Molecular biology, Cell biology, Nuclear receptor, Transcription factor and Nuclear receptor coactivator 1 are his primary areas of study. His studies deal with areas such as Transcription, Gene expression, Gene, Estrogen-related receptor gamma and Hormone response element as well as Molecular biology. The Cell biology study combines topics in areas such as Endocrinology and Thyroid hormone receptor, Receptor, Internal medicine, Steroid hormone.
His work in Thyroid hormone receptor alpha and Nuclear receptor coregulators are all subfields of Nuclear receptor research. His Transcription factor research includes themes of Estrogen receptor and Cellular differentiation. The various areas that he examines in his Nuclear receptor coactivator 1 study include Nuclear receptor coactivator 3, CREB-binding protein, Nuclear receptor coactivator 2, Transactivation and Histone acetyltransferase.
Ming-Jer Tsai mostly deals with Molecular biology, Cell biology, Internal medicine, Transcription factor and Nuclear receptor. His Molecular biology research is multidisciplinary, incorporating elements of RNA, Transcription, Gene expression, Gene and Ovalbumin. His study on Cell biology also encompasses disciplines like
In his work, COUP-TFII is strongly intertwined with Endocrinology, which is a subfield of Internal medicine. His research in Transcription factor intersects with topics in Promoter and Regulation of gene expression. Ming-Jer Tsai focuses mostly in the field of Nuclear receptor, narrowing it down to topics relating to Coactivator and, in certain cases, Proto-oncogene tyrosine-protein kinase Src and Signal transduction.
His main research concerns Computer network, Internal medicine, Endocrinology, Cell biology and COUP-TFII. His work deals with themes such as Throughput and Distributed computing, which intersect with Computer network. His Internal medicine study integrates concerns from other disciplines, such as Cell growth and Cardiology.
Ming-Jer Tsai has researched Endocrinology in several fields, including Cardiomyopathy, Metastasis, Prostate cancer and Mitochondrion. In his study, Kinase is inextricably linked to Transcription factor, which falls within the broad field of Cell biology. The subject of his COUP-TFII research is within the realm of Nuclear receptor.
His primary areas of investigation include Internal medicine, Endocrinology, Cell biology, Approximation algorithm and Computer network. His study in Internal medicine is interdisciplinary in nature, drawing from both Phenotype, COUP-TFII and Cell growth. His research integrates issues of Cancer research, Metastasis, Mitochondrion and Prostate cancer in his study of Endocrinology.
The study incorporates disciplines such as Histone H3, Transcription factor, Transcriptional regulation and Transcription factor II D in addition to Cell biology. He focuses mostly in the field of Transcription factor, narrowing it down to matters related to Immunology and, in some cases, Nuclear receptor. His Approximation algorithm research integrates issues from Routing table, Wireless sensor network, Distributed computing and Data transmission.
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MOLECULAR MECHANISMS OF ACTION OF STEROID/THYROID RECEPTOR SUPERFAMILY MEMBERS
Ming-Jer Tsai;Bert W. O'Malley.
Annual Review of Biochemistry (1994)
Sequence and Characterization of a Coactivator for the Steroid Hormone Receptor Superfamily
Sergio A. Oñate;Sophia Y. Tsai;Ming-Jer Tsai;Bert W. O'Malley.
Steroid receptor coactivator-1 is a histone acetyltransferase
T E Spencer;G Jenster;G Jenster;M M Burcin;C D Allis.
Diabetes, defective pancreatic morphogenesis, and abnormal enteroendocrine differentiation in BETA2/NeuroD-deficient mice
Francisco J. Naya;Hsiang-Po Huang;Yuhong Qiu;Hiroyuki Mutoh.
Genes & Development (1997)
A steroid receptor coactivator, SRA, functions as an RNA and is present in an SRC-1 complex.
Rainer B Lanz;Neil J McKenna;Sergio A Onate;Urs Albrecht.
Partial Hormone Resistance in Mice with Disruption of the Steroid Receptor Coactivator-1 (SRC-1) Gene
Jianming Xu;Yuhong Qiu;Francesco J. DeMayo;Sophia Y. Tsai.
Suppression of Notch signalling by the COUP-TFII transcription factor regulates vein identity
Li Ru You;Fu Jung Lin;Christopher T. Lee;Francesco J. DeMayo.
Tissue-specific regulation of the insulin gene by a novel basic helix-loop-helix transcription factor.
Francisco J. Naya;Christine M.M. Stellrecht;Ming Jer Tsai.
Genes & Development (1995)
Role of co-activators and co-repressors in the mechanism of steroid/thyroid receptor action.
H Shibata;T E Spencer;S A Oñate;G Jenster.
Recent Progress in Hormone Research (1997)
Molecular interactions of steroid hormone receptor with its enhancer element: Evidence for receptor dimer formation
Sophia Y. Tsai;Jan Carlstedt-Duke;Nancy L. Weigel;Karin Dahlman.
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