Tumor necrosis factor and interleukin 1 decrease RXRα, PPARα, PPARγ, LXRα, and the coactivators SRC-1, PGC-1α, and PGC-1β in liver cells

The nuclear receptor superfamily: the second decade

Mangelsdorf, D. J., Thummel, C., Beato, M., Herrlich, P., Schütz, G., Umesono, K., Blumberg, B., Kastner, P., Mark, M., Chambon, P., et al. (1995) · Cell · doi:10.1016/0092-8674(95)90199-x · Cited by 6,964 · see citing works

The acute phase response

Baumann, H., & Gauldie, J. (1994) · Immunology Today · doi:10.1016/0167-5699(94)90137-6 · Cited by 2,907 · see citing works

Nuclear Receptors and Lipid Physiology: Opening the X-Files

Chawla, A., Repa, J. J., Evans, R. M., & Mangelsdorf, D. J. (2001) · Science · doi:10.1126/science.294.5548.1866 · Cited by 2,085 · see citing works

THE PHENOMENON OF THE ACUTE PHASE RESPONSE*

Kushner, I. (1982) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1982.tb22124.x · Cited by 1,494 · see citing works

Thematic review series: The Pathogenesis of Atherosclerosis. Effects of infection and inflammation on lipid and lipoprotein metabolism mechanisms and consequences to the host

Khovidhunkit, W., Kim, M.-S., Memon, R. A., Shigenaga, J. K., Moser, A. H., Feingold, K. R., & Grunfeld, C. (2004) · Journal of Lipid Research · doi:10.1194/jlr.r300019-jlr200 · Cited by 1,481 · see citing works

Cytokine signal transduction

Kishimoto, T., Taga, T., & Akira, S. (1994) · Cell · doi:10.1016/0092-8674(94)90333-6 · Cited by 1,316 · see citing works

Cytokines and the hepatic acute phase response

Moshage, H. (1997) · Journal of Pathology · doi:10.1002/(sici)1096-9896(199703)181:3 · Cited by 1,035 · see citing works

The sphingomyelin pathway in tumor necrosis factor and interleukin-1 signaling

Kolesnick, R. N. (1994) · Cell · doi:10.1016/0092-8674(94)90147-3 · Cited by 932 · see citing works

Minireview: Lipid Metabolism, Metabolic Diseases, and Peroxisome Proliferator-Activated Receptors

Lee, C., Olson, P., & Evans, R. M. (2003) · Endocrinology · doi:10.1210/en.2003-0288 · Cited by 891 · see citing works

Partial Hormone Resistance in Mice with Disruption of the Steroid Receptor Coactivator-1 (SRC-1) Gene

Xu, J., Qiu, Y., DeMayo, F. J., Tsai, S. Y., Tsai, M., & O’Malley, B. W. (1998) · Science · doi:10.1126/science.279.5358.1922 · Cited by 680 · see citing works

Coordinate Regulation of the Expression of the Fatty Acid Transport Protein and Acyl-CoA Synthetase Genes by PPARα and PPARγ Activators

Martin, G., Schoonjans, K., Lefebvre, A.-M., Staels, B., & Auwerx, J. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.45.28210 · Cited by 551 · see citing works

Coregulator codes of transcriptional regulation by nuclear receptors

Rosenfeld, M. G., & Glass, C. K. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.r100041200 · Cited by 509 · see citing works

Orphan Nuclear Receptors: Shifting Endocrinology into Reverse

Kliewer, S. A., Lehmann, J. M., & Willson, T. M. (1999) · Science · doi:10.1126/science.284.5415.757 · Cited by 499 · see citing works

PPARδ regulates glucose metabolism and insulin sensitivity

Lee, C., Olson, P., Hevener, A. L., Mehl, I. R., Chong, L.-W., Olefsky, J. M., Gonzalez, F. J., Ham, J., Kang, H., Peters, J. M., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0511253103 · Cited by 495 · see citing works

Fatty Acids Activate Transcription of the Muscle Carnitine Palmitoyltransferase I Gene in Cardiac Myocytes via the Peroxisome Proliferator-activated Receptor α

Brandt, J. M., Djouadi, F., & Kelly, D. P. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.37.23786 · Cited by 456 · see citing works

CBP: A Signal-Regulated Transcriptional Coactivator Controlled by Nuclear Calcium and CaM Kinase IV

Chawla, S., Hardingham, G. E., Quinn, D. R., & Bading, H. (1998) · Science · doi:10.1126/science.281.5382.1505 · Cited by 427 · see citing works

Stat3 and Stat4: members of the family of signal transducers and activators of transcription.

Zhong, Z., Wen, Z., & Darnell, J. E. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.11.4806 · Cited by 397 · see citing works

Minireview: Nuclear Receptor Coactivators--An Update

McKenna, N. J., & O’Malley, B. W. (2002) · Endocrinology · doi:10.1210/endo.143.7.8892 · Cited by 352 · see citing works

Control of human muscle-type carnitine palmitoyltransferase I gene transcription by peroxisome proliferator-activated receptor

Mascaró, C., Acosta, E., Ortiz, J. A., Marrero, P. F., Hegardt, F. G., & Haro, D. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.15.8560 · Cited by 318 · see citing works

Histone acetyltransferase activity of CBP is controlled by cycle-dependent kinases and oncoprotein E1A

Ait‐Si‐Ali, S., Ramírez-Clavijo, S. R., Barre, F., Dkhissi, F., Magnaghi-Jaulin, L., Girault, J., Robin, P., Knibiehler, M., Pritchard, L. L., Ducommun, B., et al. (1998) · Nature · doi:10.1038/24190 · Cited by 304 · see citing works

Orphan nuclear receptors—new ligands and new possibilities: Figure 1.Preprint

Blumberg, B., & Evans, R. M. (1998) · Genes & Development · doi:10.1101/gad.12.20.3149 · Cited by 301 · see citing works

Involvement of the TRAP220 Component of the TRAP/SMCC Coactivator Complex in Embryonic Development and Thyroid Hormone Action

