scholarly article | Q13442814 |
P356 | DOI | 10.1016/J.BBADIS.2013.05.011 |
P8608 | Fatcat ID | release_rypnr5673rhwjoas4spczy3bzm |
P932 | PMC publication ID | 4435780 |
P698 | PubMed publication ID | 23688783 |
P2093 | author name string | Emilio P Mottillo | |
James G Granneman | |||
Yun-Hee Lee | |||
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Role of sympathetic innervation in brown adipocyte proliferation | Q67986322 | ||
Epididymal white adipose tissue after cold stress in rats. I. Nonmitochondrial changes | Q68107976 | ||
Tritiated thymidine autoradiographic study on postnatal development of epididymal adipose tissue in the normal mouse | Q68555012 | ||
In vivo identification of bipotential adipocyte progenitors recruited by β3-adrenoceptor activation and high-fat feeding | Q35878325 | ||
Dichotomous effects of VEGF-A on adipose tissue dysfunction. | Q35889355 | ||
Obesity-associated improvements in metabolic profile through expansion of adipose tissue | Q35945161 | ||
Assessment of oxidative metabolism in brown fat using PET imaging | Q35971423 | ||
A PPARγ-FGF1 axis is required for adaptive adipose remodelling and metabolic homeostasis | Q35981284 | ||
Intrinsic differences in adipocyte precursor cells from different white fat depots. | Q36047557 | ||
Cold but not sympathomimetics activates human brown adipose tissue in vivo | Q36056500 | ||
Programming human pluripotent stem cells into white and brown adipocytes. | Q36065868 | ||
Lipolytic products activate peroxisome proliferator-activated receptor (PPAR) α and δ in brown adipocytes to match fatty acid oxidation with supply | Q36127114 | ||
Overexpression of sPRDM16 coupled with loss of p53 induces myeloid leukemias in mice | Q36151656 | ||
Bone marrow-derived circulating progenitor cells fail to transdifferentiate into adipocytes in adult adipose tissues in mice | Q36173615 | ||
βKlotho is required for fibroblast growth factor 21 effects on growth and metabolism | Q36248720 | ||
PTEN loss in the Myf5 lineage redistributes body fat and reveals subsets of white adipocytes that arise from Myf5 precursors. | Q36368511 | ||
Stromelysin-1 regulates adipogenesis during mammary gland involution | Q36375815 | ||
Loss of perivascular adipose tissue on peroxisome proliferator-activated receptor-γ deletion in smooth muscle cells impairs intravascular thermoregulation and enhances atherosclerosis | Q36384655 | ||
Systemic β-adrenergic stimulation of thermogenesis is not accompanied by brown adipose tissue activity in humans | Q36410790 | ||
Peripheral fat loss and decline in adipogenesis in older humans | Q36492251 | ||
Natriuretic peptides enhance the oxidative capacity of human skeletal muscle. | Q36498070 | ||
Mild cold exposure modulates fibroblast growth factor 21 (FGF21) diurnal rhythm in humans: relationship between FGF21 levels, lipolysis, and cold-induced thermogenesis. | Q36508902 | ||
Adipogenic capacity and the susceptibility to type 2 diabetes and metabolic syndrome | Q36579391 | ||
Brown-fat paucity due to impaired BMP signalling induces compensatory browning of white fat. | Q36758223 | ||
Thematic review series: adipocyte biology. Sympathetic and sensory innervation of white adipose tissue | Q36802207 | ||
Macrophage infiltration into adipose tissue may promote angiogenesis for adipose tissue remodeling in obesity | Q36846149 | ||
Atrial natriuretic peptide induces postprandial lipid oxidation in humans | Q36975436 | ||
The growth of adipose tissue in children and adolescents. Cross-sectional and longitudinal studies of adipose cell number and size | Q37035696 | ||
Mesenchymal stem cells: revisiting history, concepts, and assays. | Q37036368 | ||
Control of lipolysis by natriuretic peptides and cyclic GMP. | Q37109051 | ||
Metabolic dysregulation and adipose tissue fibrosis: role of collagen VI. | Q37110569 | ||
The discovery of drugs for obesity, the metabolic effects of leptin and variable receptor pharmacology: perspectives from beta3-adrenoceptor agonists | Q37210934 | ||
Impaired preadipocyte differentiation in human abdominal obesity: role of Wnt, tumor necrosis factor-alpha, and inflammation | Q37236239 | ||
C/EBPalpha 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 gamma agonists | Q37302225 | ||
Hematopoietic stem cell origin of adipocytes | Q37340037 | ||
