Adipose tissue browning and metabolic health

Brown Adipose Tissue: Function and Physiological Significance

CANNON, B., & NEDERGAARD, J. (2004) · Physiological Reviews · doi:10.1152/physrev.00015.2003 · Cited by 6,433

A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis

Boström, P., Wu, J., Jedrychowski, M. P., Korde, A., Ye, L., Lo, J. C., Rasbach, K. A., Boström, E. A., Choi, J. H., Long, J. Z., et al. (2012) · Nature · doi:10.1038/nature10777 · Cited by 4,810

Obesity induces a phenotypic switch in adipose tissue macrophage polarization

Lumeng, C. N., Bodzin, J. L., & Saltiel, A. R. (2007) · Journal of Clinical Investigation · doi:10.1172/jci29881 · Cited by 4,664

Identification and Importance of Brown Adipose Tissue in Adult Humans

Cypess, A. M., Lehman, S., Williams, G., Tal, I., Rodman, D., Goldfine, A. B., Kuo, F. C., Palmer, E. L., Tseng, Y.-H., Doria, A., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0810780 · Cited by 4,399

Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1α

Lagouge, M., Argmann, C., Gerhart-Hines, Z., Meziane, H., Lerin, C., Daussin, F., Messadeq, N., Milne, J., Lambert, P., Elliott, P., et al. (2006) · Cell · doi:10.1016/j.cell.2006.11.013 · Cited by 4,057

Autophagy regulates lipid metabolism

Singh, R., Kaushik, S., Wang, Y., Xiang, Y., Novak, I., Komatsu, M., Tanaka, K., Cuervo, A. M., & Czaja, M. J. (2009) · Nature · doi:10.1038/nature07976 · Cited by 3,975

A Cold-Inducible Coactivator of Nuclear Receptors Linked to Adaptive Thermogenesis

Puigserver, P., Wu, Z., Park, C. W., Graves, R., Wright, M., & Spiegelman, B. M. (1998) · Cell · doi:10.1016/s0092-8674(00)81410-5 · Cited by 3,864

Cold-Activated Brown Adipose Tissue in Healthy Men

van Marken Lichtenbelt, W. D., Vanhommerig, J. W., Smulders, N. M., Drossaerts, J. M. A. F. L., Kemerink, G. J., Bouvy, N. D., Schrauwen, P., & Teule, G. J. J. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0808718 · Cited by 3,452

Beige Adipocytes Are a Distinct Type of Thermogenic Fat Cell in Mouse and Human

Wu, J., Boström, P., Sparks, L. M., Li, Y., Choi, J. H., Giang, A.-H., Khandekar, M. J., Virtanen, K. A., Nuutila, P., Schaart, G., et al. (2012) · Cell · doi:10.1016/j.cell.2012.05.016 · Cited by 3,406

AMPK regulates energy expenditure by modulating NAD+ metabolism and SIRT1 activity

Cantó, C., Gerhart-Hines, Z., Feige, J. N., Lagouge, M., Noriega, L., Milne, J. C., Elliott, P. J., Puigserver, P., & Auwerx, J. (2009) · Nature · doi:10.1038/nature07813 · Cited by 3,300

GLP-1 receptor agonist, liraglutide, protects podocytes from apoptosis in diabetic nephropathy by promoting white fat browning

Wang, J., Zhou, Y., Long, D., Wu, Y., & Liu, F. (2023) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2023.04.012 · Cited by 21

Balancing Act: Exploring the Gut Microbiota-Brown Adipose Tissue Axis in PCOS Pathogenesis and Therapeutic Frontiers

Li, Y., Fang, Y., Wang, H., & Zhang, H. (2024) · Frontiers in Bioscience-Landmark · doi:10.31083/j.fbl2906208 · Cited by 23

Non-Coding RNA Molecules Connect Calorie Restriction and Lifespan

Abraham, K. J., Ostrowski, L., & Mekhail, K. (2016) · Journal of Molecular Biology · doi:10.1016/j.jmb.2016.08.020 · Cited by 21

AT1 receptor antagonist induces thermogenic beige adipocytes in the inguinal white adipose tissue of obese mice

Graus‐Nunes, F., Rachid, T. L., Santos, F. D. O. D. S., Barbosa‐da‐Silva, S., & Souza‐Mello, V. (2016) · Endocrine · doi:10.1007/s12020-016-1213-1 · Cited by 21