Ito, M., Yuan, C., Okano, H. J., Darnell, R. B., & Roeder, R. G. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)80247-6 · Cited by 297 · see citing works

Changes in serum lipoprotein pattern induced by acute infections

Sammalkorpi, K., Valtonen, V., Kerttula, Y., Nikkilä, E. A., & Taskinen, M. (1988) · Metabolism · doi:10.1016/0026-0495(88)90120-5 · Cited by 275 · see citing works

Mice deficient in the steroid receptor co‐activator 1 (SRC‐1) are resistant to thyroid hormone

Weiss, R. E., Xu, J., Ning, G., Pohlenz, J., O’Malley, B. W., & Refetoff, S. (1999) · The EMBO Journal · doi:10.1093/emboj/18.7.1900 · Cited by 257 · see citing works

Putative Metabolic Effects of the Liver X Receptor (LXR)

Steffensen, K. R., & Gustafsson, J.-Α. (2004) · Diabetes · doi:10.2337/diabetes.53.2007.s36 · Cited by 250 · see citing works

The Acute Phase Response Is Associated with Retinoid X Receptor Repression in Rodent Liver

Beigneux, A. P., Moser, A. H., Shigenaga, J. K., Grunfeld, C., & Feingold, K. R. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m000953200 · Cited by 223 · see citing works

Regulation of somatic growth by the p160 coactivator p/CIP

Wang, Z., Rose, D. W., Hermanson, O., Liu, F. C., Herman, T., Wu, W., Szeto, D. P., Gleiberman, A. S., Krones, A., Pratt, K. L., et al. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.260463097 · Cited by 192 · see citing works

A role for fatty acids and liver fatty acid binding protein in peroxisome proliferation?

Issemann, I., Prince, R. A., Tugwood, J. D., & Green, S. (1992) · Biochemical Society Transactions · doi:10.1042/bst0200824 · Cited by 164 · see citing works

Regulation of fatty acid transport protein and fatty acid translocase mRNA levels by endotoxin and cytokines

Memon, R. A., Feingold, K. R., Moser, A. H., Fuller, J., & Grünfeld, C. (1998) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1998.274.2.e210 · Cited by 137 · see citing works

Identification of a transcriptionally active peroxisome proliferator-activated receptor α-interacting cofactor complex in rat liver and characterization of PRIC285 as a coactivator

Surapureddi, S., Yu, S., Bu, H., Hashimoto, T., Yeldandi, A. V., Kashireddy, P. V., Cherkaoui‐Malki, M., Qi, C., Zhu, Y.-J., Rao, M. S., et al. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.182426699 · Cited by 136 · see citing works

Endotoxin leads to rapid subcellular re-localization of hepatic RXRα: A novel mechanism for reduced hepatic gene expression in inflammation

Ghose, R., Zimmerman, T. L., Thevananther, S., & Karpen, S. J. (2004) · Nuclear Receptor · doi:10.1186/1478-1336-2-4 · Cited by 134 · see citing works

Sp1 Is a Component of the Cytokine-inducible Enhancer in the Promoter of Vascular Cell Adhesion Molecule-1

Neish, A. S., Khachigian, L. M., Park, A., Baichwal, V. R., & Collins, T. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.48.28903 · Cited by 119 · see citing works

Farnesol Stimulates Differentiation in Epidermal Keratinocytes via PPARα

Hanley, K., Kömüves, L. G., Ng, D., Schoonjans, K., He, S. S., Lau, P., Bikle, D. D., Williams, M. L., Elias, P. M., Auwerx, J. H., et al. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.15.11484 · Cited by 112 · see citing works

Co-regulation of Tissue-specific Alternative Human Carnitine Palmitoyltransferase Iβ Gene Promoters by Fatty Acid Enzyme Substrate

Yu, G.-S., Lu, Y., & Gulick, T. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.49.32901 · Cited by 100 · see citing works

Nuclear Export of Retinoid X Receptor α in Response to Interleukin-1β-mediated Cell Signaling

Zimmerman, T. L., Thevananther, S., Ghose, R., Burns, A. R., & Karpen, S. J. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m508277200 · Cited by 98 · see citing works

Effects of endotoxin on lipid metabolism

Harðardóttir, I., Grünfeld, C., & Feingold, K. R. (1995) · Biochemical Society Transactions · doi:10.1042/bst0231013 · Cited by 76 · see citing works

Endotoxin-induced hypertriglyceridemia is mediated by suppression of lipoprotein lipase at a post-transcriptional level.

Gouni, I., Oka, K., Etienne, J., & Chan, L. (1993) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)41327-6 · Cited by 64 · see citing works

Differential effects of interleukin-1 and tumor necrosis factor on ketogenesis

Memon, R. A., Feingold, K. R., Moser, A. H., Doerrler, W. T., Adi, S., Dinarello, C. A., & Grünfeld, C. (1992) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1992.263.2.e301 · Cited by 62 · see citing works

Fatty Acid Activation of the Peroxisome Proliferator Activated Receptor, a Member of the Nuclear Receptor Gene Superfamily ,

Gearing, K. L., Göttlicher, M., Widmark, E., Banner, C. D., Tollet, P., Strömstedt, M., Rafter, J. J., Berge, R. K., & Gustafsson, J.-Α. (1994) · Journal of Nutrition · doi:10.1093/jn/124.suppl_8.1284s · Cited by 56 · see citing works

Lipoprotein lipase activity in rat heart and adipose tissue during endotoxic shock

Bagby, G. J., & Spitzer, J. A. (1980) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1980.238.3.h325 · Cited by 54 · see citing works

In vivo regulation of acyl-CoA synthetase mRNA and activity by endotoxin and cytokines

Memon, R. A., Fuller, J., Moser, A. H., Smith, P. J., Feingold, K. R., & Grünfeld, C. (1998) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1998.275.1.e64 · Cited by 52 · see citing works

Down-regulation of liver and heart specific fatty acid binding proteins by endotoxin and cytokines in vivo

Memon, R. A., Bass, N. M., Moser, A. H., Fuller, J., Appel, R., Grünfeld, C., & Feingold, K. R. (1999) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/s1388-1981(99)00120-1 · Cited by 46 · see citing works

