lansing, Michigan, USA
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Department of Animal Sciences, Michigan State University, East Lansing, Michigan, USA
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Department of Animal Sciences, Michigan State University, East Lansing, Michigan, USA
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miR-429, miR-141-3p , and miR-126-3p promoters result in lower expression of these miRNAs that is correlated with upregulation of the genes targeted by these miRNAs, namely, XIAP (X-linked inhibitor of apoptosis protein), BRD3 (Bromodomain
Department of Physiology, The University of Melbourne, Parkville, Victoria, Australia
Tufts Medical Center, Boston, Massachusetts, USA
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Oxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Oxford, UK
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data have important implications for physiological vs pathological regulation of circadian gene targets where fluctuations between ligand availability, receptor levels and thus MR and GR homodimers or MR/GR heterodimers contribute to the net regulatory
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Acta 409 78 – 84 . ( doi:10.1016/j.cca.2009.09.003 ) Heuckeroth RO Enomoto H Grider JR Golden JP Hanke JA Jackman A Molliver DC Bardgett ME Snider WD Johnson EM Jr 1999 Gene targeting reveals a critical role for
Research Division, Department of Medicine, Department of Internal Medicine and Therapeutics, Section on Islet Transplantation and Cell Biology, Joslin Diabetes Center, One Joslin Place, Boston, Massachusetts 02215, USA
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Research Division, Department of Medicine, Department of Internal Medicine and Therapeutics, Section on Islet Transplantation and Cell Biology, Joslin Diabetes Center, One Joslin Place, Boston, Massachusetts 02215, USA
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Research Division, Department of Medicine, Department of Internal Medicine and Therapeutics, Section on Islet Transplantation and Cell Biology, Joslin Diabetes Center, One Joslin Place, Boston, Massachusetts 02215, USA
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Research Division, Department of Medicine, Department of Internal Medicine and Therapeutics, Section on Islet Transplantation and Cell Biology, Joslin Diabetes Center, One Joslin Place, Boston, Massachusetts 02215, USA
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transcription and for the terminal differentiation of islet cells ( Chae et al . 2004 ). In NeuroD gene targeting experiments, the combination of NeuroD and betacellulin selectively induced islet related genes in the liver ( Kojima et al . 2003 ). PDX-1/VP16
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important question that remains to be further addressed is what neuroanatomical and neurochemical substrates convey MC4R signaling in the control of energy homeostasis. Previous studies using the gene targeting strategy in MC4R-null mice have narrowed down
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Biophysica Acta 1346 231 –236. Walsh V , Somody L, Farrell A, Zhang B, Brown J, Pritchard C, Vincent M & Samani NJ 2003 Analysis of the Role of the SA gene in blood pressure regulation by gene targeting. Hypertension 41