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

PPARG and ADIPOQ gene polymorphisms increase type 2 diabetes mellitus risk in Asian Indian Sikhs: Pro12Ala still remains as the strongest predictor

Sanghera, D. K., Demirci, F. Y., Been, L. F., Ortega, L., Ralhan, S. K., Wander, G. S., Mehra, N. K., Singh, J., Aston, C. E., Mulvihill, J. J., et al. (2009) · Metabolism · doi:10.1016/j.metabol.2009.07.043 · Cited by 76

A Novel Antipyretic Action of 15-Deoxy-Δ12,14-Prostaglandin J2in the Rat Brain

Mouihate, A., Lomax, L. B., & Pittman, Q. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3145-03.2004 · Cited by 76

Genome-wide detection of CNVs in Chinese indigenous sheep with different types of tails using ovine high-density 600K SNP arrays

Zhu, C., Fan, H., Yuan, Z., Hu, S., Ma, X., Xuan, J., Wang, H., Zhang, L., Wei, C., Zhang, Q., et al. (2016) · Scientific Reports · doi:10.1038/srep27822 · Cited by 77

PPAR delta: an uncompletely known nuclear receptor

Fredenrich, A., & Grimaldi, P. A. (2005) · Diabetes & Metabolism · doi:10.1016/s1262-3636(07)70162-3 · Cited by 75

Modulation of PPAR Expression and Activity in Response to Polyphenolic Compounds in High Fat Diets

Domínguez-Avila, J. A., González-Aguilar, G. A., ́Álvarez-Parrilla, E., & la Rosa, L. A. D. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17071002 · Cited by 75

The therapeutic potential of inhibiting PPARγ phosphorylation to treat type 2 diabetes

Frkic, R. L., Richter, K., & Bruning, J. B. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.101030 · Cited by 79

Impairment of peroxisomal biogenesis in human colon carcinoma

Lauer, C. (1999) · Carcinogenesis · doi:10.1093/carcin/20.6.985 · Cited by 75

A critical role for p59fyn in CD2-based signal transduction

Fukai, I., Hussey, R. E., Sunder‐Plaßmann, R., & Reinherz, E. L. (2000) · European Journal of Immunology · doi:10.1002/1521-4141(2000012)30:12 · Cited by 37

Skeletal muscle metabolism in physiology and in cancer disease

Giordano, A. M., Calvani, M., Petillo, O., Carteni', M., Melone, M. A. B., & Peluso, G. (2003) · Journal of Cellular Biochemistry · doi:10.1002/jcb.10601 · Cited by 76

Effects of free fatty acids on β-cell functions: A possible involvement of peroxisome proliferator-activated receptors α or pancreatic/duodenal homeobox

Yoshikawa, H., Tajiri, Y., Yoshiyasu, S. A. K. O., Hashimoto, T., Umeda, F., & Nawata, H. (2001) · Metabolism · doi:10.1053/meta.2001.22565 · Cited by 75

PPARs and LXRs: atherosclerosis goes nuclear

Barish, G. D., & Evans, R. M. (2004) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2004.03.003 · Cited by 76

Differential regulation of the stearoyl-CoA desaturase genes by thiazolidinediones in 3T3-L1 adipocytes

Kim, Y., Gómez, F. E., Fox, B. G., & Ntambi, J. M. (2000) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)33439-8 · Cited by 75

Role of peroxisome proliferator-activated receptor-α in fasting-mediated oxidative stress

Abdelmegeed, M. A., Moon, K.-H., Hardwick, J. P., Gonzalez, F. J., & Song, B.-J. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.06.017 · Cited by 74

Ractopamine induces differential gene expression in porcine skeletal muscles1

Gunawan, A. M., Richert, B. T., Schinckel, A. P., Grant, A. L., & Gerrard, D. E. (2007) · Journal of Animal Science · doi:10.2527/jas.2006-540 · Cited by 74

A Novel Cutaneous Fatty Acid-Binding Protein-Related Signaling Pathway Leading to Malignant Progression in Prostate Cancer Cells

Bao, Z., Malki, M. I., Forootan, S. S., Adamson, J., Forootan, F. S., Chen, D., Foster, C. S., Rudland, P. S., & Ke, Y. (2013) · Genes & Cancer · doi:10.1177/1947601913499155 · Cited by 74

Nutrigenomics of ω-3 fatty acids: Regulators of the master transcription factors

Rodríguez‐Cruz, M., & Serna, D. S. (2017) · Nutrition · doi:10.1016/j.nut.2017.04.012 · Cited by 78

