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The main function of ATR CHK signaling is activating cell
2023-11-24

The main function of ATR/CHK1 signaling is activating metalloproteinase checkpoint arrest for S and G2 phases in mammalian cells. There are three checkpoints in response to DNA damage: G1/S, G2/M, and S-phase. The G2/M checkpoint can prevent cells that incur DNA damage in G2 phase or progress into
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We further evaluated the possibility
2023-11-24

We further evaluated the possibility whether letrozole mediates its effect through diverting the pathway towards 5α-DHT and further to 3α-Diol. For this purpose, we measured the concentrations of 5α-DHT and 3α-Diol in mice hippocampus and found that letrozole elevated both 5α-DHT and 3α-Diol levels
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The first and the best characterized mechanism of
2023-11-24

The first and the best-characterized mechanism of receptor-dependent internalization of Aβ is mediated via the α7-nicotinic SR 59230A hydrochloride receptor [82]. Lipoprotein receptor protein represents the second best-studied route that facilitates the uptake of Aβ by neurons, involving additional
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MAPs require divalent transition metal ions
2023-11-24

MAPs require divalent transition metal ions as cofactors for activity [21]. Previous studies on MAPs from different organisms indicate cobalt ions to be the most preferred divalent metal activator [22]. However, MAPs also exhibit activity with other divalent cations like Mn(II), Ca(II), Ni(II) or Fe
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br Materials and met http www apexbt com media diy
2023-11-24

Materials and methods Results The values for body weight are shown in Fig. 1. Body weight was measured every day. The body weight of the young mice in the control (i.e. no-stress) group was not significantly different from that of the young mice in the stress group. However, the middle-aged mi
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Another issue is that the vast majority of data from
2023-11-24

Another issue is that the vast majority of data from PET and CSF are from selected participants recruited through tertiary care dementia centers [176]. It is widely recognized that clinic-based participants differ from community-based studies, for example, the amount, type, and distribution of neuro
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Various compounds have been designed to inhibit aldose
2023-11-24

Various compounds have been designed to inhibit aldose reductase (AR) [12]. These compounds can be classified into two main categories, the first category comprises those containing a carboxylic EGTA moiety, for example, 3-thiazolidineacetic acid derivative, which has been reported to be a potent AR
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br Acetaldehyde One of the most
2023-11-24

Acetaldehyde One of the most common environmental aldehydes is acetaldehyde (CH2CHO). Acetaldehyde, which is highly volatile, has been classified as a Group I human carcinogen by the International Agency for Research on Cancer [30]. Aldehydes can form DNA adducts, including ring-open forms of cro
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The cavity volume of the binding pocket may
2023-11-24

The cavity volume of the binding pocket may differ not only between species but also among various AhR/ARNT isoforms within a single species. It is noteworthy that even a single amino GDC-0994 substitution within a binding pocket may result in a change in the cavity volume. This, in turn, may affec
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Z-Guggulsterone Adiponectin is an adipokine whose circulatin
2023-11-24

Adiponectin is an adipokine whose circulating level is depleted in a number of metabolic diseases including insulin resistance, diabetes and cancer (Khan et al., 2015, Singh et al., 2014a, Singh et al., 2014b, Yamauchi et al., 2014). Despite its importance in health and pathophysiology, adiponectin
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br ACh and ER tests hereafter Spasm provocation tests have
2023-11-24

ACh and ER tests hereafter Spasm provocation tests have self-limitations to document coronary artery spasm during daily life. In the past reports, ST elevation was reproducible in some patients with variant Fenretinide by the administration of ACh or ER. However, we now employ the ER and ACh spas
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In an effort to determine if one ARI
2023-11-24

In an effort to determine if one 5ARI was more effective than the other, the Enlarged Prostate International Comparator Study (EPICS) [17] compared treatment with finasteride and dutasteride in 1630 men over the age of 50 and concluded that after one year of treatment, both groups had statistically
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br Conflict of interest br Acknowledgements We
2023-11-23

Conflict of interest Acknowledgements We thank Ann Jackman, Mike Ormerod and members of Julian Downward's and Alan Ashworth's groups for helpful discussions. This work was supported by grant number PEM/GME/D391/40 from the Kidani Trust (S. Kaye) and by Keele University. Introduction Autota
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Another topic for research will be the combination of
2023-11-23

Another topic for research will be the combination of other cytotoxic agents with Aurora kinase inhibitors. Particularly interesting might be the combination of Aurora kinase inhibitors and agents that depend on the spindle checkpoint for their activity, such as the taxanes, given the importance of
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CHK has been reported to be the kinase responsible
2023-11-23

CHK1 has been reported to be the kinase responsible for H3.3S31 phosphorylation in human ALT cancer Ginkgolic Acid C15:1 . However, in our study, knockdown of CHK1 in HEK293F (Figs. S1c and S6) or HeLa S3 (data not shown) cells did not result in a significant decrease in H3.3S31ph, which is in agre
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