Brown adipose tissue lipoprotein and glucose disposal is not determined by thermogenesis in uncoupling protein 1-deficient mice

Fischer, A. W., Behrens, J. R., Sass, F., Schlein, C., Heine, M., Pertzborn, P., Scheja, L., & Heeren, J. (2020) · Journal of Lipid Research · doi:10.1194/jlr.ra119000455 · Cited by 21

MicroRNA-33 Inhibits Adaptive Thermogenesis and Adipose Tissue Beiging

Afonso, M. S., Verma, N., van Solingen, C., Cyr, Y., Sharma, M., Perie, L., Corr, E. M., Schlegel, M., Shanley, L. C., Peled, D., et al. (2021) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/atvbaha.120.315798 · Cited by 21

CXCL5 secreted from macrophages during cold exposure mediates white adipose tissue browning

Lee, D., Kim, D. W., Yoon, S., Nam, A.-R., Lee, K., Nam, K., Cho, S.-M., Yoon, Y.-D., & Cho, J. (2021) · Journal of Lipid Research · doi:10.1016/j.jlr.2021.100117 · Cited by 21

Isolation of Mouse Stromal Vascular Cells for Monolayer Culture

Liu, L., Zheng, L., Donnelly, S. R., Emont, M. P., Wu, J., & Cheng, Z. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6820-6_2 · Cited by 21

Inhibition of class I HDACs imprints adipogenesis toward oxidative and brown-like phenotype

Ferrari, A., Longo, R., Peri, C., Coppi, L., Caruso, D., Mai, A., Mitro, N., Fabiani, E. D., & Crestani, M. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2019.158594 · Cited by 21

CXCL13 promotes thermogenesis in mice via recruitment of M2 macrophage and inhibition of inflammation in brown adipose tissue

Xie, L., Wang, H., Wu, D., Zhang, F., Chen, W., Ye, Y., & Hu, F. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1253766 · Cited by 20

Visceral fat increase and signals of inflammation in adipose tissue after administration of titanium dioxide nanoparticles in mice

Silva, A. H., Locatelli, C., Filho, U. P. R., Gomes, B. F., JÚNIOR, R. M. D. C., de Gois, J. S., Borges, D. L. G., & Creczynski‐Pasa, T. B. (2015) · Toxicology and Industrial Health · doi:10.1177/0748233715613224 · Cited by 20

Melatonin induces fat browning by transdifferentiation of white adipocytes and de novo differentiation of mesenchymal stem cells

Salagre, D., Chayah, M., Molina‐Carballo, A., Oliveras‐López, M., Muñoz‐Hoyos, A., Navarro‐Alarcón, M., Fernández‐Vázquez, G., & Agil, A. (2022) · Food & Function · doi:10.1039/d1fo04360a · Cited by 20

Nucleophosmin3 carried by small extracellular vesicles contribute to white adipose tissue browning

Zhang, Y., Yu, M., Dong, J., Wu, Y., & Tian, W. (2022) · Journal of Nanobiotechnology · doi:10.1186/s12951-022-01381-1 · Cited by 20

Clostridium butyricum Inhibits Fat Deposition via Increasing the Frequency of Adipose Tissue‐Resident Regulatory T Cells

Li, H., Jia, Y., Weng, D., Ju, Z., Zhao, Y., Liu, S., Liu, Y., Song, M., Cui, L., Sun, S., et al. (2022) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202100884 · Cited by 20

Blockage of PPARγ T166 phosphorylation enhances the inducibility of beige adipocytes and improves metabolic dysfunctions

Yang, N., Wang, Y., Tian, Q., Wang, Q., Lu, Y., Sun, L., Wang, S., Bei, Y., Ji, J., Zhou, H., et al. (2022) · Cell Death and Differentiation · doi:10.1038/s41418-022-01077-x · Cited by 25

Role of bile acid receptor FXR in development and function of brown adipose tissue

Yang, J., de Vries, H. D., Mayeuf-Louchart, A., Stroeve, J. H. M., Bloks, V. W., Koehorst, M., Duez, H., Staels, B., Kuipers, F., & van Zutphen, T. (2022) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2022.159257 · Cited by 20

Mitochondria-associated regulation in adipose tissues and potential reagents for obesity intervention

Zheng, Y., Ni, Y., Pang, Y., Gong, Y., Yang, H., Ding, W., & Yang, H. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1132342 · Cited by 20

Specific regulation of thermosensitive lipid droplet fusion by a nuclear hormone receptor pathway