In vivo effects of interferon-alpha and interferon-gamma on lipolysis and ketogenesis

Memon, R. A., Kr, F., Moser, A. H., Doerrler, W. T., & Grünfeld, C. (1992) · Endocrinology · doi:10.1210/endo.131.4.1396316 · Cited by 43 · see citing works

The Tumor Microenvironment Represses T Cell Mitochondrial Biogenesis to Drive Intratumoral T Cell Metabolic Insufficiency and Dysfunction

Scharping, N. E., Menk, A. V., Moreci, R. S., Whetstone, R. D., Dadey, R. E., Watkins, S. C., Ferris, R. L., & Delgoffe, G. M. (2016) · Immunity · doi:10.1016/j.immuni.2016.07.009 · Cited by 848 · see citing works

The Tumor Microenvironment Represses T Cell Mitochondrial Biogenesis to Drive Intratumoral T Cell Metabolic Insufficiency and Dysfunction

Scharping, N. E., Menk, A. V., Moreci, R. S., Whetstone, R. D., Dadey, R., Watkins, S. C., Ferris, R. L., & Delgoffe, G. M. (2016) · Immunity · doi:10.1016/j.immuni.2016.08.009 · Cited by 705 · see citing works

The Inflammasome-Mediated Caspase-1 Activation Controls Adipocyte Differentiation and Insulin Sensitivity

Stienstra, R., Joosten, L. A. B., Koenen, T. B., van Tits, B. L. J. H., van Diepen, J. A., van den Berg, S. A. A., Rensen, P. C. N., Voshol, P. J., Fantuzzi, G., Hijmans, A., et al. (2010) · Cell Metabolism · doi:10.1016/j.cmet.2010.11.011 · Cited by 681 · see citing works

Kupffer Cells Promote Hepatic Steatosis Via Interleukin-1β–Dependent Suppression of Peroxisome Proliferator-Activated Receptor α Activity

Stienstra, R., Saudale, F., Duval, C., Keshtkar, S., Groener, J. E. M., van Rooijen, N., Staels, B., Kersten, S., & Müller, M. (2010) · Hepatology · doi:10.1002/hep.23337 · Cited by 452 · see citing works

Kuppfer Cells Trigger Nonalcoholic Steatohepatitis Development in Diet-induced Mouse Model through Tumor Necrosis Factor-α Production

Tosello-Trampont, A.-C., Landes, S. G., Nguyen, V., Novobrantseva, T. I., & Hahn, Y. S. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.417014 · Cited by 415 · see citing works

Peroxisome proliferator-activated receptor gamma coactivator-1 (PGC-1) family in physiological and pathophysiological process and diseases

Lu, Q., Zhu, Y., Deng, C., Liang, Z., Chen, J., Chen, Y., Wang, X., Liu, Y., Tian, Y., & Yang, Y. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01756-w · Cited by 360 · see citing works

The Role of PGC-1α and Mitochondrial Biogenesis in Kidney Diseases

Fontecha‐Barriuso, M., Martín‐Sánchez, D., Martinez-Moreno, J. M., Monsalve, M., Ramos, A. M., Sánchez-Niño, M. D., Ruiz‐Ortega, M., Ortíz, A., & Sanz, A. B. (2020) · Biomolecules · doi:10.3390/biom10020347 · Cited by 299 · see citing works

Inflammation stimulates the expression of PCSK9

Feingold, K. R., Moser, A. H., Shigenaga, J. K., Patzek, S. M., & Grünfeld, C. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.07.023 · Cited by 228 · see citing works

Hepatic metabolism of retinoids and disease associations

Shirakami, Y., Lee, S.-A., Clugston, R. D., & Blaner, W. S. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2011.06.023 · Cited by 203 · see citing works

Curcumin ameliorates renal failure in 5/6 nephrectomized rats: role of inflammation

Ghosh, S., Massey, H. D., Krieg, R. J., Fazelbhoy, Z., Ghosh, S., Sica, D. A., Fakhry, I., & Gehr, T. W. B. (2009) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.90732.2008 · Cited by 141 · see citing works

Brothers in Arms: ABCA1- and ABCG1-Mediated Cholesterol Efflux as Promising Targets in Cardiovascular Disease Treatment

Frambach, S. J. C. M., de Haas, R., Smeitink, J. A. M., Rongen, G. A. P. J. M., Rüssel, F. G. M., & Schirris, T. J. J. (2019) · Pharmacological Reviews · doi:10.1124/pr.119.017897 · Cited by 145 · see citing works

FGF21 Is Increased by Inflammatory Stimuli and Protects Leptin-Deficient ob/ob Mice from the Toxicity of Sepsis

Feingold, K. R., Grünfeld, C., Heuer, J. G., Gupta, A., Cramer, M. S., Zhang, T., Shigenaga, J. K., Patzek, S. M., Chan, Z. W., Moser, A. H., et al. (2012) · Endocrinology · doi:10.1210/en.2011-1496 · Cited by 130 · see citing works

Prolonged sleep restriction induces changes in pathways involved in cholesterol metabolism and inflammatory responses

Aho, V., Ollila, H. M., Kronholm, E., Bondia-Pons, I., Soininen, P., Kangas, A. J., Hilvo, M., Seppälä, I., Kettunen, J., Oikonen, M., et al. (2016) · Scientific Reports · doi:10.1038/srep24828 · Cited by 126 · see citing works

LPS decreases fatty acid oxidation and nuclear hormone receptors in the kidney

Feingold, K. R., Wang, Y., Moser, A. H., Shigenaga, J. K., & Grünfeld, C. (2008) · Journal of Lipid Research · doi:10.1194/jlr.m800233-jlr200 · Cited by 119 · see citing works

Daily Injection of Tumor Necrosis Factor-α Increases Hepatic Triglycerides and Alters Transcript Abundance of Metabolic Genes in Lactating Dairy Cattle

