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5(S),6(R)-7-trihydroxymethyl Heptanoate The requirement of t
2020-08-05
The requirement of the E2-SUMOB interaction for E3 activity can be tested in vitro by employing a SUMO or E2 mutant which are specifically impaired in this interaction: SUMO2 D62R abolishes, and E2 F22A weakens this particular interaction (Capili & Lima, 2007; Knipscheer et al., 2007). Here we show
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The UPP broadly involves proteolysis in biochemical processe
2020-08-05
The UPP broadly involves proteolysis in biochemical processes and is a potential target for cancer therapy. The UPP degrades unfolding or damaged proteins by an ATP-dependent mechanism (Ciechanover, Elias, Heller, Ferber, & Hershko, 1980). It also plays an important role in fk506 sale regulation, D
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br Dihydroorotate dehydrogenase DHODH Pyrimidines
2020-08-05
Dihydroorotate dehydrogenase (DHODH) Pyrimidines are obtain by the cells either through de novo in which ammonia acts as a starting material (derived from L-glu), bicarbonate, and L-asp, or by salvaging preformed pyrimidine bases (uracil, cytosine and thymine) or nucleosides (uridine, thymidine a
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The binding of collagen X
2020-08-05
The binding of collagen X to DDR2 differs from the binding of collagen X to α2β1 integrin in that the triple helical conformation is essential for DDR2 binding. We previously reported that heat denatured pepsinised collagen X supported cell adhesion via α2β1, indicating that the triple-helical confo
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In rats exposed to days of nicotine treatment h after
2020-08-05
In rats exposed to 7 days of nicotine treatment (12 h after the last nicotine administration) we observed increases in horizontal and vertical locomotor activity along with increases in the dorsal and ventral striatal dopamine release. This finding is in line with previous studies which reported loc
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After repeated intermittent exposure to
2020-08-05
After repeated, intermittent exposure to a psychostimulant an augmentation of drug response to motor activity is commonly observed, a phenomenon known as behavioral sensitization (Kalivas and Stewart, 1991, Steketee and Kalivas, 2011). On the other hand, several reports have pointed out that stress
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Each of these substrate receptors belongs to a multigene fam
2020-08-05
Each of these substrate receptors belongs to a multigene family with tens, if not hundreds of members in plants, and with in part overlapping and in part differential substrate specificities [4]. The complexity of the system is nicely illustrated by the F-box protein and auxin receptor TRANSPORT INH
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The only reported synthesis of the aminobicyclic core of
2020-08-04
The only reported synthesis of the aminobicyclic core of is based on bis-alkylation of a 4-amino-5,6-dihydroxypyrmidine with dibromoethane. The likelihood of poor regiocontrol/reactivity in utilizing such a transformation for the synthesis of compounds with a substituent on the dioxinyl ring led us
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We did not performed MD simulations of the GAPDH interaction
2020-08-04
We did not performed MD simulations of the GAPDH interaction with α-synuclein modified by glyceraldehyde-3-phosphate since the products are unclear [38], and phosphate group might split off because of lability of the connection bond. Carboxymethyl lysine was chosen since it is considered to be the m
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Lomustine Both anxiogenic and antinociceptive effects produc
2020-08-04
Both anxiogenic and antinociceptive effects produced by CRF seem to be selective for the CRF1 receptor, since intra-dPAG microinjection of ASV 30, a CRF2 receptor antagonist, altered neither the anxiety nor the antinociception response. Intra-dPAG ASV 30 was also unable to prevent the anxiogenic (ob
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Studies have shown that the dopaminergic
2020-08-04
Studies have shown that the dopaminergic system modulates working memory performance through the striatal-frontal pathway (e.g., Cools et al., 2007) and age changes in frontal lobe dopamine systems are responsible for cognitive aging (Braver and Barch, 2002). One mechanism by which this age-related
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Cyclosporine NEORAL Oral Solution Novartis is an immunosuppr
2020-08-04
Cyclosporine (NEORAL® Oral Solution, Novartis) is an immunosuppressant widely used in organ transplantation and many other clinical conditions [12]. It undergoes extensive hepatic and intestinal biotransformation mainly via the metabolizing enzyme, CYP3A4 [[12], [13], [14], [15]]. Considering the na
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In addition the kidney is
2020-08-04
In addition, the kidney is also capable of actively metabolizing many drugs, hormones and xenobiotics [4], [5], [6], [7]. Several compounds are known to be activated locally by renal biotransformation processes. For example, in male mice, chloroform, acetaminophen and 1,1-dichloroethene are bioactiv
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NTZ treatment is associated with an increased risk of
2020-08-04
NTZ treatment is associated with an increased risk of progressive multifocal leukoencephalopathy (PML), due to John Cunningham (JC) virus reactivation or infection (McGuigan et al., 2016). Because T cells are important for Moxidectin australia immune surveillance (Dubois et al., 2015), an increase
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The roles of ginsenoside in E and S proteasome inhibition
2020-08-04
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 (Unger
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