Li, S., Li, Q., Kong, Y., Wu, S., Cui, Q., Zhang, M., & Zhang, S. O. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1704277114 · Cited by 20

The role of adipose TRP channels in the pathogenesis of obesity

Gao, P., Yan, Z., & Zhu, Z. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28106 · Cited by 20

Aquaglyceroporins Are Differentially Expressed in Beige and White Adipocytes

da Silva, I. V., Díaz‐Sáez, F., Zorzano, A., Gumà, A., Camps, M., & Soveral, G. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21020610 · Cited by 20

Contrasting recruitment of skin‐associated adipose depots during cold challenge of mouse and human

Kasza, I., Kühn, J.-P., Völzke, H., Hernando, D., Xu, Y. G., Siebert, J. W., Gibson, A. L. F., Yen, C.-L. E., Nelson, D. W., MacDougald, O. A., et al. (2021) · The Journal of Physiology · doi:10.1113/jp280922 · Cited by 22

Association between Adipose Tissue Interleukin-33 and Immunometabolic Markers in Individuals with Varying Degrees of Glycemia

Hasan, A., Kochumon, S., Al‐Ozairi, E., Tuomilehto, J., & Ahmad, R. (2019) · Disease Markers · doi:10.1155/2019/7901062 · Cited by 21

Atomically precise gold nanoclusters as ROS-scavenging clusterzymes to treat high-fat diet-induced obesity

Ding, J., Zhao, M., Li, Y., Zhang, K., Chen, H., Hu, X., Li, L., Su, Y., Yuan, X. F., & Lin, Z. (2024) · Chemical Engineering Journal · doi:10.1016/j.cej.2024.153726 · Cited by 19

Lesson on obesity and anatomy of adipose tissue: new models of study in the era of clinical and translational research

Luca, T., Pezzino, S., Puleo, S., & Castorina, S. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-024-05547-3 · Cited by 19

Transdermal Delivery of Succinate Accelerates Energy Dissipation of Brown Adipocytes to Reduce Remote Fat Accumulation

Liao, F., Yao, C., Chen, S., Wu, T., & Lin, S. (2022) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.2c00628 · Cited by 19

Dietary Methionine Restriction Promotes Fat Browning and Attenuates Hepatic Lipid Accumulation in High-Choline-Fed Mice Associated with the Improvement of Thyroid Function

Yang, Y., Lu, M., Qian, J., Xu, Y., Li, B., Le, G., & Xie, Y. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.2c05535 · Cited by 20

Redox Biology in Adipose Tissue Physiology and Obesity

Yu, J., Qiu, J., Zhang, Z., Cui, X., Guo, W., Sheng, M., Gao, M., Wang, D., Xu, L., & Ma, X. (2023) · Advanced Biology · doi:10.1002/adbi.202200234 · Cited by 20

Adipocyte-derived extracellular vesicles: bridging the communications between obesity and tumor microenvironment

Zhou, C., Huang, Y., Da, M., Jin, W., & Zhou, F. (2023) · Discover Oncology · doi:10.1007/s12672-023-00704-4 · Cited by 20

A method for the automatic segmentation of brown adipose tissue

Prakash, B., Srour, H., Velan, S. S., & Chuang, K. (2016) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/s10334-015-0517-0 · Cited by 19

White Adipose Tissue Browning in the R6/2 Mouse Model of Huntington’s Disease

McCourt, A. C., Jakobsson, L., Larsson, S., Holm, C., Piel, S., Elmér, E., & Björkqvist, M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0159870 · Cited by 19

Exploring the Crosstalk between Adipose Tissue and the Cardiovascular System

Akoumianakis, I., Akawi, N. A., & Antoniades, C. A. (2017) · Korean Circulation Journal · doi:10.4070/kcj.2017.0041 · Cited by 20

Browning of the subcutaneous adipocytes in diet-induced obese mouse submitted to intermittent fasting

Marinho, T. D. S., Ornellas, F., Águila, M. B., & Mandarim‐de‐Lacerda, C. A. (2020) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2020.110872 · Cited by 19

White Adipose Tissue Expansion in Multiple Symmetric Lipomatosis Is Associated with Upregulation of CK2, AKT and ERK1/2

Sanna, M., Borgo, C., Compagnin, C., Favaretto, F., Vindigni, V., Trento, M., Bettini, S., Comin, A., Belligoli, A., Rugge, M., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21217933 · Cited by 19

