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The analysis of progression from autoantibody positivity to
2020-07-30
The analysis of progression from autoantibody positivity to clinical disease is in essence measuring the rate of this progression as long-term follow-up results indicate that close to all of the children testing positive for two or more autoantibodies progress to clinical disease within 15–20 years
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Darifenacin HBr Although there was little to no expression
2020-07-30
Although there was little to no expression change observed by TELI of the recA and ruvA genes upon CAA exposure, other specific repair pathways were induced by both CAA and SO and include the SOS-inducible gene sulA, the DNA repair gene ykfG, the mismatch repair gene mutS, the recombination and repa
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Several antimalarial drugs in clinical studies target pyrimi
2020-07-30
Several antimalarial drugs in clinical studies target pyrimidine nucleotide biosynthesis , because parasites rely on fast and large replication of DNA to infect during liver and blood stages. Dihydroorotate dehydrogenase (DHODH) catalyzes the oxidation of -dihydroorotate (L-DHO) to -orotate in the
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As a measure of target
2020-07-30
As a measure of target inhibition in vivo, a triglyceride tolerance test in mice was carried out with . Since DGAT-1 is highly expressed in the small intestine and catalyzes the rate determining step in triglyceride synthesis, co-dosing of an inhibitor with an oral Azaperone australia of lipid prov
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Predictions of enzyme topology for DGAT are more
2020-07-30
Predictions of enzyme topology for DGAT2 are more difficult since the DGAT2 polypeptide sequences are more diverse across species than those of DGAT1. The length and function of the hydrophilic N-terminus preceding the first hydrophobic segment varies with species – for example, segments in fungi ar
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Until now several CYP genes are identified in human CYPs
2020-07-30
Until now, several CYP genes are identified in human (57 CYPs), mouse (108 CYPs), nematode (75 CYPs, Caenorhabiditis elegans), sea urchin (120 CYPs, Strongylocentrotus purpuratus), water flea (83 CYPs, Daphnia magna), and yeast (2–3 CYPs) (Nelson, 2013). In the phylum Ciliophora which is one of the
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br Acknowledgement AM and SK thank ICMR New
2020-07-30
Acknowledgement AM and SK thank ICMR, New Delhi, India for the financial assistance BIC/12(32)/2012. SK is the recipient of JRF from the project. RK and GJ thank Bristol-Myer Squibb (Grant # 34003085), USA for financial support. Introduction Proliferating Cell Nuclear Antigen (PCNA) is a high
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The phenomenon of SIRT phosphorylation was
2020-07-30
The phenomenon of SIRT6 phosphorylation was first reported by Thirumurthi et al. They found that SIRT6 was phosphorylated at Ser (338) by the kinase AKT1, which induced the interaction and ubiquitination of SIRT6 by MDM2, targeting SIRT6 for protease-dependent degradation in various breast cancer ce
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Several different information items can be recommended to su
2020-07-30
Several different information items can be recommended to support the software engineer in his/her task according to his/her needs. These items types include source code within a project, reusable source code, code examples, operations and people (Robillard et al., 2014). We witness several works on
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br Acknowledgements The present work was funded by National
2020-07-30
Acknowledgements The present work was funded by National Natural Science Foundation of China (No. 816712276 and No. 81771147), Natural Science Foundation of Shandong Province (ZR2016HM30), Medical and Health Development Program of Shandong Province (2016WSB33025), 2015 Science and Technology Deve
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Classical DHFR inhibitors such as methotrexate MTX bind tigh
2020-07-29
Classical DHFR inhibitors such as methotrexate (MTX) bind tightly to the enzyme and possess adequate clinical pharmacokinetics. MTX bind to the DHFR binding site through the formation of hydrogen bonds with Asn64, Lys68, Arg28, Arg70, Val115 and Ile7 amino tranylcypromine residues as well as hydrop
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In conclusion MEN behave as
2020-07-29
In conclusion, MEN91507 behave as a potent and selective CysLT1antagonist in guinea-pigs and human in vitro assays. In vivo, MEN91507 shares with the other CysLT1 antagonists anti-bronchospastic and anti-inflammatory effects; since these effects are long-lasting and are also observed following the o
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2 deoxy d glucose In the present study we isolated a
2020-07-29
In the present study, we isolated a full-length GluCl cDNA (named as CsGluCl) from C. suppressalis. We report the expression patterns of three CsGluCl variants and document the role of CsGluCl in abamectin toxicity and C. suppressalis development. Our results are pivotal to the discovery of new chem
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The roles of ginsenoside in
2020-07-28
The roles of ginsenoside in E1 and 26S proteasome inhibition are shown in Table 2. The nitro substitute on the furan ring may be important for PYR-41 inhibition of the E1 enzyme (Yang et al., 2007). The macrocycle core and aliphatic tail of Largazole are responsible for inhibiting E1 activity (Unge
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The CysLT receptor is highly expressed
2020-07-28
The CysLT1 receptor is highly expressed in the lung, which may be relevant for its implication in pulmonary diseases like asthma. In fact, specific antagonists of the CysLT1 receptor (pranlukast, montelukast and zafirlukast) are used in the clinic to control bronchoconstriction and inflammation in a
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