Postprandial Oxidative Metabolism of Human Brown Fat Indicates Thermogenesis

Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

Benjamini, Y., & Hochberg, Y. (1995) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1995.tb02031.x · Cited by 109,482

Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2

Love, M. I., Huber, W., & Anders, S. (2014) · Genome Biology · doi:10.1186/s13059-014-0550-8 · Cited by 95,106

New methods for calculating metabolic rate with special reference to protein metabolism

Weir, J. B. D. V. (1949) · The Journal of Physiology · doi:10.1113/jphysiol.1949.sp004363 · Cited by 5,688

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

Functional Brown Adipose Tissue in Healthy Adults

Virtanen, K. A., Lidell, M. E., Orava, J., Heglind, M., Westergren, R., Niemi, T., Taittonen, M., Laine, J., Savisto, N.-J., Enerbäck, S., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0808949 · Cited by 3,058

Graphical Evaluation of Blood-to-Brain Transfer Constants from Multiple-Time Uptake Data. Generalizations

Patlak, C. S., & Blasberg, R. G. (1985) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1985.87 · Cited by 1,673

A role for brown adipose tissue in diet-induced thermogenesis

Rothwell, N. J., & Stock, M. J. (1979) · Nature · doi:10.1038/281031a0 · Cited by 1,606

UCP1 Ablation Induces Obesity and Abolishes Diet-Induced Thermogenesis in Mice Exempt from Thermal Stress by Living at Thermoneutrality

Feldmann, H. M., Golozoubova, V., Cannon, B., & Nedergaard, J. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2008.12.014 · Cited by 1,318

Brown adipose tissue oxidative metabolism contributes to energy expenditure during acute cold exposure in humans

Ouellet, V., Labbé, S. M., Blondin, D. P., Phoenix, S., Guérin, B., Haman, F., Turcotte, É. E., Richard, D., & Carpentier, A. C. (2012) · Journal of Clinical Investigation · doi:10.1172/jci60433 · Cited by 985

Different Metabolic Responses of Human Brown Adipose Tissue to Activation by Cold and Insulin

Orava, J., Nuutila, P., Lidell, M. E., Oikonen, V., Noponen, T., Viljanen, T., Scheinin, M., Taittonen, M. T., Niemi, T. S., Enerbäck, S., et al. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.06.012 · Cited by 745

Remodeling of Adipose Tissues by Fatty Acids: Mechanistic Update on Browning and Thermogenesis by n-3 Polyunsaturated Fatty Acids

Raj, R. R., Lofquist, S., & Lee, M. (2022) · Pharmaceutical Research · doi:10.1007/s11095-022-03377-w · Cited by 16

Environmental toxicants, brown adipose tissue, and potential links to obesity and metabolic disease

Wang, B., & Steinberg, G. R. (2022) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2022.102314 · Cited by 14

The obesity‐linked human lncRNA AATBC stimulates mitochondrial function in adipocytes

Giroud, M., Kotschi, S., Kwon, Y., Thuc, O. L., Hoffmann, A., Gil‐Lozano, M., Karbiener, M., Higareda‐Almaraz, J. C., Khani, S., Tews, D., et al. (2023) · EMBO Reports · doi:10.15252/embr.202357600 · Cited by 16

Association between dietary factors and brown adipose tissue volume/18F-FDG uptake in young adults

Jurado‐Fasoli, L., Merchán-Ramírez, E., Martínez‐Téllez, B., Acosta, F. M., Sánchez‐Delgado, G., Amaro‐Gahete, F. J., Muñoz-Hernández, V., Martinez-Avila, W. D., Ortiz-Alvarez, L., Xu, H., et al. (2020) · Clinical Nutrition · doi:10.1016/j.clnu.2020.09.020 · Cited by 14

Sleep duration and quality are not associated with brown adipose tissue volume or activity—as determined by 18F-FDG uptake, in young, sedentary adults

Acosta, F. M., Sánchez‐Delgado, G., Martínez‐Téllez, B., Migueles, J. H., Amaro‐Gahete, F. J., Rensen, P. C. N., Elvira, J. M. L., Blondin, D. P., & Ruiz, J. R. (2019) · SLEEP · doi:10.1093/sleep/zsz177 · Cited by 15

