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The mechanism of protein degradation mediated by ubiquitin h
2020-08-05
The mechanism of protein degradation mediated by ubiquitin has been well studied; meanwhile, there are growing evidences that reveal the non-proteolytic roles of ubiquitin modification. Deubiquitination counteracts the ubiquitin cascade, including inhibiting E2 ubiquitin conjugating hippo signaling
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We next examined the possibility that the
2020-08-05
We next examined the possibility that the hepatic CYP3A expression level was decreased via an indirect effect of EGCG. Previously, it has been reported that EGCG suppressed the growth of intestinal bacteria of Clostridium spp., which are involved in the production of secondary bile acids (Okubo et a
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Its auto inhibited structure contain N
2020-08-05
Its auto-inhibited structure contain N-terminus packed between residues of the glycine-rich loop, the activation loop and the αC helix. Both its N and C termini wrapping around the αC helix and the JM domain adopts a twisted hairpin conformation (Fig. 2.1B). The exclusive and unphosphorylated tyrosi
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Previous studies have shown the harmful effects of
2020-08-05
Previous studies have shown the harmful effects of NEFA on ovarian functionality, such as inhibition of bovine granulosa cell survival and proliferation, steroidogenesis, and follicular development and alteration in oocyte development [36,45,46]. Therefore, the higher levels of NEFA found in the fol
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ApoBrdU DNA Fragmentation Assay Kit The results of our study
2020-08-05
The results of our study demonstrated that HSL activation by kinsenoside-mediated PKA activation was coordinated with perilipin phosphorylation and facilitated efficient lipolysis, resulting in increased glycerol release and decreased lipid accumulation. The localization and interplay of perilipin a
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QNRF grant number NPRP Qatar National
2020-08-05
QNRF grant number NPRP6-065-3-012, Qatar National Research Fund, Doha Qatar for funding this work with grant number NPRP No.: NPRP6-065-3-012. Introduction Preeclampsia (PE) affects 3–5 % of pregnancies worldwide and is one of the leading causes of maternal and fetal morbidity and mortality [1].
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In this regard some attempts have been made to reduce
2020-08-05
In this regard, some attempts have been made to reduce the presence of those radicals. In presence of fluorine source, it seems that the fluorine atoms can substitute the hydrogen atoms linked to silicon atoms, forming Si-F bonds with a higher bonding Oltipraz australia (536 kJ mo1−1) than the Si-H
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There were tumors with EWS
2020-08-05
There were 72 tumors with EWS-FLI1 transcripts: 44 type 1 fusions and 28 grouped into the non-type 1 group. Fourteen tumors had EWS-ERG fusions. Patients having EWS-FLI1 fusions had similar age, stage at diagnosis, and tumor volume with respect to those bearing EWS-ERG fusion NHS-12-Biotin (results
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Another emerging approach is the
2020-08-04
Another emerging approach is the live cell imaging, tracking the behavior of the fluorescently labeled proteins after laser micro irradiation [2]. Mari et al. demonstrated that the accumulation of XRCC4 in irradiated area was dependent on Ku but not on DNA-PKcs [23]. Yano et al. showed that the accu
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Death associated protein kinase DAPK a known apoptosis
2020-08-04
Death-associated protein kinase (DAPK), a known apoptosis regulator, is shown to be up-regulated in atherosclerotic lesions (Arab et al., 2008). DAPK up-regulation leads to increased cell turnover and arterial wall instability, which provides increase susceptibility to LDL GDC-0349 (Schumacher et al
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To the best of our
2020-08-04
To the best of our knowledge, this is the first report on the effect of chronic SSRI treatment on the acquisition and Cladribine of fear-potentiated startle in rodents. The lack of effect on expression of cued fear is in line with the single human fear-potentiated startle study available (Grillon e
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Tylosin tartrate The reference standards methyl difluoro dio
2020-08-04
The reference standards methyl 3-((2,2-difluoro-5-[1,3]dioxolo[4′,5′:4,5]benzo[1,2-]imidazol-6-yl)carbamoyl)benzoate () and -(2,2-difluoro-5-[1,3]dioxolo[4′,5′:4,5]benzo[1,2-]imidazol-6-yl)-3-methoxybenzamide (), and their corresponding desmethylated precursors 3-((2,2-difluoro-5-[1,3]dioxolo[4′,5′:
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Udenafil Zydena Dong A Seoul Korea a recently
2020-08-04
Udenafil (Zydena®; Dong-A, Seoul, Korea), a recently developed selective PDE-5I, showed promising pharmacokinetic characteristics for use in a once-daily strategy with a peak plasma concentration at 0.8–1.3 hours, which then declines monoexponentially with a HC-030031 (T1/2) ranging from 9.9 to 12.
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Recent studies indicated that nuclear
2020-08-04
Recent studies indicated that nuclear hormone receptor super family has been linked directly or indirectly to oncogenesis (Marino et al., 2006). ERR family, a nuclear receptor super family which acts as transcription factor, has been determined in various cancer types at the RNA or protein level (Bi
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Historically covalent drugs have had
2020-08-04
Historically, covalent drugs have had great success (e.g., aspirin and penicillin), and covalent drugs have become a focus in anticancer and antiviral drug discovery (Kalgutkar and Dalvie, 2012, Singh et al., 2011). These compounds contain low reactivity warheads that allow covalent adducts to form
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