Differential expression of peroxisome proliferator-activated receptors (PPARs): tissue distribution of PPAR-alpha, -beta, and -gamma in the adult rat

Hepatic peroxisome proliferator-activated receptor α may have an important role in the toxic effects of di(2-ethylhexyl)phthalate on offspring of mice

Hayashi, Y., Ito, Y., Yamagishi, N., Yanagiba, Y., Tamada, H., Wang, D., Ramdhan, D. H., Naito, H., Harada, Y., Kamijima, M., et al. (2011) · Toxicology · doi:10.1016/j.tox.2011.02.007 · Cited by 46

Expression of peroxisome proliferator-activated receptors in the liver of gray mullet (Mugil cephalus)

Ibabe, A., Grabenbauer, M., Baumgart‐Vogt, E., Völkl, A., Fahimi, H. D., & Cajaraville, M. P. (2004) · Acta Histochemica · doi:10.1016/j.acthis.2003.09.002 · Cited by 46

Peroxisome proliferator-activated receptor-? as a target for wound healing drugs

Tan, N. S., Michalik, L., Desvergne, B., & Wahli, W. (2004) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.8.1.39 · Cited by 46

Renoprotective effect of a novel selective PPARα modulator K-877 in db/db mice: A role of diacylglycerol-protein kinase C-NAD(P)H oxidase pathway

Maki, T., Maeda, Y., Sonoda, N., Makimura, H., Kimura, S., Maeno, S., Takayanagi, R., & Inoguchi, T. (2017) · Metabolism · doi:10.1016/j.metabol.2017.02.013 · Cited by 44

Obesity-Mediated Immune Modulation: One Step Forward, (Th)2 Steps Back

Schmidt, V., Hogan, A. E., Fallon, P. G., & Schwartz, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.932893 · Cited by 51

Peroxisome Proliferator-Activated Receptor γ Ligands Enhance Human B Cell Antibody Production and Differentiation

García-Bates, T. M., Baglole, C. J., Bernard, M. P., Murant, T. I., Simpson‐Haidaris, P. J., & Phipps, R. P. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900324 · Cited by 45

Modulation of Peroxisome Proliferator-Activated Receptor-α Activity by Bile Acids Causes Circadian Changes in the Intestinal Expression of Octn1/Slc22a4 in Mice

Wada, E., Koyanagi, S., Kusunose, N., Akamine, T., Masui, H., Hashimoto, H., Matsunaga, N., & Ohdo, S. (2014) · Molecular Pharmacology · doi:10.1124/mol.114.094979 · Cited by 45

Alzheimer’s Disease, a Lipid Story: Involvement of Peroxisome Proliferator-Activated Receptor α

Sáez-Orellana, F., Octave, J., & Pierrot, N. (2020) · Cells · doi:10.3390/cells9051215 · Cited by 47

Gene-Gene, Gene-Environment & Multiple Interactions in Colorectal Cancer

Ahmed, F. (2006) · Journal of Environmental Science and Health Part C · doi:10.1080/10590500600614295 · Cited by 45

Protective effect of bezafibrate on streptozotocin-induced oxidative stress and toxicity in rats

Anwer, T., Sharma, M., Pillai, K. K., Haque, S. E., Alam, M. M., & Zaman, M. S. (2006) · Toxicology · doi:10.1016/j.tox.2006.10.016 · Cited by 45

PPARδ expression is influenced by muscle activity and induces slow muscle properties in adult rat muscles after somatic gene transfer

Lunde, I. G., Ekmark, M., Rana, Z. A., Buonanno, A., & Gundersen, K. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.133025 · Cited by 48

Hyperammonemia: regulation of argininosuccinate synthetase and argininosuccinate lyase genes in aggregating cell cultures of fetal rat brain

Braissant, O., Honegger, P., Loup, M., Iwase, K., Takiguchi, M., & Bachmann, C. (1999) · Neuroscience Letters · doi:10.1016/s0304-3940(99)00274-8 · Cited by 45

