Metabolic and cellular plasticity in white adipose tissue I: effects of β3-adrenergic receptor activation

The Database of Interacting Proteins: 2004 update

Salwinski, L. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh086 · Cited by 2,271

The changing global patterns of female breast cancer incidence and mortality

Bray, F., McCarron, P., & Parkin, D. M. (2004) · Breast Cancer Research · doi:10.1186/bcr932 · Cited by 1,006

Emergence of brown adipocytes in white fat in mice is under genetic control. Effects on body weight and adiposity.

Guerra, C., Koza, R. A., Yamashita, H., Walsh, K., & Kozak, L. P. (1998) · Journal of Clinical Investigation · doi:10.1172/jci3155 · Cited by 635

Multilocular fat cells in WAT of CL-316243-treated rats derive directly from white adipocytes

Himms-Hagen, J., Melnyk, A., Zingaretti, M. C., Ceresi, E., Barbatelli, G., & Cinti, S. (2000) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2000.279.3.c670 · Cited by 593

Free Fatty Acids and Cytokines Induce Pancreatic β-Cell Apoptosis by Different Mechanisms: Role of Nuclear Factor-κB and Endoplasmic Reticulum Stress

Kharroubi, I., Ladrière, L., Cardozo, A. K., Doğusan, Z., Cnop, M., & Eizirik, D. L. (2004) · Endocrinology · doi:10.1210/en.2004-0478 · Cited by 582

The peroxisome proliferator-activated receptor regulates mitochondrial fatty acid oxidative enzyme gene expression.

Gulick, T., Cresci, S., Caira, T., Moore, D. D., & Kelly, D. P. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.23.11012 · Cited by 567

Profiling Gene Expression Using Onto-Express

Khatri, P., Drăghici, S., Ostermeier, G. C., & Krawetz, S. A. (2002) · Genomics · doi:10.1006/geno.2002.6698 · Cited by 459

Regulation of mammary gland branching morphogenesis by the extracellular matrix and its remodeling enzymes

Fata, J. E., Werb, Z., & Bissell, M. J. (2003) · Breast Cancer Research · doi:10.1186/bcr634 · Cited by 406

Transcriptional repression of the GLUT4 and C/EBP genes in 3T3-L1 adipocytes by tumor necrosis factor-alpha.

Stephens, J. M., & Pekala, P. H. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)54714-1 · Cited by 370

Effect of fatty acids on energy coupling processes in mitochondria

Wojtczak, L., & Schönfeld, P. (1993) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(93)90004-y · Cited by 363

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

Cancer Stem Cells: Emergent Nature of Tumor Emergency

Efremov, Y. R., Proskurina, A. S., Potter, E. A., Долгова, Е. В., Efremova, O. V., Taranov, O. S., Ostanin, A., Chernykh, E. R., Kolchanov, N. A., & Bogachev, S. S. (2018) · Frontiers in Genetics · doi:10.3389/fgene.2018.00544 · Cited by 16

Aerobic exercise and lipolysis: A review of the β-adrenergic signaling pathways in adipose tissue

Rodrigues, A. C., Prímola‐Gomes, T. N., Pelúzio, M. D. C. G., Hermsdorff, H. H. M., & Natali, A. J. (2020) · Science & Sports · doi:10.1016/j.scispo.2020.04.006 · Cited by 16

Prolonged treatment with the β3-adrenergic agonist CL 316243 induces adipose tissue remodeling in rat but not in guinea pig: 1) fat store depletion and desensitization of β-adrenergic responses

Ferrand, C., Redonnet, A., Prévot, D., Carpéné, C., & Atgié, C. (2006) · Journal of Physiology and Biochemistry · doi:10.1007/bf03174070 · Cited by 15

Natural Histogel-Based Bio-Scaffolds for Sustaining Angiogenesis in Beige Adipose Tissue

Somma, M. D., Schaafsma, W., Grillo, E., Vliora, M., Dakou, E., Corsini, M., Ravelli, C., Ronca, R., Sakellariou, P., Vanparijs, J., et al. (2019) · Cells · doi:10.3390/cells8111457 · Cited by 15

Metabolic effects of antihypertensive agents: role of sympathoadrenal and renin-angiotensin systems

Ernsberger, P. R., & Koletsky, R. J. (2006) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-006-0080-3 · Cited by 15

Comparison of visceral fat lipolysis adaptation to high-intensity interval training in obesity-prone and obesity-resistant rats

