| P50 | author | Anne-Laure Poher | Q37373111 |
| P2093 | author name string | Christelle Veyrat-Durebex | |
| | Françoise Rohner-Jeanrenaud | |
| | Jordi Altirriba | |
| P2860 | cites work | Identification of a novel FGF, FGF-21, preferentially expressed in the liver | Q22254289 |
| | BMP8B increases brown adipose tissue thermogenesis through both central and peripheral actions | Q24321265 |
| | Identification and importance of brown adipose tissue in adult humans | Q24632425 |
| | Diet, nutrition and the prevention of chronic diseases | Q73440494 |
| | CL-316,243, a beta3-specific adrenoceptor agonist, enhances insulin-stimulated glucose disposal in nonobese rats | Q73531700 |
| | Differential effects of leptin on thermoregulation and uncoupling protein abundance in the neonatal lamb | Q74694792 |
| | Cellular mechanisms for insulin resistance in normal pregnancy and gestational diabetes | Q80538214 |
| | Substrate cycling between de novo lipogenesis and lipid oxidation: a thermogenic mechanism against skeletal muscle lipotoxicity and glucolipotoxicity | Q81127020 |
| | UCP1 deficiency increases susceptibility to diet-induced obesity with age | Q81797596 |
| | Beige differentiation of adipose depots in mice lacking prolactin receptor protects against high-fat-diet-induced obesity. | Q50577860 |
| | Differences in the metabolic status of healthy adults with and without active brown adipose tissue. | Q51191301 |
| | The adipose organ: morphological perspectives of adipose tissues. | Q51546421 |
| | Impact of brown adipose tissue on body fatness and glucose metabolism in healthy humans. | Q53089250 |
| | An essential role for Tbx15 in the differentiation of brown and "brite" but not white adipocytes. | Q54295743 |
| | Reduced beta cell function in offspring of mothers with young-onset type 2 diabetes | Q57920431 |
| | Intrauterine exposure to diabetes conveys risks for type 2 diabetes and obesity: a study of discordant sibships | Q59150834 |
| | Different Metabolic Responses of Human Brown Adipose Tissue to Activation by Cold and Insulin | Q60714047 |
| | Triiodothyronine Induces the Transcription of the Uncoupling Protein Gene and Stabilizes Its mRNA in Fetal Rat Brown Adipocyte Primary Cultures | Q61776588 |
| | Prognostic significance of birth of large infant for subsequent development of maternal non-insulin-dependent diabetes mellitus: a prospective study over 20-27 years | Q69589295 |
| | Brown adipose tissue uncoupling protein content in human infants, children and adults | Q69615952 |
| | Brown adipose tissue in the parametrial fat pad of the mouse | Q71273619 |
| | Effects of novel beta-adrenoceptor agonists on carbohydrate metabolism: relevance for the treatment of non-insulin-dependent diabetes | Q72602463 |
| | New role of bone morphogenetic protein 7 in brown adipogenesis and energy expenditure | Q24652521 |
| | The type 2 iodothyronine deiodinase is essential for adaptive thermogenesis in brown adipose tissue | Q24670736 |
| | The brain and brown fat | Q26865368 |
| | Bile acids induce energy expenditure by promoting intracellular thyroid hormone activation | Q28290455 |
| | Thyroid hormone--sympathetic interaction and adaptive thermogenesis are thyroid hormone receptor isoform--specific | Q28343412 |
| | Mice lacking mitochondrial uncoupling protein are cold-sensitive but not obese | Q28510931 |
| | UCP1 ablation induces obesity and abolishes diet-induced thermogenesis in mice exempt from thermal stress by living at thermoneutrality | Q28513102 |
| | A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis | Q28588558 |
| | Cold-activated brown adipose tissue in healthy men | Q29547382 |
| | Brown adipose tissue: function and physiological significance | Q29547448 |
| | Functional brown adipose tissue in healthy adults | Q29547687 |
| | New insights into tumor suppression: PTEN suppresses tumor formation by restraining the phosphoinositide 3-kinase/AKT pathway | Q29616144 |
| | Beige adipocytes are a distinct type of thermogenic fat cell in mouse and human | Q29617382 |
| | Bone morphogenetic proteins: multifunctional regulators of vertebrate development | Q29618986 |
| | Unexpected evidence for active brown adipose tissue in adult humans | Q29619030 |
| | The chronic inflammatory hypothesis for the morbidity associated with morbid obesity: implications and effects of weight loss. | Q30341777 |
| | From cytokine to myokine: the emerging role of interleukin-6 in metabolic regulation. | Q30361595 |
