Search Results
Search for other papers by Yanli Miao in
Google Scholar
PubMed
Search for other papers by Haojie Qin in
Google Scholar
PubMed
Search for other papers by Yi Zhong in
Google Scholar
PubMed
Search for other papers by Kai Huang in
Google Scholar
PubMed
Search for other papers by Caijun Rao in
Google Scholar
PubMed
asprosin mediated inhibition of adipose browning To uncover the underlying mechanism of the aforementioned observations, we explored whether Nrf2, a crucial antioxidant transcription factor, was involved in the process. Nrf2 is a transcription factor
Search for other papers by Robin Kristófi in
Google Scholar
PubMed
Search for other papers by Jan W Eriksson in
Google Scholar
PubMed
action. This includes activation of Dicer, iPFK2 and miRNA leading to lower expression of several pro-inflammatory cytokines such as TNF-α and IL-6. AMPK, AMP kinase; ATF3, activating transcription factor 3; ChREBP, carbohydrate-responsive element
Search for other papers by Andre Sarmento-Cabral in
Google Scholar
PubMed
Search for other papers by Mercedes del Rio-Moreno in
Google Scholar
PubMed
Search for other papers by Mari C Vazquez-Borrego in
Google Scholar
PubMed
Search for other papers by Mariyah Mahmood in
Google Scholar
PubMed
Search for other papers by Elena Gutierrez-Casado in
Google Scholar
PubMed
Search for other papers by Natalie Pelke in
Google Scholar
PubMed
Search for other papers by Grace Guzman in
Google Scholar
PubMed
Search for other papers by Papasani V Subbaiah in
Google Scholar
PubMed
Search for other papers by Jose Cordoba-Chacon in
Google Scholar
PubMed
Search for other papers by Shoshana Yakar in
Google Scholar
PubMed
Search for other papers by Rhonda D Kineman in
Google Scholar
PubMed
( Cd36 )), and esterification (monoacylglycerol O-acyltransferase 1 ( Mogat1 )). The expression of sterol regulatory element-binding transcription factor 1 ( Srebf1) , a major downstream regulator of insulin-mediated induction of lipogenesis, was not
Search for other papers by Wenjuan Liu in
Google Scholar
PubMed
Search for other papers by Harry Kevin Lau in
Google Scholar
PubMed
Search for other papers by Dong Ok Son in
Google Scholar
PubMed
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
Search for other papers by Tianru Jin in
Google Scholar
PubMed
Search for other papers by Yehong Yang in
Google Scholar
PubMed
Search for other papers by Zhaoyun Zhang in
Google Scholar
PubMed
Search for other papers by Yiming Li in
Google Scholar
PubMed
Search for other papers by Gerald J Prud’homme in
Google Scholar
PubMed
Search for other papers by Qinghua Wang in
Google Scholar
PubMed
/or function. Pancreatic duodenal homeobox (PDX-1) and NK6 homeobox 1 (Nkx6.1) are two widely studied transcription factors that regulate pancreatic ontogeny and fetal β-cell development ( Baeyens et al. 2018 ). In particular, PDX-1, also known as insulin
Search for other papers by Nicole G Barra in
Google Scholar
PubMed
Search for other papers by Fernando F Anhê in
Google Scholar
PubMed
Search for other papers by Joseph F Cavallari in
Google Scholar
PubMed
Search for other papers by Anita M Singh in
Google Scholar
PubMed
Search for other papers by Darryl Y Chan in
Google Scholar
PubMed
Search for other papers by Jonathan D Schertzer in
Google Scholar
PubMed
uptake, and by inhibiting the expression of FOXO transcription factors, gluconeogenic enzymes (phosphoenolpyruvate, glucose-6-phosphatase), and negative regulators of PI3K/Akt signaling like phosphatase and tensin homolog protein (PTEN) ( Cameron et al