Liu, Y., Li, Y., Cheng, B., Feng, S., Zhu, X., Chen, W., & Zhang, H. (2022) · Diabetology & Metabolic Syndrome · doi:10.1186/s13098-022-00834-9 · Cited by 14

Mechanism of Fatty Acid Metabolism and Regulation by Lactate During Exercise in White Adipose and Skeletal Muscle Tissue: A Review

Huang, S., Shangguan, R., Chen, S., Lai, X., Han, H., & Sun, J. (2025) · Sports Medicine - Open · doi:10.1186/s40798-025-00862-5 · Cited by 14

Thermogenesis and Related Metabolic Targets in Anti-Diabetic Therapy

Arch, J. R. S. (2011) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-17214-4_10 · Cited by 14

Renaissance of brown adipose tissue research: integrating the old and new

Granneman, J. G. (2015) · International Journal of Obesity Supplements · doi:10.1038/ijosup.2015.3 · Cited by 12

The Adipose Organ: Morphological Perspectives of Adipose Tissues

Smorlesi, A., Frontini, A., & Cinti, S. (2014) · Springer eBooks · doi:10.1007/978-3-642-45207-9_8 · Cited by 14

Adipose targets for obesity drug development

Boss, O., & Bergenhem, N. C. H. (2006) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.10.1.119 · Cited by 12

Is the β3-Adrenoceptor a Valid Target for the Treatment of Obesity and/or Type 2 Diabetes?

Dwaib, H. S., & Michel, M. C. (2023) · Biomolecules · doi:10.3390/biom13121714 · Cited by 14

Influence of prolonged fasting on monoamine oxidase and semicarbazide-sensitive amine oxidase activities in rat white adipose tissue

Iffiú-Soltész, Z., Prévot, D., & Carpéné, C. (2009) · Journal of Physiology and Biochemistry · doi:10.1007/bf03165965 · Cited by 12

The Histone Methyltransferase SMYD1 is Induced by Thermogenic Stimuli in Adipose Tissue

Cicatiello, A. G., Nappi, A., Franchini, F., Nettore, I. C., Raia, M., Rocca, C., Angelone, T., Dentice, M., Ungaro, P., & Macchia, P. (2024) · Epigenomics · doi:10.2217/epi-2023-0381 · Cited by 11

Role of uncoupling protein 1 in the anti-obesity effect of β3-adrenergic agonist in the dog

OMACHI, A., Matsushita, Y., Kimura, K., & Saito, M. (2008) · Research in Veterinary Science · doi:10.1016/j.rvsc.2007.11.003 · Cited by 11

Prolonged treatment with the β3-adrenergic agonist CL 316243 induces adipose tissue remodeling in rat but not in guinea pig: 2) modulation of glucose uptake and monoamine oxidase activity

Duffaut, C., Bour, S., Prévot, D., Marti, L., Testar, X., Zorzano, A., & Carpéné, C. (2006) · Journal of Physiology and Biochemistry · doi:10.1007/bf03174071 · Cited by 10

Patch-Clamp Analysis of the Mitochondrial H+ Leak in Brown and Beige Fat

Bertholet, A. M., & Kirichok, Y. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00326 · Cited by 11

Development of an adipocyte differentiation protocol using 3T3-L1 cells for the investigation of the browning process: identification of the PPAR-γ agonist rosiglitazone as a browning reference drug

Flori, L., Galgani, G., Bray, G., Ippolito, C., Segnani, C., Pellegrini, C., Citi, V., Bernardini, N., Martelli, A., & Calderone, V. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1546456 · Cited by 10

Astrocytic circadian clock control of energy expenditure by transcriptional stress responses in the ventromedial hypothalamus

Mendoza-Viveros, L., Marmolejo‐Gutierrez, C., Cid‐Castro, C., Escalante‐Covarrubias, Q., Montellier, E., Carreño‐Vázquez, E., Noriega, L. G., Velázquez‐Villegas, L. A., Tovar, A. R., Sassone‐Corsi, P., et al. (2023) · Glia · doi:10.1002/glia.24360 · Cited by 10

Reversible transdifferentiation in the adipose organ

Cinti, S. (2008) · International Journal of Pediatric Obesity · doi:10.1080/17477160802404665 · Cited by 9

Pathway crosstalk effects: shrinkage and disentanglement using a Bayesian hierarchical model