Selective activation of PPARγ in breast, colon, and lung cancer cell lines

Allred, C. D., & Kilgore, M. W. (2005) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2005.02.003 · Cited by 73

The Effect of PPAR α , PPAR δ , PPAR γ , and PPARpan Agonists on Body Weight, Body Mass, and Serum Lipid Profiles in Diet-Induced Obese AKR/J Mice

Harrington, W. W., Britt, C. S., Wilson, J. G., Milliken, N. O., Binz, J. G., Lobe, D. C., Oliver, W. R., Lewis, M. C., & Ignar, D. M. (2007) · PPAR Research · doi:10.1155/2007/97125 · Cited by 74

Conditionally-immortalized astrocytic cell line expresses GAD and secretes GABA under tetracycline regulation

Behrstock, S. P., Anantharam, V., Thompson, K. W., Schweitzer, E. S., & Tobin, A. J. (2000) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(20000501)60:3 · Cited by 17

PPAR γ activators induce growth arrest and process extension in B12 oligodendrocyte‐like cells and terminal differentiation of cultured oligodendrocytes

Roth, A. D., Leisewitz, A. V., Jung, J. E., Cassina, P., Barbeito, L., Inestrosa, N. C., & Bronfman, M. (2003) · Journal of Neuroscience Research · doi:10.1002/jnr.10596 · Cited by 75

Modulation of peroxisome proliferator-activated receptors (PPARs) by PPARα- and PPARγ-specific ligands and by 17β-estradiol in isolated zebrafish hepatocytes

Ibabe, A., Herrero, A., & Cajaraville, M. P. (2005) · Toxicology in Vitro · doi:10.1016/j.tiv.2005.03.019 · Cited by 74

Increased Expression of Peroxisome Proliferator-Activated Receptor-α and -γ in Blood Vessels of Spontaneously Hypertensive Rats

Diep, Q. N., & Schiffrin, E. L. (2001) · Hypertension · doi:10.1161/01.hyp.38.2.249 · Cited by 74

Macrophage-derived lipid agonists of PPAR-αas intrinsic controllers of inflammation

Pontis, S., Ribeiro, A., Sasso, O., & Piomelli, D. (2015) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.3109/10409238.2015.1092944 · Cited by 75

Transcriptional control of physiological and pathological processes by the nuclear receptor PPARβ/δ

Tan, N. S., Vázquez‐Carrera, M., Montagner, A., Sng, M. K., Guillou, H., & Wahli, W. (2016) · Progress in Lipid Research · doi:10.1016/j.plipres.2016.09.001 · Cited by 75

Characterization of cholesterol metabolism in Sertoli cells and spermatogenesis (Review)

Shi, J., Li, Y., Ren, K., Xie, Y., Yin, W., & Mo, Z. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.8000 · Cited by 74

Peroxisome proliferators: mechanisms of adverse effects in rodents and molecular basis for species differences

Roberts, R. A. (1999) · Archives of Toxicology · doi:10.1007/s002040050629 · Cited by 74

Peroxisome proliferator-activated receptor subtype- and cell-type-specific activation of genomic target genes upon adenoviral transgene delivery

Nielsen, R., Grøntved, L., Stunnenberg, H. G., & Mandrup, S. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.02266-05 · Cited by 77

Potential Health-modulating Effects of Isoflavones and Metabolites via Activation of PPAR and AhR

Medjakovic, S., Mueller, M., & Jungbauer, A. (2010) · Nutrients · doi:10.3390/nu2030241 · Cited by 76

PPARα Protects Proximal Tubular Cells from Acute Fatty Acid Toxicity

Kamijo, Y., Hora, K., Kono, K., Takahashi, K., Higuchi, M., Ehara, T., Kiyosawa, K., Shigematsu, H., Gonzalez, F., & Aoyama, T. (2007) · Journal of the American Society of Nephrology · doi:10.1681/asn.2007020238 · Cited by 64

Differential involvement of peroxisome-proliferator-activated receptors α and δ in fibrate and fatty-acid-mediated inductions of the gene encoding liver fatty-acid-binding protein in the liver and the small intestine

Poirier, H., Niot, I., MONNOT, M.-C., Braissant, O., Durmort, C., Costet, P., Pineau, T., Wahli, W., Willson, T. M., & Besnard, P. (2001) · Biochemical Journal · doi:10.1042/0264-6021:3550481 · Cited by 73