Effects of Nutrition/Diet on Brown Adipose Tissue in Humans: A Systematic Review and Meta-Analysis

Heenan, K. A., Carrillo, A. E., Fulton, J. L., Ryan, E. J., Edsall, J. R., Rigopoulos, D., Markofski, M. M., Flouris, A. D., & Dinas, P. C. (2020) · Nutrients · doi:10.3390/nu12092752 · Cited by 15

Mechanism of cold exposure delaying wound healing in mice

Li, F., Liu, J.-J., Lei, L.-M., Li, Y.-H., Xu, F., Lin, X., Cui, R., Zheng, M.-H., Guo, B., Shan, S., et al. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-03009-y · Cited by 13

Acute/Chronic Responses of Combined Training on Serum Pro-thermogenic/Anti-inflammatory Inducers and Its Relation With Fed and Fasting State in Overweight Type 2 Diabetic Individuals

Bonfante, I. L. P., Duft, R. G., Mateus, K. C. D. S., Trombeta, J. C. D. S., Finardi, E. A. R., Ramkrapes, A. P. B., Brunelli, D. T., Mori, M. A., Chacon‐Mikahil, M. P. T., Velloso, L. A., et al. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2021.736244 · Cited by 13

Brown Adipose Tissue, Adiposity, and Metabolic Profile in Preschool Children

Tint, M. T., Michael, N., Sadananthan, S. A., Huang, J. Y., Khoo, C. M., Godfrey, K. M., Shek, L. P., Lek, N., Tan, K. H., Yap, F. K. P., et al. (2021) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgab447 · Cited by 12

Myoglobin in Brown Adipose Tissue: A Multifaceted Player in Thermogenesis

Aboouf, M. A., Gorr, T. A., Hamdy, N. Μ., Gassmann, M., & Thiersch, M. (2023) · Cells · doi:10.3390/cells12182240 · Cited by 14

Cold-stimulated brown adipose tissue activation is related to changes in serum metabolites relevant to NAD+ metabolism in humans

U-Din, M., de Mello, V. D., Tuomainen, M. H., Raiko, J. R. H., Niemi, T. S., Fromme, T., Klåvus, A., Gautier, N., Haimilahti, K., Lehtonen, M., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113131 · Cited by 17

Neuropeptide Y – Its role in human performance and extreme environments

Kienast, C., Gunga, H., & Steinach, M. (2019) · REACH · doi:10.1016/j.reach.2019.100032 · Cited by 12

Different Protein Sources Enhance 18FDG-PET/MR Uptake of Brown Adipocytes in Male Subjects

Maliszewska, K., Adamska-Patruno, E., Miniewska, K., Bauer, W., Buczyńska, A., Mojsak, M. N., & Kretowski, A. J. (2022) · Nutrients · doi:10.3390/nu14163411 · Cited by 11

Semaphorin 4B is an ADAM17-cleaved adipokine that inhibits adipocyte differentiation and thermogenesis

Amin, A., Badenes, M., Tüshaus, J., de Carvalho, É., Burbridge, E., Faísca, P., Trávníčková, K., Barros, A., Carobbio, S., Domingos, P. M., et al. (2023) · Molecular Metabolism · doi:10.1016/j.molmet.2023.101731 · Cited by 12

Secretin as a Satiation Whisperer With the Potential to Turn into an Obesity-curbing Knight

Schnabl, K., Li, Y., U-Din, M., & Klingenspor, M. (2021) · Endocrinology · doi:10.1210/endocr/bqab113 · Cited by 11

Brown Adipose Tissue: A Protective Mechanism Against “Preprediabetes”?

Crandall, J. P., Fraum, T. J., & Wahl, R. L. (2022) · Journal of Nuclear Medicine · doi:10.2967/jnumed.121.263357 · Cited by 12

Compensation for cold-induced thermogenesis during weight loss maintenance and regain

Presby, D. M., Jackman, M. R., Rudolph, M. C., Sherk, V. D., Foright, R. M., Houck, J. A., Johnson, G. C., Orlicky, D. J., Melanson, E. L., HIGGINS, J. A., et al. (2019) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00543.2018 · Cited by 11

Oxygenic metabolism in nutritional obesity induced by olive oil. The influence of vitamin C