| | Thyroid hormone induced brown adipose tissue and amelioration of diabetes in a patient with extreme insulin resistance | Q33586783 |
| | A smooth muscle-like origin for beige adipocytes | Q33738053 |
| | Hepatic FGF21 expression is induced at birth via PPARalpha in response to milk intake and contributes to thermogenic activation of neonatal brown fat. | Q33762194 |
| | PTEN mutations as a cause of constitutive insulin sensitivity and obesity. | Q33811688 |
| | FGF21 as a Hepatokine, Adipokine, and Myokine in Metabolism and Diseases | Q33851027 |
| | Perinatal environment and its influences on metabolic programming of offspring | Q33915422 |
| | Chronic peroxisome proliferator-activated receptor gamma (PPARgamma) activation of epididymally derived white adipocyte cultures reveals a population of thermogenically competent, UCP1-containing adipocytes molecularly distinct from classic [...] | Q34089543 |
| | The distribution of brown adipose tissue in the human | Q34228011 |
| | Pten positively regulates brown adipose function, energy expenditure, and longevity | Q34260134 |
| | Brown adipose tissue regulates glucose homeostasis and insulin sensitivity. | Q34316238 |
| | Brown and beige fat: development, function and therapeutic potential | Q34375850 |
| | Temperature-acclimated brown adipose tissue modulates insulin sensitivity in humans. | Q34393361 |
| | Irisin and FGF21 are cold-induced endocrine activators of brown fat function in humans | Q34403054 |
| | The anti-inflammatory effect of exercise | Q34403605 |
| | Prdm16 determines the thermogenic program of subcutaneous white adipose tissue in mice | Q34428994 |
| | Brown adipose tissue improves whole-body glucose homeostasis and insulin sensitivity in humans | Q34430537 |
| | Subcutaneous adipose tissue releases interleukin-6, but not tumor necrosis factor-alpha, in vivo. | Q34449273 |
| | Identification of inducible brown adipocyte progenitors residing in skeletal muscle and white fat. | Q34472039 |
| | Fibroblast growth factor 21 corrects obesity in mice | Q34805555 |
| | Increased brown adipose tissue oxidative capacity in cold-acclimated humans | Q42262593 |
| | Medicine. Beige can be slimming | Q42716947 |
| | Adipose fibroblast growth factor 21 is up-regulated by peroxisome proliferator-activated receptor gamma and altered metabolic states. | Q42813296 |
| | Prevention of brown adipose tissue activation in 18F-FDG PET/CT of breast cancer patients receiving neoadjuvant systemic therapy | Q43160257 |
| | Thyroid hormone effects on whole-body energy homeostasis and tissue-specific fatty acid uptake in vivo. | Q43255420 |
| | Exercise as a new physiological stimulus for brown adipose tissue activity | Q43488931 |
| | White-to-brown transdifferentiation of omental adipocytes in patients affected by pheochromocytoma | Q43546622 |
| | Interleukin-6-deficient mice develop mature-onset obesity | Q43851625 |
| | BMP4 and BMP7 induce the white-to-brown transition of primary human adipose stem cells | Q43911045 |
| | Induction of uncoupling protein 1 by central interleukin-6 gene delivery is dependent on sympathetic innervation of brown adipose tissue and underlies one mechanism of body weight reduction in rats | Q44219031 |
| | Comparison of the release of adipokines by adipose tissue, adipose tissue matrix, and adipocytes from visceral and subcutaneous abdominal adipose tissues of obese humans | Q44730563 |
| | AMPK activity is diminished in tissues of IL-6 knockout mice: the effect of exercise | Q44953597 |
| | The Lou/C rat: a model of spontaneous food restriction associated with improved insulin sensitivity and decreased lipid storage in adipose tissue | Q46125862 |
| | Offspring from mothers fed a 'junk food' diet in pregnancy and lactation exhibit exacerbated adiposity that is more pronounced in females | Q46604434 |
| | Diet-induced obesity in female mice leads to offspring hyperphagia, adiposity, hypertension, and insulin resistance: a novel murine model of developmental programming | Q46845260 |
| | Nebivolol induces, via β3 adrenergic receptor, lipolysis, uncoupling protein 1, and reduction of lipid droplet size in human adipocytes | Q47198817 |
| | Mechanisms of the antidiabetic effects of the beta 3-adrenergic agonist CL-316243 in obese Zucker-ZDF rats | Q47918259 |
| | Brown adipose tissue. More than an effector of thermogenesis? | Q48300475 |
| | ASC-1, PAT2, and P2RX5 are cell surface markers for white, beige, and brown adipocytes. | Q35166610 |