Bradford, B. J., Mamedova, L. K., Minton, J. E., Drouillard, J. S., & Johnson, B. J. (2009) · Journal of Nutrition · doi:10.3945/jn.109.108233 · Cited by 117 · see citing works

Down-regulation of SREBP-1c is associated with the development of burned-out NASH

Nagaya, T., Tanaka, N., Suzuki, T., Sano, K., Horiuchi, A., Komatsu, M., Nakajima, T., Nishizawa, T., Joshita, S., Umemura, T., et al. (2010) · Journal of Hepatology · doi:10.1016/j.jhep.2010.04.033 · Cited by 111 · see citing works

Steroid receptor coactivators: servants and masters for control of systems metabolism

Stashi, E., York, B., & O’Malley, B. W. (2014) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2014.05.004 · Cited by 105 · see citing works

Thyroid axis function and dysfunction in critical illness

Mebis, L., & Van den Berghe, G. (2011) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2011.03.002 · Cited by 99 · see citing works

Fine metabolic regulation in ruminants via nutrient–gene interactions: saturated long-chain fatty acids increase expression of genes involved in lipid metabolism and immune response partly through PPAR-α activation

Bionaz, M., Thering, B. J., & Loor, J. J. (2011) · British Journal Of Nutrition · doi:10.1017/s0007114511002777 · Cited by 100 · see citing works

Sepsis-induced inhibition of neutrophil chemotaxis is mediated by activation of peroxisome proliferator-activated receptor-γ

Reddy, R. C., Narala, V. R., Keshamouni, V. G., Milam, J. E., Newstead, M. W., & Standiford, T. J. (2008) · Blood · doi:10.1182/blood-2007-12-128967 · Cited by 99 · see citing works

Liver gene expression analysis reveals endoplasmic reticulum stress and metabolic dysfunction in SCD1-deficient mice fed a very low-fat diet

Flowers, M. T., Keller, M. P., Choi, Y., Hong, L., Kendziorski, C. M., Ntambi, J. M., & Attie, A. (2008) · Physiological Genomics · doi:10.1152/physiolgenomics.00139.2007 · Cited by 92 · see citing works

Peroxisome Proliferator-Activated Receptor δ Regulates Inflammation via NF-κB Signaling in Polymicrobial Sepsis

Zingarelli, B., Piraino, G., Hake, P. W., O’Connor, M. P., Denenberg, A. G., Fan, H., & Cook, J. A. (2010) · American Journal Of Pathology · doi:10.2353/ajpath.2010.091010 · Cited by 86 · see citing works

PPAR-γ Activation As an Anti-inflammatory Therapy for Respiratory Virus Infections

Bassaganya-Riera, J., Song, R., Roberts, P. C., & Hontecillas, R. (2010) · Viral Immunology · doi:10.1089/vim.2010.0016 · Cited by 83 · see citing works

Nuclear Control of the Inflammatory Response in Mammals by Peroxisome Proliferator-Activated Receptors

Mandard, S., & Patsouris, D. (2013) · PPAR Research · doi:10.1155/2013/613864 · Cited by 83 · see citing works

Some new aspects of nutrition, health conditions and fertility of intensively reared dairy cows

Bertoni, G., Trevisi, E., & Lombardelli, R. (2009) · Italian Journal of Animal Science · doi:10.4081/ijas.2009.491 · Cited by 82 · see citing works

Role of the Nuclear Receptors HNF4α, PPARα, and LXRs in the TNFα-Mediated Inhibition of Human Apolipoprotein A-I Gene Expression in HepG2 Cells

Mogilenko, D. A., Dizhe, E. B., Shavva, V. S., Lapikov, I. A., Orlov, S., & Ap, P. (2009) · Biochemistry · doi:10.1021/bi9015742 · Cited by 79 · see citing works

The liver X receptor: A master regulator of the gut–liver axis and a target for non alcoholic fatty liver disease

Ducheix, S., Montagner, A., Théodorou, V., Ferrier, L., & Guillou, H. (2013) · Biochemical Pharmacology · doi:10.1016/j.bcp.2013.03.016 · Cited by 75 · see citing works

Pathogenesis of alcoholic liver disease: the role of nuclear receptors

Gyamfi, M. A., & Wan, Y. Y. (2010) · Experimental Biology and Medicine · doi:10.1258/ebm.2009.009249 · Cited by 74 · see citing works

Dynamic molecular and histopathological changes in the extracellular matrix and inflammation in the transition to heart failure in isolated volume overload

Chen, Y., Pat, B., Gladden, J. D., Zheng, J., Powell, P. C., Wei, C., Cui, X., Husain, A., & Dell’Italia, L. J. (2011) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01104.2010 · Cited by 71 · see citing works

Crosstalk between TNF and glucocorticoid receptor signaling pathways

Bogaert, T. V., Bosscher, K. D., & Libert, C. (2010) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2010.04.003 · Cited by 69 · see citing works

Topical Rosiglitazone Treatment Improves Ulcerative Colitis by Restoring Peroxisome Proliferator-Activated Receptor-γ Activity

Pedersen, G., & Brynskov, J. (2010) · The American Journal of Gastroenterology · doi:10.1038/ajg.2009.749 · Cited by 67 · see citing works

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 66 · see citing works

Molecular mechanism underlying the suppression of lipid oxidation during endotoxemia

Maitra, U., Chang, S., Singh, N., & Li, L. (2009) · Molecular Immunology · doi:10.1016/j.molimm.2009.08.023 · Cited by 64 · see citing works

Tumor Necrosis Factor Inhibits Glucocorticoid Receptor Function in Mice

Bogaert, T. V., Vandevyver, S., Dejager, L., Hauwermeiren, F. V., Pinheiro, I., Πέττα, Ι., Engblom, D., Kleyman, A., Schütz, G., Tuckermann, J. P., et al. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.212365 · Cited by 64 · see citing works

The nuclear receptors NUR77, NURR1 and NOR1 in obesity and during fat loss

Veum, V. L., Dankel, S. N., Gjerde, J., Nielsen, H. J., Solsvik, M. H., Haugen, C., Christensen, B. J., Hoang, T., Fadnes, D. J., Busch, C., et al. (2011) · International Journal of Obesity · doi:10.1038/ijo.2011.240 · Cited by 63 · see citing works

