PGC-1α coactivates PDK4 gene expression via the orphan nuclear receptor ERRα: a mechanism for transcriptional control of muscle glucose metabolism

AR Wende, JM Huss, PJ Schaeffer… - … and cellular biology, 2005 - Am Soc Microbiol
The transcriptional coactivator PGC-1α is a key regulator of energy metabolism, yet little is
known about its role in control of substrate selection. We found that physiological stimuli …

[HTML][HTML] PGC-1α Coactivates PDK4 Gene Expression via the Orphan Nuclear Receptor ERRα: a Mechanism for Transcriptional Control of Muscle Glucose Metabolism

AR Wende, JM Huss, PJ Schaeffer… - … and Cellular Biology, 2005 - ncbi.nlm.nih.gov
The transcriptional coactivator PGC-1α is a key regulator of energy metabolism, yet little is
known about its role in control of substrate selection. We found that physiological stimuli …

PGC-1alpha coactivates PDK4 gene expression via the orphan nuclear receptor ERRalpha: a mechanism for transcriptional control of muscle glucose metabolism.

AR Wende, JM Huss, PJ Schaeffer… - … and Cellular Biology, 2005 - europepmc.org
The transcriptional coactivator PGC-1α is a key regulator of energy metabolism, yet little is
known about its role in control of substrate selection. We found that physiological stimuli …

PGC-1α Coactivates PDK4 Gene Expression via the Orphan Nuclear Receptor ERRα: a Mechanism for Transcriptional Control of Muscle Glucose Metabolism

AR Wende, JM Huss, PJ Schaeffer, V Giguère… - Molecular and Cellular …, 2005 - cir.nii.ac.jp
抄録< jats: title> ABSTRACT</jats: title>< jats: p> The transcriptional coactivator PGC-1α is a
key regulator of energy metabolism, yet little is known about its role in control of substrate …

[PDF][PDF] PGC-1α coactivates PDK4 gene expression via the orphan nuclear receptor ERRα: A mechanism for transcriptional control of muscle glucose metabolism

AR Wende, JM Huss, PJ Schaeffer, V Giguere… - Citeseer
The transcriptional coactivator PGC-1 is a key regulator of energy metabolism, yet little is
known about its role in control of substrate selection. We found that physiological stimuli …

[PDF][PDF] PGC-1α coactivates PDK4 gene expression via the orphan nuclear receptor ERRα: A mechanism for transcriptional control of muscle glucose metabolism

AR Wende, JM Huss, PJ Schaeffer, V Giguere… - core.ac.uk
The transcriptional coactivator PGC-1 is a key regulator of energy metabolism, yet little is
known about its role in control of substrate selection. We found that physiological stimuli …

PGC-1alpha coactivates PDK4 gene expression via the orphan nuclear receptor ERRalpha: a mechanism for transcriptional control of muscle glucose metabolism

AR Wende, JM Huss, PJ Schaeffer… - Molecular and …, 2005 - pubmed.ncbi.nlm.nih.gov
The transcriptional coactivator PGC-1alpha is a key regulator of energy metabolism, yet little
is known about its role in control of substrate selection. We found that physiological stimuli …

[PDF][PDF] PGC-1 Coactivates PDK4 Gene Expression via the Orphan Nuclear Receptor ERR: a Mechanism for Transcriptional Control of Muscle Glucose Metabolism

AR Wende, JM Huss, PJ Schaeffer… - MOLECULAR AND …, 2005 - researchgate.net
The transcriptional coactivator PGC-1 is a key regulator of energy metabolism, yet little is
known about its role in control of substrate selection. We found that physiological stimuli …

[PDF][PDF] PGC-1α coactivates PDK4 gene expression via the orphan nuclear receptor ERRα: A mechanism for transcriptional control of muscle glucose metabolism

AR Wende, JM Huss, PJ Schaeffer, V Giguere… - 2005 - digitalcommons.wustl.edu
The transcriptional coactivator PGC-1 is a key regulator of energy metabolism, yet little is
known about its role in control of substrate selection. We found that physiological stimuli …

PGC-1α Coactivates PDK4 Gene Expression via the Orphan Nuclear Receptor ERRα: a Mechanism for Transcriptional Control of Muscle Glucose Metabolism

AR Wende, JM Huss, PJ Schaeffer… - … and Cellular Biology, 2005 - Taylor & Francis
The transcriptional coactivator PGC-1α is a key regulator of energy metabolism, yet little is
known about its role in control of substrate selection. We found that physiological stimuli …