PPARα deficiency increases secretion and serum levels of apolipoprotein B-containing lipoproteins

Lindén, D., Alsterholm, M., Wennbo, H., & Oscarsson, J. (2001) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)31509-1 · Cited by 73

An aPPARent functional consequence in skeletal muscle physiology via peroxisome proliferator-activated receptors

Phua, W. W. T., Wong, M. X. Y., Liao, Z., & Tan, N. S. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19051425 · Cited by 72

Chromatin recruitment of activated AMPK drives fasting response genes co-controlled by GR and PPARα

Ratman, D., Mylka, V., Bougarne, N., Pawlak, M., Caron, S., Hennuyer, N., Paumelle, R., Cauwer, L. D., Thommis, J., Rider, M. H., et al. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw742 · Cited by 73

Skeletal muscle mitochondrial remodeling in heart failure: An update on mechanisms and therapeutic opportunities

Lv, J., Li, Y., Shi, S., Xu, X., Wu, H., Zhang, B., & Song, Q. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113833 · Cited by 74

Endocrine disruptors and endometriosis

Dutta, S., Banu, S. K., & Arosh, J. A. (2022) · Reproductive Toxicology · doi:10.1016/j.reprotox.2022.11.007 · Cited by 78

Peroxisome Proliferator-Activated Receptor-α-Null Mice Have Increased White Adipose Tissue Glucose Utilization, GLUT4, and Fat Mass: Role in Liver and Brain

Knauf, C., Rieusset, J., Foretz, M., Cani, P. D., Uldry, M., Hosokawa, M., Martinez, E., Bringart, M., Waget, A., Kersten, S., et al. (2006) · Endocrinology · doi:10.1210/en.2005-1536 · Cited by 75

Combination therapy with PPARγ and PPARα agonists increases glucose-stimulated insulin secretion in db/dbmice

Yajima, K., Hirose, H., Fujita, H., Seto, Y., Fujita, H., Ukeda, K., Miyashita, K., Kawai, T., Yamamoto, Y., Ogawa, T., et al. (2003) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00149.2002 · Cited by 72

Eicosapentaenoic acid, but not oleic acid, stimulates β‐oxidation in adipocytes

Guo, W., Xie, W., Lei, T., & Hamilton, J. A. (2005) · Lipids · doi:10.1007/s11745-005-1443-8 · Cited by 72

Modulating Microglia Activity with PPAR-γ Agonists: A Promising Therapy for Parkinson’s Disease?

Carta, A. R., & Pisanu, A. (2012) · Neurotoxicity Research · doi:10.1007/s12640-012-9342-7 · Cited by 72

Peroxisome Proliferator–Activated Receptor-γ Regulates Expression of PDX-1 and NKX6.1 in INS-1 Cells

Moibi, J. A., Gupta, D., Jetton, T. L., Peshavaria, M., Desai, R., & Leahy, J. L. (2006) · Diabetes · doi:10.2337/db06-0948 · Cited by 71

PPAR α in Obesity: Sex Difference and Estrogen Involvement

Yoon, M. (2010) · PPAR Research · doi:10.1155/2010/584296 · Cited by 74

Peroxisome Proliferator-Activated Receptor α Deficiency Increases the Risk of Maternal Abortion and Neonatal Mortality in Murine Pregnancy with or without Diabetes Mellitus: Modulation of T Cell Differentiation

Yessoufou, A., Hichami, A., Besnard, P., Moutairou, K. A., & Khan, N. A. (2006) · Endocrinology · doi:10.1210/en.2006-0067 · Cited by 74

PPARG: Gene Expression Regulation and Next-Generation Sequencing for Unsolved Issues

Costa, V., Gallo, M. A., Letizia, F., Aprile, M., Casamassimi, A., & Ciccodicola, A. (2010) · PPAR Research · doi:10.1155/2010/409168 · Cited by 75

Association Study of Wnt Signaling Pathway Genes in Bipolar Disorder

Zandi, P. P. (2008) · Archives of General Psychiatry · doi:10.1001/archpsyc.65.7.785 · Cited by 72

PPARs and pain

Okine, B. N., Gaspar, J. C., & Finn, D. P. (2018) · British Journal of Pharmacology · doi:10.1111/bph.14339 · Cited by 70

The dual PPARα/γ agonist, ragaglitazar, improves insulin sensitivity and metabolic profile equally with pioglitazone in diabetic and dietary obese ZDF rats