A chronic high-cholesterol diet paradoxically suppresses hepatic CYP7A1 expression in FVB/NJ mice

Henkel, A. S., Anderson, K. A., Dewey, A. M., Kavesh, M. H., & Green, R. M. (2010) · Journal of Lipid Research · doi:10.1194/jlr.m012781 · Cited by 63 · see citing works

TNF-α interferes with lipid homeostasis and activates acute and proatherogenic processes

Tacer, K. F., Kuzman, D., Seliškar, M., Pompon, D., & Rozman, D. (2007) · Physiological Genomics · doi:10.1152/physiolgenomics.00264.2006 · Cited by 62 · see citing works

Hepatocyte Retinoid X Receptor α-Dependent Regulation of Lipid Homeostasis and Inflammatory Cytokine Expression Contributes to Alcohol-Induced Liver Injury

Gyamfi, M. A., He, L., French, S. W., Damjanov, I., & Wan, Y. Y. (2007) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.107.132258 · Cited by 60 · see citing works

Genetic polymorphisms of tumor necrosis factor-α modify the association between dietary polyunsaturated fatty acids and fasting HDL-cholesterol and apo A-I concentrations

Fontaine‐Bisson, B., Wolever, T. M. S., Chiasson, J., RABASA-LHORET, R. P. R., Maheux, P., Josse, R. G., Leiter, L. A., Rodger, N., Ryan, E. A., Connelly, P. W., et al. (2007) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/86.3.768 · Cited by 60 · see citing works

Infection decreases fatty acid oxidation and nuclear hormone receptors in the diaphragm

Feingold, K. R., Moser, A., Patzek, S. M., Shigenaga, J. K., & Grunfeld, C. (2009) · Journal of Lipid Research · doi:10.1194/jlr.m800655-jlr200 · Cited by 59 · see citing works

LPS and proinflammatory cytokines decrease lipin-1 in mouse adipose tissue and 3T3-L1 adipocytes

Lü, B., Lu, Y., Moser, A. H., Shigenaga, J. K., Grünfeld, C., & Feingold, K. R. (2008) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.90323.2008 · Cited by 58 · see citing works

Cisplatin-Induced Downregulation of OCTN2 Affects Carnitine Wasting

Lancaster, C. S., Hu, C., Franke, R. M., Filipski, K. K., Orwick, S. J., Chen, Z., Zuo, Z., Loos, W. J., & Sparreboom, A. (2010) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-10-1239 · Cited by 55 · see citing works

A fish protein hydrolysate alters fatty acid composition in liver and adipose tissue and increases plasma carnitine levels in a mouse model of chronic inflammation

Bjørndal, B., Berge, C., Ramsvik, M. S., Svardal, A. M., Bohov, P., Skorve, J., & Berge, R. K. (2013) · Lipids in Health and Disease · doi:10.1186/1476-511x-12-143 · Cited by 51 · see citing works

Involvement of caspase-4 in IL-1 beta production and pyroptosis in human macrophages during dengue virus infection

Cheung, K. T., Sze, D., Chan, K. H., & Leung, P. H. M. (2017) · Immunobiology · doi:10.1016/j.imbio.2017.10.044 · Cited by 48 · see citing works

Epigenetic modifications of gene promoter DNA in the liver of adult female mice masculinized by testosterone

Dkhil, M. A., Al‐Quraishy, S., Abdel‐Baki, A. S., Ghanjati, F., Araúzo-Bravo, M. J., Delić, D., & Wunderlich, F. T. (2014) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2014.11.006 · Cited by 47 · see citing works

Urinary excretion of carnitine as a marker of proximal tubular damage associated with platin-based antineoplastic drugs

Haschke, M., Vitins, T., Lude, S., Todesco, L., Novakova, K., Herrmann, R., & Krähenbühl, S. (2009) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfp456 · Cited by 46 · see citing works

Targets for TNFα-induced lipolysis in gilthead sea bream(Sparus aurata L.) adipocytes isolated from lean and fat juvenile fish

Cruz-Garcia, L., Saera-Vila, A., Navarro, I., Calduch-Giner, J. À., & Pérez‐Sánchez, J. (2009) · Journal of Experimental Biology · doi:10.1242/jeb.029025 · Cited by 45 · see citing works

Profound gene expression changes in the epithelial monolayer of active ulcerative colitis and Crohn’s disease

Sæterstad, S., Østvik, A. E., Røyset, E. S., Bakke, I., Sandvik, A. K., & Granlund, A. V. B. (2022) · PLoS ONE · doi:10.1371/journal.pone.0265189 · Cited by 42 · see citing works

Retinal Vascular Abnormalities and Microglia Activation in Mice with Deficiency in Cytochrome P450 46A1–Mediated Cholesterol Removal

Saadane, A., Mast, N., Trichonas, G., Chakraborty, D., Hammer, S. S., Busik, J. V., Grant, M. B., & Pikuleva, I. A. (2018) · American Journal Of Pathology · doi:10.1016/j.ajpath.2018.10.013 · Cited by 41 · see citing works

Liver-inherent immune system: its role in blood-stage malaria

Wunderlich, F. T., Al‐Quraishy, S., & Dkhil, M. A. (2014) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00559 · Cited by 41 · see citing works

Coordinating Role of RXRα in Downregulating Hepatic Detoxification during Inflammation Revealed by Fuzzy-Logic Modeling

Keller, R., Klein, M., Thomas, M., Dräger, A., Metzger, U., Templin, M. F., Joos, T. O., Thasler, W. E., Zell, A., & Zanger, U. M. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004431 · Cited by 40 · see citing works

Rat Urinary Bladder Carcinogenesis by Dual‐Acting PPARα + γ Agonists

Oleksiewicz, M. B., Southgate, J., Iversen, L., & Egerod, F. L. (2008) · PPAR Research · doi:10.1155/2008/103167 · Cited by 41 · see citing works

Analysis of Common and Specific Mechanisms of Liver Function Affected by Nitrotoluene Compounds

