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Changes in gene expression in primary human white preadipocytes in response to knockdown of DPP4

ChEBI2015-11-24 更新2026-07-12 收录

脂肪代谢调控

DPP4基因功能研究

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-75328 数据链接链接失效反馈

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Changes in gene expression in primary human white preadipocytes in response to knockdown of DPP4

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创建时间：

2015-11-24

脂肪代谢调控

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Table3_Genetic association-based functional analysis detects HOGA1 as a potential gene involved in fat accumulation.XLSX

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Although there are a number of discoveries from genome-wide association studies (GWAS) for obesity, it has not been successful in linking GWAS results to biology. We sought to discover causal genes fo

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The GIP receptor activates futile calcium cycling in white adipose tissue to increase energy expenditure and drive weight loss in mice

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Obesity is a chronic disease that contributes to the development of insulin resistance, type 2 diabetes (T2D), and cardiovascular risk. GIP receptor (GIPR) and GLP-1 receptor (GLP-1R) co-agonism provi

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Functional study and epigenetic targets analyses of SIRT1 in intramuscular preadipocytes via ChIP-seq and mRNA-seq

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The SIRT1 epigenetic regulator is involved in hepatic lipid homoeostasis. However, the role of SIRT1 in regulating intramuscular fat deposition as well as the pathways and potential epigenetic targets

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Detailed genotypes.

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Knowledge of adipogenetic mechanisms is essential to understand and treat conditions affecting organismal metabolism and adipose tissue health. In Drosophila, mature adipose tissue (fat body) exists i

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Changes in gene expression in primary human white preadipocytes in response to knockdown of DPP4

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