Tomoiaga, A. S., Westfall, P. H., Donato, M., Drăghici, S., Hassan, S., Romero, R. J., & Tellaroli, P. (2016) · Statistics in Biosciences · doi:10.1007/s12561-016-9160-1 · Cited by 9

Adipose Tissue Inflammation and Insulin Resistance

Francisco, L., Miriam, H., de Oliveira, A. C., & Alonso‐Vale, M. I. C. (2012) · InTech eBooks · doi:10.5772/53974 · Cited by 9

Metabolic Effect of an Oriental Herbal Medicine on Obesity and Its Comorbidities with Transcriptional Responses in Diet-Induced Obese Mice

Choi, J., Kim, Y.-S., Cho, S.-J., Kwon, E., Ryu, R., & Choi, M. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18040747 · Cited by 9

Molecular evolution of thermogenic uncoupling protein 1 and implications for medical intervention of human disease

Gaudry, M. J., Keuper, M., & Jastroch, M. (2019) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2019.06.006 · Cited by 9

Nav1.8-expressing neurons control daily oscillations of food intake, body weight and gut microbiota in mice

Bullich‐Vilarrubias, C., Romaní‐Pérez, M., López‐Almela, I., Rubio, T., García, C. J., Tomás-Barberán, F. A., & Sanz, Y. (2024) · Communications Biology · doi:10.1038/s42003-024-05905-3 · Cited by 8

Quantifying Biochemical Alterations in Brown and Subcutaneous White Adipose Tissues of Mice Using Fourier Transform Infrared Widefield Imaging

Aboualizadeh, E., Carmichael, O. T., He, P., Albarado, D. C., Morrison, C. D., & Hirschmugl, C. J. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00121 · Cited by 8

CL316243 treatment mitigates the inflammation in white adipose tissues of juvenile adipocyte-specific Nfe2l1 knockout mice

Wang, Z., Hou, Y., Ren, S., Liu, Z., Zuo, Z., Huang, S., Wang, W., Wang, H., Chen, Y., Xu, Y., et al. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.01.043 · Cited by 8

CELL BIOLOGY SYMPOSIUM: Imaging the organization and trafficking of lipolytic effectors in adipocytes12

Granneman, J. G., Kimler, V. A., & Moore, H. P. (2010) · Journal of Animal Science · doi:10.2527/jas.2010-3370 · Cited by 9

Adipose Tissue

Eckel, J. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809518-8.00002-7 · Cited by 11

β3-adrenergic receptor methylation mediates fine particulate matter inhalation-impaired white adipose tissue browning

Hu, R., Pan, J., Zhu, J., Li, S., Zhang, G., Wang, P., Zhang, W., Zhang, L., Li, Q., Li, R., et al. (2024) · Nano Today · doi:10.1016/j.nantod.2024.102167 · Cited by 6

Adipose Tissue and Central Nervous System Crosstalk: Roles in Pain and Cognitive Dysfunction

Li, J., Li, Z., Chen, K., Wu, Y., Yang, X., He, Z., & Xiang, H. (2025) · Biomedicines · doi:10.3390/biomedicines14010054 · Cited by 8

Transgenic Adipose-specific Expression of the Nuclear Receptor RORα Drives a Striking Shift in Fat Distribution and Impairs Glycemic Control

Tuong, Z. K., Fitzsimmons, R. L., Wang, S.-C., Oh, T. G., Lau, P., Steyn, F. J., Thomas, G. P., & Muscat, G. E. O. (2016) · EBioMedicine · doi:10.1016/j.ebiom.2016.08.027 · Cited by 6

MLR-1023 Treatment in Mice and Humans Induces a Thermogenic Program, and Menthol Potentiates the Effect

Rebello, C. J., Coulter, A. A., Reaume, A. G., Cong, W.-N., Cusimano, L. A., & Greenway, F. L. (2021) · Pharmaceuticals · doi:10.3390/ph14111196 · Cited by 6

Mercaptoacetate fails to block the feeding-inhibitory effect of the β3-adrenergic receptor agonist CGP 12177A

Brandt, K., Geary, N., Langhans, W., & Leonhardt, M. (2006) · Physiology & Behavior · doi:10.1016/j.physbeh.2006.06.015 · Cited by 6

Protein Kinase SGK2 Is Induced by the β3 Adrenergic Receptor-cAMP-PKA-PGC-1α/NT-PGC-1α Axis but Dispensable for Brown/Beige Adipose Tissue Thermogenesis