Have we entered the brown adipose tissue renaissance? | Q37379239 | ||
Preadipocyte apoptosis is prevented by macrophage-conditioned medium in a PDGF-dependent manner. | Q42803013 | ||
The spatiotemporal development of adipose tissue | Q42803974 | ||
Involvement of matrix metalloproteinases in the adipose conversion of 3T3-L1 preadipocytes. | Q42814385 | ||
Fibronectin modulation of cell shape and lipogenic gene expression in 3T3-adipocytes | Q42820082 | ||
Role of hormone-sensitive lipase in beta-adrenergic remodeling of white adipose tissue | Q42825407 | ||
Mesenchymal progenitors distinct from satellite cells contribute to ectopic fat cell formation in skeletal muscle | Q42830262 | ||
Alpha 2-adrenergic stimulation promotes preadipocyte proliferation. Involvement of mitogen-activated protein kinases. | Q42831985 | ||
Hypoxia-inducible factor 1alpha induces fibrosis and insulin resistance in white adipose tissue. | Q43071652 | ||
Characterization of the adipocyte cellular lineage in vivo | Q43077735 | ||
Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis | Q43203009 | ||
Characterization of structure and cellular components of aspirated and excised adipose tissue | Q43236453 | ||
Depot-specific differences in adipogenic progenitor abundance and proliferative response to high-fat diet | Q43297876 | ||
Altered expression of C/EBP family members results in decreased adipogenesis with aging | Q43608324 | ||
Human adipose tissue endothelial cells promote preadipocyte proliferation | Q43762958 | ||
Lineage tracing and genetic ablation of ADAM12(+) perivascular cells identify a major source of profibrotic cells during acute tissue injury | Q43777578 | ||
Adipose tissue triglyceride turnover, de novo lipogenesis, and cell proliferation in humans measured with2H2O | Q44643865 | ||
Mechanisms of early insulin-sensitizing effects of thiazolidinediones in type 2 diabetes | Q44909485 | ||
Sensory or sympathetic white adipose tissue denervation differentially affects depot growth and cellularity | Q45154794 | ||
Effect of pioglitazone on body composition and energy expenditure: a randomized controlled trial | Q45161685 | ||
Obesity short-circuits stemness gene network in human adipose multipotent stem cells. | Q45743932 | ||
VE-cadherin-CreERT2 transgenic mouse: a model for inducible recombination in the endothelium. | Q46289913 | ||
Macrophage plasticity and polarization: in vivo veritas | Q29547620 | ||
Obesity induces a phenotypic switch in adipose tissue macrophage polarization | Q29547686 | ||
Stimulation of adipogenesis in fibroblasts by PPAR gamma 2, a lipid-activated transcription factor | Q29547912 | ||
Macrophage-specific PPARgamma controls alternative activation and improves insulin resistance | Q29614354 | ||
Dynamics of fat cell turnover in humans | Q29615688 | ||
Beige adipocytes are a distinct type of thermogenic fat cell in mouse and human | Q29617382 | ||
Inflammatory mechanisms in obesity | Q29617932 | ||
The relationship between the spleen colony-forming cell and the haemopoietic stem cell | Q29620090 | ||
Mechanisms of fibrosis: therapeutic translation for fibrotic disease | Q29620307 | ||
CCR2 modulates inflammatory and metabolic effects of high-fat feeding | Q29622869 | ||
Adipocyte death defines macrophage localization and function in adipose tissue of obese mice and humans | Q29622900 | ||
White adipose tissue contributes to UCP1-independent thermogenesis | Q30979912 | ||
p38 mitogen-activated protein kinase is the central regulator of cyclic AMP-dependent transcription of the brown fat uncoupling protein 1 gene | Q33199648 | ||
What causes the insulin resistance underlying obesity? | Q33684984 | ||
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 | ||
A history of the first uncoupling protein, UCP1. | Q33827372 | ||
Defining stem and progenitor cells within adipose tissue | Q33834898 | ||
Rapid cellular turnover in adipose tissue | Q33847015 | ||
Adipocyte dysfunctions linking obesity to insulin resistance and type 2 diabetes | Q33918445 | ||
Coexistence of quiescent and active adult stem cells in mammals | Q33926891 | ||
Pro-inflammatory CD11c+CD206+ adipose tissue macrophages are associated with insulin resistance in human obesity | Q33930230 | ||
beta3-adrenergic receptor induction of adipocyte inflammation requires lipolytic activation of stress kinases p38 and JNK | Q34005459 | ||
