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7 ne these issues without the complexities of living tissues, we treated cell-free strips of onion epidermal walls with var
8 the production of IL-6 and other proinflammatory cytokines, we treated COVID-19 patients early in the disease with the IL
9 ocellular IL-6 on skeletal muscle mitochondrial physiology, we treated differentiated myotubes with exogenous IL-6 to eva
12 itself might contribute to dysbiosis or immune dysfunction, we treated healthy rhesus macaques with protease, integrase,
15 relationship between ER stress and beta-cell function, here we treated insulin-secreting INS-1(832/13) cells or isolated
16 to asparaginase changes during maturity to adulthood, here we treated juvenile (2-week), young adult (8-week), and matur
17 DL) receptor as a target for cholesterol depleting therapy, we treated lymphoma cell lines known to be sensitive to the r
18 In an attempt to replicate those observations, we treated macaques infected with the same virus and with the
19 or require the synergistic effects of several antibiotics, we treated male APPPS1-21 transgenic mice with either individ
20 To study SCR in vivo in a genome-wide manner, we treated mammalian cells with aminoglycosides and performed
21 To test if inflammation was necessary for this effect, we treated melanoma transplants with nonsteroid anti-inflamma
24 dependent on colony-stimulating factor 1 receptor (CSF1R), we treated mice with a CSF1R inhibitor, PLX5622.
25 if the combination is efficacious in inhibiting metastasis, we treated mice with intracardially inoculated TNBC cells and
28 eficiency impairs mitochondrial respiration/ATP production, we treated mixed-sex embryonic mouse hippocampal neuron cultu
30 al regulators whose suppression accounts for these effects, we treated multiple CRPC cell lines with the BET bromodomain
32 he relationship between macrophages and decorin expression, we treated obese mice with either IgG control or anti-F4/80 a
33 To corroborate these findings in vivo, we treated Parkin knockout mice with simvastatin for 2 wk.
37 ressants impact the molecular composition in these tissues, we treated stress-exposed mice with imipramine and repeated o
38 nvestigate the role of IL-1R signaling pathways during IRI, we treated syngeneic cardiac transplant recipients at 1-hour
40 ut microbiota on diabetes development in this model system, we treated the A22Calpha(-/-)PI2(-/-) NOD mice with enrofloxa
42 In the corresponding theoretical model, we treated the proteins as limited-valence (patchy) particles
47 rstand the role of IL-15 in SIV infection and pathogenesis, we treated two cohorts of SIVmac239-infected rhesus macaques
50 fects of ethanol on early transcripts during embryogenesis, we treated zebrafish embryos with ethanol during pre-gastrula