Park, C., Moon, J., Park, M., Cheng, H., Lee, J., & Chang, J. S. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.780312 · Cited by 5

Plasticity of the Adipose Organ

Cinti, S. (2010) · Wiley eBooks · doi:10.1002/9783527629527.ch3 · Cited by 4

Mature white adipocyte plasticity during mammary gland remodelling and cancer

Singh, P., & Ali, S. A. (2023) · Cell Insight · doi:10.1016/j.cellin.2023.100123 · Cited by 4

Adipose tissue plasticity mediated by the counterregulatory axis of the renin‐angiotensin system: Role of Mas and MrgD receptors

Proença, A. B., Medeiros, G. R., Reis, G. D. S., Losito, L. D. F., Ferraz, L. M., Bargut, T. C. L., Soares, N. P., Alexandre‐Santos, B., Campagnole‐Santos, M. J., Magliano, D. C., et al. (2024) · Journal of Cellular Physiology · doi:10.1002/jcp.31265 · Cited by 4

The early transition to cold-induced browning in mouse subcutaneous white adipose tissue (scWAT) involves proteins related to nerve remodeling, cytoskeleton, mitochondria, and immune cells

Blaszkiewicz, M., Johnson, C. P., Willows, J. W., Gardner, M. L., Taplin, D. R., Freitas, M. A., & Townsend, K. L. (2024) · Adipocyte · doi:10.1080/21623945.2024.2428938 · Cited by 4

Mitochondrial Actions for Fat Browning and Energy Expenditure in White Adipose Tissue

de Andrade, P. B. M., Lopes, A. B., & Alonso‐Vale, M. I. C. (2016) · Journal of Obesity and Overweight · doi:10.15744/2455-7633.2.201 · Cited by 4

Beta‐adrenergic agonist induces unique transcriptomic signature in inguinal white adipose tissue

Paz, H. A., Pilkington, A., Loy, H. D., Zhong, Y., Shankar, K., & Wankhade, U. D. (2023) · Physiological Reports · doi:10.14814/phy2.15646 · Cited by 4

Transcriptome analysis of norepinephrine-induced lipolysis in differentiated adipocytes of Bama pig

Li, H., Li, H., Zhang, J., Zhang, J., Zhang, G., Tong, X., Zhang, T., Wu, Y., Li, M., & Jin, L. G. (2023) · Gene · doi:10.1016/j.gene.2023.147753 · Cited by 4

Distinctive Roles and Molecular Regulation of CTP:Phosphoethanolamine Cytidylyltransferase Alpha and Gamma Splice Variants

Pavlovic, Z. (2014) · The Atrium (University of Guelph) · Cited by 4

Insulin and adipocyte IRF4 promote fat retention over muscle preservation during intermittent fasting in obesity.

Marko, D. M., Conn, M. O., Cavallari, J. F., Neudorf, H., Steele, A. P., Duggan, B. M., McAlpin, B. T., Barra, N. G., Hawke, T., Little, J., et al. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117023 · Cited by 1

Brown and Beige Fat: Therapeutic Potential in Obesity

Meiliana, A., & Wijaya, A. (2014) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v6i2.32 · Cited by 3

Inducible UCP1 silencing: A lentiviral RNA-interference approach to quantify the contribution of beige fat to energy homeostasis

Khor, N. W. M., Swarbrick, M. M., & Gunton, J. E. (2019) · PLoS ONE · doi:10.1371/journal.pone.0223987 · Cited by 3

TNF / TNFR1 is a Key Regulator of Prolonged Fasting‐Induced Decrease in Adipose Tissue

de Oliveira, A. C. C., Babêtto, A. M., Silva, M. L., Lacerda, L. D. S. B., Rodrigues, T. D. S., Oliveira, M. C., Rouault, C., Gautier, E. L., de Oliveira, A. G., Clément, K., et al. (2026) · The FASEB Journal · doi:10.1096/fj.202501928rr · Cited by 2

Brown Adipose Tissue and Obesity

Jiménez, G., López‐Ruiz, E., Griñán‐Lisón, C., Antich, C., & Marchal, J. A. (2015) · Springer eBooks · doi:10.1007/978-3-319-19821-7_2 · Cited by 2

Childhood obesity treatment and prevention. Psychological perspectives of clinical approaches