Pickavance, L. C., Brand, C. L., Wassermann, K., & Wilding, J. P. H. (2005) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0706041 · Cited by 71

Branched Chain Fatty Acids Induce Nitric Oxide-dependent Apoptosis in Vascular Smooth Muscle Cells

Idel, S., Ellinghaus, P., Wolfrum, C., Nofer, J., Gloerich, J., Assmann, G., Spener, F., & Seedorf, U. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m204639200 · Cited by 71

Peroxisome proliferator-activated receptor (PPAR) alpha activation and its consequences in humans

Hertz, R., & Bar‐Tana, J. (1998) · Toxicology Letters · doi:10.1016/s0378-4274(98)00290-2 · Cited by 71

Fibrate induction of the adrenoleukodystrophy‐related gene (ABCD2): Promoter analysis and role of the peroxisome proliferator‐activated receptor PPARα

Fourcade, S., Savary, S., Albet, S., Gauthé, D., Gondcaille, C., Pineau, T., Bellenger, J., Bentejac, M., Holzinger, A., Berger, J., et al. (2001) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.2001.02249.x · Cited by 70

PPARγ, a Lipid‐Activated Transcription Factor as a Regulator of Dendritic Cell Function

Szatmári, I., Rajnavölgyi, É., & Nagy, L. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1366.013 · Cited by 70

Antiepileptic popular ketogenic diet: emerging twists in an ancient story

Vamecq, J., Vallée, L., Lesage, F., Gressèns, P., & Stables, J. P. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.11.003 · Cited by 70

Sesamol ameliorates diet‐induced obesity in C57BL/6J mice and suppresses adipogenesis in 3T3‐L1 cells via regulating mitochondria‐lipid metabolism

Liu, Z., Qiao, Q., Sun, Y., Chen, Y., Ren, B., & Liu, X. (2016) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201600717 · Cited by 71

Synthetic and natural Peroxisome Proliferator-Activated Receptor (PPAR) agonists as candidates for the therapy of the metabolic syndrome

Tan, C. K., Zhuang, Y., & Wahli, W. (2017) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2017.1280467 · Cited by 74

Ligand‐dependent contribution of RXRβ to cholesterol homeostasis in Sertoli cells

Mascrez, B., Ghyselinck, N. B., 渡辺, 光., Annicotte, J., Chambon, P., Auwerx, J. H., & Mark, M. P. (2004) · EMBO Reports · doi:10.1038/sj.embor.7400094 · Cited by 70

Energy metabolism and cytotoxicity

Portilla, D. (2003) · Seminars in Nephrology · doi:10.1016/s0270-9295(03)00088-3 · Cited by 70

Peroxisome proliferator-activated receptors: Lipid binding proteins controling gene expression

van Bilsen, M., Vusse, G. J., Gilde, A. J., Lindhout, M., & van der Lee, K. A. J. M. (2002) · Springer eBooks · doi:10.1007/978-1-4419-9270-3_17 · Cited by 71

PPARγ Ligand Troglitazone Lowers Cholesterol Synthesis in HepG2 and Caco-2 Cells via a Reduced Concentration of Nuclear SREBP-2

Klopotek, A., Hirche, F., & Eder, K. (2006) · Experimental Biology and Medicine · doi:10.1177/153537020623100810 · Cited by 69

Megalin/LRP2 Expression Is Induced by Peroxisome Proliferator-Activated Receptor -Alpha and -Gamma: Implications for PPARs' Roles in Renal Function

Cabezas, F., Lagos, J., Céspedes, C., Vio, C. P., Bronfman, M., & Marzolo, M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016794 · Cited by 67

Enhanced anti-ulcer effect of pioglitazone on gastric ulcers in cirrhotic rats: The role of nitric oxide and IL-1β

Moezi, L., Heidari, R., Amirghofran, Z., Nekooeian, A. A., Monabati, A., & Dehpour, A. R. (2013) · Pharmacological Reports · doi:10.1016/s1734-1140(13)70971-x · Cited by 69

Angiopoietin-like protein 4: health effects, modulating agents and structure–function relationships

Grootaert, C., de Wiele, T. V., Verstraete, W., Bracke, M., & Vanhoecke, B. W. A. (2012) · Expert Review of Proteomics · doi:10.1586/epr.12.12 · Cited by 69