Deng, Y., Meyer, S. A., Guan, X., Escalon, B. L., Ai, J., Wilbanks, M. S., Welti, R., García‐Reyero, N., & Perkins, E. J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0014662 · Cited by 39 · see citing works

Peroxisome Proliferator‐Activated Receptor and Retinoic X Receptor in Alcoholic Liver Disease

Mello, T., Polvani, S., & Galli, A. (2009) · PPAR Research · doi:10.1155/2009/748174 · Cited by 38 · see citing works

Disturbed hepatic carbohydrate management during high metabolic demand in medium-chain acyl–CoA dehydrogenase (MCAD)–deficient mice

Herrema, H., Derks, T. G. J., van Dijk, T. H., Bloks, V. W., Gerding, A., Havinga, R., Tietge, U. J. F., Müller, M. M., Smit, P. G. A., Kuipers, F., et al. (2008) · Hepatology · doi:10.1002/hep.22284 · Cited by 38 · see citing works

PPARα Ligands Reduce PCB-Induced Endothelial Activation: Possible Interactions in Inflammation and Atherosclerosis

Arzuaga, X., Reiterer, G., Májková, Z., Kilgore, M. W., Toborek, M. J., & Hennig, B. (2007) · Cardiovascular Toxicology · doi:10.1007/s12012-007-9005-8 · Cited by 36 · see citing works

Subacute Endotoxemia Induces Adipose Inflammation and Changes in Lipid and Lipoprotein Metabolism in Cats

Osto, M., Zini, E., Franchini, M., Wolfrum, C., Guscetti, F., Häfner, M., Ackermann, M., Reusch, C. E., & Lutz, T. A. (2011) · Endocrinology · doi:10.1210/en.2010-0999 · Cited by 35 · see citing works

Liver X Receptors, Atherosclerosis and Inflammation

Michael, D., Ashlin, T. G., Buckley, M. L., & Ramji, D. (2012) · Current Atherosclerosis Reports · doi:10.1007/s11883-012-0239-y · Cited by 22 · see citing works

Induction of gene pattern changes associated with dysfunctional lipid metabolism induced by dietary fat and exposure to a persistent organic pollutant

Arzuaga, X., Na, R., Stromberg, A. J., Black, E. P., Arsenescu, V., Cassis, L. A., Májková, Z., Toborek, M. J., & Hennig, B. (2009) · Toxicology Letters · doi:10.1016/j.toxlet.2009.05.008 · Cited by 35 · see citing works

Liver X receptor-dependent inhibition of microglial nitric oxide synthase 2

Secor McVoy, J. R., Oughli, H. A., & Oh, U. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-015-0247-2 · Cited by 34 · see citing works

Retinoid X Receptor Agonists Impair Arterial Mononuclear Cell Recruitment through Peroxisome Proliferator-Activated Receptor-γ Activation

Sanz, M., Albertos, F., Otero, E., Juez, M., Morcillo, E. J., & Piqueras, L. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1102942 · Cited by 33 · see citing works

Keratinocyte‐derived IL‐1β induces PPARG downregulation and PPARD upregulation in human reconstructed epidermis following barrier impairment

Blunder, S., Krimbacher, T., Moosbrugger‐Martinz, V., Gruber, R. W., Schmuth, M., & Dubrac, S. (2021) · Experimental Dermatology · doi:10.1111/exd.14323 · Cited by 32 · see citing works

HDL and innate immunity: a tale of two apolipoproteins

Grünfeld, C., & Feingold, K. R. (2008) · Journal of Lipid Research · doi:10.1194/jlr.e800011-jlr200 · Cited by 32 · see citing works

Differential pulmonary transcriptomic profiles in murine lungs infected with low and highly virulent influenza H3N2 viruses reveal dysregulation of TREM1 signaling, cytokines, and chemokines

Ivan, F. X., Rajapakse, J. C., Welsch, R. E., Rozen, S., Narasaraju, T., Xiong, G. M., Engelward, B. P., & Chow, V. T. K. (2011) · Functional & Integrative Genomics · doi:10.1007/s10142-011-0247-y · Cited by 31 · see citing works

Treatment of mouse liver slices with cholestatic hepatotoxicants results in down-regulation of Fxr and its target genes

Szalowska, E., Stoopen, G. M., Groot, M., Hendriksen, P. J. M., & Peijnenburg, A. (2013) · BMC Medical Genomics · doi:10.1186/1755-8794-6-39 · Cited by 31 · see citing works

Peroxisome proliferator-activated receptor gamma co-activator-1 alpha in depression and the response to electroconvulsive therapy

Ryan, K. M., Patterson, I., & McLoughlin, D. M. (2018) · Psychological Medicine · doi:10.1017/s0033291718002556 · Cited by 30 · see citing works

Downregulation of OCTN2 by cytokines plays an important role in the progression of inflammatory bowel disease

Li, P., Wang, Y., Luo, J. F., Zeng, Q., Wang, M., Bai, M., Zhou, H., Wang, J., & Jiang, H. (2020) · Biochemical Pharmacology · doi:10.1016/j.bcp.2020.114115 · Cited by 30 · see citing works

Thyroid hormone receptors are down-regulated in skeletal muscle of patients with non-thyroidal illness syndrome secondary to non-septic shock

Lado-Abeal, J., Romero, A., Castro-Piedras, I., Rodriguez-Perez, A., & Alvarez-Escudero, J. (2010) · European Journal of Endocrinology · doi:10.1530/eje-10-0376 · Cited by 29 · see citing works

The HIF-2α/PPARα pathway is essential for liraglutide-alleviated, lipid-induced hepatic steatosis

Wang, H., Wang, L., Li, Y., Luo, S., Ye, J., Lu, Z., Li, X., & Lu, H. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.111778 · Cited by 29 · see citing works

Krill powder increases liver lipid catabolism and reduces glucose mobilization in tumor necrosis factor-alpha transgenic mice fed a high-fat diet

