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br Ataxia telangiectasia and Rad
2023-01-16

Ataxia–telangiectasia and Rad3 related as a therapeutic target Several concerns revolving around functional inhibition of ATR have hindered the exploitation of ATR as therapeutic target in cancer therapy and delayed the development of specific ATR kinase inhibitors. It was anticipated that pharma
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In conclusion we report that the widely prescribed drug VPA
2023-01-16

In conclusion, we report that the widely prescribed drug VPA exerts therapeutic effects on optic nerve demyelination and retinal degeneration in a mouse model of MS. Our findings raise an interesting possibility that combination therapy of VPA and ASK1 inhibition may be useful for treatment of autoi
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br Dysregulated aromatase expression the link between obesit
2023-01-16

Dysregulated aromatase expression: the link between obesity and breast cancer Obesity has been associated with abnormally high expression of the enzyme aromatase in the breast, influencing the local production and bioavailability of estrogens (Morris et al, 2011, Subbaramaiah et al, 2012). Bowers
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Although the earlier studies focused on
2023-01-16

Although the earlier studies focused on the antioxidant capacity of tocopherols, ascorbic Vandetanib australia and carotenoids, then it was noticed that phenolic compounds were more powerful than others (Rice-Evans, Miller, & Paganga, 1996). Phenolic compounds, the most numerous and ubiquitous group
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br Nanoparticle Conjugated Topoisomerase Inhibitors The safe
2023-01-16

Nanoparticle-Conjugated Topoisomerase Inhibitors The safety and efficacy of topotecan administered as LDM or MTD have been evaluated in several preclinical studies and a few clinical trials whose results showed that there can be significant adverse effects likely precluding its use in patients [5
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Regarding progression free survival analyzing
2023-01-16

Regarding progression free-survival, analyzing 12 clinical trials, we demonstrated that the use of antiangiogenic treatment results in a statistically longer PFS with a pooled HR of 0.76 (95% CI 0.65–0.89, pAI-10-49 australia of improvement of PFS only is that after antiangiogenic therapy glioblasto
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br Combination Effective RAS inhibition which is
2023-01-16

Combination Effective RAS inhibition, which is important for ONC201 receptor control as well for the management of associated illnesses, can be produced through proper selection and dose maintenance and also by the combination with other antihypertensive agents along with continuous monitoring f
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Circular dichroism CD provides useful information about prot
2023-01-14

Circular dichroism (CD) provides useful information about protein structure, the extent and rate of structural changes and ligand binding. CD is a form of light JWH 015 spectroscopy that measures differences in the absorbance of right- and left-circularly polarized light (rather than the commonly u
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br Conflicts of interest br Funding br Introduction
2023-01-14

Conflicts of interest Funding Introduction Brassicaceae is an economically important family of plants containing rapeseed, cabbage, broccoli, brussels, radish and mustard. Among them rapeseed plays a crucial role, because of its application in food and also in fuel industry. According to th
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br MHCI peptide editing N
2023-01-14

MHCI peptide editing, N-terminal extensions and the peptide loading complex Conventionally, peptide-MHCI binding is thought to require both amino- and carboxyl-termini for stable interaction (Madden, 1995; Bouvier and Wiley, 1994). Peptides with longer than optimal length (10–13 residues) have be
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Decrease in soluble protein content in diabetic lenses compa
2023-01-14

Decrease in soluble protein content in diabetic lenses compared with those in control lenses in present study could be due to leakage of proteins and insolubilization. T. purpurea treatment could increase the levels of soluble proteins in diabetic lenses may be by preventing cross-linking/aggregatio
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The lack of specific PARP inhibitors prevents our
2023-01-14

The lack of specific PARP inhibitors prevents our understanding of how TIPARP or perhaps other PARPs affect AHR signaling. Current inhibitors are based on NAM and were designed to inhibit PARP1 [59]. Many of them do not effectively inhibit mono-ADP-ribosyltransferases and their ability to inhibit TI
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Octreotide acetate Luciferase Immunoprecipitation Systems LI
2023-01-13

Luciferase Immunoprecipitation Systems (LIPS), which utilizes recombinant antigens fused to the enzyme reporter Renilla luciferase (Ruc) to detect patient antibodies, provides a unique platform to investigate Octreotide acetate directed against a variety of antigenic targets [25]. Previously, LIPS h
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Octreotide acetate Luciferase Immunoprecipitation Systems LI
2023-01-13

Luciferase Immunoprecipitation Systems (LIPS), which utilizes recombinant antigens fused to the enzyme reporter Renilla luciferase (Ruc) to detect patient antibodies, provides a unique platform to investigate Octreotide acetate directed against a variety of antigenic targets [25]. Previously, LIPS h
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a66 sale Derivatives of M that possess either an
2023-01-13

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 a66 sale to maintain 5-HTR antagonist properties as (+)-M100907 was demonstrated
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