review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Antonio Vidal-Puig | Q61080073 |
P2093 | author name string | Vivian Peirce | |
P2860 | cites work | BMP8B increases brown adipose tissue thermogenesis through both central and peripheral actions | Q24321265 |
FGF-21 as a novel metabolic regulator | Q24523933 | ||
Identification and importance of brown adipose tissue in adult humans | Q24632425 | ||
New role of bone morphogenetic protein 7 in brown adipogenesis and energy expenditure | Q24652521 | ||
PRDM16 controls a brown fat/skeletal muscle switch | Q24657178 | ||
Beyond the sympathetic tone: the new brown fat activators | Q26995845 | ||
Brown adipose tissue-specific insulin receptor knockout shows diabetic phenotype without insulin resistance | Q28361848 | ||
A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis | Q28588558 | ||
Lipocalin prostaglandin D synthase and PPARγ2 coordinate to regulate carbohydrate and lipid metabolism in vivo | Q28727526 | ||
Brown adipose tissue: function and physiological significance | Q29547448 | ||
Functional brown adipose tissue in healthy adults | Q29547687 | ||
Hepatic fibroblast growth factor 21 is regulated by PPARalpha and is a key mediator of hepatic lipid metabolism in ketotic states | Q29615208 | ||
Endocrine regulation of the fasting response by PPARalpha-mediated induction of fibroblast growth factor 21 | Q29615209 | ||
Ablation of the leptin receptor in the hypothalamic arcuate nucleus abrogates leptin-induced sympathetic activation | Q42712856 | ||
Brown adipose tissue transplantation improves whole-body energy metabolism | Q43137936 | ||
Blunted metabolic responses to cold and insulin stimulation in brown adipose tissue of obese humans. | Q43429671 | ||
White-to-brown transdifferentiation of omental adipocytes in patients affected by pheochromocytoma | Q43546622 | ||
Banting lecture 2001: dysregulation of fatty acid metabolism in the etiology of type 2 diabetes | Q43833528 | ||
Interleukin-6-deficient mice develop mature-onset obesity | Q43851625 | ||
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 | ||
Cardiovascular responses to weight management and sibutramine in high-risk subjects: an analysis from the SCOUT trial | Q44471524 | ||
Evidence for two types of brown adipose tissue in humans. | Q44667691 | ||
Role of the sympathetic nervous system and insulin in enhancing glucose uptake in peripheral tissues after intrahypothalamic injection of leptin in rats | Q48116737 | ||
Cold exposure reverses the diabetogenic effects of high-fat feeding. | Q54432192 | ||
Brown adipose tissue activity controls triglyceride clearance. | Q55053878 | ||
β3-Adrenergic Receptors on White and Brown Adipocytes Mediate β3-Selective Agonist-induced Effects on Energy Expenditure, Insulin Secretion, and Food Intake | Q60564113 | ||
Different Metabolic Responses of Human Brown Adipose Tissue to Activation by Cold and Insulin | Q60714047 | ||
CL-316,243, a beta3-specific adrenoceptor agonist, enhances insulin-stimulated glucose disposal in nonobese rats | Q73531700 | ||
beta-Adrenergic stimulation of interleukin-1alpha and interleukin-6 expression in mouse brown adipocytes | Q73564574 | ||
Increase in insulin action and fat oxidation after treatment with CL 316,243, a highly selective beta3-adrenoceptor agonist in humans | Q77349144 | ||
Lipotoxicity, an imbalance between lipogenesis de novo and fatty acid oxidation | Q81127015 | ||
Outdoor Temperature, Age, Sex, Body Mass Index, and Diabetic Status Determine the Prevalence, Mass, and Glucose-Uptake Activity of 18F-FDG-Detected BAT in Humans | Q85189481 | ||
High incidence of metabolically active brown adipose tissue in healthy adult humans: effects of cold exposure and adiposity | Q29615454 | ||
Beige adipocytes are a distinct type of thermogenic fat cell in mouse and human | Q29617382 | ||
Unexpected evidence for active brown adipose tissue in adult humans | Q29619030 | ||