Evaluation of Browning Agents on the White Adipogenesis of Bone Marrow Mesenchymal Stromal Cells: A Contribution to Fighting Obesity

Maio, G. D., Alessio, N., Demirsoy, İ. H., Peluso, G., Perrotta, S., Monda, M., & Bernardo, G. D. (2021) · Cells · doi:10.3390/cells10020403 · Cited by 19

Differential effects of Roux-en-Y gastric bypass surgery on brown and beige adipose tissue thermogenesis

Hankir, M. K., Bronisch, F., Hintschich, C. A., Krügel, U., Seyfried, F., & Fenske, W. K. (2015) · Metabolism · doi:10.1016/j.metabol.2015.06.010 · Cited by 21

Dietary control of peripheral adipose storage capacity through membrane lipid remodelling

Tol, M. J., Shimanaka, Y., Bedard, A. H., Sapia, J. L., Cui, L., Colaço-Gaspar, M., Hofer, P., Ferrari, A., Qian, K., Kennelly, J. P., et al. (2025) · Nature Metabolism · doi:10.1038/s42255-025-01320-y · Cited by 21

Erythropoietin reduces fat mass in female mice lacking estrogen receptor alpha

Lee, J., Walter, M. F., Korach, K. S., & Noguchi, C. T. (2020) · Molecular Metabolism · doi:10.1016/j.molmet.2020.101142 · Cited by 18

A PPAR-alpha agonist and DPP-4 inhibitor mitigate adipocyte dysfunction in obese mice

Santana-Oliveira, D. A., Fernandes‐da‐Silva, A., Miranda, C. S., Martins, F. F., Mandarim‐de‐Lacerda, C. A., & Souza‐Mello, V. (2022) · Journal of Molecular Endocrinology · doi:10.1530/jme-21-0084 · Cited by 18

Adipose Tissue Dysfunction: Impact on Metabolic Changes?

Morais, J. B. S., Dias, T. M. D. S., Cardoso, B. E. P., Sousa, M. D. P., de Sousa, T. G. V., de Araújo, D. S. C., & Marreiro, D. D. N. (2022) · Hormone and Metabolic Research · doi:10.1055/a-1922-7052 · Cited by 20

Circular RNA- and microRNA-Mediated Post-Transcriptional Regulation of Preadipocyte Differentiation in Adipogenesis: From Expression Profiling to Signaling Pathway

Huang, C.-J., & Choo, K. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054549 · Cited by 19

Browning of Mesenteric White Adipose Tissue in Crohn’s Disease: A New Pathological Change and Therapeutic Target

Zuo, L., Geng, Z., Song, X., Li, J., Wang, Y., Zhang, X., Ge, S., Wang, L. Y., Liu, G., Zhang, L., et al. (2023) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjad046 · Cited by 18

Lactate shuttling drives the browning of white adipose tissue after burn

Barayan, D., Abdullahi, A., Knuth, C. M., Khalaf, F., Rehou, S., Screaton, R. A., & Jeschke, M. G. (2023) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00084.2023 · Cited by 18

A microneedle patch realizes weight loss through photothermal induction of fat browning

Gao, Z., Liu, Y., Lin, W., Lian, H., & Meng, Z. (2024) · Biomaterials Science · doi:10.1039/d3bm01767b · Cited by 18

An Emerging Role of Natriuretic Peptides

Palmer, B. F., & Clegg, D. J. (2015) · Mayo Clinic Proceedings · doi:10.1016/j.mayocp.2015.08.006 · Cited by 19

Loss of miR-146b-3p Inhibits Perivascular Adipocyte Browning with Cold Exposure During Aging

Pan, X., Cao, J., Cai, F., Ruan, C., Wu, F., & Gao, P. (2018) · Cardiovascular Drugs and Therapy · doi:10.1007/s10557-018-6814-x · Cited by 18

LIGHT/TNFSF14 signaling attenuates beige fat biogenesis

Kou, Y., Liu, Q., Liu, W., Sun, H., Liang, M., Kong, F., Zhang, B., Wei, Y., Liu, Z., & Wang, Y. (2018) · The FASEB Journal · doi:10.1096/fj.201800792r · Cited by 18

The Transcription Factor ATF7 Controls Adipocyte Differentiation and Thermogenic Gene Programming

Liu, Y., Maekawa, T., Yoshida, K., Muratani, M., Chatton, B., & Ishii, S. (2019) · iScience · doi:10.1016/j.isci.2019.02.013 · Cited by 17

