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In a recent study a CMV DNA load
2020-08-10

In a recent study, a CMV DNA load cut-off of 500 IU/ml in BAL fluid was found to have a positive predictive value of ∼50% for the presence of probable CMV pneumonia (considering a prevalence of this event of 10% among patients at risk and undergoing BAL testing). Tan et al., in contrast, found CMV D
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br Materials and methods br Results br Discussion For many
2020-08-10

Materials and methods Results Discussion For many years, oral PDE5-Is have been prescribed as an on-demand regimen for treating ED. Several studies have reported on the efficacy and safety of such a regimen, with an overall efficacy rate of 60–70% [21]. However, many patients complain of a
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Despite the sources of error discussed above several
2020-08-10

Despite the sources of error discussed above, several trends have emerged and much valuable data are available regarding binding affinities of progestogens for different steroid receptors. All the progestogens bind to the PR with a high affinity, typically in the nanomolar range. For example the syn
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ascorbic acid sale Enlarging the ligand binding pocket by re
2020-08-10

Enlarging the ligand-binding pocket by reduction of the size of the residue F435 switched DES to an agonist indicating that F435 is involved in mediating the antagonistic effect of DES (Fig. 7E) [13]. The conformation of the smaller side chain of L435 was either not altered by DES or was too small t
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DL-TBOA Furan analogs and N methylpyrrole analogs had comple
2020-08-10

Furan analogs and N-methylpyrrole analogs had completely different SARs. For example, replacement of the furan-2-sulfonyl moiety of 6 with the furan-3-sulfonyl moiety resulted in 8 with a decreased EP1 DL-TBOA affinity and an increased antagonist activity, while the corresponding chemical modificat
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340 7 Enzyme mimics belong to a type
2020-08-10

Enzyme mimics belong to a type of rising catalysts which show the similar function with their corresponding natural enzymes [20], [21], [22], [23], [24], [25], [26], [27], although their structures are different from natural enzymes. In the area of prodrug activation, the widely-used enzyme mimics a
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Simulation methods In our study
2020-08-10

Simulation methods In our study, the TIP3P model is applied for water, AMBER99sb force field [24] is used to describe three types of EGFR, including the wild type (PDB: 2ITY) [25], its mutant G719S (PDB: 2ITO) [25] and mutant T790M (PDB: 3IKA) [26]. The force field of Tubemoside molecule is paramet
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Peficitinb br Progestogens and venous thromboembolism
2020-08-08

Progestogens and venous thromboembolism: clinical data Progestogens and haemostatis: biological studies For many years, the effect of HT on haemostatis has been largely investigated in observational studies as well as in high evidence level studies among users of oral and transdermal estrogens
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br Introduction When women reach the menopause they experien
2020-08-08

Introduction When women reach the menopause they experience a number of physical complaints such as hot flushes, vaginal dryness and mood changes [1]. Bone loss also becomes manifest at this time [1], [2], but women will often not suffer from back pain before a vertebral fracture occurs. Women wh
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It is interesting to note that
2020-08-06

It is interesting to note that Ciclopirox synthesis our results show a very similar behavior in binding of DDR2 ECD to immobilized a-telo (bovine-dermal) versus telo- (rat-tail) collagen I as a function of its oligomeric state. Thus, the telopeptide region of tropocollagen exerts little influence o
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In the functional assay measuring inhibition of PGD mediated
2020-08-06

In the functional assay measuring inhibition of PGD2-mediated GTPγS binding, LAS191589 depressed the agonist binding capacity producing a progressive reduction of maximal response at 2h of incubation that was observed even after 22h of incubation time therefore showing a clear functional insurmounta
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Tetrahydroquinoline discovered in a high throughput screen i
2020-08-06

Tetrahydroquinoline (), discovered in a high throughput screen, inhibited the binding of H-PGD to hCRTH2 receptors on 293 cells with an IC of 0.043μM (). Compound also inhibited CRTH2 mediated cell migration in response to PGD with an EC of 11nM using hCRTH2 stably transfected CEM cells. The struc
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As indicated in the Introduction several research groups
2020-08-06

As indicated in the Introduction, several research groups reported that the CRF2 knockout mouse exhibits alterations in anxiety behavior [2], [9], [27]. However, the direction of the behavioral alterations was not always consistent across laboratories. Although the present results do not reconcile t
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Defactinib synthesis br Methods and materials br Results
2020-08-06

Methods and materials Results Discussion The data reported herein establishes that the human CRF2(a) receptor is stringently regulated by a rapid and strong desensitization mechanism following activation by the urocortins or related stresscopin peptides but not CRF. Furthermore, UCN2 and UC
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The chemokine receptor CXCR plays a
2020-08-05

The chemokine receptor CXCR5 plays a significant role in CLL/SLL pathogenesis. The receptor protein has been identified on greater than 90% of patient samples [3], [4], [10], [72] and shown not to be affected by IGHV mutation status [90]. Depending on the study, CXCR5 protein was either similarly ex
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