Brown fat as a therapy for obesity and diabetes

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High Incidence of Metabolically Active Brown Adipose Tissue in Healthy Adult Humans

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Transcriptional Control of Brown Fat Determination by PRDM16

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The presence of UCP1 demonstrates that metabolically active adipose tissue in the neck of adult humans truly represents brown adipose tissue

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Brown adipose tissue: a factor to consider in symmetrical tracer uptake in the neck and upper chest region

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Regulation of the brown and white fat gene programs through a PRDM16/CtBP transcriptional complex

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Nuclear receptor corepressor RIP140 regulates fat accumulation

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The occurrence of brown adipose tissue in outdoor workers

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Retinoblastoma protein functions as a molecular switch determining white versus brown adipocyte differentiation

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Ectopic brown adipose tissue in muscle provides a mechanism for differences in risk of metabolic syndrome in mice

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Bone morphogenic protein-7 (BMP-7), a novel therapy for diabetic nephropathy11Professor Robert Chevalier served as a guest editor for this paper.

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Prediction of preadipocyte differentiation by gene expression reveals role of insulin receptor substrates and necdin

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Rb and p107 regulate preadipocyte differentiation into white versus brown fat through repression of PGC-1α

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C/EBPα and the Corepressors CtBP1 and CtBP2 Regulate Repression of Select Visceral White Adipose Genes during Induction of the Brown Phenotype in White Adipocytes by Peroxisome Proliferator-Activated Receptor γ Agonists

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Butyrate reduces appetite and activates brown adipose tissue via the gut-brain neural circuit

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