T
Thomas E. Spencer
Researcher at University of Missouri
Publications - 403
Citations - 35585
Thomas E. Spencer is an academic researcher from University of Missouri. The author has contributed to research in topics: Conceptus & Endometrium. The author has an hindex of 98, co-authored 383 publications receiving 32248 citations. Previous affiliations of Thomas E. Spencer include Baylor College of Medicine & Texas A&M University System.
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Journal ArticleDOI
Steroid receptor coactivator-1 is a histone acetyltransferase
Thomas E. Spencer,Guido Jenster,Guido Jenster,Mark M. Burcin,C D Allis,Jun Zhou,C A Mizzen,Neil J. McKenna,Sergio A. Onate,Sophia Y. Tsai,Ming-Jer Tsai,Bert W. O'Malley +11 more
TL;DR: It is shown that SRC-1 possesses intrinsic histone acetyltransferase activity and that it also interacts with another HAT, p300/CBP-associated factor (PCAF), which could be a mechanism by which the activation functions of steroid receptors and associated coactivators enhance formation of a stable preinitiation complex, thereby increasing transcription of specific genes from transcriptionally repressed chromatin templates.
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Arginine metabolism and nutrition in growth, health and disease
Guoyao Wu,Guoyao Wu,Fuller W. Bazer,Teresa A. Davis,Sung Woo Kim,Peng Li,J. Marc Rhoads,M. Carey Satterfield,Stephen B. Smith,Thomas E. Spencer,Yulong Yin +10 more
TL;DR: The results of both experimental and clinical studies indicate that Arg is a nutritionally essential amino acid (AA) for spermatogenesis, embryonic survival, fetal and neonatal growth, as well as maintenance of vascular tone and hemodynamics and novel and effective therapies for obesity, diabetes, and the metabolic syndrome.
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Board-invited review: intrauterine growth retardation: implications for the animal sciences.
TL;DR: There is growing evidence that maternal nutritional status can alter the epigenetic state (stable alterations of gene expression through DNA methylation and histone modifications) of the fetal genome, which may provide a molecular mechanism for the role of maternal nutrition on fetal programming and genomic imprinting.
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Maternal Nutrition and Fetal Development
TL;DR: There is growing evidence that maternal nutritional status can alter the epigenetic state (stable alterations of gene expression through DNA methylation and histone modifications) of the fetal genome, which may provide a molecular mechanism for the impact of maternal nutrition on both fetal programming and genomic imprinting.
Journal Article
Role of co-activators and co-repressors in the mechanism of steroid/thyroid receptor action.
H Shibata,Thomas E. Spencer,Sergio A. Onate,Guido Jenster,Sophia Y. Tsai,Ming-Jer Tsai,Bert W. O'Malley +6 more
TL;DR: A ternary complex-consisting of CBP, SRC-1, and liganded steroid receptors-may form to increase the rate of hormone-responsive gene transcription and enhance transactivation of steroid hormone-dependent target genes.