Bjørndal, B., Vik, R., Brattelid, T., Vigerust, N. F., Burri, L., Bohov, P., Nygard, O. K., Skorve, J., & Berge, R. K. (2012) · Metabolism · doi:10.1016/j.metabol.2012.03.012 · Cited by 29 · see citing works

Gene Expression Profiles in Livers from Diclofenac-Treated Rats Reveal Intestinal Bacteria-Dependent and -Independent Pathways Associated with Liver Injury

Deng, X., Liguori, M. J., Sparkenbaugh, E., Waring, J. F., Blomme, E. A. G., Ganey, P. E., & Roth, R. A. (2008) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.108.140335 · Cited by 29 · see citing works

Foxa2-dependent hepatic gene regulatory networks depend on physiological state

Bochkis, I. M., Schug, J., Rubins, N. E., Chopra, A. R., O’Malley, B. W., & Kaestner, K. H. (2009) · Physiological Genomics · doi:10.1152/physiolgenomics.90376.2008 · Cited by 28 · see citing works

Liver X Receptor α Activation with the Synthetic Ligand T0901317 Reduces Lung Injury and Inflammation After Hemorrhage and Resuscitation Via Inhibition of the Nuclear Factor κB Pathway

Solan, P. D., Piraino, G., Hake, P. W., Denenberg, A. G., O’Connor, M. P., Lentsch, A. B., & Zingarelli, B. (2010) · Shock · doi:10.1097/shk.0b013e3181f7d742 · Cited by 29 · see citing works

Luteolin potentiates the sensitivity of colorectal cancer cell lines to oxaliplatin through the PPARγ/OCTN2 pathway

Qu, Q., Qu, J., Guo, Y. G., Zhou, B., & Zhou, H. (2014) · Anti-Cancer Drugs · doi:10.1097/cad.0000000000000125 · Cited by 28 · see citing works

Transcription of Liver X Receptor Is Down-Regulated by 15-Deoxy-Δ12,14-Prostaglandin J2 through Oxidative Stress in Human Neutrophils

Álba, G., Reyes-Quiróz, M. E., Santa‐María, C., Ramírez, R., Geniz, I., Jiménez, J., Martín‐Nieto, J., Pintado, E., & Sobrino, F. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042195 · Cited by 27 · see citing works

Peroxisome Proliferator-Activated Receptor Gamma, Coactivator 1α Enhances Local Estrogen Biosynthesis by Stimulating Aromatase Activity in Endometriosis

Suganuma, I., Mori, T., Ito, F., Tanaka, Y., Sasaki, A., Matsuo, S., Kusuki, I., & Kitawaki, J. (2014) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2013-2525 · Cited by 27 · see citing works

Molecular mechanisms underlying the inhibition of IFN‐γ‐induced, STAT1‐mediated gene transcription in human macrophages by simvastatin and agonists of PPARs and LXRs

Li, N., Salter, R., & Ramji, D. (2011) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22976 · Cited by 29 · see citing works

The bidirectional interaction of COVID-19 infections and lipoproteins

Feingold, K. R. (2023) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2023.101751 · Cited by 26 · see citing works

Celastrol alleviates metabolic disturbance in high‐fat diet‐induced obese mice through increasing energy expenditure by ameliorating metabolic inflammation

Yang, X., Wu, F., Li, L., Lynch, E. C., Xie, L., Zhao, Y. Q., Fang, K., Li, J., Luo, J., Xu, L., et al. (2020) · Phytotherapy Research · doi:10.1002/ptr.6800 · Cited by 26 · see citing works

Microarray analysis suggests that burn injury results in mitochondial dysfunction in human skeletal muscle

Tzika (2009) · International Journal of Molecular Medicine · doi:10.3892/ijmm_00000244 · Cited by 26 · see citing works

Tumour necrosis factor alpha down-regulates the expression of peroxisome proliferator activated receptor alpha (PPARα) in human hepatocarcinoma HepG2 cells by activation of NF-κB pathway

Lim, W. S., Ng, D. L., Kor, S. B., Wong, H. K., Muhammad, T. S. T., Choo, Q.-C., & Chew, C.-H. (2012) · Cytokine · doi:10.1016/j.cyto.2012.10.007 · Cited by 25 · see citing works

Hepatic interleukin‐1 receptor type 1 signalling regulates insulin sensitivity in the early phases of nonalcoholic fatty liver disease

Gehrke, N., Hofmann, L. J., Straub, B. K., Rühle, F., Waisman, A., Galle, P. R., & Schattenberg, J. M. (2022) · Clinical and Translational Medicine · doi:10.1002/ctm2.1048 · Cited by 23 · see citing works

Nuclear receptors: mediators and modifiers of inflammation-induced cholestasis

Mulder, J. (2009) · Frontiers in bioscience · doi:10.2741/3400 · Cited by 23 · see citing works

Alterations in Hepatic FGF21, Co-Regulated Genes, and Upstream Metabolic Genes in Response to Nutrition, Ketosis and Inflammation in Peripartal Holstein Cows

Akbar, H., Batistel, F., Drackley, J. K., & Loor, J. J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0139963 · Cited by 23 · see citing works

Alteration of Canalicular Transporters in a Mouse Model of Total Parenteral Nutrition

Tazuke, Y., & Teitelbaum, D. H. (2009) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0b013e3181852201 · Cited by 23 · see citing works

Redundant roles for cJun-N-terminal kinase 1 and 2 in interleukin-1β-mediated reduction and modification of murine hepatic nuclear retinoid X receptor α

Kosters, A., White, D., Sun, H., Thevananther, S., & Karpen, S. J. (2009) · Journal of Hepatology · doi:10.1016/j.jhep.2009.06.029 · Cited by 22 · see citing works

Inflammatory Mediators Increase SUMOylation of Retinoid X Receptor α in a c-Jun N-Terminal Kinase–Dependent Manner in Human Hepatocellular Carcinoma Cells

Aguirre, R. S., & Karpen, S. J. (2013) · Molecular Pharmacology · doi:10.1124/mol.113.085555 · Cited by 22 · see citing works

