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clusters that separated the genes with similar actions were detected: retinol, arachidonic acid and linoleic acid metabolism; FA oxidation; metabolic pathways with anti-inflammatory actions ( Table 5 ). Table 3 Hepatic up- and downregulated genes in
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MH Sullivan LM Ingram C O’Donnell CJ Keaney JF Vasan RS 2012 Cardiometabolic correlates and heritability of fetuin-A, retinol-binding protein 4, and fatty-acid binding protein 4 in the Framingham Heart Study . Journal of
School of Medicine, Conjoint Endocrine Laboratory, Disciplines of Medicine, Royal Brisbane and Women's Hospital, The University of Queensland, Herston, Brisbane, Queensland 4029, Australia
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School of Medicine, Conjoint Endocrine Laboratory, Disciplines of Medicine, Royal Brisbane and Women's Hospital, The University of Queensland, Herston, Brisbane, Queensland 4029, Australia
School of Medicine, Conjoint Endocrine Laboratory, Disciplines of Medicine, Royal Brisbane and Women's Hospital, The University of Queensland, Herston, Brisbane, Queensland 4029, Australia
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School of Medicine, Conjoint Endocrine Laboratory, Disciplines of Medicine, Royal Brisbane and Women's Hospital, The University of Queensland, Herston, Brisbane, Queensland 4029, Australia
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recently reported that human trophoblast cells produce the T 4 and retinol-binding protein, TTR ( McKinnon et al . 2005 ). Studies on polarised choriocarcinoma JEG-3 cells maintained in bicameral chambers indicate that TTR is secreted apically and basally
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family member 8-like 9.57 432384 rbp2b Retinol binding protein 2b, cellular 9.48 100003412 zgc:172139 Uncharacterized KIAA0930-like Differential immune response against an inflammatory stimulus in normal and overfed fish A total of 902 genes demonstrated
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result in generation of circulating factors that are responsible for cross-organ communication. Retinol-binding protein-4 (RBP4) was recently identified as one candidate for that crosstalk in the adipose tissue of adipose-specific Glut4 knockout mice
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- cis -Retinol dehydrogenase (RDH5) 5′-CTGATCTGTGACCCGGACCTAA-3′ 5′-GGGGCAGAAATAAATCAAAGTCCTT-3′ 5α-Reductase-1 5′-TGGCGATTATGTTCTGTACCTGTA-3′ 5′-AACCACAAGCCAAAACCTATTAGA-3′ P450 aromatase 5′-CGACAGGCTGGTACCGCATGCTC-3′ 5′-AAGAGGCAATAATAAAGGAAATCCAGAC-3
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. Huang X-F & Luu-The V 2001 Modulation of the androgenic response by recombinant human 11-cis retinol dehydrogenase. Journal of Steroid Biochemistry 77 129 –133. Kelly PA , Asselin J & Labrie F 1979 Endocrine
Monash Institute for Medical Research, Monash University, Clayton, Victoria, 3168, Australia
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.g. cadherin, cathepsin L), while others are known to function in signal transduction (e.g. HNF3, MAPKKK, Smad 3, rat retinol-binding protein) and to participate in regulation of hormonal inputs (StAR and androgen binding protein). However, because the
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Department of Cellular and Integrative Physiology, Section of Nephrology, Department of Internal Medicine, University of Nebraska Medical Center, 985850 Nebraska Medical Center, Omaha, Nebraska 68198-5850, USA
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. Diabetologia 47 1541 – 1549 . Yang Q Graham TE Mody N Preitner F Peroni OD Zabolotny JM Kotani K Quadro L Kahn BB 2005 Serum retinol binding protein 4 contributes to insulin resistance in obesity and type 2 diabetes . Nature 436
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syndrome (PCOS) since PCOS ovaries have enhanced expression of genes and proteins of the alternate pathway ( Marti et al. 2017 ). The aldo-keto reductases ( AKR1C1 /AKR1C4), 5α-reductases ( SRD5A1/2 ) and retinol dehydrogenase ( RoDH ) are all expressed