Hepatic Steatosis and Peroxisomal Fatty Acid Beta-oxidation

Cherkaoui‐Malki, M., Surapureddi, S., Hajj, H. I. E., Vamecq, J., & Andreoletti, P. (2012) · Current Drug Metabolism · doi:10.2174/138920012803762765 · Cited by 71

Characterization of the Species-Specificity of Peroxisome Proliferators in Rat and Human Hepatocytes

Ammerschlaeger, M. (2004) · Toxicological Sciences · doi:10.1093/toxsci/kfh071 · Cited by 70

On the pivotal role of PPARa in adaptation of the heart to hypoxia and why fat in the diet increases hypoxic injury

Cole, M. A., Jamil, A. H. A., Heather, L. C., Murray, A. J., Sutton, E. R., Slingo, M., Sebag‐Montefiore, L., Tan, S. C., Aksentijević, D., Gildea, O. S., et al. (2016) · The FASEB Journal · doi:10.1096/fj.201500094r · Cited by 71

Peroxisome Proliferator-Activated Receptors and Skin Development

Rosenfield, R. L., Deplewski, D., & Greene, M. E. (2000) · Hormone Research in Paediatrics · doi:10.1159/000053270 · Cited by 69

Role of Peroxisome Proliferator-Activated Receptor-α in the Mechanism Underlying Changes in Renal Pyruvate Dehydrogenase Kinase Isoform 4 Protein Expression in Starvation and after Refeeding

Sugden, M. C., Bulmer, K., Gibbons, G. F., & Holness, M. J. (2001) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2001.2586 · Cited by 69

Regulation of Peroxisome Proliferator-Activated Receptors

Sørensen, H. N., Treuter, E., & Gustafsson, J.-Å. (1998) · Vitamins and hormones · doi:10.1016/s0083-6729(08)60924-3 · Cited by 68

Molecular effects of ER alpha- and beta-selective agonists on regulation of energy homeostasis in obese female Wistar rats

Weigt, C., Hertrampf, T., Kluxen, F. M., Flenker, U., Hülsemann, F., Fritzemeier, K. H., & Diel, P. R. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.07.007 · Cited by 70

The Ubiquitin Ligase Siah2 Regulates PPARγ Activity in Adipocytes

Kilroy, G. E., Kirk-Ballard, H., Carter, L. E., & Floyd, Z. E. (2012) · Endocrinology · doi:10.1210/en.2011-1725 · Cited by 68

Interactions between Human Liver Fatty Acid Binding Protein and Peroxisome Proliferator Activated Receptor Selective Drugs

Velkov, T. (2013) · PPAR Research · doi:10.1155/2013/938401 · Cited by 68

PPARs as therapeutic targets in cardiovascular disease

van Bilsen, M., & van Nieuwenhoven, F. A. (2010) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2010.512917 · Cited by 67

PPARγ is involved in the hyperglycemia‐induced inflammatory responses and collagen degradation in human chondrocytes and diabetic mouse cartilages

Chen, Y., Chan, D., Lan, K., Wang, C., Chen, C., Chao, S., Tsai, K., Yang, R., & Liu, S. (2014) · Journal of Orthopaedic Research® · doi:10.1002/jor.22770 · Cited by 67

Activation of PPARα inhibits IGF‐I‐mediated growth and survival responses in medulloblastoma cell lines

Urbańska, K., Pannizzo, P., Grabacka, M., Croul, S. E., Valle, L. D., Khalili, K., & Reiss, K. (2008) · International Journal of Cancer · doi:10.1002/ijc.23588 · Cited by 68

Peroxisome Proliferator‐Activated Receptor‐γ in Amyotrophic Lateral Sclerosis and Huntington′s Disease

Kiaei, M. (2008) · PPAR Research · doi:10.1155/2008/418765 · Cited by 67

In Vivo and in Vitro Studies of a Functional Peroxisome Proliferator-activated Receptor γ Response Element in the Mouse pdx-1 Promoter

Gupta, D., Jetton, T. L., Mortensen, R. M., Duan, S. Z., Peshavaria, M., & Leahy, J. L. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m801813200 · Cited by 67

Bezafibrate, a lipid-lowering pharmaceutical, as a potential endocrine disruptor in male zebrafish (Danio rerio)

Velasco‐Santamaría, Y. M., Korsgaard, B., Madsen, S. S., & Bjerregaard, P. (2011) · Aquatic Toxicology · doi:10.1016/j.aquatox.2011.05.018 · Cited by 74