Effects of Pharmacological Thermogenic Adipocyte Activation on Metabolism and Atherosclerotic Plaque Regression

Worthmann, A., Schlein, C., Berbée, J. F. P., Rensen, P. C. N., Heeren, J., & Bartelt, A. (2019) · Nutrients · doi:10.3390/nu11020463 · Cited by 18

Preadipocyte factor 1 regulates adipose tissue browning via TNF-α-converting enzyme-mediated cleavage

Rhee, M., Kim, J.-W., Lee, M.-W., Yoon, K.-H., & Lee, S. (2019) · Metabolism · doi:10.1016/j.metabol.2019.153977 · Cited by 18

Chronic arsenic exposure impairs adaptive thermogenesis in male C57BL/6J mice

Castriota, F., Zushin, P. H., Sanchez, S. S., Phillips, R. V., Hubbard, A., Stahl, A., Smith, M. T., Wang, J.-C., & Merrill, M. A. L. (2020) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00282.2019 · Cited by 18

Effects of BMP7 produced by group 2 innate lymphoid cells on adipogenesis

Miyajima, Y., Ealey, K. N., Motomura, Y., Mochizuki, M., Takeno, N., Yanagita, M., Economides, A. N., Nakayama, M., Koseki, H., & Moro, K. (2020) · International Immunology · doi:10.1093/intimm/dxaa013 · Cited by 19

Grape pomace reduces the severity of non-alcoholic hepatic steatosis and the development of steatohepatitis by improving insulin sensitivity and reducing ectopic fat deposition in mice

Daniel, T., Ben‐Shachar, M., Drori, E., Hamad, S., Permyakova, A., Ben-Cnaan, E., Tam, J., Kerem, Z., & Rosenzweig, T. (2021) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2021.108867 · Cited by 18

LETMD1 is required for mitochondrial structure and thermogenic function of brown adipocytes

Snyder, M. M., Yue, F., Zhang, L., Shang, R., Qiu, J., Chen, J., Kim, K. H., Peng, Y., Oprescu, S. N., Donkin, S. S., et al. (2021) · The FASEB Journal · doi:10.1096/fj.202100597r · Cited by 18

Juvenile dermato/polymyositis: a retrospective analysis of 33 cases with special focus on initial CPK levels.

van Rossum, M. A. J., Hiemstra, I., Prieur, A., Rijkers, G. T., & Kuis, W. (1994) · PubMed · Cited by 18

Brown Algae Ecklonia cava Extract Modulates Adipogenesis and Browning in 3T3-L1 Preadipocytes through HO-1/Nrf2 Signaling

Suryaningtyas, I. T., Lee, D.-S., & Je, J. (2024) · Marine Drugs · doi:10.3390/md22080330 · Cited by 17

Browning of Pig White Preadipocytes by Co-Overexpressing Pig PGC-1α and Mice UCP1

Hou, L., Xie, M.-Y., Cao, L., Shi, J., Xu, G., Hu, C. Y., & Wang, C. (2018) · Cellular Physiology and Biochemistry · doi:10.1159/000491885 · Cited by 17

Co-Evolution of Breast Milk Lipid Signaling and Thermogenic Adipose Tissue

Rőszer, T. (2021) · Biomolecules · doi:10.3390/biom11111705 · Cited by 17

Linker histone variant H1.2 is a brake on white adipose tissue browning

Yuan, Y.-M., Fan, Y., Zhou, Y.-H., Qiu, R., Kang, W., Liu, Y., Chen, Y., Wang, C.-Y., Shi, J.-J., Liu, C., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-39713-w · Cited by 14

Roles of citrus fruits on energy expenditure, body weight management, and metabolic biomarkers: a comprehensive review

ASLAN, M. N., Sukan-Karaçağıl, B., & Tek, N. A. (2023) · Nutrition Reviews · doi:10.1093/nutrit/nuad116 · Cited by 22

Adipose Tissue-Derived Extracellular Vesicles: A Promising Biomarker and Therapeutic Strategy for Metabolic Disorders

Liu, W., Liu, T., Zhao, Q., Ma, J., Jiang, J., & Shi, H. (2023) · Stem Cells International · doi:10.1155/2023/9517826 · Cited by 21

Exercise differentially affects metabolic functions and white adipose tissue in female letrozole- and dihydrotestosterone-induced mouse models of polycystic ovary syndrome