Drehmer, E., Moreno, M. Á. N., Carrera, S., Villar, V. M., & Moreno, M. L. (2019) · Food & Function · doi:10.1039/c8fo02550a · Cited by 11

Brown fat-associated postprandial thermogenesis in humans: Different effects of isocaloric meals rich in carbohydrate, fat, and protein

Aita, S., Matsushita, M., Yoneshiro, T., Hatano, T., Kameya, T., Ohkubo, I., & Saito, M. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1040444 · Cited by 10

Promoting metabolic inefficiency for metabolic disease

Kazak, L. (2023) · iScience · doi:10.1016/j.isci.2023.107843 · Cited by 10

Associations Between Brain Gray Matter Volumes and Adipose Tissue Metabolism in Healthy Adults

Raiko, J. R. H., Tuulari, J. J., Saari, T., Parkkola, R. K., Savisto, N., Nuutila, P., & Virtanen, K. A. (2021) · Obesity · doi:10.1002/oby.23094 · Cited by 10

Low‐Level Radiofrequency Exposure Induces Vasoconstriction in Rats

Cuc, T., Braun, A., Bach, V., Pelletier, A., & de Sèze, R. (2021) · Bioelectromagnetics · doi:10.1002/bem.22350 · Cited by 10

Measurement of Futile Creatine Cycling Using Respirometry

Rahbani, J. F., Chouchani, E. T., Spiegelman, B. M., & Kazak, L. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2087-8_10 · Cited by 10

Computational modelling of energy balance in individuals with Metabolic Syndrome

Wesseling-Rozendaal, Y. J. W., Wang, Y., Hilbers, P. A. J., & van Riel, N. A. W. (2019) · BMC Systems Biology · doi:10.1186/s12918-019-0705-z · Cited by 10

Association of shivering threshold time with body composition and brown adipose tissue in young adults

Mishre, A. S. D. S., Martínez‐Téllez, B., Acosta, F. M., Sánchez‐Delgado, G., Straat, M. E., WEBB, A. G., Kan, H. E., Rensen, P. C. N., & Ruiz, J. R. (2022) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2022.103277 · Cited by 9

Is stimulation of browning of human adipose tissue a relevant therapeutic target?

Carpentier, A. C., & Blondin, D. P. (2024) · Annales d Endocrinologie · doi:10.1016/j.ando.2024.05.006 · Cited by 8

Novel effects of the gastrointestinal hormone secretin on cardiac metabolism and renal function

Laurila, S., Rebelos, E., Lahesmaa, M., Sun, L., Schnabl, K., Peltomaa, T.-M., Klén, R., U-Din, M., Honka, M., Eskola, O., et al. (2021) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00260.2021 · Cited by 8

Overexpressing the hydroxycarboxylic acid receptor 1 in mouse brown adipose tissue restores glucose tolerance and insulin sensitivity in diet-induced obese mice

Min, H.-Y., Hwang, J., Choi, Y., & Jo, Y. (2022) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00084.2022 · Cited by 7

PGC-1β-expressing POMC neurons mediate the effect of leptin on thermoregulation in the mouse

Delezie, J., Gill, J. F., Santos, G., Karrer‐Cardel, B., & Handschin, C. (2020) · Scientific Reports · doi:10.1038/s41598-020-73794-7 · Cited by 9

Changes in electrocardiogram parameters during acute nonshivering cold exposure and associations with brown adipose tissue activity, plasma catecholamine levels, and brachial blood pressure in healthy adults

Raiko, J. R. H., Saari, T., Orava, J., Savisto, N., Parkkola, R. K., Haaparanta‐Solin, M., Nuutila, P., & Virtanen, K. A. (2021) · Physiological Reports · doi:10.14814/phy2.14718 · Cited by 8

Regulatory networks determining substrate utilization in brown adipocytes

Onogi, Y., & Ussar, S. (2022) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2022.04.001 · Cited by 8

Adverse cardiac remodeling augments adipose tissue ß-adrenergic signaling and lipolysis counteracting diet-induced obesity

Kolleritsch, S., Pajed, L., Tilp, A., Hois, V., Pototschnig, I., Kien, B., Diwoky, C., Höefler, G., Schoiswohl, G., & Haemmerle, G. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.104788 · Cited by 7

Radiation induced oxidation of [18F]fluorothia fatty acids under cGMP manufacturing conditions

