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tivozanib In contrast to TPX members of the CPC
2023-09-21
In tivozanib to TPX2, members of the CPC (Figure 1B), such as survivin, borealin, and INCEN-P, which associate with Aurora B/C in animals, do not appear to have obvious homologs in plants. Recently, however, a putative INCEN-P homolog, termed WYRD, has been identified [34]. Sequence comparison betw
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Beside estrogen several classes of compounds have
2023-09-21
Beside estrogen, several Cetrorelix of compounds have shown significant neuroprotective efficacy when administered shortly after the induction of animal models of stroke, including glutamate (NMDA) receptor antagonists and zinc chelators [25], [26], [27]. Effects of these or other neuroprotective a
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Another interesting aspect of neutralizing
2023-09-21
Another interesting aspect of neutralizing AP-1 is the inhibition of interactions between AP-1 and Smad proteins, which synergize to activate the TGF-β1-responsive genes involved in hypertrophic growth of the heart muscle and in the development of cardiac fibrosis. Through preventing AP-1 activation
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For all three fluorescent dyes used the
2023-09-21
For all three fluorescent dyes used, the double-labeled UQ-bodies showed higher antigen responses. A plausible mechanism for the higher quenching observed for the double-labeled UQ-bodies is the dye-dye quenching due to H-dimer formation [19] between the two dyes introduced into the Fd and L chains.
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Modulating the ability of tumor cells to detoxify ROS
2023-09-20
Modulating the ability of tumor Ac-Endothelin-1 (16-21), human to detoxify ROS is a key mechanism by which cysteine metabolism affects tumor cell survival. One study observed hypermethylation of cysteine dioxygenase (CDO1) in 60% of tested breast cancer samples, leading to increased ROS detoxificat
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Gliomas and Aldehyde Dehydrogenase Aldehyde dehydrogenases A
2023-09-20
Gliomas and Aldehyde Dehydrogenase Aldehyde dehydrogenases (ALDHs) are key metabolic enzymes involved in regulation of glycolysis/gluconeogenesis pathways as well as in the detoxification of endogenous and exogenous aldehydes, regulating cell function and homeostasis. ALDHs play important roles in
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Studies on both TCDD treated mice and AhR null mice
2023-09-20
Studies on both TCDD treated mice and AhR null mice have also pointed to a role of AhR in hematopoiesis [65], [66]. Singh et al. showed that AhR is a negative regulator of HSC (hematopoietic stem cell) proliferation, while deletion of AhR leads to spleen enlargement in juvenile and adult mice [67].
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This chemistry paved way for multi gram synthesis of which
2023-09-20
This chemistry paved way for multi-gram synthesis of which was utilized for extensive piperazine benzamide SAR exploration. Depicted in , the two-step operation towards final targets involved standard amide coupling conditions with EDC or HATU followed by Boc deprotection under acidic conditions.
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AMG 487 Tension within the network could
2023-09-20
Tension within the network could be explained by two potential mechanisms: the more classical contractility that is dependent on motor proteins that are pulling AMG 487 filaments towards each other [10]; or contractility that is caused by disassembly of a crosslinked network of actin filaments [2].
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Ten strains of lactobacilli TMW isogenic with strain F TMW
2023-09-20
Ten strains of lactobacilli: TMW 1.1434 (isogenic with strain F19 ), TMW 1.1733 (isolated from fermented food), TMW 1.1628 (isolated from baby feces), TMW 1.1609 (isolated from baby feces), TMW 1.1734 (isolated from fermented food), TMW 1.313 (isolated from non-pasteurized Heineken beer), TMW 1.465
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However there are studies revealing the dark side of autopha
2023-09-20
However, there are studies revealing the “dark side” of autophagy at later stages in cancers, when oncogenes (mainly K-ras and B-raf) are activated and/or tumour suppressors such as PTEN and p53 are inactivated. These studies are based on the use of GEMM and deletions of essential autophagy genes (A
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Evidences have suggested that impairment of CK activity
2023-09-20
Evidences have suggested that impairment of CK activity contributes to inhibition of Na+, K+-ATPase and H+-ATPase activities during infectious diseases, since these ATPases are dependent of ATP, as observed by Baldissera et al. [31] in fish experimentally infected by Aeromonas caviae. We observed th
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Illustrated in is the protocol we
2023-09-20
Illustrated in is the protocol we applied for the screens of novel furoic acids as ACL inhibitors. We constructed our furan carboxylate library that contained 1446 2-furoic PD0332991 Isethionate derivatives and 501 3-furoic acid derivatives by performing substructural searches of the ZINC database.
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Previous studies have demonstrated ATR
2023-09-20
Previous studies have demonstrated ATR inhibition is effective for treating cancers combining with chemotherapies in lung adenocarcinoma, gastric cancer, HER2 positive breast cancer and chronic lymphocytic leukemia BGJ 398 to enhance chemotherapy sensitivity [[16], [17], [18],[20], [21], [22]]. VE-
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br Conclusions br Acknowledgements We
2023-09-20
Conclusions Acknowledgements We would like to thank the members of the Bergmann lab for fruitful discussions in the course of this work. This work was supported by the National Institute of General Medical Sciences (NIGMS) under award number R35 GM118330. The content is solely the responsibili
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