Marcondes, R. R., Maliqueo, M. A., Fornes, R., Benrick, A., Hu, M., Ivarsson, N., Carlström, M., Cushman, S. W., Stenkula, K. G., Maciel, G. A. R., et al. (2017) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2017.03.025 · Cited by 16

Leptin deficiency reverses high metabolic state and weight loss without affecting central pathology in the R6/2 mouse model of Huntington's disease

Sjögren, M., Soylu-Kucharz, R., Dandunna, U., Stan, T. L., Cavalera, M., Sandelius, Å., Zetterberg, H., & Björkqvist, M. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.104560 · Cited by 17

Browning capabilities of human primary adipose-derived stromal cells compared to SGBS cells

Halbgebauer, D., Dahlhaus, M., Wabitsch, M., Fischer‐Posovszky, P., & Tews, D. (2020) · Scientific Reports · doi:10.1038/s41598-020-64369-7 · Cited by 17

HAND2 is a novel obesity-linked adipogenic transcription factor regulated by glucocorticoid signalling

Giroud, M., Tsokanos, F., Caratti, G., Kotschi, S., Khani, S., Jouffe, C., Vogl, E. S., Irmler, M., Glantschnig, C., Gil‐Lozano, M., et al. (2021) · Diabetologia · doi:10.1007/s00125-021-05470-y · Cited by 16

Transcriptional Landscaping Identifies a Beige Adipocyte Depot in the Newborn Mouse

Hoang, A. C., Yu, H., & Rőszer, T. (2021) · Cells · doi:10.3390/cells10092368 · Cited by 20

Gene expression in WAT from healthy humans and monkeys correlates with FGF 21‐induced browning of WAT in mice

Schlessinger, K., Li, W., Tan, Y., Liu, F., Souza, S. C., Tozzo, E., Liu, K., Thompson, J. R., Wang, L., & Muise, E. S. (2015) · Obesity · doi:10.1002/oby.21153 · Cited by 17

Implications of thermogenic adipose tissues for metabolic health

Schlein, C., & Heeren, J. (2016) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2016.08.002 · Cited by 18

Is Neuronal Histamine Signaling Involved in Cancer Cachexia? Implications and Perspectives

Zwickl, H., Zwickl-Traxler, E., & Pecherstorfer, M. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.01409 · Cited by 18

What induces watts in WAT?

Forest, C. D., Joffin, N., Jaubert, A., & Noirez, P. (2016) · Adipocyte · doi:10.1080/21623945.2016.1187345 · Cited by 16

Lancing Drug Reservoirs into Subcutaneous Fat to Combat Obesity and Associated Metabolic Diseases

Than, A., Duong, P. K., Zan, P., Liu, J., Leow, M. K., & Chen, P. (2020) · Small · doi:10.1002/smll.202002872 · Cited by 16

Excessive fat expenditure in cachexia is associated with dysregulated circadian rhythm: a review

Ma, D., Li, X., Wang, Y., Cai, L., & Wang, Y. (2021) · Nutrition & Metabolism · doi:10.1186/s12986-021-00616-6 · Cited by 15

Exercise Improves Redox Homeostasis and Mitochondrial Function in White Adipose Tissue

Matta, L., de Faria, C. C., de Oliveira, D. F., Andrade, I. S., Lima-Junior, N. C., Gregório, B. M., Takiya, C. M., Ferreira, A. C. F., Nascimento, J. H. M., de Carvalho, D. P., et al. (2022) · Antioxidants · doi:10.3390/antiox11091689 · Cited by 18

NRF2 is essential for adaptative browning of white adipocytes

Bauzá-Thorbrügge, M., Peris, E., Zamani, S., Micallef, P., Paul, A., Bartesaghi, S., Benrick, A., & Asterholm, I. W. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102951 · Cited by 20

Transgenic Mice Overexpressing SREBP-1a in Male ob/ob Mice Exhibit Lipodystrophy and Exacerbate Insulin Resistance

Ohno, H., Matsuzaka, T., Tang, N., Sharma, R., Motomura, K., Shimura, T., Satoh, A., Han, S., Takeuchi, Y., Aita, Y., et al. (2018) · Endocrinology · doi:10.1210/en.2017-03179 · Cited by 16

Enoyl coenzyme A hydratase 1 combats obesity and related metabolic disorders by promoting adipose tissue browning

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ESRRG and PERM1 Govern Mitochondrial Conversion in Brite/Beige Adipocyte Formation

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