IL-1β-Induced Downregulation of the Multifunctional PDZ Adaptor PDZK1 Is Attenuated by ERK Inhibition, RXRα, or PPARα Stimulation in Enterocytes

Luo, M., Yeruva, S., Liu, Y., Chodisetti, G., Riederer, B., Menon, M., Tachibana, K., Doi, T., & Seidler, U. E. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00061 · Cited by 22 · see citing works

Roles of NF-κB Activation and Peroxisome Proliferator-Activated Receptor Gamma Inhibition in the Effect of Rifampin on Inducible Nitric Oxide Synthase Transcription in Human Lung Epithelial Cells

Yuhas, Y., Berent, E., Cohen, R., & Ashkenazi, S. (2008) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00961-08 · Cited by 22 · see citing works

Modulation of Cellular Redox Parameters for Improving Therapeutic Responses in Multiple Myeloma

Allegra, A., Petrarca, C., Gioacchino, M. D., Casciaro, M., Musolino, C., & Gangemi, S. (2022) · Antioxidants · doi:10.3390/antiox11030455 · Cited by 21 · see citing works

Genetic Polymorphisms of Tumor Necrosis Factor-Alpha Modify the Association between Dietary Polyunsaturated Fatty Acids and Plasma High-Density Lipoprotein-Cholesterol Concentrations in a Population of Young Adults

Fontaine‐Bisson, B., & El‐Sohemy, A. (2008) · Lifestyle Genomics · doi:10.1159/000149825 · Cited by 21 · see citing works

Environmental pollutants directly affect the liver X receptor alpha activity: Kinetic and thermodynamic characterization of binding

Mozzicafreddo, M., Cuccioloni, M., Bonfili, L., Cecarini, V., Palermo, F. A., Cocci, P., Mosconi, G., Capone, A., Ricci, I., Eleuteri, A. M., et al. (2015) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2015.04.011 · Cited by 21 · see citing works

Kupffer cells modulate hepatic fatty acid oxidation during infection with PR8 influenza

Tarasenko, T. N., Singh, L. N., Chatterji-Len, M., Zerfas, P. M., Cusmano‐Ozog, K. P., & McGuire, P. J. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2015.08.021 · Cited by 20 · see citing works

Endometrial expression of various genes (ISGs, PPARs, RXRs and MUC1) on day 16 post-ovulation in repeat breeder cows, with or without subclinical endometritis

Kasimanickam, R. K., Kasimanickam, V. R., & Grende, K. (2019) · Theriogenology · doi:10.1016/j.theriogenology.2019.10.036 · Cited by 20 · see citing works

Fisetin, a dietary flavonoid, promotes transintestinal cholesterol excretion through the activation of PPARδ

Guo, Y., Liu, B., Geng, Y., Chen, K., Li, J., Yin, X., & Zhang, S. (2023) · Food Research International · doi:10.1016/j.foodres.2023.113783 · Cited by 19 · see citing works

Liver X receptor-α and miR-130a-3p regulate expression of sphingosine 1-phosphate receptor 2 in human umbilical vein endothelial cells

Fan, A., Wang, Q., Yuan, Y., Cheng, J.-L., Chen, L., Guo, X., Li, Q., Chen, B., Huang, X., & Huang, Q. (2015) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00102.2015 · Cited by 19 · see citing works

Peroxisome Proliferator-Activated Receptor-γGene Expression and Its Association with Oxidative Stress in Patients with Metabolic Syndrome

حاتمی, م., Saidijam, M., Yadegarzari, R., Borzuei, S., Soltanian, A. R., Arian, M. S., & Goodarzi, M. T. (2016) · Chonnam Medical Journal · doi:10.4068/cmj.2016.52.3.201 · Cited by 19 · see citing works

Correlation between porcinePPARGC1A mRNA expression and its downstream target genes in backfat andlongissimus dorsi muscle

Erkens, T., Vandesompele, J., Zeveren, A. V., & Peelman, L. J. (2009) · Journal of Applied Genetics · doi:10.1007/bf03195694 · Cited by 18 · see citing works

PPARγ Represses Apolipoprotein A‐I Gene but Impedes TNFα‐Mediated ApoA‐I Downregulation in HepG2 Cells

Shavva, V. S., Mogilenko, D. A., Bogomolova, A. M., Nikitin, A. A., Dizhe, E. B., Efremov, A. M., Oleinikova, G. N., Ap, P., & Orlov, S. (2016) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25498 · Cited by 18 · see citing works

Inflammatory reactions and drug response: importance of cytochrome P450 and membrane transporters

Dumais, G., Iovu, M. O., & du Souich, P. (2008) · Expert Review of Clinical Pharmacology · doi:10.1586/17512433.1.5.627 · Cited by 18 · see citing works

Downregulation of liver X receptor-α in mouse kidney and HK-2 proximal tubular cells by LPS and cytokines

Wang, Y., Moser, A. H., Shigenaga, J. K., Grünfeld, C., & Feingold, K. R. (2005) · Journal of Lipid Research · doi:10.1194/jlr.m500134-jlr200 · Cited by 81 · see citing works

Type II nuclear hormone receptors, coactivator, and target gene repression in adipose tissue in the acute-phase response

Lü, B., Moser, A. H., Shigenaga, J. K., Feingold, K. R., & Grünfeld, C. (2006) · Journal of Lipid Research · doi:10.1194/jlr.m500540-jlr200 · Cited by 47 · see citing works

The Acute Phase Response Is Associated with Retinoid X Receptor Repression in Rodent Liver

Beigneux, A. P., Moser, A. H., Shigenaga, J. K., Grunfeld, C., & Feingold, K. R. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m000953200 · Cited by 223 · see citing works

Repression of Farnesoid X Receptor during the Acute Phase Response

Kim, M. S., Shigenaga, J. K., Moser, A., Feingold, K. R., & Grünfeld, C. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m212633200 · Cited by 151 · see citing works

Role of Toll‐like receptor signaling in hepatocytes in regulating the gene expression of drug metabolizing enzymes

Ghose, R., & Guo, T. (2010) · The FASEB Journal · doi:10.1096/fasebj.24.1_supplement.757.3