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Osteoblasts have been thought to
2024-10-18
Osteoblasts have been thought to be the major cell type that expresses RANKL (Suda et al., 1999) which is a ligand for osteoprotegerin (OPG) and which functions as a key factor for osteoclast differentiation and activation. Recently, Nakashima and his colleagues (Nakashima et al., 2011) demonstrated
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Search sphere This sphere includes the acetylcholine binding
2024-10-18
Search sphere 1: This sphere includes the dna diamonds binding site between the α–γ subunits. The center point of the search area was located at x=35.26, y=77.67, z=137.74 and the initial search radius was set to 27Å which assures that the corresponding area outside the channel pore of the two subu
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Our results suggest that plasma membrane and a containing
2024-10-17
Our results suggest that plasma membrane and a3-containing V-ATPases represent an important and novel target in the development of drugs to limit breast cancer metastasis. That knock-down of a3 has been shown to reduce metastasis of melanoma cells in an in vivo mouse model suggests that this role ma
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Recent studies have demonstrated significant cross talk
2024-10-17
Recent studies have demonstrated significant cross-talk between XRCC1 (a key player in 7-Nitroindazole sale excision repair (BER) and single strand break repair) and DDR [30], [31], [32]. ATM and DNA-PKcs are known to be involved in the phosphorylation of XRCC1 to promote BER [30], [31]. We have re
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Although the role of apelin and
2024-10-17
Although the role of apelin and APJ receptor in cardiovascular functions has been well-elucidated, little is known for the effect of the central apelinergic system on gastrointestinal (GI) functions. In mice, it has been found previously that central exogenous apelin-13 decreased gastric emptying (G
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There are several AP binding sites in the
2024-10-17
There are several AP-1 EHNA hydrochloride mg in the sequence of TIMP-1 promoter [18,19]. EBV could up-regulate TIMP-1 expression by binding to the AP-1 site in the TIMP-1 promoter [18]. IL-32, a newly multi-function cytokine, could activate AP-1, NF-κβ, p38MAPK signal pathways, and induce cytokine
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br Antioxidant polymers conjugates Natural
2024-10-17
Antioxidant-polymers conjugates Natural antioxidants are usually used as a substitute for synthetics but some degradation phenomena could influence their applications. For example, ascorbic 1400W dihydrochloride as a natural antioxidant undergoes yellowish coloration as a result of oxidation [29
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Terfenadine Tetracyclines constitute one of the most importa
2024-10-17
Tetracyclines constitute one of the most important antibiotic groups used as veterinary and human medicine and as feed additives in the agricultural sector (Li et al., 2011a, Simon, 2005). Annual worldwide production of tetracyclines is estimated to be in the thousands of tons (Michalova et al., 200
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Thus we presumed that ALDH A might play an important
2024-10-17
Thus, we presumed that ALDH1A3 might play an important role in TMZ-chemoresistance in glioblastoma patients. As we expected, the glioblastoma cell lines and primary glioma Tylosin tartrate were more sensitive to TMZ treatment when ALDH1A3 was inhibited or depleted. Consistently, it has been shown t
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The excellent potencies selectivities and improved PK associ
2024-10-16
The excellent potencies, selectivities and improved PK associated with the piperazine class triggered more extensive off-target screenings of the highlighted compounds. A screen of more than 100 enzymes, receptors, and ion channels resulted in activity at the norepinephrine transporter (NET). This m
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To assess relative metabolic activity and proliferation of c
2024-10-16
To assess relative metabolic activity and proliferation of GSK481 australia attached to various substrates we used the MTT assay [29], [30]. In order to compare the metabolic activity of cells under the various conditions irrespective of the number or viability of the cells, we performed a PicoGreen
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Despite these efforts to prevent oxidative metabolic degrada
2024-10-16
Despite these efforts to prevent oxidative metabolic degradation, and showed only marginal improvements in metabolic stability and still exhibited high plasma clearances as shown in . High molecular weight as well as relative high log values could be contributing factors to the poor PK profiles of a
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Derivatives of M that possess
2024-10-16
Derivatives of (+)-M100907 that possess either an alkyne or an azide have been synthesized. The most active enantiomer was obtained by resolution of a relatively early intermediate in the synthesis. The ability of these acpt receptor to maintain 5-HTR antagonist properties as (+)-M100907 was demonst
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Over the past decade extensive research has been directed
2024-10-16
Over the past decade, extensive research has been directed toward the discovery of Aurora-selective small-molecule inhibitors. As a result, a handful of Aurora inhibitors has been identified. Among them, 1 (VX-680) and 2 (SNS-314) have entered human clinical trials as pan-Aurora kinase inhibitors (F
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Another contributor for the G M arrest in
2024-10-16
Another contributor for the G2/M arrest in A549 and H1299 cells might be p21WAF1/CIP1 which was up-regulated upon ovatodiolide treatment. p21WAF1/CIP1 is a common CDKs inhibitor which blocks Cilengitide G2/M phase progression in various types of cancer cells (Kim et al., 2015, Liberio et al., 2015)
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