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Exercise training enhances white adipose tissue metabolism in rats selectively bred for low- or high-endurance running capacity

Stephenson, E. J., Lessard, S. J., Rivas, D. A., Watt, M. J., Yaspelkis, B. B., Koch, L. G., Britton, S. L., & Hawley, J. A. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00544.2012 · Cited by 41

Oxidative Phosphorylation Flexibility in the Liver of Mice Resistant to High-Fat Diet–Induced Hepatic Steatosis

Poussin, C., Ibberson, M. R., Hall, D., Ding, J., Soto, J. E., Abel, E. D., & Thorens, B. (2011) · Diabetes · doi:10.2337/db11-0338 · Cited by 40

STAT1 Dissociates Adipose Tissue Inflammation From Insulin Sensitivity in Obesity

Admin, A., Cox, A. R., Chernis, N., Bader, D., Saha, P. K., Masschelin, P. M., Felix, J. B., Sharp, R., 连泽勤, Putluri, V., et al. (2020) · Diabetes · doi:10.2337/db20-0384 · Cited by 42

Mitochondrial aconitase controls adipogenesis through mediation of cellular ATP production

Chen, Y., Cai, G. H., Xia, B., Wang, X., Zhang, C. C., Xie, B., Shi, X., Liu, H., Lu, J. F., Zhang, R. X., et al. (2020) · The FASEB Journal · doi:10.1096/fj.201903224rr · Cited by 39

Immune Cells Gate White Adipose Tissue Expansion

Cox, A. R., Chernis, N., Masschelin, P. M., & Hartig, S. M. (2019) · Endocrinology · doi:10.1210/en.2019-00266 · Cited by 39

Physical exercise remodels visceral adipose tissue and mitochondrial lipid metabolism in rats fed a high‐fat diet

Rocha‐Rodrigues, S., Rodríguez, A., Becerril, S., Ramírez, B., Gonçalves, I. O., Beleza, J., Frühbeck, G., Ascensão, A. A. M. R., & Magalhães, J. (2016) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.12706 · Cited by 40

Metabolomics Profiling of Visceral Adipose Tissue: Results From MESA and the NEO Study

Neeland, I. J., Boone, S. C., Mook‐Kanamori, D. O., Ayers, C. R., Smit, R. A. J., Tzoulaki, I., Karaman, İ., Boulangé, C. L., Vaidya, D. M., Punjabi, N. M., et al. (2019) · Journal of the American Heart Association · doi:10.1161/jaha.118.010810 · Cited by 37

Impaired Mitochondrial Fusion and Oxidative Phosphorylation Triggered by High Glucose Is Mediated by Tom22 in Endothelial Cells

Zeng, Y., Pan, Q., Wang, X., Li, D., Lin, Y., Man, F., Xiao, F., & Guo, L. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/4508762 · Cited by 39

Adipose tissue failure and mitochondria as a possible target for improvement by bioactive food components

Keijer, J., & van Schothorst, E. M. (2008) · Current Opinion in Lipidology · doi:10.1097/mol.0b013e3282f39f95 · Cited by 36

BNIP3 is essential for mitochondrial bioenergetics during adipocyte remodelling in mice

Choi, J. W., Jo, A., Kim, M., Park, H. S., Chung, S. S., Kang, S., & Park, K. S. (2015) · Diabetologia · doi:10.1007/s00125-015-3836-9 · Cited by 36

Global transcriptome profiling identifies KLF15 and SLC25A10 as modifiers of adipocytes insulin sensitivity in obese women

Kulyté, A., Ehrlund, A., Arner, P., & Dahlman, I. A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0178485 · Cited by 34

Impaired mitochondrial oxidative phosphorylation capacity in epicardial adipose tissue is associated with decreased concentration of adiponectin and severity of coronary atherosclerosis

Nakajima, T., Yokota, T., Shingu, Y., Yamada, A., Iba, Y., Ujihira, K., Wakasa, S., Ōoka, T., Takada, S., Shirakawa, R., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-40419-7 · Cited by 37

Gene expression profile of subcutaneous adipose tissue in BMI-discordant monozygotic twin pairs unravels molecular and clinical changes associated with sub-types of obesity

Muniandy, M., Heinonen, S., Yki‐Järvinen, H., Hakkarainen, A., Lundbom, J., Lundbom, N. M. I., Kaprio, J. A., Rissanen, A., Ollikainen, M., & Pietiläinen, K. H. (2017) · International Journal of Obesity · doi:10.1038/ijo.2017.95 · Cited by 35

The metabolic response to a high-fat diet reveals obesity-prone and -resistant phenotypes in mice with distinct mRNA-seq transcriptome profiles