| | Myogenic gene expression signature establishes that brown and white adipocytes originate from distinct cell lineages. | Q35663501 |
| | FGF21 regulates PGC-1α and browning of white adipose tissues in adaptive thermogenesis | Q35755169 |
| | Ectopic brown adipose tissue in muscle provides a mechanism for differences in risk of metabolic syndrome in mice | Q35844663 |
| | Coupling of lipolysis and de novo lipogenesis in brown, beige, and white adipose tissues during chronic β3-adrenergic receptor activation | Q36196794 |
| | Mild cold exposure modulates fibroblast growth factor 21 (FGF21) diurnal rhythm in humans: relationship between FGF21 levels, lipolysis, and cold-induced thermogenesis. | Q36508902 |
| | Liver-specific deletion of negative regulator Pten results in fatty liver and insulin hypersensitivity [corrected] | Q36604703 |
| | Brown-fat paucity due to impaired BMP signalling induces compensatory browning of white fat. | Q36758223 |
| | Anatomical localization, gene expression profiling and functional characterization of adult human neck brown fat. | Q36831935 |
| | FGF21 regulates metabolism and circadian behavior by acting on the nervous system | Q37161082 |
| | Receptor-mediated regional sympathetic nerve activation by leptin. | Q37369894 |
| | Emergence of brown adipocytes in white fat in mice is under genetic control. Effects on body weight and adiposity | Q37383979 |
| | Renaissance of brown adipose tissue | Q37849516 |
| | Adipose tissue and fetal programming. | Q37992001 |
| | The adipose organ: white-brown adipocyte plasticity and metabolic inflammation. | Q38056234 |
| | The hypothalamus-adipose axis is a key target of developmental programming by maternal nutritional manipulation | Q38056405 |
| | Bone morphogenic proteins signaling in adipogenesis and energy homeostasis | Q38077033 |
| | Brown adipose tissue thermogenesis: β3-adrenoreceptors as a potential target for the treatment of obesity in humans | Q38109463 |
| | Understanding the brown adipocyte as a contributor to energy homeostasis | Q38109726 |
| | Brown adipose tissue: research milestones of a potential player in human energy balance and obesity. | Q38117251 |
| | Nutritional manipulations in the perinatal period program adipose tissue in offspring | Q38138831 |
| | Regulation of glucose homoeostasis by brown adipose tissue. | Q38195448 |
| | Browning of white fat: does irisin play a role in humans? | Q38208190 |
| | The different shades of fat. | Q38217767 |
| | Does exposure to hyperglycaemia in utero increase the risk of obesity and diabetes in the offspring? A critical reappraisal. | Q38266316 |
| | Central leptin regulates the UCP1 and ob genes in brown and white adipose tissue via different beta-adrenoceptor subtypes | Q38309535 |
| | Leptin alters metabolic rates before acquisition of its anorectic effect in developing neonatal mice | Q38320718 |
| | Effect of age on brown adipose tissue activity in the obese (ob/ob) mouse | Q38339279 |
| | A classical brown adipose tissue mRNA signature partly overlaps with brite in the supraclavicular region of adult humans | Q39421041 |
| | Luxuskonsumption, Diet-Induced Thermogenesis and Brown Fat: The Case in Favour | Q40144246 |
| | Multilocular fat cells in WAT of CL-316243-treated rats derive directly from white adipocytes | Q40861453 |
| | Fibroblast growth factor-21 regulates PPARγ activity and the antidiabetic actions of thiazolidinediones. | Q40895648 |
| | Hepatic PTEN deficiency improves muscle insulin sensitivity and decreases adiposity in mice | Q41733861 |
| | Recruited brown adipose tissue as an antiobesity agent in humans | Q41890383 |
| | Identification of a domain within peroxisome proliferator-activated receptor gamma regulating expression of a group of genes containing fibroblast growth factor 21 that are selectively repressed by SIRT1 in adipocytes | Q41910885 |
| | A preadipocyte clonal line from mouse brown adipose tissue. Short- and long-term responses to insulin and beta-adrenergics. | Q42201790 |
| | Grizzly bears exhibit augmented insulin sensitivity while obese prior to a reversible insulin resistance during hibernation | Q42202924 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | insulin resistance | Q1053470 |
| | preproinsulin | Q7240673 |
| | obesity | Q12174 |
| P304 | page(s) | 4 | |
| P577 | publication date | 2015-01-30 | |
| P1433 | published in | Frontiers in Physiology | Q2434141 |
| P1476 | title | Brown adipose tissue activity as a target for the treatment of obesity/insulin resistance | |
| P478 | volume | 6 | |