Quattropani, M. C. A., & Buccheri, T. (2013) · Mediterranean Journal of Clinical Psychology · doi:10.6092/2282-1619/2013.1.887 · Cited by 2

Calorie restriction-mediated restoration of hypothalamic signal transducer and activator of transcription 3 (STAT3) phosphorylation is not effective for lowering the body weight set point in IRS-2 knockout obese mice

Senda, S., Inoue, A., Mahmood, A., Suzuki, R., Kamei, N., Kubota, N., Watanabe, T., Aoyama, M., Nawaz, A., Ohkuma, Y., et al. (2015) · Diabetology International · doi:10.1007/s13340-015-0205-3 · Cited by 2

Potential novel therapeutic strategies from understanding adipocyte transdifferentiation mechanisms

Sartini, L., & Frontini, A. (2014) · Expert Review of Endocrinology & Metabolism · doi:10.1586/17446651.2015.983474 · Cited by 2

A method for analysis and correction of cross-talk effects in pathway analysis

Donato, M., Drăghici, S., Tomoiaga, A. S., Westfall, P. H., Xu, Z., & Romero, R. J. (2012) · International Joint Conference on Neural Networks (IJCNN) · doi:10.1109/ijcnn.2012.6252654 · Cited by 2

Adipose Tissue and Fat Cell Biology

Kopecký, J. (2014) · Springer eBooks · doi:10.1007/978-3-319-09943-9_13 · Cited by 2

Fueling or Fighting Cancer? The Thermogenic Paradox of Brown Adipose Tissue

Guerrero, J. J. G., Encarnacion, P. C., Wang, C., del Rosario, M. A. S., Notarte, K. I., Zhou, J., Hsieh, Y.-T., Wang, W.-Y., Chang, C.-W., & Li, W.-C. (2026) · Current Obesity Reports · doi:10.1007/s13679-026-00699-3 · Cited by 2

Neural Innervation of Adipose Tissue: Current Understanding and Future Perspective

Wang, C.-N., & Yang, C. (2026) · Neuroendocrinology · doi:10.1159/000551952 · Cited by 1

Local Macrophage Proliferation in Adipose Tissue Is a Characteristic of Obesity-Associated Inflammation: A Dissertation

Amano, S. U. (2013) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/m2bw2z · Cited by 1

Yin and Yang of Pluripotency: Results of Analysis of Genes Overexpressed In Tumor-Initiating Cells of Krebs-2 Ascites Carcinoma

Efremov, Y. R., Proskurina, A. S., Potter, E. A., Долгова, Е. В., Efremova, O. V., Kolchanov, N. A., & Bogachev, S. S. (2019) · Mathematical Biology and Bioinformatics · doi:10.17537/2019.14.160 · Cited by 1

METABOLIC AND ENDOCRINE ADAPTATIONS TO HEAT STRESS IN LACTATING DAIRY COWS

Xie, G. (2015) · Cited by 1

The Adipose Organ

Cinti, S. (2019) · Endocrinology · doi:10.1007/978-3-319-46933-1_5 · Cited by 1

Molecular Mechanisms of Adipocyte Lipolysis

Granneman, J. G., & Moore, H. H. (2010) · Wiley eBooks · doi:10.1002/9783527629527.ch5 · Cited by 1

L’organo endocrino adiposo

Cinti, S. (2006) · L Endocrinologo · doi:10.1007/bf03345942

Adipose Tissue and Skeletal Muscle Plasticity in Obesity and Metabolic Disease

Ukropec, J., & Ukropcov, B. (2012) · InTech eBooks · doi:10.5772/28506

Cellular plasticity in white adipose tissue: in vivo identification of bipotent adipocyte progenitors in adult white adipose tissue

Lee, Y.-H. (2012) · Human Biology

Browning of Adipose Organ

Cinti, S. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1203-2_6

Origin of White and Brown Adipose Cells From Vascular Endothelium: A Dissertation

Tran, K. (2012) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/e746-pp32

The effect of beta-adrenergic and peroxisome proliferator-activated receptor gamma stimulation on target genes related to lipid metabolism in human subcutaneous adipose tissue. Received for publication 20 November 2006 and accepted in revised form 13 February 2007. Clinical Trial Number: NCT00377975

Bogacka, I., Gettys, T. W., de Jonge, L., Nguyen, T., Smith, J. M., Greenway, F. L., Smith, S. R., & Rouge, B. (2007)

