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Drug resistance to both pathogens and cancer has been a
2021-06-02
Drug resistance to both pathogens and cancer has been a big hindrance in healthcare. Integrated research undertakings are being pursued to find the exact causes of the lack of response towards drugs. Surprisingly, host pumps are the key factors in failure of most drugs. The pumps either do not allow
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br Early developments Historically the advent of SMEPT
2021-06-02
Early developments Historically, the advent of SMEPT can be traced to the 1980′s, where the first example of localized prodrug conversion was achieved using a judiciously placed enzyme – in order to achieve a localized feed of 5-fluorouracil (5-FU). Immobilization of E. coli-derived cytosine deam
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br Experimental section br Acknowledgments
2021-06-02
Experimental section Acknowledgments MIN6 cells were kindly provided by Dr. Junichi Miyazaki, Osaka University. This research was supported in part by the Ministry of Education, Culture, Sports, Science and Technology of Japan (JP16H05099 and JP18H04609 to K.H., and JP16H06574 to T.U.), SENTAN
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br Experimental procedures br Acknowledgments br Introductio
2021-06-01
Experimental procedures Acknowledgments Introduction Receptor tyrosine kinases (RTKs) control many fundamental cellular processes, such as cell proliferation, differentiation, migration, and metabolism (Lemmon and Schlessinger, 2010). RTK activity is normally tightly controlled, and dysregu
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Ubiquitination is a reversible posttranslational modificatio
2021-06-01
Ubiquitination is a reversible posttranslational modification. The removal of Ub is carried out by enzymes known as deubiquitinases (DUBs). The antagonistic role played by these enzymes in the Ub pathway regulates the function of the ubiquitinated proteins, while maintaining the free Ub pool in euka
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To determine whether the same concentration of humic
2021-06-01
To determine whether the same concentration of humic Lauric Acid synthesis causes changes in PCR efficiency, we performed another experiment in which the humic acid was added to the PCR mix after bisulfite conversion. All samples that were amplified in the presence of humic acid (thick lines) show
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Acknowledgments We acknowledge the Danish Council for Indepe
2021-06-01
Acknowledgments We acknowledge the Danish Council for Independent Research (Grant no. 11-105250) and the Carlsberg Foundation (Grant no. 2011-01-0567) for funding this work. Introduction DNA is vital as a biological target to design diagnostic agents as well as therapeutic drugs. The recognitio
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In contrast to DDR the role of
2021-06-01
In 3'-Azido-3'-deoxythymidine β-D-glucuronide sodium salt to DDR1, the role of oligomerization and/or clustering of DDR2 in mediating its interactions with collagen is less understood. Current data show that in DDR2, like in DDR1, (i) dimerization [7] and higher-order oligomerization of its ECD [11
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br Materials and methods br Results br Discussion Although
2021-06-01
Materials and methods Results Discussion Although no increase in DAPK activity was detected at early time points associated with neuronal apoptosis, it is possible that the spread of apoptosis through the ion channel following HI is not synchronized enough to yield a large, consistent fluc
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Substitutions on the benzene ring of the phenyl
2021-06-01
Substitutions on the benzene ring of the phenyl acetic HQNO receptor moiety were evaluated to study their effect on DP and CRTH2 selectivity (). Compound has strong affinity for CRTH2, but it only has moderate affinity for DP. Small substitutions such as methoxy () and fluorine () next to the arylox
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Notochord is a transient structure differentiating
2021-06-01
Notochord is a transient structure differentiating at early stage during embryogenesis that is at the origin of vertebral bodies in all vertebrates. In zebrafish, it is composed of vacuolated XEN445 surrounded by a unique ECM structure improperly called notochordal BM. As in chicken and amphibians,
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Pomalidomide Hymenialdisine the most potent inhibitor of par
2021-06-01
Hymenialdisine, the most potent inhibitor of parasite TgCK1 enzymes in vitro has no whole cell anti-parasitic activity (Table 2). Like purvalanol B however, this Pomalidomide also displays poor activity against target enzymes in cultured cells. For example, in vitro IC50 values for inhibition of CDK
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No effect on the A production
2021-06-01
No effect on the Aβ production by γ-secretase was observed at 50μM, the highest effective concentration used in cultured PF-431396 by the study of Flajolet et al. IC261 did also not exert a modulatory effect on the production of Aβ, Aβ and Aβ species in the cell-free assay at this concentration. γ-
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MK-8245 The four other mutations S T
2021-06-01
The four other mutations (S281T, V317I, T328A and A329S) were not detected in the absence of the A286S. This could suggest that when all of them are present, there would be a tri-dimensional structural modification that would interfere with the binding of the insecticide and produce different levels
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br Methods and materials br Results br Discussion Many
2021-05-31
Methods and materials Results Discussion Many small molecules have been individually explored to enhance endothelial barrier both in vitro and in vivo, including S1P, forskolin, cAMP analogs, ROCK inhibitors, statins, and imatinib [[10], [11], [12],25,26]. In the current study, we applied t
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