Adipose tissue mass can be regulated through the vasculature | Q34075818 | ||
Peroxisome proliferator-activated receptors (PPARs): nuclear receptors at the crossroads between lipid metabolism and inflammation | Q34088380 | ||
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 | ||
Drosophila genome-wide obesity screen reveals hedgehog as a determinant of brown versus white adipose cell fate | Q34092765 | ||
De novo generation of white adipocytes from the myeloid lineage via mesenchymal intermediates is age, adipose depot, and gender specific | Q34093108 | ||
Lipotoxic diseases | Q34111950 | ||
Proteolytic cleavage product of 30-kDa adipocyte complement-related protein increases fatty acid oxidation in muscle and causes weight loss in mice | Q34118282 | ||
Fat tissue, aging, and cellular senescence | Q34130783 | ||
Regulatory motifs for CREB-binding protein and Nfe2l2 transcription factors in the upstream enhancer of the mitochondrial uncoupling protein 1 gene | Q34135481 | ||
Weight loss and lipolysis promote a dynamic immune response in murine adipose tissue | Q34162171 | ||
PDGFRβ signaling regulates mural cell plasticity and inhibits fat development. | Q34191687 | ||
Mir193b-365 is essential for brown fat differentiation | Q34199261 | ||
Effect of early nutrition on the development of rat epididymal fat pads: cellularity and metabolism | Q34278536 | ||
Regulation of DNA synthesis in fat cells and stromal elements from rat adipose tissue | Q34280266 | ||
A morphological study of the adipocyte precursor | Q70202713 | ||
Local sympathetic denervation of white adipose tissue in rats induces preadipocyte proliferation without noticeable changes in metabolism | Q70492752 | ||
DNA synthesis and differentiation in developing white adipose tissue | Q70580475 | ||
The chronology of adipose tissue appearance and distribution in the human fetus | Q70671603 | ||
Changes in adipose tissue of the rat due early undernutrition followed by rehabilitation. 3. Changes in cell replication studied with tritiated thymidine | Q71178074 | ||
Growth and development of human adipose tissue during early gestation | Q71736835 | ||
Extracellular matrix components secreted by microvascular endothelial cells stimulate preadipocyte differentiation in vitro | Q72054192 | ||
Effect of CL-316,243, a thermogenic beta 3-agonist, on energy balance and brown and white adipose tissues in rats | Q72677930 | ||
Anti-obesity and anti-diabetic effects of CL 316,243, a highly specific beta 3-adrenoceptor agonist, in yellow KK mice | Q72776174 | ||
Appearance of brown adipocytes in white adipose tissue during CL 316,243-induced reversal of obesity and diabetes in Zucker fa/fa rats | Q73435770 | ||
Extracellular matrix development during differentiation into adipocytes with a unique increase in type V and VI collagen | Q74702096 | ||
Distribution of adipose tissue in the newborn | Q75185464 | ||
Plasticity of human adipose lineage cells toward endothelial cells: physiological and therapeutic perspectives | Q75302855 | ||
Fibronectins and basal lamina molecules expression in human subcutaneous white adipose tissue | Q77697507 | ||
Matrix metalloproteinase inhibition impairs adipose tissue development in mice | Q77743242 | ||
Committed subcutaneous preadipocytes are reduced in human obesity | Q79345667 | ||
Involvement of adipose tissues in the early hypolipidemic action of PPARgamma agonism in the rat | Q79434384 | ||
Adipogenesis in obesity requires close interplay between differentiating adipocytes, stromal cells, and blood vessels | Q80049800 | ||
Role of proteolysis in development of murine adipose tissue | Q80710162 | ||
Different autonomous myogenic cell populations revealed by ablation of Myf5-expressing cells during mouse embryogenesis | Q80958958 | ||
A population of multipotent CD34-positive adipose stromal cells share pericyte and mesenchymal surface markers, reside in a periendothelial location, and stabilize endothelial networks | Q81514904 | ||
Metabolic and cellular plasticity in white adipose tissue II: role of peroxisome proliferator-activated receptor-alpha | Q81823210 | ||
Metabolic and cellular plasticity in white adipose tissue I: effects of beta3-adrenergic receptor activation | Q81823213 | ||