Expression of Genes Associated with Bone Resorption is Increased and Bone Formation is Decreased in Mice Fed a High‐Fat Diet

Xiao, Y., Cui, J., Li, Y., Shi, Y., & Le, G. (2010) · Lipids · doi:10.1007/s11745-010-3397-0 · Cited by 44

PPAR Activation Induces M1 Macrophage Polarization via cPLA2-COX-2 Inhibition, Activating ROS Production againstLeishmania mexicana

Díaz‐Gandarilla, J. A., Osorio‐Trujillo, C., Hernández‐Ramírez, V. I., & Talamás‐Rohana, P. (2013) · BioMed Research International · doi:10.1155/2013/215283 · Cited by 44

Molecular cloning, characterization and expression analysis of PPAR gamma in the orange-spotted grouper (Epinephelus coioides) after the Vibrio alginolyticus challenge

Luo, S., Huang, Y., Xie, F., Huang, X., Liu, Y., Wang, W.-N., & Qin, Q. (2015) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2015.01.003 · Cited by 44

The intestinal bioavailability of vaccenic acid and activation of peroxisome proliferator‐activated receptor‐α and ‐γ in a rodent model of dyslipidemia and the metabolic syndrome

Wang, Y., Jacome‐Sosa, M. M., Ruth, M. R., Lu, Y., Shen, J., Reaney, M. J. T., Scott, S. L., Dugan, M. E. R., Anderson, H. D., Field, C. J., et al. (2012) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201100517 · Cited by 44

Mat1 Inhibits Peroxisome Proliferator-Activated Receptor γ-Mediated Adipocyte Differentiation

Helenius, K., Ying, Y., Alasaari, J., & Mäkelä, T. P. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.00347-08 · Cited by 47

Sports genetics: the PPARA gene and athletes' high ability in endurance sports. A systematic review and meta-analysis.

López‐León, S., Tuvblad, C., & Forero, D. A. (2016) · Europe PMC (PubMed Central) · doi:10.5604/20831862.1180170 · Cited by 44

PPARγ maintains the metabolic heterogeneity and homeostasis of renal tubules

Lyu, Z., Mao, Z., Li, Q., Xia, Y., Liu, Y., He, Q., Wang, Y., Zhao, H., Lu, Z., & Zhou, Q. (2018) · EBioMedicine · doi:10.1016/j.ebiom.2018.10.072 · Cited by 44

Targeting PPARα for the Treatment and Understanding of Cardiovascular Diseases

Li, S., Yang, B., Du, Y., Lin, Y., Liu, J., Huang, S., Zhang, A.-H., Jia, Z., & Zhang, Y. (2018) · Cellular Physiology and Biochemistry · doi:10.1159/000495969 · Cited by 48

Peroxisome Proliferator-Activated Receptor α Activation during Pregnancy Severely Impairs Mammary Lobuloalveolar Development in Mice

Yang, Q., Kurotani, R., Yamada, A., Kimura, S., & Gonzalez, F. J. (2006) · Endocrinology · doi:10.1210/en.2006-0437 · Cited by 44

PPARγ2Pro12Ala Polymorphism and Human Health

He, W. (2009) · PPAR Research · doi:10.1155/2009/849538 · Cited by 46

Differential expression of glucagon and glucagon-like peptide 1 receptors in mouse pancreatic alpha and beta cells in two models of alpha cell hyperplasia

Kedees, M. H., Grigoryan, M., Guz, Y., & Teitelman, G. (2009) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2009.07.024 · Cited by 44

Emerging role of PPAR ligands in the management of diabetic nephropathy

Balakumar, P., Arora, M. K., & Singh, M. (2009) · Pharmacological Research · doi:10.1016/j.phrs.2009.01.010 · Cited by 46

Regulation of triacylglycerol hydrolase expression by dietary fatty acids and peroxisomal proliferator-activated receptors

Dolinsky, V. W., Gilham, D., Hatch, G. M., Agellon, L. B., Lehner, R. S., & Vance, D. E. (2003) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2003.09.007 · Cited by 44