Pandey, M. K., Jacobson, M., Groth, E. K., Tran, N. G., Lowe, V. J., & DeGrado, T. R. (2019) · Nuclear Medicine and Biology · doi:10.1016/j.nucmedbio.2019.11.004 · Cited by 6

Extracts of Dunkelfelder Grape Seeds and Peel Increase the Metabolic Rate and Reduce Fat Deposition in Mice Maintained on a High-Fat Diet

Yang, C., Tian, X., Han, Y., Shi, X., Wang, H., & Hua, L. (2023) · Foods · doi:10.3390/foods12173251 · Cited by 6

MiR-143 Targets SYK to Regulate NEFA Uptake and Contribute to Thermogenesis in Male Mice

Liu, J., Wei, L., Chen, T., Wang, H., Luo, J., Chen, X., Jiang, Q., Xi, Q., Sun, J., Zhang, L., et al. (2023) · Endocrinology · doi:10.1210/endocr/bqad114 · Cited by 6

Human brown adipose tissue function: insights from current in vivo techniques

Kwok, T. C., & Stimson, R. H. (2023) · Journal of Endocrinology · doi:10.1530/joe-23-0017 · Cited by 6

Energy Expenditure and Macronutrient Oxidation in Response to an Individualized Nonshivering Cooling Protocol

Sánchez‐Delgado, G., Alcántara, J. M. A., Acosta, F. M., Martínez‐Téllez, B., Amaro‐Gahete, F. J., Merchán-Ramírez, E., Löf, M., Labayen, I., Ravussin, É., & Ruiz, J. R. (2020) · Obesity · doi:10.1002/oby.22972 · Cited by 5

Human Brown Adipose Tissue—A Decade Later

Lichtenbelt, W. D. V. M. (2021) · Obesity · doi:10.1002/oby.23166 · Cited by 5

The effects of physical activity on rehabilitation for acute hepatitis.

Ishida, A., SUMIYA, N., & Ueno, F. (1996) · PubMed · Cited by 5

Multidisciplinary Therapy to Target Obesity and Its Complications in Adult Population: A Narrative Review

Dâmaso, A. R., Corgosinho, F. C., Masquio, D. C. L., Figueiredo, N., Kattah, F. M., Cercato, C., Tock, L., & Campos, R. M. D. S. (2026) · Obesity Reviews · doi:10.1111/obr.70093 · Cited by 6

Local large arterial perivascular adipose tissue metabolic and anatomical features are associated with hypertensive clinical outcomes: a PET/CT-based study

Long, H.-Y., Chen, G., Liu, J., Cheng, K., Yu, W.-J., & Chen, B.-Q. (2025) · Annals of Medicine · doi:10.1080/07853890.2025.2578724 · Cited by 4

Sex-specific response of the human plasma lipidome to short-term cold exposure

Höring, M., Brunner, S. P., Scheiber, J., Honecker, J., Liebisch, G., Seeliger, C., Schinhammer, L., Claussnitzer, M., Burkhardt, R., Hauner, H., et al. (2024) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2024.159567 · Cited by 4

Thermogenic Capacity of Human Supraclavicular Brown Fat and Cold-Stimulated Brain Glucose Metabolism

U-Din, M., Rebelos, E., Saari, T., Niemi, T. S., Kuellmer, K., Eskola, O., Fromme, T., Rajander, J., Taittonen, M. T., Klingenspor, M., et al. (2023) · Metabolites · doi:10.3390/metabo13030387 · Cited by 4

Beiging Modulates Inflammatory Adipogenesis in Salt-Treated and MEK6–Transfected Adipocytes

Kang, S., & Lee, M. (2021) · Cells · doi:10.3390/cells10051106 · Cited by 4

Multimodal epigenetic and enhancer network remodeling shape the transcriptional landscape of human beige adipocytes

Pickering, S. H., Galigniana, N. M., Abdelhalim, M., Sørensen, A. L., Madsen‐Østerbye, J., Zucknick, M., Collas, P., & Briand, N. (2026) · Communications Biology · doi:10.1038/s42003-025-09469-8 · Cited by 3

Sustained effect of habitual feeding time on daily rhythm of core body temperature in mice

