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Publication : Knockdown of slincRAD leads to defective adipose development in vivo.

First Author  Zhang P Year  2019
Journal  Biochem Biophys Res Commun Volume  513
Issue  4 Pages  983-989
PubMed ID  31005260 Mgi Jnum  J:291791
Mgi Id  MGI:6443504 Doi  10.1016/j.bbrc.2019.04.035
Citation  Zhang P, et al. (2019) Knockdown of slincRAD leads to defective adipose development in vivo. Biochem Biophys Res Commun 513(4):983-989
abstractText  The development of adipose tissue is a precisely coordinated cellular process, in which both protein-coding and non-coding genes are involved. To characterize the in vivo function of a novel long non-coding RNA (lncRNAs), loss-of-function assays were performed with slincRAD knockdown mice. Down-regulation of slincRAD expression was found to impair the development of adipose tissue, leading to a slim phenotype for both of the male and female mice. Compared to normal adipocytes, slincRAD knockdown cells had defective differentiation features, such as smaller sizes and decreased lipid production. For elder mice, slincRAD knockdown led to abnormal glucose and lipid metabolism. Therefore, a physiologically important lncRNA was characterized in the development of adipose tissue.
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