Environmental and Endogenous Peroxisome Proliferator-Activated Receptor γ Agonists Induce Bone Marrow B Cell Growth Arrest and Apoptosis: Interactions between Mono(2-ethylhexyl)phthalate, 9-cis-Retinoic Acid, and 15-Deoxy-Δ12,14-prostaglandin J2

Schlezinger, J. J., Howard, G. J., Hurst, C. H., Emberley, J. K., Waxman, D. J., Webster, T. F., & Sherr, D. H. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.5.3165 · Cited by 44

Effects of the PPAR-β agonist GW501516 in an in vitro model of brain inflammation and antibody-induced demyelination

Defaux, A., Zurich, M., Braissant, O., Honegger, P., & Monnet‐Tschudi, F. (2009) · Journal of Neuroinflammation · doi:10.1186/1742-2094-6-15 · Cited by 44

Troglitazone Inhibits the Progression of Chronic Pancreatitis and the Profibrogenic Activity of Pancreatic Stellate Cells via a PPARγ-Independent Mechanism

Shimizu, K., Shiratori, K., Kobayashi, M., & Kawamata, H. (2004) · Pancreas · doi:10.1097/00006676-200407000-00058 · Cited by 45

Contamination and Effects of Perfluorochemicals in Baikal Seal (Pusa sibirica). 2. Molecular Characterization, Expression Level, and Transcriptional Activation of Peroxisome Proliferator-Activated Receptor α

Ishibashi, H., Iwata, H., Kim, E., Lin, T., Kannan, K., Tanabe, S., Batoev, V. B., & Petrov, E. A. (2008) · Environmental Science & Technology · doi:10.1021/es0720558 · Cited by 44

Peroxisome proliferator‐activated receptors are expressed in mouse bone marrow‐derived mast cells

Sugiyama, H., Nonaka, T., Kishimoto, T., Komoriya, K., Tsuji, K., & Nakahata, T. (2000) · FEBS Letters · doi:10.1016/s0014-5793(00)01169-8 · Cited by 45

Evidence for a novel regulatory pathway activated by (carba)prostacyclin in preadipose and adipose cells

Aubert, J., Ailhaud, G. P., & Négrel, R. (1996) · FEBS Letters · doi:10.1016/s0014-5793(96)01152-0 · Cited by 44

Chemical Probes That Differentially Modulate Peroxisome Proliferator-activated Receptor α and BLTR, Nuclear and Cell Surface Receptors for Leukotriene B4

Devchand, P. R., Hihi, A. K., Perroud, M., Schleuning, W.-D. D., Spiegelman, B. M., & Wahli, W. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.33.23341 · Cited by 44

Mechanistic insights into the potential role of dietary polyphenols and their nanoformulation in the management of Alzheimer’s disease

Albadrani, H. M., Chauhan, P., Ashique, S., Babu, M. A., Iqbal, D., Almutary, A. G., Abomughaid, M. M., Kamal, M., Paiva‐Santos, A. C., Alsaweed, M., et al. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116376 · Cited by 46

The human peroxisome in health and disease: The story of an oddity becoming a vital organelle

Vamecq, J., Cherkaoui‐Malki, M., Andreoletti, P., & Latruffe, N. (2013) · Biochimie · doi:10.1016/j.biochi.2013.09.019 · Cited by 46

Peroxisome proliferator‐activated receptor‐γ cofactors in neurodegeneration

Katsouri, L., Blondrath, K., & Sastre, M. (2012) · IUBMB Life · doi:10.1002/iub.1097 · Cited by 46

Pioglitazone, a synthetic ligand for PPARγ, induces apoptosis in RB-deficient human colorectal cancer cells

Lee, C. J., Han, J. S., Seo, C., Park, T. H., Kwon, H.-C., Jeong, J., Kim, I. H., Yun, J., Bae, Y., Kwak, J., et al. (2006) · APOPTOSIS · doi:10.1007/s10495-006-4003-z · Cited by 43

