Bio-AMS enhances the activity of rifampicin and ethambutol in vitro

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Fig. 1 CSF1 is increased in blood of melanoma patients and correlates with disease progression. CSF1 is increased in blood of melanoma patients and correlates.
LTB4 production is elevated in preclinical and clinical lymphedema
Fig. 2. Effects of AZD4785 on proliferation and MAPK pathway signaling in KRAS mutant and wild-type cancer cells in vitro. Effects of AZD4785 on proliferation.
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Fig. 4. Biomechanical properties of treated tibiae.
JQ1 directly represses the promoter activities of BRCA1 and RAD51
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PVSRIPO-mediated APC activation occurs in immunosuppressive conditions
Fig. 3. Serum HBsAg and liver HBV mRNA reduction in chimpanzees dosed with ARC-520. Serum HBsAg and liver HBV mRNA reduction in chimpanzees dosed with.
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Workflow of a sample-to-answer AST performed in less than 30 min
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Fig. 5 Early and modest immune response at day 3 after exposure in Delayed animals. Early and modest immune response at day 3 after exposure in Delayed.
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Fig. 2. BET inhibition enhances PARPi-induced DNA damage.
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Bio-AMS enhances the activity of rifampicin and ethambutol in vitro
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Fig. 5 Bio-AMS enhances the activity of rifampicin and ethambutol in vitro. Bio-AMS enhances the activity of rifampicin and ethambutol in vitro. (A to E) Impact of Bio-AMS on the activities of the TB drugs rifampicin (A and D), ethambutol (B and E), and isoniazid (C). The Mtb H37Rv strain was grown in standard liquid culture with Bio-AMS (1 μM in DMSO) or DMSO alone for 3 days, after which the bacteria were exposed to the other anti-TB drugs. Data are representative of two independent experiments with three samples per time point. Data are means ± SEM. Divya Tiwari et al., Sci Transl Med 2018;10:eaal1803 Published by AAAS