CHRONIC ETHANOL FEEDING DISRUPTS BOTH LIPID AND GLUCOSE HOMEOSTASIS IN RAT ADIPOSE TISSUE

Kang, L. (2007) · OhioLink ETD Center (Ohio Library and Information Network)

Mitochondrial function in metabolic health

Stephenson, E. J. (2013) · RMIT Research Repository (RMIT University Library) · doi:10.25439/rmt.27351021

Adipose Drug Targets for Obesity Treatment

Giacobino, J., Lehr, L., & Boss, O. (2007) · CRC Press eBooks · doi:10.1201/9781420005479.pt4

A Role of Visceral Adipose and Gastric Tissue in Inflammatory Conditions Associated With Metabolic Syndrome

Mehta, R. (2013) · doi:10.13021/mars/7304

Effect of acute exercise on whole body fat oxidation: contributions of abdominal subcutaneous adipose tissue

Smith, M. M. W. (2013) · QSpace (Queen's University Library)

Effects of dietary polyphenols on aspects of cell molecular physiology relevant to metabolic health and ageing

Aziz, S. A. (2015)

Novel aspects of metabolic regulation and inflammation in human adipocytes

Pettersson, A. M. L. (2015) · Figshare

The Effects Of Bone Marrow Adipocytes On Metabolic Regulation In Metastatic Prostate Cancer

Diedrich, J. D. (2017) · Human Biology

The Role of Adrenergic Intervention on Thoracic and Abdominal Perivascular Adipose Tissue Expansion in Rats with and without Heart Failure

Rekhtman, D. (2019) · University Libraries (University of Maryland) · doi:10.13016/hqfs-jcru

Role of Epicardial Adipose Tissue in Heart Failure: From Basic to Clinical Perspectives

Zhang, H., Gheblawi, M., Zhong, J., & Oudit, G. Y. (2020) · Springer eBooks · doi:10.1007/978-3-030-47336-5_10

The Nutritional System

Cinti, S. (2021) · Perspectives in nursing management and care for older adults · doi:10.1007/978-3-030-63892-4_17

Cold-Induced Adaptations to the Proteome of Mouse Subcutaneous White Adipose Tissue (scWAT) Reveal Proteins Relevant for Tissue Remodeling and PlasticityPreprint

Johnson, C. P., Taplin, D. R., Gardner, M. L., Freitas, M. A., & Townsend, K. L. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3924636

The Adipose Organ

Cinti, S. (2017) · Endocrinology · doi:10.1007/978-3-319-47685-8_5-1

The Adipose Organ

Vettor, R., & Cinti, S. (2009) · Oxidative stress and disease · doi:10.1201/9781420091311.ch1

Role of Taurine Supplementation in Obesity: Stimulating Fats to Burn in Cellular Power Plants

Heidari, R., & Ommati, M. M. (2023) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815124484123010013

Fatty Acylcarnitine Metabolism in Brown/Beige and White Fats by 13C HRMAS NMR Spectroscopy With Metabolic Interventions

Yaligar, J., Anantharaj, R., Le, G. T. T., Leow, M. K., Eriksson, J. G., Ashokkumar, B., & Velan, S. S. (2025) · NMR in Biomedicine · doi:10.1002/nbm.70040

Insulin Prevents Fat Loss and Promotes Muscle Loss During Intermittent Fasting in ObesityPreprint

Marko, D. M., Conn, M. O., Cavallari, J. F., Neudorf, H., Steele, A. P., Duggan, B. M., McAlpin, B. T., Barra, N., Hawke, T., Little, J. P., et al. (2025) · bioRxiv · doi:10.1101/2025.06.21.660875

Excessive lipolysis and inflammatory response in adipose tissue are associated with elevated serum growth hormone in dairy cows with clinical ketosis

Gao, X., Yu, H., Shi, Z., Song, C., Fang, Z., Gao, W., Lei, L., Song, Y., Li, X., Du, X., et al. (2025) · Journal of Dairy Science · doi:10.3168/jds.2025-27422

Fatty acid fate in determining oxidation and inflammation in adipose tissue

Mottillo, E. P. (2013) · Human Biology

Additional file 1 of Transcriptomic profiling of adipose tissue inflammation, remodeling, and lipid metabolism in periparturient dairy cows (Bos taurus)