Effects of d-α-tocopherol supplements on lipid metabolism in a high-fat diet-fed animal model

Kim, D. Y., Kim, J., Ham, H. J., & Choue, R. (2013) · Nutrition Research and Practice · doi:10.4162/nrp.2013.7.6.481 · Cited by 43

Colon OCTN2 Gene Expression Is Up-regulated by Peroxisome Proliferator-activated Receptor γ in Humans and Mice and Contributes to Local and Systemic Carnitine Homeostasis

D’Argenio, G., Petillo, O., Margarucci, S., Torpedine, A., Calarco, A., Koverech, A., Boccia, A. S., Paolella, G., & Peluso, G. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.109678 · Cited by 43

Characterization of a cDNA sequence encoding the peroxisome proliferator activated receptor alpha in the chicken

Diot, C., & Douaire, M. (1999) · Poultry Science · doi:10.1093/ps/78.8.1198 · Cited by 43

Effect of reduced maternal protein consumption during pregnancy in the rat on plasma lipid concentrations and expression of peroxisomal proliferator–activated receptors in the liver and adipose tissue of the offspring

Burdge, G. C., Phillips, E. S., Dunn, R. L., Jackson, A. A., & Lillycrop, K. A. (2004) · Nutrition Research · doi:10.1016/j.nutres.2003.12.009 · Cited by 43

Cyclic Stretch Facilitates Myogenesis in C2C12 Myoblasts and Rescues Thiazolidinedione-Inhibited Myotube Formation

Chang, Y., Chen, Y., Huang, C.-W., Fan, S.-C., Huang, B., Chang, W., Tsai, Y.-S., Su, F., & Wu, C. (2016) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2016.00027 · Cited by 43

A PPARγ mutant serves as a dominant negative inhibitor of PPAR signaling and is localized in the nucleus

Berger, J. P., Patel, H. V., Woods, J. W., Hayes, N. S., Parent, S. A., Clemas, J. A., Leibowitz, M. D., Elbrecht, A., Rachubinski, R. A., Capone, J. P., et al. (2000) · Molecular and Cellular Endocrinology · doi:10.1016/s0303-7207(00)00211-2 · Cited by 42

Troglitazone does not protect rat pancreatic β cells against free fatty acid-induced cytotoxicity

Cnop, M., Hannaert, J. C., & PIPELEERS, D. G. (2002) · Biochemical Pharmacology · doi:10.1016/s0006-2952(02)00860-2 · Cited by 43

Effect of the peroxisome proliferator‐activated receptor β activator GW0742 in rat cultured cerebellar granule neurons

Smith, S. A., Monteith, G. R., Robinson, J. A., Venkata, N. G., May, F. J., & Roberts‐Thomson, S. J. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20153 · Cited by 43

Platelets as a Novel Target for PPAR?? Ligands

Ray, D. M., Spinelli, S. L., Brien, J. J. O., Blumberg, N., & Phipps, R. P. (2006) · BioDrugs · doi:10.2165/00063030-200620040-00004 · Cited by 43

Peroxisome-Proliferator Regulates Key Enzymes of the Tryptophan-NAD+ Pathway

Shin, M., Ohnishi, M., Iguchi, S., Sano, K., & Umezawa, C. Y. (1999) · Toxicology and Applied Pharmacology · doi:10.1006/taap.1999.8683 · Cited by 43

Nuclear Orphan Receptors

Willy, P. J., & Mangelsdorf, D. J. (1998) · Elsevier eBooks · doi:10.1016/b978-012312411-1/50011-1 · Cited by 43

Loss of PPARγ expression in mammary secretory epithelial cells creates a pro‐breast tumorigenic environment

Apostoli, A. J., Skelhorne‐Gross, G., Rubino, R. E., Peterson, N. T., Lena, M. A. D., Schneider, M. M., Sengupta, S., & Nicol, C. J. B. (2013) · International Journal of Cancer · doi:10.1002/ijc.28432 · Cited by 42

