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Aleksandra Strokach,Polina Zoruk,Daria Boldyreva et al. Aleksandra Strokach et al.
This study systematically evaluates these factors in mouse gut microbiota analysis, comparing 16S rRNA gene sequencing and metagenome sequencing (MS) across both platforms.
Yutong Zhang,Jingyi Liu,Xiaoai Chen et al. Yutong Zhang et al.
Although resistant starch (RS) isolated from raw starch exhibits established regulatory effects on the mouse gut microbiota and associated hyperlipidemia, critical questions persist regarding RS in heated foods - the predominant form in the human diets, namely, the role of RS from heated food in the
Xinqi Fan,Yingjun Zhou,Wenjuan Bai et al. Xinqi Fan et al.
Here we report an in vivo fluorogenic labeling method, which enables in situ imaging of mouse gut microbiota and real-time tracking of the translocated bacteria.
Joon-Ha Lee,Hyojung Son,Sathiyamoorthy Subramaniyam et al. Joon-Ha Lee et al.
The increasing global population and the environmental consequences of meat consumption have led to the exploration of alternative sources of protein. Edible insects have gained attention as a sustainable and nutritionally rich meat alterna...
Huibin Lin,Xinying Zheng,Liyuan Lin et al. Huibin Lin et al.
In vivo labeling revealed that ∼13.7% of the mouse gut microbiota (mostly Gram-positive) was selectively labeled. We then identified Oscillibacter and several other Gram-positive genera in this population, most of which were previously unknown m-DAP-type bacteria.
Yu-Han Lin,Wei-Shiung Lian,Re-Wen Wu et al. Yu-Han Lin et al.
Notably, transplantation of mouse gut microbiota counteracts obesity- or estrogen deficiency-induced TMAO overproduction and mitigates key features of osteoporosis. Mechanistically, excessive TMAO intake augments bone mass loss by inhibiting bone mineral acquisition and osteogenic differentiation.
Jie Zhang,Ming Guan,Suling Wu et al. Jie Zhang et al.
In addition, 16S rRNA sequencing and ultra-performance liquid chromatography-tandem mass spectrometry were used to detect the changes in the mouse gut microbiota and serum metabolites.
Dandan Yi,Xia Liu,Menghui Wang et al. Dandan Yi et al.
Moreover, RA relieved the increase in intestinal permeability, reversed the structural damage to the mouse gut microbiota caused by E. coli, and increased the abundance of beneficial bacteria, including Lachnospiraceae_NK4136_group.
Manjin Xu,Huixia Niu,Lizhi Wu et al. Manjin Xu et al.
Furthermore, the composition and diversity of the mouse gut microbiota were significantly altered following microplastic exposure, with 11 gut genera exhibiting a differential presence between mice fed a high-fat diet combined with microplastic exposure compared to those fed a normal diet with microplastic
Xianzhang Zeng,Can Ma,Wenchao Fu et al. Xianzhang Zeng et al.
Fecal 16SrRNA sequencing indicated that T1D mice and mice with transplantation of T1D mouse gut microbiota had lower relative abundance of butyric acid producers, f_Erysipelotrichaceae and g_Allobaculum, and lower content of butyric acid in feces.
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