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1. Full Text TNF-α and adipocyte biology
by Cawthorn, William P and Sethi, Jaswinder K
FEBS letters, ISSN 0014-5793, 2008, Volume 582, Issue 1, pp. 117 - 131
Type 2 diabetes | Obesity | Dyslipidemia | Insulin resistance | Lipid metabolism | Antiadipogenesis | Metabolic syndrome | TNF signalling | C/EBPα | extracellular signal-regulated kinase | white adipose tissue | JNK | inhibitor of NFκB | LPL | WAT | IKKβ | IκB kinase beta | AMP-activated protein kinase | hormone sensitive lipase | IκB | sTNF-α | c-jun N-terminal kinase | tumour necrosis factor-alpha | HSL | NFκB | mTNF-α | transmembrane tumour necrosis factor-alpha | T2D | TNFR2 | nuclear factor-kappa B | soluble tumour necrosis factor-alpha | tumour necrosis factor-alpha receptor 1 | PPARγ | TNFR1 | tumour necrosis factor-alpha receptor 2 | CCAAT/enhancer binding protein | ERK1/2 | type 2 diabetes | TNF-α | brown adipose tissue | BAT | lipoprotein lipase | AMPK | peroxisome proliferator-activated receptor gamma | Biochemistry & Molecular Biology | Biophysics | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Animals | Body Temperature Regulation - physiology | Adipocytes - metabolism | Humans | Tumor Necrosis Factor-alpha - physiology | Adipocytes - cytology | Lipid Metabolism | Cell Differentiation - physiology | Index Medicus
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2. Full Text Chronic peroxisome proliferator-activated receptor γ (PPARγ) activation of epididymally derived white adipocyte cultures reveals a population of thermogenically competent, UCP1-containing adipocytes molecularly distinct from classic brown adipocytes
by Petrovic, Natasa and Walden, Tomas B and Shabalina, Irina G and Timmons, James A and Cannon, Barbara and Nedergaard, Jan
The Journal of biological chemistry, ISSN 0021-9258, 03/2010, Volume 285, Issue 10, pp. 7153 - 7164
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Adipocytes, White - cytology | Coculture Techniques | Ion Channels - genetics | Male | Epididymis - cytology | Mitochondrial Proteins - genetics | PPAR gamma - metabolism | Oxygen Consumption - physiology | Thermogenesis - physiology | Adipocytes, White - drug effects | Mitochondrial Proteins - metabolism | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Trans-Activators - genetics | Thiazolidinediones - pharmacology | Cell Differentiation - physiology | PPAR gamma - genetics | Biomarkers - metabolism | Adipocytes, Brown - drug effects | Mice, Inbred C57BL | Cells, Cultured | Gene Expression Regulation | Hypoglycemic Agents - pharmacology | Mice, Knockout | Adipocytes, White - physiology | Voltage-Dependent Anion Channels - genetics | Adipocytes, Brown - physiology | Animals | Ion Channels - metabolism | PPAR gamma - agonists | Rosiglitazone | Trans-Activators - metabolism | Mice | Transcription Factors | Uncoupling Protein 1 | Adipocytes, Brown - cytology | Voltage-Dependent Anion Channels - metabolism | Index Medicus | Adipocyte | Subcellular Organelles | UCP1 | Brown Adipocytes | Microscopic Imaging | PPARγ | Cell Biology | Receptors | Mitochondria | Nuclear | Mouse | Development Differentiation | White Adipocytes
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3. Full Text Pink Adipocytes
by Cinti, Saverio
Trends in endocrinology and metabolism, ISSN 1043-2760, 09/2018, Volume 29, Issue 9, pp. 651 - 666
transdifferentiation | pink | mammary gland | white | brown | adipocytes | Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Index Medicus
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4. Full Text Characterization of the adipocyte cellular lineage in vivo
by Berry, Ryan and Rodeheffer, Matthew S
Nature cell biology, ISSN 1465-7392, 03/2013, Volume 15, Issue 3, pp. 302 - 308
Life Sciences & Biomedicine | Science & Technology | Cell Biology | Adipocytes, White - cytology | Endothelium, Vascular - cytology | Cell Proliferation | Mice, Inbred C57BL | RNA, Messenger - genetics | Male | Mice, Transgenic | Cadherins - physiology | Hematopoietic Stem Cells - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Adipogenesis - physiology | Cell Lineage | Receptor, Platelet-Derived Growth Factor alpha - physiology | Animals | Flow Cytometry | Endothelium, Vascular - metabolism | Hematopoietic Stem Cells - cytology | Antigens, CD - physiology | Cell Differentiation | Mice | Real-Time Polymerase Chain Reaction | Adipocytes, White - metabolism | Physiological aspects | Fat cells | Genetic aspects | Platelet-derived growth factor | Research | Cell differentiation | Index Medicus
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5. Full Text CD206 + M2-like macrophages regulate systemic glucose metabolism by inhibiting proliferation of adipocyte progenitors
by Nawaz, Allah and Aminuddin, Aminuddin and Kado, Tomonobu and Takikawa, Akiko and Yamamoto, Seiji and Tsuneyama, Koichi and Igarashi, Yoshiko and Ikutani, Masashi and Nishida, Yasuhiro and Nagai, Yoshinori and Takatsu, Kiyoshi and Imura, Johji and Sasahara, Masakiyo and Okazaki, Yukiko and Ueki, Kohjiro and Okamura, Tadashi and Tokuyama, Kumpei and Ando, Akira and Matsumoto, Michihiro and Mori, Hisashi and Nakagawa, Takashi and Kobayashi, Norihiko and Saeki, Kumiko and Usui, Isao and Fujisaka, Shiho and Tobe, Kazuyuki
Nature communications, ISSN 2041-1723, 12/2017, Volume 8, Issue 1, pp. 286 - 16
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Mannose-Binding Lectins - metabolism | Cell Proliferation | Adipose Tissue, White - metabolism | Diet, High-Fat - adverse effects | Adipocytes - cytology | Stem Cells - cytology | Lectins, C-Type - genetics | Stem Cells - metabolism | Lectins, C-Type - metabolism | Adipose Tissue, White - cytology | Cell Differentiation | Signal Transduction | Mice, Inbred C57BL | Insulin Resistance | Receptors, Cell Surface - metabolism | Mice, Transgenic | Obesity - metabolism | Macrophages - metabolism | Adipocytes, White - pathology | Animals | Mannose-Binding Lectins - genetics | Adipocytes - metabolism | Glucose - metabolism | Transforming Growth Factor beta - metabolism | Adipocytes, White - metabolism | Receptors, Cell Surface - genetics | Glucose metabolism | Adipose tissue | Adipocytes | Cytokines | Macrophages | Metabolism | Index Medicus
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