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sacrificed and tissues were collected to further examine the expression of asprosin and histomorphology. Adenovirus was recommended a period of 3–7 days following infection to assess effects on gene expression or physiology ( Gomez-Banoy & Lo 2017 ). HFD
The Third Xiangya Hospital of Central South University, Changsha, Hunan, China
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Animal Core Facility, Nanjing Medical University, Nanjing, Jiangsu, China
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genetic defects, abnormal gene expression, and metabolic anomalies has been extensively investigated ( Escobar-Morreale et al . 2011 , Azziz 2016 , Streiter et al. 2016 ). Theoretically, intervention measures that reverse the neuroendocrinological
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vector expressing rat IGF1, targeted specifically to hepatocytes (AAV8-TBGp-rIGF1) and the impact on systemic metabolism, liver fat content and composition, liver injury and gene expression profile was determined. Materials and methods Animal
Lifelong Health Theme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, South Australia, Australia
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Lifelong Health Theme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, South Australia, Australia
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Lifelong Health Theme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, South Australia, Australia
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Lifelong Health Theme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, South Australia, Australia
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-hydroxyacyl CoA dehydrogenase activity were measured in 6–10 mg liver tissue homogenates by kinetic assay as previously described ( Srere 1969 , Bergmeyer 1974 ). Gene expression analysis Total RNA was extracted from liver using Trizol (Invitrogen) and
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-terminal kinase (JNK) p46 and lipopolysaccharide-induced gene expression of IL-1β and TNF-α ( Qi et al. 2017 ). Interestingly, these anti-inflammatory effects seemed to be mediated by inducible 6-phosphofructokinase-2 (iPFK2) as they were not seen in iPFK2
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with hyperexpression of HLA class I molecules and insulitis ( Richardson et al. 2009 , 2013 ). There is evidence that enterovirus infections impair beta-cell function ( Gallagher et al. 2015 ), their gene expression, and microRNA regulation ( Kim
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Division of Advanced Diagnostics, Toronto General Research Institutes, University Health Network, Toronto, Ontario, Canada
Banting and Best Diabetes Centre, University of Toronto, Toronto, Ontario, Canada
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diabetes . Diabetes 64 4298 – 4 311 . ( https://doi.org/10.2337/db15-0066 ) Lin Y Sun Z 2015b In vivo pancreatic beta-cell-specific expression of antiaging gene klotho: a novel approach for preserving beta-cells in type 2 diabetes . Diabetes
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microbial composition, increased microbial metabolites such as short-chain fatty acid (SCFA) levels in the colon, increased adipose tissue mass, and changed hepatic gene expression related to carbohydrate and lipid metabolism ( Cho et al. 2012 ). Studies
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European Associated Laboratory (EAL) ‘NeuroMicrobiota’, Brussels/Toulouse, Belgium
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European Associated Laboratory (EAL) ‘NeuroMicrobiota’, Brussels/Toulouse, Belgium
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309 G528 – G 541 . ( https://doi.org/10.1152/ajpgi.00172.2015 ) Chassaing B Van de Wiele T De Bodt J Marzorati M Gewirtz AT 2017 Dietary emulsifiers directly alter human microbiota composition and gene expression ex vivo potentiating