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of 6
pro vyhledávání: '"Jiling Liao"'
Autor:
Jieying Zhang, Kunlu Wu, Xiaojuan Xiao, Jiling Liao, Qikang Hu, Huiyong Chen, Jing Liu, Xiuli An
Publikováno v:
International Journal of Molecular Sciences, Vol 16, Iss 2, Pp 4083-4094 (2015)
Autophagy is a process that leads to the degradation of unnecessary or dysfunctional cellular components and long-lived protein aggregates. Erythropoiesis is a branch of hematopoietic differentiation by which mature red blood cells (RBCs) are generat
Externí odkaz:
https://doaj.org/article/9e21a0c1d44840a68ad5ecd1c3befbc5
Autor:
Yiming Li, Stéphane Richard, Heejin Jun, Kezhou Zhu, Yingxu Ma, Min-Jung Park, Alexander J. Knights, Jay H Lipinski, Jiling Liao, Steven A. Weinman, Xiaona Qiao, Dong-Il Kim, Jun Wu
Publikováno v:
Endocrinology
Protein arginine methyltransferases (PRMTs) are enzymes that regulate the evolutionarily conserved process of arginine methylation. It has been reported that PRMTs are involved in many metabolic regulatory pathways. However, until now, their roles in
Publikováno v:
FEBS lettersReferences. 594(17)
We previously reported the involvement of protein arginine methyltransferase 1 (PRMT1) in adipocyte thermogenesis. Here, we investigate the effects of PRMT1 inhibitors on thermogenesis. Unexpectedly, we find that the PRMT1 inhibitor TC-E 5003 (TC-E)
Publikováno v:
Endocrinology. 159:2520-2527
It has been reported that class I histone deacetylase (HDAC) inhibition increases thermogenesis in fat, but adipocyte-specific Hdac3 deletions have presented inconsistent results. In this study, we observed that HDAC3 protein levels were lower in bro
Publikováno v:
Metabolism. 77:58-64
Cinnamaldehyde (CA) is a food compound that has previously been observed to be protective against obesity and hyperglycemia in mouse models. In this study, we aimed to elucidate the mechanisms behind this protective effect by assessing the cell-auton
Publikováno v:
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences. 41(12)
To demonstrate the effect of AB serum on terminal erythroid differentiation ex vivo. Methods: After separation of CD34+ cells from cord blood, the cells were cultured and divided into a control group and an experimental group. The effects of AB serum