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The CRF receptors are listed in Table A
2020-08-06

The CRF2 receptors are listed in Table 1A and B. The corresponding Class II cytokines are organized by families in Table 2, and are diagrammatically paired with their receptors in Fig. 1. All the receptors except TF appear to function as heterodimers (see below). Although this review will focus on
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br Materials and methods br Results br Discussion Evidence
2020-08-06

Materials and methods Results Discussion Evidence of the role of CHK inhibition in the therapeutic setting in ovarian cancer has been provided in several studies. PARP inhibition in PEO1 BRCA-mutated serous carcinoma cells was shown to activate the ATR/CHK1 pathway, preventing cell death an
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Asb genes are characterized by the presence of a
2020-08-05

Asb genes are characterized by the presence of a conserved SOCS box motif and a variable number of ankyrin repeats. The SOCS box is a structural C-terminal domain that interacts with Elongin C via its B/C box conserved motif. In turn, Elongin C binds Elongin B to form a dimer that bridges the substr
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The use of manganese as divalent
2020-08-05

The use of manganese as divalent cofactor instead of magnesium increased TLS across abasic sites (Figure 3C) as well as de novo DNA synthesis (Figures 4C and 5; Figure S5). Although the roles of divalent metal ions in DNA synthesis have been controversial, a number of recent findings suggest a physi
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Aldehyde dehydrogenase has been characterized as
2020-08-05

Aldehyde dehydrogenase has been characterized as a cancer stem cell marker, which plays a key role in various biological processes in tumor, including cell proliferation, invasiveness and chemoresistance. Recent data of Abourbih et al reported that ALDH1 expression did not correlate with primary tum
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Recent studies have reported the co localization
2020-08-05

Recent studies have reported the co-localization of total and pDDRs in iwr synthesis with collagen [20], [21], [35]. Our results expand these observations by showing that higher-order assembly of DDRs into receptor clusters and/or filamentous structures may associate with different morphological st
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br Introduction Adenotonsillar hypertrophy is the
2020-08-05

Introduction Adenotonsillar hypertrophy is the most frequent cause of sleep-disordered breathing (SDB) in childhood, so it is widely accepted that the first line of treatment is tonsillectomy and adenoidectomy (T&A) [1]. However, many mild patients that do not fulfill the polysomnographic criteri
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In the present study it was found that HepG
2020-08-05

In the present study, it was found that HepG2, H4IIE and LMH cells were inclined to remove S-metalaxyl and lead to decrease of ERs of metalaxyl, while L8824 cells were inclined to attenuate R-metalaxyl and resulted in an inverse shift of ER. These findings indicate the enantioselective accumulation
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Stimulation of the VSMC with
2020-08-04

Stimulation of the VSMC with Ang II also resulted in a time-dependent decrease in gp130-related mRNA but the maximal decrease occurred four hours after stimulation and level remained markedly low within 12 hours after stimulation . Again, our results show that stimulation of the VSMCs with Ang II fo
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The in vitro studies support
2020-08-04

The in vitro studies support our previous observations of a bimodal expression pattern of B. malayi transcripts after tetracycline treatment, including the two enzymes we studied here. We hypothesize that this bimodal expression may be due to stage-specific responses of the host in response to Wolba
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br Results br Discussion LNX was first identified as a
2020-08-04

Results Discussion LNX1 was first identified as a binding partner of Numb and interacts with c-Src in a PDZ-dependent manner, triggering its ubiquitination [18]. Until recently, no structure-based mechanism had been established for the LNX family of proteins. Here, we identified the ubiquitina
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br Discussion Several DPP inhibitors are currently available
2020-08-04

Discussion Several DPP-4 inhibitors are currently available for use in the treatment of type 2 diabetes mellitus. Due to the different chemical structures there are marked differences both in the binding kinetics on the target enzyme [10] and also different pathways of elimination [13] exist. In
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br Discussion Several DPP inhibitors are currently available
2020-08-04

Discussion Several DPP-4 inhibitors are currently available for use in the treatment of type 2 diabetes mellitus. Due to the different chemical structures there are marked differences both in the binding kinetics on the target enzyme [10] and also different pathways of elimination [13] exist. In
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Conversely P Y receptors are GPCRs responsive to both adenin
2020-08-03

Conversely, P2Y receptors are GPCRs responsive to both CJ-42794 mg (ATP, ADP) and uracil (UTP, UDP) nucleotides, or to sugar nucleotides (UDP-glucose and UDP-galactose) [25]. Eight P2Y receptor subtypes are currently recognized: the P2Y1,2,4,6,11,12,13,14 receptors (ibidem). These receptors are wid
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br Materials and methods br Results br Discussion
2020-08-03

Materials and methods Results Discussion Field populations of the P. xylostella pest have evolved various levels of resistance to 95 active ingredients (APRD, 2018), including abamectin (Pu et al., 2010) and fipronil (Wang et al., 2016b) pesticides that act on GluCls. We previously identifi
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