Malcolm Parker

Affiliations: 
Metabolism, Digestion and Reproduction Imperial College London, London, England, United Kingdom 
Area:
Molecular Endocrinology
Website:
https://www.imperial.ac.uk/people/m.parker
Google:
"Malcolm Parker"
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Publications

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Morganstein DL, Parker MG. (2019) Role of nuclear receptor coregulators in metabolism. Expert Review of Endocrinology & Metabolism. 2: 797-807
Blondrath K, Steel JH, Katsouri L, et al. (2016) The nuclear cofactor receptor interacting protein-140 (RIP140) regulates the expression of genes involved in Aβ generation. Neurobiology of Aging. 47: 180-191
Nikolopoulou E, Papacleovoulou G, Jean-Alphonse F, et al. (2014) Arachidonic acid-dependent gene regulation during preadipocyte differentiation controls adipocyte potential. Journal of Lipid Research. 55: 2479-90
Rosell M, Nevedomskaya E, Stelloo S, et al. (2014) Complex formation and function of estrogen receptor α in transcription requires RIP140. Cancer Research. 74: 5469-79
Lapierre M, Bonnet S, Bascoul-Mollevi C, et al. (2014) RIP140 increases APC expression and controls intestinal homeostasis and tumorigenesis. The Journal of Clinical Investigation. 124: 1899-913
Rosell M, Kaforou M, Frontini A, et al. (2014) Brown and white adipose tissues: intrinsic differences in gene expression and response to cold exposure in mice. American Journal of Physiology. Endocrinology and Metabolism. 306: E945-64
Kiskinis E, Chatzeli L, Curry E, et al. (2014) RIP140 represses the "brown-in-white" adipocyte program including a futile cycle of triacylglycerol breakdown and synthesis. Molecular Endocrinology (Baltimore, Md.). 28: 344-56
Nautiyal J, Christian M, Parker MG. (2013) Distinct functions for RIP140 in development, inflammation, and metabolism. Trends in Endocrinology and Metabolism: Tem. 24: 451-9
Nautiyal J, Steel JH, Mane MR, et al. (2013) The transcriptional co-factor RIP140 regulates mammary gland development by promoting the generation of key mitogenic signals. Development (Cambridge, England). 140: 1079-89
Percharde M, Lavial F, Ng JH, et al. (2012) Ncoa3 functions as an essential Esrrb coactivator to sustain embryonic stem cell self-renewal and reprogramming. Genes & Development. 26: 2286-98
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