Ando, H., Nagata, N., Hosono, T., Hasan, N., Morishige, J., Daikoku, T., Maida, Y., Ono, M., Fujiwara, T., & Fujiwara, H. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.966788 · Cited by 3

Cold-induction of afadin in brown fat supports its thermogenic capacity

Lundh, M., Altıntaş, A., Tozzi, M., Fabre, O., Ma, T., Shamsi, F., Gerhart‐Hines, Z., Barrès, R., Tseng, Y., & Emanuelli, B. (2021) · Scientific Reports · doi:10.1038/s41598-021-89207-2 · Cited by 3

Commentary: Tracing the fate of metabolic substrates during changes in whole-body energy expenditure in mice

Lyons, S. A., & McClelland, G. B. (2024) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2024.111008 · Cited by 3

Cold Stress Regulates Muscle Development and Promotes Muscle Fiber Transformation by Regulating Mib1/Notch Pathway

Zheng, M., Qi, J., Wang, X., Fu, T., Chang, Z., Zhao, T. M., Sun, Y., Lu, J., Yan, Y., & Wang, H. (2025) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl40141 · Cited by 2

Effects of boysenberry on postprandial energy metabolism in healthy adults: A randomized controlled crossover trial

Furuuchi, R., Kato, S., Maejima, D., Amano, T., Shimizu, I., & Minamino, T. (2025) · PLoS ONE · doi:10.1371/journal.pone.0330683 · Cited by 2

Deciphering the Presence of Active Interscapular Brown Adipose Tissue in Humans

Sanchez‐Gomez, J., Ruiz-Campos, S., Chica‐Pérez, A., Baena‐Raya, A., Acosta, F. M., Wolfrum, C., Rensen, P. C. N., Romacho, T., & Martínez‐Téllez, B. (2026) · Acta Physiologica · doi:10.1111/apha.70190 · Cited by 2

Deep learning enables the quantification of browning capacity of human adipose samples

Wang, Y., Zuo, S., Yang, N., Jian, A., Zheng, W., Hua, Z., & Shen, P. (2024) · Journal Of Big Data · doi:10.1186/s40537-024-00879-9 · Cited by 2

Not feeling the heat? Effects of dietary protein on satiation and satiety in mice are not due to its impact on body temperature

Jazmin Osorio, M., Mitchell, S. E., Hambly, C., Allison, D. B., & Speakman, J. R. (2024) · Appetite · doi:10.1016/j.appet.2024.107421 · Cited by 3

Preliminary study on the effects of boysenberry juice intake on brown adipose tissue activity in healthy adults

Furuuchi, R., Kato, S., Maejima, D., Amano, T., Fujiki, S., Shimizu, I., & Minamino, T. (2024) · Scientific Reports · doi:10.1038/s41598-024-76452-4 · Cited by 2

Brucella secretory protein VceA promotes FOXO1 entry into the nucleus to shift host cell metabolism toward glycolysis

Cao, S., Han, X., Deng, X., Guo, J., Liu, L., Zhang, Y., Suleimenov, M., Zhao, T., Li, W., Ding, J., et al. (2024) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2024203 · Cited by 2

Prolonged or Repeated Cold Exposure: From Basic Physiological Adjustment to Therapeutic Effects

Fontana, J. M., Dugué, B., & Capodaglio, P. (2024) · Springer eBooks · doi:10.1007/978-3-031-18545-8_1 · Cited by 2

Secretin Links Brown Fat to Food Intake: New Perspectives for Targeting Energy Balance in Humans

Klingenspor, M. (2019) · Obesity · doi:10.1002/oby.22477 · Cited by 2

Rearing mice at 22°C programs increased capacity to respond to chronic exposure to cold but not high fat diet

Neri, D., Ramos-Lobo, A. M., Lee, S., Lafond, A., & Zeltser, L. M. (2023) · Molecular Metabolism · doi:10.1016/j.molmet.2023.101740 · Cited by 1

CircRNAs: Orchestrating Obesity, Thermogenesis, and Obesity-Associated Cancer Pathways

Hamdy, N. Μ., Zaki, M. B., El‐Daly, S. M., Ali, M. T., Sanad, E. F., Noureldein, M. H., & Aboouf, M. A. (2024) · Interdisciplinary cancer research · doi:10.1007/16833_2024_468 · Cited by 1

