George E.O. Muscat focuses on Nuclear receptor, Molecular biology, Endocrinology, Internal medicine and Myogenesis. His Nuclear receptor study combines topics in areas such as Receptor and Signal transduction, Cell biology. George E.O. Muscat interconnects Gene expression, Myogenin and Histone deacetylase, Histone deacetylase 2, HDAC4 in the investigation of issues within Molecular biology.
His research in the fields of Molecular cloning overlaps with other disciplines such as Multiple cloning site. His work on Skeletal muscle, Lipid metabolism and Carbohydrate metabolism as part of general Endocrinology study is frequently linked to Solution hybridization, bridging the gap between disciplines. His study in Myogenesis is interdisciplinary in nature, drawing from both Regulation of gene expression and Cellular differentiation.
George E.O. Muscat spends much of his time researching Molecular biology, Nuclear receptor, Internal medicine, Endocrinology and Cell biology. His Molecular biology research incorporates elements of Gene expression, Myogenesis, Transcription factor, Messenger RNA and Gene. His Transcription factor study integrates concerns from other disciplines, such as Consensus sequence and Regulation of gene expression.
His Nuclear receptor research incorporates themes from Cancer research, Coactivator, Orphan receptor, Receptor and Signal transduction. His Endocrinology research is multidisciplinary, incorporating elements of Inflammation and Retinoic acid. The various areas that George E.O. Muscat examines in his Cell biology study include Angiogenesis and Immunology.
George E.O. Muscat mainly focuses on Cancer research, Nuclear receptor, Internal medicine, Endocrinology and Gene expression. His studies in Cancer research integrate themes in fields like Carcinogenesis, Cancer, Breast cancer, DNA repair and Epigenetics. His Nuclear receptor research integrates issues from Peroxisome proliferator-activated receptor, Receptor, Orphan receptor, Signal transduction and Skeletal muscle.
Many of his research projects under Endocrinology are closely connected to Autophagy Protein 5 with Autophagy Protein 5, tying the diverse disciplines of science together. His Gene expression research includes elements of Molecular biology, Transcription factor, Gene knockdown and Cell biology. His research links Phosphorylase kinase with Molecular biology.
The scientist’s investigation covers issues in Molecular biology, Cancer research, Skeletal muscle, Nuclear receptor and Nucleotide excision repair. Molecular biology and Gene expression are frequently intertwined in his study. George E.O. Muscat combines subjects such as Glycogen, Glycogen synthase and Oxidative phosphorylation with his study of Skeletal muscle.
The Glycogen synthase study which covers Mitochondrion that intersects with Glycolysis, Internal medicine and Endocrinology. His Nuclear receptor study combines topics from a wide range of disciplines, such as Peroxisome proliferator-activated receptor and Signal transduction. His studies deal with areas such as Carcinogenesis, Regulation of gene expression, Histone and Pyrimidine dimer as well as Nucleotide excision repair.
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A human beta-actin expression vector system directs high-level accumulation of antisense transcripts
Peter Gunning;John Leavitt;George Muscat;Sun-Yu Ng.
Proceedings of the National Academy of Sciences of the United States of America (1987)
SOX9 Binds DNA, Activates Transcription, and Coexpresses with Type II Collagen during Chondrogenesis in the Mouse
Ling-Jim Ng;Susan Wheatley;George E.O Muscat;John Conway-Campbell.
Developmental Biology (1997)
Sox18 induces development of the lymphatic vasculature in mice
Mathias Francois;Andrea Caprini;Brett Hosking;Fabrizio Orsenigo.
Nature (2008)
The Peroxisome Proliferator-Activated Receptor β/δ Agonist, GW501516, Regulates the Expression of Genes Involved in Lipid Catabolism and Energy Uncoupling in Skeletal Muscle Cells
Uwe Dressel;Tamara L. Allen;Jyotsna B. Pippal;Paul R. Rohde.
Molecular Endocrinology (2003)
The NR4A subgroup: immediate early response genes with pleiotropic physiological roles.
Megan A. Maxwell;George E.O. Muscat.
Nuclear Receptor Signaling (2006)
Minireview: Nuclear Hormone Receptor 4A Signaling: Implications for Metabolic Disease
Michael A. Pearen;George E. O. Muscat.
Molecular Endocrinology (2010)
A dynamic role for HDAC7 in MEF2-mediated muscle differentiation.
Uwe Dressel;Peter J. Bailey;Shu-Ching M. Wang;Michael Downes.
Journal of Biological Chemistry (2001)
Class I histone deacetylases sequentially interact with MyoD and pRb during skeletal myogenesis
Pier Lorenzo Puri;Pier Lorenzo Puri;Simona Iezzi;Peter Stiegler;Tung Ti Chen.
Molecular Cell (2001)
International Union of Pharmacology. LXVI. Orphan Nuclear Receptors
Gérard Benoit;Austin Cooney;Vincent Giguere;Holly Ingraham.
Pharmacological Reviews (2006)
Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice.
David J. Pennisi;Jennifer Gardner;Doreen Chambers;Brett Hosking.
Nature Genetics (2000)
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