Improved insulin sensitivity and islet function after PPARδ activation in diabetic db/db mice

Winzell, M. S., Wulff, E. M., Olsen, G. S., Sauerberg, P., Gotfredsen, C. F., & Åhrén, B. (2009) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2009.09.053 · Cited by 42

Tau hyperphosphorylation and increased BACE1 and RAGE levels in the cortex of PPARβ/δ-null mice

Barroso, E., del Valle, J., Porquet, D., Santos, A. M. V., Salvadó, L., Rodríguez‐Rodríguez, R., Gutiérrez, P., Anglada‐Huguet, M., Alberch, J., Camins, A., et al. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2013.03.006 · Cited by 42

Fibrates: Therapeutic potential for diabetic nephropathy?

Kouroumichakis, I., Παπάνας, Ν., Zarogoulidis, P., Liakopoulos, V., Maltezos, E. S., & Mikhailidis, D. P. (2012) · European Journal of Internal Medicine · doi:10.1016/j.ejim.2011.12.007 · Cited by 43

PPARα Agonist Oral Therapy in Diabetic Retinopathy

Tomita, Y., Lee, D., Tsubota, K., & Kurihara, T. (2020) · Biomedicines · doi:10.3390/biomedicines8100433 · Cited by 42

PPARγ stimulation promotes neurite outgrowth in SH-SY5Y human neuroblastoma cells

Miglio, G., Rattazzi, L., Rosa, A. C., & Fantozzi, R. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.03.014 · Cited by 43

Biochemical and Physiological Characteristics of Fat Cell.

Kawada, T., Takahashi, N., & Fushiki, T. (2001) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.47.1 · Cited by 42

Di(2-ethylhexyl) phthalate inhibits B cell proliferation and reduces the abundance of IgM-secreting cells in cultured immune tissues of the rainbow trout

Martins, K. F., Applegate, B., Hagedorn, B., Kennish, J. M., & Zwollo, P. (2015) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2015.02.037 · Cited by 42

Dietary fish oil n-3 polyunsaturated fatty acids and alpha-linolenic acid differently affect brain accretion of docosahexaenoic acid and expression of desaturases and sterol regulatory element-binding protein 1 in mice

Zhu, H., Fan, C., Xu, F., Tian, C., Zhang, F., & Qi, K. (2009) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2009.07.011 · Cited by 41

Involvement of PPARα and PPARγ in apoptosis and proliferation of human hepatocarcinoma HepG2 cells

Maggiora, M., Oraldi, M., Muzio, G., & Canuto, R. A. (2010) · Cell Biochemistry and Function · doi:10.1002/cbf.1691 · Cited by 42

Lactoferrin suppress the adipogenic differentiation of MC3T3-G2/PA6 cells

Yagi, M., Suzuki, N., Takayama, T., Arisue, M., Kodama, T., Yoda, Y., Numasaki, H., Otsuka, K., & Ito, K. (2008) · Journal of Oral Science · doi:10.2334/josnusd.50.419 · Cited by 42

Emerging roles of PPARδ in metabolism

Seedorf, U., & Aberle, J. (2007) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2007.04.017 · Cited by 41

Fatty Acids, Eicosanoids, and Hypolipidemic Agents Regulate Gene Expression Through Direct Binding to Peroxisome Proliferator-Activated Receptors

Wahli, W., Devchand, P. R., Jpenberg, A. I., & Desvergne, B. (1999) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-4861-4_19 · Cited by 44

15‐Deoxy‐Δ12,14‐prostaglandin J2regulates the functional state and the survival of microglial cells through multiple molecular mechanisms

Bernardo, A., Ajmone‐Cat, M. A., Levi, G., & Minghetti, L. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.02045.x · Cited by 45

Thiazolidinediones are associated with a reduced risk of COPD exacerbations

Rinne, S. T., Feemster, L. C., Collins, B. F., Liu, C., Bryson, C. L., O’Riordan, T. G., & Au, D. H. (2015) · International Journal of COPD · doi:10.2147/copd.s82643 · Cited by 41

