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Five alternatively spliced isoforms of ATX have been
2025-02-25
Five alternatively-spliced isoforms of ATX have been described and all are catalytically active [16], [17]. The original ATX described in 1992 is termed ATXα, whereas the most abundant isoform is ATXβ and is the same isoform responsible for plasma lysoPLD activity [18]. Full length ATX is synthesize
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The phylogenetic relationship demonstrates that both bovine
2025-02-24
The phylogenetic relationship demonstrates that both bovine and porcine 12/15-LO is more related to the human enzyme than the rabbit enzyme, despite the fact that the rabbit reticulocyte enzyme is a 15-lipoxygenase. The rabbit is one single species that expresses a 12/15 LO with 15-LO activity while
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Compound was synthesized by reacting
2025-02-24
Compound 31 was synthesized by reacting 5-amino-2-methoxybenzoate (28) with ethanesulfonyl chloride in the presence of pyridine in DCM to give sulfonamide 29. Hydrolysis of 29 by aqueous sodium hydroxide afforded the porcn 30 which was converted to the acid chloride by heating in thionyl chloride. R
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br Future directions outlook Peptide based macrocycles are
2025-02-24
Future directions-outlook Peptide-based macrocycles are among the privileged scaffolds in antibiotic drug discovery. Many compounds were discovered by natural product screening and developed unchanged, or as semi-synthetic derivatizations. Since the golden age of antibiotic discovery (1940s-mid 1
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br Brain Angiotensin II receptors The information above leav
2025-02-24
Brain Angiotensin II receptors The information above leaves Angiotensin II receptors as the only RAAS components for which localization, regulation of expression and function in the GSK212 has been convincingly demonstrated, with the use of quantitative film and emulsion autoradiography to study
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br Results and discussion br Conclusion
2025-02-24
Results and discussion Conclusion The tyrosine kinase ALK represents one of the most successful molecular targets for the development of precise medicine to treat stratified subgroups of cancer patients. Three generations of ALK inhibitors have been awarded the FDA's approval or are being exte
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An important observation is that this patient has been
2025-02-24
An important observation is that this patient has been on ALK inhibitor for more than 4 years (51 months: 27 months on crizotinib+24 months on alectinib and on-going) and there was no evidence of disease progression in the central nervous system. The other potential driver mutation in this patient’s
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Previous studies to investigate the functions of
2025-02-24
Previous studies to investigate the functions of AHR in Treg z vad fmk have employed a loss-of-function approach, using AHR complete-null mice, or a gain-of-function approach by ligand administration. However, these approaches may confound the interpretation of the results. For example, the broad e
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br ABCA and cancer drug response Overall the expression of
2025-02-24
ABCA2 and cancer drug response Overall, the expression of ABC transporters has been linked with multidrug resistance phenotypes through the efflux of drugs via ATP-dependent transport. For example, 13 distinct transporters (ABCA2, ABCB1, ABCB4, ABCB11, ABCC1–6 ABCC10, ABCC11 and ABCG2) have been
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Fulvestrant AdipoR and AdipoR have been reported to
2025-02-24
AdipoR1 and AdipoR2 have been reported to be present in almost all type of tissues and low Fulvestrant levels have been observed in white adipose tissue (Inukai et al., 2005). These receptors have been observed to become deregulated with the onset of obesity, resulting in a reduced level of APN exp
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Tension within the network could
2025-02-21
Tension within the network could be explained by two potential mechanisms: the more classical contractility that is dependent on motor proteins that are pulling KU-60019 filaments towards each other [10]; or contractility that is caused by disassembly of a crosslinked network of actin filaments [2]
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The biological characteristics of cancer
2025-02-21
The biological characteristics of cancer invasion and metastasis are mainly attributed to the poor prognosis in cancer. It has been reported that overexpression of Ack1 promoted the migratory and invasive properties of breast cancer JIB-04 in lung cancer research by sustaining expression of epiderm
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It is worth pointing out that phenotypes
2025-02-21
It is worth pointing out that phenotypes of in vivo HSP90β inhibition were not identical to those observed in rapsyn mutant mice (Gautam et al., 1995). Postsynaptically, junctional AChR clusters appeared fragmented, in addition to expected reduction in AChR intensity, in muscles injected with 17-AAG
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Phenazine methyl sulfate Finasteride has been shown to
2025-02-21
Finasteride has been shown to be a mechanism-based inhibitor of 5AR-2 [9]. Finasteride acts as an alternate substrate for 5AR-2 and is initially bound in an extremely stable enzyme-bound NADP-dihydrofinasteride adduct which is ultimately processed to dihydrofinasteride. The NADP-dihydrofinasteride a
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GTS-21 dihydrochloride CK is considered a central controller
2025-02-21
CK is considered a central controller of cellular energy homeostasis that catalyzes the reversible transfer of a phosphoryl group from ATP to adenosine diphosphate (ADP) and creatine to produce PCr [5]. This enzyme builds up a large pool of rapidly diffusing PCr for temporal and spatial buffering of
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