Retinoid X receptor γ interacts with peroxisome proliferator-activated receptor-γ to promote browning during adipose tissue differentiation

Chen, D., Woraikat, S., Guo, X., Yang, F., Tang, C., He, F., & Qian, K. (2025) · Adipocyte · doi:10.1080/21623945.2025.2548780 · Cited by 1

Gabpα‐Pparγ Complex Determines Glycolytic Capacity and Lactic Acid Homeostasis in Brown Fat

Wang, Z., Wang, H., Kang, Q., Pan, R., He, R., Yang, M., Liu, J., Peng, X., Xie, Y., Deng, H., et al. (2025) · Advanced Science · doi:10.1002/advs.202517426 · Cited by 1

Diet and temperature interactively impact brown adipose tissue gene regulation controlled by DNA methylation

Hagemann, T., Hoffmann, A., Rohde‐Zimmermann, K., Broghammer, H., Massier, L., Kovacs, P., Stümvoll, M., Blüher, M., Heiker, J. T., & Weiner, J. (2026) · Molecular Metabolism · doi:10.1016/j.molmet.2025.102315 · Cited by 1

Brown Adipose Tissue Thermogenesis

Blondin, D. P. (2026) · Physiology · doi:10.1152/physiol.00002.2026 · Cited by 1

Brown adipose tissue and beyond: lipolysis and glycerolipid cycling in thermogenesis

Langin, D., & Carpentier, A. C. (2026) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2026.01.009 · Cited by 1

Adipose tissue development and metabolic regulation

Nguyen, H. P., Yi, D., & Sul, H. S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819404-1.00025-7 · Cited by 1

Relationship between Brown Adipose Tissue and Cardiovascular Disease

田, 源. (2024) · Advances in Clinical Medicine · doi:10.12677/acm.2024.14102761 · Cited by 1

The obesity-linked human lncRNA AATBC regulates adipocyte plasticity by stimulating mitochondrial dynamics and respirationPreprint

Giroud, M., Kotschi, S., Kwon, Y., Thuc, O. L., Hoffmann, A., Gil‐Lozano, M., Karbiener, M., Higareda‐Almaraz, J. C., Khani, S., Tews, D., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.09.455681 · Cited by 1

Postprandial metabolism of infant formulas containing different fat sources : digestion, absorption, and metabolic responses

Hageman, J. H. J. (2019) · doi:10.18174/496799

Tissus adipeux brun et beige

Carrière, A., Casteilla, L., & Valet, P. (2021) · Elsevier eBooks · doi:10.1016/b978-2-294-76753-1.00032-1

Brown adipose tissue–associated postprandial thermogenesis in humans: Different effects of isocaloric meals rich in carbohydrate, fat, and proteinPreprint

Aita, S., Matsushita, M., Yoneshiro, T., Hatano, T., Kameya, T., Ohkubo, I., & Saito, M. (2022) · Research Square · doi:10.21203/rs.3.rs-1762974/v1

Semaphorin 4B is an ADAM17-cleaved inhibitor of adipocyte thermogenesisPreprint

Amin, A., Badenes, M., Tüshaus, J., de Carvalho, É., Burbridge, E., Faísca, P., Trávníčková, K., Barros, A., Carobbio, S., Domingos, P. M. D. N., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.11.511765

Respostas do treinamento combinado sobre marcadores inflamatórios, metabólicos, autofágicos e de remodelamento do tecido adiposo em diabéticos tipo 2 com excesso de peso

Bonfante, I. L. P. (2019) · doi:10.47749/t/unicamp.2019.1231335

Metabolites, Bioactive Compounds, and Browning: Unveiling the Therapeutic Potential of Whole-Body Cryostimulation for Metabolic Health

Cancello, R. (2024) · Springer eBooks · doi:10.1007/978-3-031-18545-8_8

Advances in imaging studies to assess thermogenic fat

Chen, B.-Q., & Li, J. (2024) · Chinese Journal of Academic Radiology · doi:10.1007/s42058-024-00167-8

Polycystic ovary syndrome: a multisystemic approach to metabolic dysfunctions – review