Mast cell tryptase stimulates myoblast proliferation; a mechanism relying on protease-activated receptor-2 and cyclooxygenase-2

Duchesne, É., Tremblay, M.-H., & Côt́e, C. H. (2011) · BMC Musculoskeletal Disorders · doi:10.1186/1471-2474-12-235 · Cited by 41

Biochemical and histological evaluation of kidney damage after sub-acute exposure to 2,4-dichlorophenoxyacetic herbicide in rats: involvement of oxidative stress

Tayeb, W., Nakbi, A., Trabelsi, M., Miled, A., & Hammami, M. (2012) · Toxicology Mechanisms and Methods · doi:10.3109/15376516.2012.717650 · Cited by 41

Association of Variants in PPARγ2, IGF2BP2, and KCNQ1 with a Susceptibility to Gestational Diabetes Mellitus in a Korean Population

Chon, S. J., Kim, S. Y., Cho, N. R., Min, D. L., Hwang, Y. J., & Mamura, M. (2013) · Yonsei Medical Journal · doi:10.3349/ymj.2013.54.2.352 · Cited by 41

Beneficial effect of dietary Ephedra sinica on obesity and glucose intolerance in high-fat diet-fed mice

Song, M.-K., Um, J., Jang, H.-J., & Lee, B.-C. (2012) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2012.462 · Cited by 40

Osthol regulates hepatic PPARα-mediated lipogenic gene expression in alcoholic fatty liver murine

Sun, F., Xie, M.-L., Xue, J., & Wang, H.-B. (2009) · Phytomedicine · doi:10.1016/j.phymed.2009.10.021 · Cited by 41

PPARγ Pro12Ala and ACE ID polymorphisms are associated with BMI and fat distribution, but not metabolic syndrome

Passaro, A., Nora, E. D., Marcello, C., Vece, F. D., Morieri, M. L., Sanz, J. M., Bosi, C., Fellin, R., & Zuliani, G. (2011) · Cardiovascular Diabetology · doi:10.1186/1475-2840-10-112 · Cited by 41

Muscle unloading-induced metabolic remodeling is associated with acute alterations in PPARδ and UCP-3 expression

Mazzatti, D. J., Smith, M. A., Oita, R. C., Lim, F.-L., White, A., & Reid, M. B. (2008) · Physiological Genomics · doi:10.1152/physiolgenomics.00281.2007 · Cited by 41

Pioglitazone Protected against Cardiac Hypertrophy via Inhibiting AKT/GSK3βand MAPK Signaling Pathways

Wei, W., Ma, Z., Xu, S., Zhang, N., & Tang, Q. (2016) · PPAR Research · doi:10.1155/2016/9174190 · Cited by 41

Idebenone and coenzyme Q10 are novel PPARα/γ ligands, with potential for treatment of fatty liver diseases

Tiefenbach, J., Magomedova, L., Liu, J., Reunov, A., Tsai, R., Eappen, N. S., Jockusch, R. A., Nislow, C., Cummins, C. L., & Krause, H. M. (2018) · Disease Models & Mechanisms · doi:10.1242/dmm.034801 · Cited by 41

Relationships between the functional PPARα Leu162Val polymorphism and obesity, type 2 diabetes, dyslipidaemia, and related quantitative traits in studies of 5799 middle-aged white people

Sparsø, T., Hussain, M. S., Andersen, G., Hainerová, I. A., Borch‐Johnsen, K., Jørgensen, T., Hansen, T. F., & Pedersen, O. B. (2006) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2006.10.007 · Cited by 41

Advanced glycation end products downregulates peroxisome proliferator-activated receptor γ expression in cultured rabbit chondrocyte through MAPK pathway

Yang, Q., Chen, C., Wu, S., Zhang, Y., Mao, X., & Wang, W. (2010) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2010.09.025 · Cited by 41

GDF-3 is an adipogenic cytokine under high fat dietary condition

Wang, W., Yang, Y., Meng, Y., & Shi, Y. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.07.058 · Cited by 41