Identification of white adipocyte progenitor cells in vivo | Q82206003 | ||
Plasticity of human adipose stem cells toward endothelial cells and cardiomyocytes | Q82662208 | ||
Activation of the cold-sensing TRPM8 channel triggers UCP1-dependent thermogenesis and prevents obesity | Q83225129 | ||
A crucial role for adipose tissue p53 in the regulation of insulin resistance | Q84491291 | ||
Human adipose CD34+ CD90+ stem cells and collagen scaffold constructs grafted in vivo fabricate loose connective and adipose tissues | Q85368478 | ||
Ephedrine activates brown adipose tissue in lean but not obese humans | Q87440877 | ||
Adipocyte macrophage colony-stimulating factor is a mediator of adipose tissue growth | Q37380502 | ||
PPARgamma activation in adipocytes is sufficient for systemic insulin sensitization | Q37478987 | ||
Mitochondrial remodeling in adipose tissue associated with obesity and treatment with rosiglitazone | Q37591975 | ||
The development and endocrine functions of adipose tissue. | Q37660587 | ||
Gluttony, sloth and the metabolic syndrome: a roadmap to lipotoxicity | Q37707665 | ||
Brown fat and the myth of diet-induced thermogenesis | Q37726542 | ||
The changed metabolic world with human brown adipose tissue: therapeutic visions. | Q37726545 | ||
Compartmentalized organization: a common and required feature of stem cell niches? | Q37739680 | ||
Positive and negative control of Ucp1 gene transcription and the role of β-adrenergic signaling networks | Q37799247 | ||
Alternative Macrophage Activation and Metabolism | Q37804862 | ||
Developmental origins of the adipocyte lineage: new insights from genetics and genomics studies. | Q37848703 | ||
Architecture and the extracellular matrix: the still unappreciated components of the adipose tissue | Q37848921 | ||
Forming functional fat: a growing understanding of adipocyte differentiation | Q37939532 | ||
Orchestration of metabolism by macrophages | Q38000642 | ||
Inflammation and lipid signaling in the etiology of insulin resistance | Q38007632 | ||
The genetics of brown adipocyte induction in white fat depots | Q38015366 | ||
Complementary action of the PGC-1 coactivators in mitochondrial biogenesis and brown fat differentiation | Q38313575 | ||
Mice lacking adiponectin show decreased hepatic insulin sensitivity and reduced responsiveness to peroxisome proliferator-activated receptor gamma agonists | Q38318111 | ||
The role of thermoregulatory thermogenesis in the development of obesity in genetically-obese (ob/ob) mice pair-fed with lean siblings | Q38357342 | ||
Aging leads to a programmed loss of brown adipocytes in murine subcutaneous white adipose tissue | Q38456892 | ||
MyomiR-133 regulates brown fat differentiation through Prdm16. | Q39246512 | ||
Electron microscopical studies on the genesis of white adipocytes: Differentiation of immature pericytes into adipocytes in transplanted preadipose tissue | Q39290430 | ||
Brown adipose tissue responds to cold and adrenergic stimulation by induction of FGF21. | Q39581682 | ||
Growth and development of adipose tissue | Q39648694 | ||
Human multipotent adipose-derived stem cells differentiate into functional brown adipocytes | Q39809960 | ||
Central players in inherited lipodystrophies | Q39858385 | ||
Peroxisome proliferator-activated receptor gamma activation promotes infiltration of alternatively activated macrophages into adipose tissue. | Q39973799 | ||
A futile metabolic cycle activated in adipocytes by antidiabetic agents | Q40700524 | ||
Adipocyte produces matrix metalloproteinases 2 and 9: involvement in adipose differentiation | Q40783644 | ||
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 | ||
The vascular endothelium of the adipose tissue gives rise to both white and brown fat cells | Q41087356 | ||
White fat progenitor cells reside in the adipose vasculature. | Q41145314 | ||
Peroxisome proliferator-activated receptor (PPAR) gamma: adipose-predominant expression and induction early in adipocyte differentiation | Q41451147 | ||
A Review of the Microcirculation of Adipose Tissue: Anatomic, Metabolic, and Angiogenic Perspectives | Q41528456 | ||
PPAR-gamma: adipogenic regulator and thiazolidinedione receptor | Q41755813 | ||
Alternatively activated macrophages produce catecholamines to sustain adaptive thermogenesis. | Q41807977 | ||