Adiponectin and adiponectin receptors in insulin resistance, diabetes, and the metabolic syndrome | Q29619211 | ||
Glycemic durability of rosiglitazone, metformin, or glyburide monotherapy | Q29620534 | ||
Imaging cold-activated brown adipose tissue using dynamic T2*-weighted magnetic resonance imaging and 2-deoxy-2-[18F]fluoro-D-glucose positron emission tomography | Q30630382 | ||
Thyroid hormone induced brown adipose tissue and amelioration of diabetes in a patient with extreme insulin resistance | Q33586783 | ||
Molecular mechanisms regulating hormone-sensitive lipase and lipolysis | Q34001474 | ||
beta-Adrenergic regulation of IL-6 release from adipose tissue: in vivo and in vitro studies | Q34104598 | ||
Leptin and its role in lipid metabolism | Q34251173 | ||
The role of lipids in the pathogenesis of muscle insulin resistance and beta cell failure in type II diabetes and obesity | Q34312028 | ||
Brown adipose tissue regulates glucose homeostasis and insulin sensitivity. | Q34316238 | ||
beta(3)-Adrenoceptor agonists: potential, pitfalls and progress | Q34635446 | ||
Lessons from obesity management programmes: greater initial weight loss improves long-term maintenance | Q34741841 | ||
Leptin-receptor-expressing neurons in the dorsomedial hypothalamus and median preoptic area regulate sympathetic brown adipose tissue circuits | Q34753919 | ||
Thermogenic activation induces FGF21 expression and release in brown adipose tissue. | Q34787051 | ||
The relationship between patients' serum glucose levels and metabolically active brown adipose tissue detected by PET/CT. | Q35155623 | ||
Lipotoxicity: when tissues overeat | Q35168828 | ||
BRL 35135, a potent and selective atypical beta-adrenoceptor agonist | Q35249868 | ||
Myogenic gene expression signature establishes that brown and white adipocytes originate from distinct cell lineages. | Q35663501 | ||
Brown adipose tissue oxidative metabolism contributes to energy expenditure during acute cold exposure in humans. | Q35698990 | ||
FGF21 regulates PGC-1α and browning of white adipose tissues in adaptive thermogenesis | Q35755169 | ||
Reversal of type 1 diabetes in mice by brown adipose tissue transplant. | Q35766895 | ||
Cardiac natriuretic peptides act via p38 MAPK to induce the brown fat thermogenic program in mouse and human adipocytes | Q35780260 | ||
In vivo identification of bipotential adipocyte progenitors recruited by β3-adrenoceptor activation and high-fat feeding | Q35878325 | ||
Cold but not sympathomimetics activates human brown adipose tissue in vivo | Q36056500 | ||
A new role for lipocalin prostaglandin d synthase in the regulation of brown adipose tissue substrate utilization. | Q36410683 | ||
Cellular localization of interleukin 6 mRNA and interleukin 6 receptor mRNA in rat brain | Q36760462 | ||
Anatomical localization, gene expression profiling and functional characterization of adult human neck brown fat. | Q36831935 | ||
15O PET measurement of blood flow and oxygen consumption in cold-activated human brown fat. | Q37444605 | ||
Nonshivering thermogenesis and its adequate measurement in metabolic studies | Q37823045 | ||
Endoplasmic reticulum stress, pancreatic β-cell degeneration, and diabetes | Q38040992 | ||
Pharmacological strategies for targeting BAT thermogenesis. | Q38104512 | ||
Brown adipose tissue: development, metabolism and beyond | Q38117395 | ||
A classical brown adipose tissue mRNA signature partly overlaps with brite in the supraclavicular region of adult humans | Q39421041 | ||
The antidiabetic beta 3-adrenoceptor agonist BRL 26830A works by release of endogenous insulin | Q41088986 | ||
Alternatively activated macrophages produce catecholamines to sustain adaptive thermogenesis. | Q41807977 | ||
P433 | issue | 4 | |
P921 | main subject | glycobiology | Q899224 |
P304 | page(s) | 353-360 | |
P577 | publication date | 2013-08-27 | |