Popa, E., Chiş-Şerban, A.-A., Poroch, M., Popa, A.-E., Avram, R.-I., & Coman, A. E. (2024) · Medic ro · doi:10.26416/med.160.4.2024.10047

miR-196a-5p and miR-342-3p mediate skeletal muscle and thermogenic adipose tissue crosstalk through extracellular vesiclesPreprint

Tischer, D., Schranner, D., Kallabis, S., Braunsperger, A., Schönfelder, M., Gnad, T., Jost, P. J., Nesic, S., Renziehausen, F., Fester, L., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.28.656129

Additional file 9 of Deep learning enables the quantification of browning capacity of human adipose samples

Wang, Y., Zuo, S., Yang, N., Jian, A., Zheng, W., Hua, Z., & Shen, P. (2024) · Figshare · doi:10.6084/m9.figshare.26679626

Additional file 3 of Deep learning enables the quantification of browning capacity of human adipose samples

Wang, Y., Zuo, S., Yang, N., Jian, A., Zheng, W., Hua, Z., & Shen, P. (2024) · Figshare · doi:10.6084/m9.figshare.26679608

Additional file 2 of Deep learning enables the quantification of browning capacity of human adipose samples

Wang, Y., Zuo, S., Yang, N., Jian, A., Zheng, W., Hua, Z., & Shen, P. (2024) · Figshare · doi:10.6084/m9.figshare.26679605

Additional file 1 of Deep learning enables the quantification of browning capacity of human adipose samples

Wang, Y., Zuo, S., Yang, N., Jian, A., Zheng, W., Hua, Z., & Shen, P. (2024) · Figshare · doi:10.6084/m9.figshare.26679602

Additional file 5 of Deep learning enables the quantification of browning capacity of human adipose samples

Wang, Y., Zuo, S., Yang, N., Jian, A., Zheng, W., Hua, Z., & Shen, P. (2024) · Figshare · doi:10.6084/m9.figshare.26679614

Additional file 8 of Deep learning enables the quantification of browning capacity of human adipose samples

Wang, Y., Zuo, S., Yang, N., Jian, A., Zheng, W., Hua, Z., & Shen, P. (2024) · Figshare · doi:10.6084/m9.figshare.26679623

Additional file 7 of Deep learning enables the quantification of browning capacity of human adipose samples

Wang, Y., Zuo, S., Yang, N., Jian, A., Zheng, W., Hua, Z., & Shen, P. (2024) · Figshare · doi:10.6084/m9.figshare.26679620

Additional file 4 of Deep learning enables the quantification of browning capacity of human adipose samples

Wang, Y., Zuo, S., Yang, N., Jian, A., Zheng, W., Hua, Z., & Shen, P. (2024) · Figshare · doi:10.6084/m9.figshare.26679611

Additional file 6 of Deep learning enables the quantification of browning capacity of human adipose samples

Wang, Y., Zuo, S., Yang, N., Jian, A., Zheng, W., Hua, Z., & Shen, P. (2024) · Figshare · doi:10.6084/m9.figshare.26679617

Burning fast & slow: a review of the differential metabolic routes of brown adipose tissue activity during cold exposure and their implications for populational variation

Ocobock, C. J., Niclou, A. M., Stenbäck, V., & McElreavy, D. (2025) · Lipids in Health and Disease · doi:10.1186/s12944-025-02838-6

NCOA1 is a gatekeeper of the sexually dimorphic thermogenic activity of white adipose tissue

Tannour‐Louet, M., Pisani, D. F., Bouguerra, H., Zedda, A., Bourcier, M., Lamghari, N., Gautier, N., Chaput, B., Riant, É., Bouloumié, A., et al. (2026) · Nature Communications · doi:10.1038/s41467-025-65229-6

Functional and metabolomic analyses of brown adipose tissue during cold-deacclimation reveal rapid N-acetylated amino acid adaptations

Pileggi, C. A., McIlroy, E., Hamilton, L. E., Kuksal, N., Kennedy, L. S., Vasilyeva, V., Kanaan, M. N., Hankouri, Z. E., Burelle, Y., Čuperlović‐Culf, M., et al. (2026) · iScience · doi:10.1016/j.isci.2026.115146

In vitro derivation of human brown adipose tissue from pluripotent and mesenchymal stem cell sources: A systematic review of genetic and non-genetic differentiation strategies

Dharmendhran, P., Subramanian, K., & Parameswaran, S. (2026) · Differentiation · doi:10.1016/j.diff.2026.100954

