Additional file 6: of Transcriptional analysis of abdominal fat in chickens divergently selected on bodyweight at two ages reveals novel mechanisms controlling adiposity: validating visceral adipose tissue as a dynamic endocrine and metabolic organ
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https://figshare.com/articles/dataset/Additional_file_6_of_Transcriptional_analysis_of_abdominal_fat_in_chickens_divergently_selected_on_bodyweight_at_two_ages_reveals_novel_mechanisms_controlling_adiposity_validating_visceral_adipose_tissue_as_a_dynamic_endocrine_and_metabolic_organ/5318737
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资源简介:
Top pathways and biological functions identified by IPA from time-course microarray analysis of abdominal fat in HG and LG cockerels (1-11 wk). A Microsoft Excel file containing eight worksheets [i.e., “Upstream Regulators, Oxidative Phosphorylation, LXR/RXR Activation, Fatty Acid Metabolism, Adipogenesis Pathway, Insulin Resistance, VEGF Signaling, and Protein Metabolism”]. Top canonical pathways and biological functions were identified by Ingenuity Pathway Analysis (IPA) of 647 “Analysis Ready” (AR)-DE genes (FDR ≤ 0.05) from time-course (1-11 wk) microarray analysis. (XLSX 49 kb)
本数据集源自对高生长(HG)与低生长(LG)公鸡1~11周龄腹部脂肪的时序微阵列分析,经Ingenuity通路分析(Ingenuity Pathway Analysis)鉴定得到核心经典通路与生物学功能。本数据集以Microsoft Excel文件形式存储,内含8个工作表,分别为:上游调控因子(Upstream Regulators)、氧化磷酸化(Oxidative Phosphorylation)、LXR/RXR激活(LXR/RXR Activation)、脂肪酸代谢(Fatty Acid Metabolism)、成脂通路(Adipogenesis Pathway)、胰岛素抵抗(Insulin Resistance)、VEGF信号通路(VEGF Signaling)以及蛋白质代谢(Protein Metabolism)。本次分析的基因集为647个经时序(1~11周龄)微阵列分析得到的「分析就绪(Analysis Ready, AR)」差异表达基因(differentially expressed genes, DE genes),其错误发现率(False Discovery Rate, FDR)≤0.05,通过上述分析鉴定得到核心经典通路与生物学功能。本数据集文件格式为XLSX,大小为49 KB。
创建时间:
2017-08-17