P1433 | published in | The Lancet: Diabetes & Endocrinology | Q27725107 |
P1476 | title | Regulation of glucose homoeostasis by brown adipose tissue | |
P478 | volume | 1 |
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Q90288151 | Association between brown adipose tissue and bone mineral density in humans |
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Q38809663 | Brown adipose tissue: The heat is on the heart. |
Q38926160 | Brown and Beige Adipose Tissue: Therapy for Obesity and Its Comorbidities? |
Q34137164 | Brown fat in humans: consensus points and experimental guidelines |
Q27335000 | Browning of white adipose tissue uncouples glucose uptake from insulin signaling |
Q90124201 | Browning of white fat: agents and implications for beige adipose tissue to type 2 diabetes |
Q27316188 | Central chronic apelin infusion decreases energy expenditure and thermogenesis in mice. |
Q38552228 | Could burning fat start with a brite spark? Pharmacological and nutritional ways to promote thermogenesis |
Q40142078 | Cyanidin-3-glucoside increases whole body energy metabolism by upregulating brown adipose tissue mitochondrial function |
Q92667186 | Dysregulation of PP2A-Akt interaction contributes to Sucrose non-fermenting related kinase (SNRK) deficiency induced insulin resistance in adipose tissue |
Q38980163 | Epigenomic and transcriptional control of insulin resistance |
Q92825488 | Glucose metabolism in brown adipose tissue determined by deuterium metabolic imaging in rats |
Q36516921 | High intensity interval training improves liver and adipose tissue insulin sensitivity. |
Q42824278 | Insufficient glucose supply is linked to hypothermia upon cold exposure in high-fat diet-fed mice lacking PEMT. |
Q55090115 | Intracellular glycolysis in brown adipose tissue is essential for optogenetically induced nonshivering thermogenesis in mice. |
Q39270549 | Lsd1 Ablation Triggers Metabolic Reprogramming of Brown Adipose Tissue |
Q26995325 | Mitochondrial uncoupling proteins and energy metabolism |
Q38923829 | Mulberry and mulberry wine extract increase the number of mitochondria during brown adipogenesis |
Q89338990 | Near-Infrared Spatially Resolved Spectroscopy as an Indirect Technique to Assess Brown Adipose Tissue in Young Women |
Q37219488 | Obesity and related consequences to ageing |
Q64966800 | Pharmacological Action of a Pregnane Glycoside, Russelioside B, in Dietary Obese Rats: Impact on Weight Gain and Energy Expenditure. |
Q57065546 | Regulation and Metabolic Significance of Lipogenesis in Adipose Tissues |
Q92468516 | Relationship between the Daily Rhythm of Distal Skin Temperature and Brown Adipose Tissue 18F-FDG Uptake in Young Sedentary Adults |
Q90589347 | Resveratrol enhances brown adipose tissue activity and white adipose tissue browning in part by regulating bile acid metabolism via gut microbiota remodeling |
Q47850115 | Role of brown adipose tissue in metabolic syndrome, aging, and cancer cachexia |
Q42488894 | Searching for Classical Brown Fat in Humans: Development of a Novel Human Fetal Brown Stem Cell Model. |
Q33858968 | Significance of Microbiota in Obesity and Metabolic Diseases and the Modulatory Potential by Medicinal Plant and Food Ingredients |
Q27308719 | Stress-induced activation of brown adipose tissue prevents obesity in conditions of low adaptive thermogenesis |
Q38852204 | Targeting adipose tissue in the treatment of obesity-associated diabetes |
Q54942140 | The impact of using BARCIST 1.0 criteria on quantification of BAT volume and activity in three independent cohorts of adults. |
Q38613383 | Type 2 diabetes in migrant south Asians: mechanisms, mitigation, and management |
Q26778658 | Vascular repair strategies in type 2 diabetes: novel insights |
Q88531202 | β-Adrenergic receptors control brown adipose UCP-1 tone and cold response without affecting its circadian rhythmicity |
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