Salcedo-Tacuma, D., Parales-Girón, J., Prom, C., Chirivi, M., Laguna, J., Lock, A. L., & Contreras, G. A. (2020) · Figshare · doi:10.6084/m9.figshare.13279521

Dysfunctional white adipose tissue in the progression of endometriosis: The role of the renin-angiotensin system

Medeiros, G. R., Silva-Veiga, F. M., Vieira, A. L. L. D. S., Lisboa, M. J. A., de Souza, R., Prodel, E., Frantz, E. D. C., & Souza‐Mello, V. (2026) · Life Sciences · doi:10.1016/j.lfs.2026.124341

Effects of the periparturient period and parity on local innervation markers in subcutaneous adipose tissue of dairy cows

Sparks, B. B., Lima, A. F. S., Osorio, J. S., & Strieder‐Barboza, C. (2026) · Journal of Dairy Science · doi:10.3168/jds.2025-27515 · Cited by 1

Inflammation du tissu adipeux au cours de l'obésité humaine : implication des lymphocytes Th17

Caër, C. (2016) · theses.fr (ABES) · doi:10.70675/65eca5dczaa63z4e9az82dbzb223bfe8ef82 · Cited by 1

La fraction vasculaire stromale issue du tissu adipeux en urologie : propriétés thérapeutiques et modèle d'évaluation de la vasculocompétence du transplant rénal

Boissier, R. (2019) · theses.fr (ABES) · doi:10.70675/6756b876z32e2z4980zabb7z0026dfb2fc72

Role of adipose tissue macrophages in Beta 3-adrenergic receptor-mediated beige adipogenesis and thermogenesis

Manuel, R. (2024) · theses.fr (ABES) · doi:10.70675/c53ff99dz9779z4859zaddezf6262c18b2b9

ETS-2 deficiency impairs brown adipose tissue function through Prdm16 repression

Chen, H., Zhai, X., Zhang, Y., Chen, K., Fu, L., Hu, D., Zheng, Z., Guan, S., Qu, X., & Ye, M. (2026) · Metabolism · doi:10.1016/j.metabol.2026.156788

Adipocyte lipolysis is a determinant of skeletal muscle size during fasting and feeding

Marko, D. M., Vemula, R. V., Conn, M. O., Robin, N., Schmidt, A., Rebalka, I. A., & Schertzer, J. D. (2026) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00262.2026

Importància de l’estimulació del teixit adipós marró i de la remodelació del teixit adipós blanc en marró com a perspectiva per al tractament de l’obesitat i les seves complicacions

Rigo, C. S. (2014)

Environmental Manipulation and Neuropeptide Effects on Energy Balance and Cancer

Cao, L. (2015) · Energy balance and cancer · doi:10.1007/978-3-319-16733-6_2

Endothelial Driven Inflammation in Metabolic Disease: A Dissertation

Matevossian, A. (2015) · eScholarship@UMassChan · doi:10.13028/m2qs3q

Metabolic changes in adipose tissues in response to β3‐adrenergic receptor activation in mice

Fujimoto, Y., Hashimoto, O., Shindo, D., Sugiyama, M., Tomonaga, S., Murakami, M., Matsui, T., & Funaba, M. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.27443 · Cited by 20

Metabolic and cellular plasticity in white adipose tissue II: role of peroxisome proliferator-activated receptor-α

Li, P., Zhu, Z., Lu, Y., & Granneman, J. G. (2005) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00010.2005 · Cited by 143

Suppression of estrogen receptor beta classical genomic activity enhances systemic and adipose-specific response to chronic beta-3 adrenergic receptor (β3AR) stimulation

Queathem, E. D., Fitzgerald, M., Welly, R. J., Rowles, C. C., Schaller, K., Bukhary, S., Baines, C. P., Rector, R. S., Padilla, J., Manrique‐Acevedo, C., et al. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.920675 · Cited by 5

Apparent histological changes of adipocytes after treatment with CL 316,243, a ß-3-adrenergic receptor agonist

Ghorbani, M., Teimourian, S., Farzad, R., & Asl, N. N. (2015) · Drug Design Development and Therapy · doi:10.2147/dddt.s73891 · Cited by 15

Chronic β3 adrenergic stimulation induced remodeling of white adipose tissue in mice

Lindholm, C. R., Bauwens, J. D., Ertel, R. L., Mulligan, J. D., Schmuck, E. G., & Saupe, K. W. (2010) · The FASEB Journal · doi:10.1096/fasebj.24.1_supplement.502.3