PPARγ agonists induce a white-to-brown fat conversion through stabilization of PRDM16 protein. | Q41893963 | ||
Zfp423 expression identifies committed preadipocytes and localizes to adipose endothelial and perivascular cells | Q41911584 | ||
Increased mitochondrial activity in BMP7-treated brown adipocytes, due to increased CPT1- and CD36-mediated fatty acid uptake | Q42173526 | ||
PPAR-γ is a major driver of the accumulation and phenotype of adipose tissue Treg cells | Q42183814 | ||
Genome-wide profiling of peroxisome proliferator-activated receptor γ in primary epididymal, inguinal, and brown adipocytes reveals depot-selective binding correlated with gene expression | Q42281547 | ||
TNF-alpha-induced insulin resistance in vivo and its prevention by troglitazone | Q42446456 | ||
Transcriptional synergy and the regulation of Ucp1 during brown adipocyte induction in white fat depots | Q42537485 | ||
RIP140-targeted repression of gene expression in adipocytes | Q42590169 | ||
Occurrence of brown adipocytes in rat white adipose tissue: molecular and morphological characterization | Q42601829 | ||
Is irisin a human exercise gene? | Q34296647 | ||
FNDC5 and irisin in humans: I. Predictors of circulating concentrations in serum and plasma and II. mRNA expression and circulating concentrations in response to weight loss and exercise | Q34302332 | ||
Angiogenesis inhibitor, TNP-470, prevents diet-induced and genetic obesity in mice | Q34322120 | ||
Neural crest cell formation and migration in the developing embryo | Q34331556 | ||
Adipose lineage specification of bone marrow-derived myeloid cells | Q34346254 | ||
The adipose organ | Q34423808 | ||
Adipose tissue macrophages in insulin-resistant subjects are associated with collagen VI and fibrosis and demonstrate alternative activation. | Q34426034 | ||
Prdm16 determines the thermogenic program of subcutaneous white adipose tissue in mice | Q34428994 | ||
Identification of inducible brown adipocyte progenitors residing in skeletal muscle and white fat. | Q34472039 | ||
Stem cells and their niches | Q34507142 | ||
A pericellular collagenase directs the 3-dimensional development of white adipose tissue | Q34522343 | ||
Evidence for a role of developmental genes in the origin of obesity and body fat distribution | Q34597959 | ||
Thematic review series: Adipocyte Biology. Lipodystrophies: windows on adipose biology and metabolism | Q34610713 | ||
beta(3)-Adrenoceptor agonists: potential, pitfalls and progress | Q34635446 | ||
Angiogenesis modulates adipogenesis and obesity | Q34677131 | ||
Developmental origin of fat: tracking obesity to its source. | Q34705822 | ||
The biology of white adipocyte proliferation | Q34742765 | ||
Adipose-specific peroxisome proliferator-activated receptor gamma knockout causes insulin resistance in fat and liver but not in muscle | Q34790967 | ||
A role for central nervous system PPAR-γ in the regulation of energy balance | Q34949080 | ||
Adipose tissue remodeling and obesity | Q35015740 | ||
Inducible lineage tracing of Pax7-descendant cells reveals embryonic origin of adult satellite cells | Q35040766 | ||
Desnutrin/ATGL is regulated by AMPK and is required for a brown adipose phenotype | Q35140891 | ||
Transplantation of adipose tissue and stem cells: role in metabolism and disease | Q35184552 | ||
Rosiglitazone promotes development of a novel adipocyte population from bone marrow-derived circulating progenitor cells | Q35191054 | ||
Native human adipose stromal cells: localization, morphology and phenotype | Q35211725 | ||
BRL 35135, a potent and selective atypical beta-adrenoceptor agonist | Q35249868 | ||
The implication of brown adipose tissue for humans | Q35502624 | ||
Therapeutic approaches to target inflammation in type 2 diabetes | Q35581498 | ||
ATGL-mediated fat catabolism regulates cardiac mitochondrial function via PPAR-α and PGC-1. | Q35630386 | ||
Myogenic gene expression signature establishes that brown and white adipocytes originate from distinct cell lineages. | Q35663501 | ||
Adipose tissue stem cells meet preadipocyte commitment: going back to the future | Q35715553 | ||
FGF21 regulates PGC-1α and browning of white adipose tissues in adaptive thermogenesis | Q35755169 | ||
Cardiac natriuretic peptides act via p38 MAPK to induce the brown fat thermogenic program in mouse and human adipocytes | Q35780260 | ||
