Ontology highlight
ABSTRACT:
INSTRUMENT(S): Q Exactive
ORGANISM(S): Homo Sapiens (human)
SUBMITTER: Rongli Zhao
LAB HEAD: Junhua Li
PROVIDER: PXD013452 | Pride | 2019-09-11
REPOSITORIES: Pride
Action | DRS | |||
---|---|---|---|---|
meta_rep1.dat | Other | |||
meta_rep1.mgf | Mgf | |||
meta_rep1.mzid.gz | Mzid | |||
meta_rep1.pride.mgf.gz | Mgf | |||
meta_rep1.pride.mztab.gz | Mztab |
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Zhong Huanzi H Ren Huahui H Lu Yan Y Fang Chao C Hou Guixue G Yang Ziyi Z Chen Bing B Yang Fangming F Zhao Yue Y Shi Zhun Z Zhou Baojin B Wu Jiegen J Zou Hua H Zi Jin J Chen Jiayu J Bao Xiao X Hu Yihe Y Gao Yan Y Zhang Jun J Xu Xun X Hou Yong Y Yang Huanming H Wang Jian J Liu Siqi S Jia Huijue H Madsen Lise L Brix Susanne S Kristiansen Karsten K Liu Fang F Li Junhua J
EBioMedicine 20190903
<h4>Background</h4>The gut microbiota plays important roles in modulating host metabolism. Previous studies have demonstrated differences in the gut microbiome of T2D and prediabetic individuals compared to healthy individuals, with distinct disease-related microbial profiles being reported in groups of different age and ethnicity. However, confounding factors such as anti-diabetic medication hamper identification of the gut microbial changes in disease development.<h4>Method</h4>We used a combi ...[more]