Anti-inflammatory effect of antidiabetic thiazolidinediones prevents bone resorption rather than cartilage changes in experimental polyarthritis

Koufany, M., Moulin, D., Bianchi, A., Muresan, M., Sébillaud, S., Netter, P., Weryha, G., & Jouzeau, J. (2008) · Arthritis Research & Therapy · doi:10.1186/ar2354 · Cited by 67

Identification of Functions of Peroxisome Proliferator-Activated Receptor α in Proximal Tubules

Kamijo, Y., Hora, K., Tanaka, N., Usuda, N., Kiyosawa, K., Nakajima, T., Gonzalez, F. J., & Aoyama, T. (2002) · Journal of the American Society of Nephrology · doi:10.1097/01.asn.0000018403.61042.56 · Cited by 67

Effects of fenofibrate on lipid parameters in obese rhesus monkeys

Winegar, D. A., Brown, P. J., Wilkison, W. O., Lewis, M. C., Ott, R. J., Tong, W. Q., Brown, H. R., Lehmann, J. M., Kliewer, S. A., Plunket, K. D., et al. (2001) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)32207-0 · Cited by 67

Peroxisome proliferator‐activated receptor (PPAR) modulators: Diabetes and beyond*

Jones, A. B. (2001) · Medicinal Research Reviews · doi:10.1002/med.1025 · Cited by 67

Phthalate Induction of CYP3A4 is Dependent on Glucocorticoid Regulation of PXR Expression

Cooper, B. W., Cho, T. M., Thompson, P. M., & Wallace, A. D. (2008) · Toxicological Sciences · doi:10.1093/toxsci/kfn047 · Cited by 68

Induction of differentiation and peroxisome proliferator-activated receptor ? expression in colon cancer cell lines by troglitazone

Kato, M., Kusumi, T., Tsuchida, S., Tanaka, M., Sasaki, M., & Kudo, H. (2004) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-003-0510-2 · Cited by 67

Thermodynamics in Gliomas: Interactions between the Canonical WNT/Beta-Catenin Pathway and PPAR Gamma

Vallée, A., Lecarpentier, Y., Guillevin, R., & Vallée, J.-N. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00352 · Cited by 68

The peroxisome proliferator‐activated receptors in cardiovascular diseases: experimental benefits and clinical challenges

Cheang, W. S., Tian, X. Y., Wong, W. T., & Huang, Y. (2014) · British Journal of Pharmacology · doi:10.1111/bph.13029 · Cited by 66

Cranberries (Oxycoccus quadripetalus) inhibit adipogenesis and lipogenesis in 3T3-L1 cells

Kowalska, K., Olejnik, A. M., Rychlik, J., & Grajek, W. (2013) · Food Chemistry · doi:10.1016/j.foodchem.2013.10.032 · Cited by 66

Telmisartan ameliorates germ cell toxicity in the STZ-induced diabetic rat: Studies on possible molecular mechanisms

Kushwaha, S., & Jena, G. (2013) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2013.04.013 · Cited by 68

Modification in Oxidative Stress, Inflammation, and Lipoprotein Assembly in Response to Hepatocyte Nuclear Factor 4α Knockdown in Intestinal Epithelial Cells

Marcil, V., Seidman, E. G., Sinnett, D., Boudreau, F., Gendron, F., Beaulieu, J., Ménard, D., Précourt, L., Amre, D. K., & Levy, E. H. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.155358 · Cited by 64

Regulation of Peroxisome Proliferator-activated Receptor α-Induced Transactivation by the Nuclear Orphan Receptor TAK1/TR4

Yan, Z. H., Karam, W. G., Staudinger, J. L., Medvedev, A. V., Ghanayem, B. I., & Jetten, A. M. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.18.10948 · Cited by 66

Peroxisome Proliferator-Activated Receptors as Novel Targets in Lung Disease *

Belvisi, M. G., & Hele, D. J. (2008) · CHEST Journal · doi:10.1378/chest.07-0019 · Cited by 66

Low-fat, high-carbohydrate and high-fat, low-carbohydrate diets decrease primary bile acid synthesis in humans

Bisschop, P. H. L. T., Bandsma, R., Stellaard, F., ter Harmsel, A., Meijer, A. J., Sauerwein, H. P., Kuipers, F., & Romijn, J. A. (2004) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/79.4.570 · Cited by 66

Oleic acid causes apoptosis and dephosphorylates Bad

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