Stereospecific Regulation of Tyrosine Hydroxylase and Proenkephalin Genes by Short-Chain Fatty Acids in Rat PC12 Cells

Mally, P., Mishra, R., Gandhi, S., DeCastro, M., Nankova, B. B., & LaGamma, E. F. (2004) · Pediatric Research · doi:10.1203/01.pdr.0000119365.21770.45 · Cited by 40

Optimization of in vitro conditions for bovine subcutaneous and intramuscular preadipocyte differentiation1

GRANT, A., Ortiz-Colón, G., Doumit, M. E., & Buskirk, D. D. (2007) · Journal of Animal Science · doi:10.2527/jas.2007-0379 · Cited by 41

PPARγ as a potential therapeutic target in pulmonary hypertension

Sutliff, R. L., Kang, B., & Hart, C. M. (2010) · Therapeutic Advances in Respiratory Disease · doi:10.1177/1753465809369619 · Cited by 44

Genetic Manipulations of PPARs: Effects on Obesity and Metabolic Disease

Barak, Y., & Kim, S. (2007) · PPAR Research · doi:10.1155/2007/12781 · Cited by 43

Regulation of Cytochrome P-450 4A Activity by Peroxisome Proliferator-Activated Receptors in the Rat Kidney

Ishizuka, T., Ito, O., Tan, L., Ogawa, S., Kohzuki, M., Omata, K., Takeuchi, K., & Ito, S. (2003) · Hypertension Research · doi:10.1291/hypres.26.929 · Cited by 41

Localization and Expression of Messenger RNAs for the Peroxisome Proliferator-Activated Receptors in Ovarian Tissue from Naturally Cycling and Pseudopregnant Rats1

Komar, C. M., & Curry, T. E. (2002) · Biology of Reproduction · doi:10.1095/biolreprod66.5.1531 · Cited by 41

Tissue-specific actions of antidiabetic thiazolidinediones on the reduced fatty acid oxidation in skeletal muscle and liver of zucker diabetic fatty rats

Ide, T., NAKAZAWA, T., Mochizuki, T., & Murakami, K. (2000) · Metabolism · doi:10.1016/s0026-0495(00)80019-0 · Cited by 41

PPARs and Female Reproduction: Evidence from Genetically Manipulated Mice

Yang, J., Chen, L., Zhang, X., Zhou, Y., Zhang, D., Huo, M., & Guan, Y. (2008) · PPAR Research · doi:10.1155/2008/723243 · Cited by 40

PPAR-α and PPARGC1A gene variants have strong effects on aerobic performance of Turkish elite endurance athletes

Tural, E., Kara, N., Ağaoğlu, S. A., Elbistan, M., Taşmektepligil, M. Y., & İmamoğlu, O. (2014) · Molecular Biology Reports · doi:10.1007/s11033-014-3453-6 · Cited by 40

Orphan Nuclear Receptors as Targets for Drug Development

Mukherjee, S., & Mani, S. (2010) · Pharmaceutical Research · doi:10.1007/s11095-010-0117-7 · Cited by 42

N-Palmitoylethanolamide protects the kidney from hypertensive injury in spontaneously hypertensive rats via inhibition of oxidative stress

Raso, G. M., Simeoli, R., Russo, R., Santoro, A. N., Pirozzi, C., Bianca, R. D. D. V., Mitidieri, E., Paciello, O., Pagano, T. B., Orefice, N. S., et al. (2013) · Pharmacological Research · doi:10.1016/j.phrs.2013.07.007 · Cited by 40

Ligand activation of peroxisome proliferator-activated receptor β/δ (PPARβ/δ) inhibits chemically induced skin tumorigenesis

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Printed in U.S.A. Copyright © 1998 by The Endocrine Society Differential Expression of Peroxisome Proliferator- Activated Receptor-�,-�, and- � during Rat

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Differential Expression of Peroxisome Proliferator-Activated Receptor- , - , and - during Rat Embryonic Development

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