Choi, J. Y., McGregor, R. A., Kwon, E.-Y., Kim, Y. J., Han, Y., Park, J. H. Y., Lee, K. W., Kim, S.-J., Kim, J., Yun, J. W., et al. (2016) · International Journal of Obesity · doi:10.1038/ijo.2016.70 · Cited by 33

Roux-en-Y Gastric Bypass Acutely Decreases Protein Carbonylation and Increases Expression of Mitochondrial Biogenesis Genes in Subcutaneous Adipose Tissue

Jahansouz, C., Serrot, F. J., Frohnert, B. I., Foncea, R. E., Dorman, R. B., Slusarek, B., Leslie, D. B., Bernlohr, D. A., & Ikramuddin, S. (2015) · Obesity Surgery · doi:10.1007/s11695-015-1708-5 · Cited by 32

High-throughput proteomics uncovers exercise training and type 2 diabetes–induced changes in human white adipose tissue

Larsen, J. K., Kruse, R., Sahebekhtiari, N., Moreno‐Justicia, R., Jorba, G. G., Petersen, M. H., de Almeida, M. E., Ørtenblad, N., Deshmukh, A. S., & Højlund, K. (2023) · Science Advances · doi:10.1126/sciadv.adi7548 · Cited by 35

Assessment of Metabolic Flexibility of Old and Adult Mice Using Three Noninvasive, Indirect Calorimetry-Based Treatments

Duivenvoorde, L. P. M., van Schothorst, E. M., Swarts, H. J. M., & Keijer, J. (2014) · The Journals of Gerontology Series A · doi:10.1093/gerona/glu027 · Cited by 31

AMPK/Mitochondria in Metabolic Diseases

Bullón, P., Marín‐Aguilar, F., & Román-Malo, L. (2016) · Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions · doi:10.1007/978-3-319-43589-3_6 · Cited by 31

Analysis of the Human Proteome in Subcutaneous and Visceral Fat Depots in Diabetic and Non-diabetic Patients with Morbid Obesity

Kojima, L. F. K. (2015) · Journal of Proteomics & Bioinformatics · doi:10.4172/jpb.1000361 · Cited by 30

What distinguishes adipose tissue of severely obese humans who are insulin sensitive and resistant?

Xu, X. J., Pories, W. J., Dohm, L. G., & Ruderman, N. B. (2013) · Current Opinion in Lipidology · doi:10.1097/mol.0b013e32835b465b · Cited by 28

Adipose-Specific Deficiency of Fumarate Hydratase in Mice Protects Against Obesity, Hepatic Steatosis, and Insulin Resistance

Yang, H., Wu, J. W., Wang, S. P., Severi, I., Sartini, L., Frizzell, N., Cinti, S., Yang, G., & Mitchell, G. A. (2016) · Diabetes · doi:10.2337/db16-0136 · Cited by 28

Original Article Downregulation of Electron Transport Chain Genes in Visceral Adipose Tissue in Type 2 Diabetes Independent of Obesity and Possibly Involving Tumor Necrosis Factor-

Dahlman, I. A., Forsgren, M., Nordström, E. A., Kaaman, M., Atters, A., & Arner, P. (2016)

Downregulation of electron transport chain genes in visceral adipose tissue in type 2 diabetes independent of obesity and possibly involving tumor necrosis factor-a

Dahlman, I. A. (n.d.) · UCLA - Biblioteca de Ciencias de la Salud · Cited by 1

Impaired mitochondrial oxidative phosphorylation in multiple insulin-sensitive tissues of humans with type 2 diabetes mellitus.

Wang, M., Xc, W., Zy, Z., Mou, B., & Rm, H. (2010) · PubMed · Cited by 33

A Signature of Exaggerated Adipose Tissue Dysfunction in Type 2 Diabetes Is Linked to Low Plasma Adiponectin and Increased Transcriptional Activation of Proteasomal Degradation in Muscle

Sabaratnam, R., Skov, V., Paulsen, S. K., Petersson, S. J., Kruse, R., Hansen, T. T., Halkier, C., Kristensen, J. M., Vind, B. F., Richelsen, B., et al. (2022) · Cells · doi:10.3390/cells11132005 · Cited by 15

PO9-213 MYELOPEROXIDASE OXIDIZED-LDL AND TNF-ALPHA ACT IN SYNERGY IN THE TRIGGERING OF INFLAMMATORY RESPONSE

Legssyer, I., Boudjeltia, K. Z., Babar, S., Nuyens, V., Antwerpen, P. V., Vanhaeverbeek, M., Ducobu, J., & Brohée, D. (2007) · Atherosclerosis Supplements · doi:10.1016/s1567-5688(07)71223-0 · Cited by 1