Lv7
3580 积分 2020-10-24 加入
Qingjin Huatan decoction protects mice against influenza a virus pneumonia via the chemokine signaling pathways
1个月前
已完结
Zuogui pills maintain the stemness of oogonial stem cells and alleviate cyclophosphamide-induced ovarian aging through Notch signaling pathway
1个月前
已完结
Natural products targeting the gut-brain axis for the treatment of post-cardiac procedures anxiety or depression
1个月前
已完结
Targeting ferroptosis in the treatment of ulcerative colitis by traditional Chinese medicine: A novel therapeutic strategies
1个月前
已完结
Global, regional, and national burden of chronic respiratory diseases and impact of the COVID-19 pandemic, 1990–2023: a Global Burden of Disease study
1个月前
已完结
Melatonin alleviates rheumatoid arthritis by promoting Src/Fundc1-mediated mitophagy to regulate macrophage polarization
1个月前
已完结
Fenofibrate inhibits activation of cGAS-STING pathway by alleviating mitochondrial damage to attenuate inflammatory response in diabetic dry eye
2个月前
已完结
Ceramides increase mitochondrial permeabilization to trigger mtDNA-dependent inflammation in astrocytes during brain ischemia
2个月前
已完结
A methionine-choline-deficient diet induces nonalcoholic steatohepatitis and alters the lipidome, metabolome, and gut microbiome profile in the C57BL/6J mouse
2个月前
已完结
Differentiation and Polarization of THP-1 Cells into M1 and M2 Macrophages for Cancer Research
2个月前
已完结
酪氨酸酶基因在HEK293细胞表达的MRI评价
7个月前
已采纳
防止再造外耳道再闭锁与狭窄的新策略和方法
7个月前
已采纳
Preliminary application of the Radimetrics system in CT radiation dose evaluation
7个月前
已采纳
[A novel mutation of the LYST gene in a Chinese family with Chediak-Higashi syndrome]
7个月前
已采纳
[Mutations of the STK11 and FHIT genes among patients with Peutz-Jeghers syndrome]
7个月前
已采纳
[Analysis of SLC39A4 gene mutation in a patient with acrodermatitis enteropathica]
7个月前
已采纳
SIS3逆转多药耐药肝癌细胞的干性作用
7个月前
已采纳
Clinical researches of coenzyme Q10 in diabetes mellitus
7个月前
已采纳
[Clinical and mutation analysis of a Chinese family with muscle eye brain disease]
7个月前
已采纳
[Analysis of phenotypes and genetic mutations in two pedigrees affected with hereditary protein C deficiency]
7个月前
已采纳
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