A comparison of the effects of thiazolidinediones and metformin on metabolic control in patients with type 2 diabetes mellitus | Q35840613 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 358-369 | |
P577 | publication date | 2013-05-17 | |
P1433 | published in | Biochimica et Biophysica Acta | Q864239 |
P1476 | title | Adipose tissue plasticity from WAT to BAT and in between | |
P478 | volume | 1842 |
Q51277508 | 3,5-diiodothyronine (3,5-T2) reduces blood glucose independently of insulin sensitization in obese mice. |
Q42248250 | 3D brown adipogenesis to create "Brown-Fat-in-Microstrands". |
Q35160062 | Adipocytes in both brown and white adipose tissue of adult mice are functionally connected via gap junctions: implications for Chagas disease |
Q36699664 | Adipogenic role of alternatively activated macrophages in β-adrenergic remodeling of white adipose tissue |
Q28080748 | Adipose tissue dysfunction and its effects on tumor metabolism |
Q38286500 | Adipose tissue dysregulation and metabolic consequences in childhood and adolescent obesity: potential impact of dietary fat quality |
Q37028404 | Adrenergic regulation of cellular plasticity in brown, beige/brite and white adipose tissues |
Q92811904 | Aquaglyceroporins Are Differentially Expressed in Beige and White Adipocytes |
Q90598383 | Arsenite exposure suppresses adipogenesis, mitochondrial biogenesis and thermogenesis via autophagy inhibition in brown adipose tissue |
Q39182807 | BROWN AND BEIGE ADIPOSE TISSUES: PHENOTYPE AND METABOLIC POTENTIAL IN MICE AND MEN. |
Q47689981 | Brown adipocytes postnatally arise through both differentiation from progenitors and conversion from white adipocytes in Syrian hamster |
Q42629530 | CIDE Family-Mediated Unique Lipid Droplet Morphology in White Adipose Tissue and Brown Adipose Tissue Determines the Adipocyte Energy Metabolism |
Q39720531 | Characterization of Eicosanoids Produced by Adipocyte Lipolysis: IMPLICATION OF CYCLOOXYGENASE-2 IN ADIPOSE INFLAMMATION |
Q89736197 | Chronic Adipose Tissue Inflammation Linking Obesity to Insulin Resistance and Type 2 Diabetes |
Q64119240 | Connecting Metainflammation and Neuroinflammation Through the PTN-MK-RPTPβ/ζ Axis: Relevance in Therapeutic Development |
Q42054611 | Contribution of Maladaptive Adipose Tissue Expansion to Development of Cardiovascular Disease |
Q38769110 | Convertible visceral fat as a therapeutic target to curb obesity. |
Q36196794 | Coupling of lipolysis and de novo lipogenesis in brown, beige, and white adipose tissues during chronic β3-adrenergic receptor activation |
Q58699640 | Curcumin, Cardiometabolic Health and Dementia |
Q52721051 | De novo reconstruction of human adipose transcriptome reveals conserved lncRNAs as regulators of brown adipogenesis. |
Q91971416 | Deciphering the Anti-obesity Benefits of Resveratrol: The "Gut Microbiota-Adipose Tissue" Axis |
Q92662926 | Dietary Silk Peptide Prevents High-Fat Diet-Induced Obesity and Promotes Adipose Browning by Activating AMP-Activated Protein Kinase in Mice |
Q41700242 | Disruption of beta3 adrenergic receptor increases susceptibility to DIO in mouse. |
Q37278838 | Dynamic DNA methylation landscape defines brown and white cell specificity during adipogenesis |
Q89959164 | Early-life programming of adipose tissue |
Q53668858 | Editorial: Fate of fat tissue adipocytes: do they transform into myofibroblasts in scleroderma? |
Q45057994 | Fasting rapidly increases fatty acid oxidation in white adipose tissue of young broiler chickens |
Q91595419 | Fibroblast feeder layer supports adipogenic differentiation of human adipose stromal/progenitor cells |
Q35936105 | Glutathione Decrement Drives Thermogenic Program In Adipose Cells. |
Q37593267 | HO-1 inhibits preadipocyte proliferation and differentiation at the onset of obesity via ROS dependent activation of Akt2. |
Q48042365 | Impact of dietary ω3 polyunsaturated fatty acid supplementation on brown and brite adipocyte function. |
Q34439535 | Inducible brown adipocytes in subcutaneous inguinal white fat: the role of continuous sympathetic stimulation |
Q92823826 | Irisin as a Multifunctional Protein: Implications for Health and Certain Diseases |
Q39270549 | Lsd1 Ablation Triggers Metabolic Reprogramming of Brown Adipose Tissue |
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