Effets d'une exposition répétée aux ondes radiofréquences sur la régulation thermique chez les rongeurs

Mai, T. C. (2020) · doi:10.70675/11bc0dedz4ba0z4f09z8216z37c7ef5e01ae

Early postnatal antibiotic-associated gut microbiota alterations might promote long-term lipid metabolism via brown adipose tissue metabolic programming

Liang, H., Jiang, F., Ren, L., Li, X., Wu, S., Li, J., Li, L., Ze, X., Shen, X., & He, F. (2026) · Gut Microbes · doi:10.1080/19490976.2026.2665885

Adipose Tissue Engineering

Wang, L., Nie, Y., Xu, X., Zhou, Y., Zhang, J., Wang, W., Tang, J., Wang, W., & Ma, N. (2026) · Springer eBooks · doi:10.1007/978-3-032-01711-6_14

Beta2-adrenergic stimulation by fenoterol increases energy expenditure without activating human brown adipose tissue

Füchtbauer, L. M., Senn, J. R., Baumann, C., Isenrich, A., Gaynor, T. L., Schläfli, R., Sharma, A. K., Horváth, C., Maushart, C. I., Ghosh, A., et al. (2026) · Cell Metabolism · doi:10.1016/j.cmet.2026.07.012

Human brown fat metabolism associates with systemic branched-chain amino acids homeostasis

U-Din, M., Acosta, F. M., Saari, T., de Mello, V. D., van der Kolk, B. W., Monfort‐Pires, M., Clemente‐Postigo, M., Niemi, T., Taittonen, M. T., Tuomainen, M. H., et al. (2026) · Molecular Metabolism · doi:10.1016/j.molmet.2026.102434

Increased energy expenditure through intermittent cold exposure does not enhance tirzepatide-induced weight loss in obese mice

Bellucci, A., Alfares, H., Gale, C., Akcan, M., Waters, B., Eisner, K., Baranowski, B. J., Jeromson, S., Babicki-Moore, A., & Wright, D. C. (2026) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00220.2026

Brown adipocyte Acss1 restoration ameliorates redox-metabolic dysfunction and systemic metabolic decline during aging

Luo, Y., Zhang, Y., Song, Y., Li, X., Liang, J., Xing, H., Lai, Y., Chen, Y., Zeng, M., Zhou, C., et al. (2026) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2026.09.016

Meal‐Induced Proton Density Fat Fraction and T2∗ Decrease in Supraclavicular Adipose Tissue

Raspe, J., Du, T., Wu, M., Stelter, J., Klingenspor, M., Junker, D., Skurk, T., & Karampinos, D. C. (2026) · NMR in Biomedicine · doi:10.1002/nbm.70414

Fasting and Postprandial Activity of Brown Adipose Tissue in Healthy Men

Vrieze, A., Schopman, J. E., Admiraal, W. M., Soeters, M. R., Nieuwdorp, M., Verberne, H. J., & Holleman, F. (2012) · Journal of Nuclear Medicine · doi:10.2967/jnumed.111.100701 · Cited by 52

Brown adipose tissue activity after a high-calorie meal in humans

Vosselman, M. J., Brans, B. T., van der Lans, A. A. J. J., Wierts, R., van Baak, M. A., Mottaghy, F. M., Schrauwen, P., & Lichtenbelt, W. D. V. M. (2013) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.113.059022 · Cited by 172

Quantification of brown adipose tissue fatty acid metabolism in lean and obese subjects using 18F-FTHA positron emission tomography

Saari, T. (2018) · UTUPub (University of Turku)

Effect of Prandial Glucose on Brown Fat Thermogenesis in Rats: Possible Implications for Dietary Obesity

Glick, Z., Bray, G. A., & Teague, R. J. (1984) · Journal of Nutrition · doi:10.1093/jn/114.2.286 · Cited by 12

Brown adipose tissue–associated postprandial thermogenesis in humans: Different effects of isocaloric meals rich in carbohydrate, fat, and proteinPreprint

Aita, S., Matsushita, M., Yoneshiro, T., Hatano, T., Kameya, T., Ohkubo, I., & Saito, M. (2022) · Research Square · doi:10.21203/rs.3.rs-1762974/v1