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Imatinib was first approved for
2025-02-13
Imatinib was first approved for the treatment of Philadelphia chromosome positive chronic myelogenous leukemia in 2001 [25]. This first approved small molecule antagonist is quite unusual in that it provides a durable response that lasts for more than a decade in the majority of patients. Imatinib h
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The lack of specific PARP inhibitors prevents
2025-02-13
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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Moreover an increase of extracellular calcium stimulates BMP
2025-02-13
Moreover, an increase of extracellular calcium stimulates BMP-2 expression of pulp docetaxel drug via L-type calcium channel and ERK signaling, which can be attenuated by PD98059 and nifedipine . Dental pulp cells expressed little calcium-sensing receptors . immunohistochemistry staining also show
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Numerous studies have shown that PUFA incorporation into
2025-02-13
Numerous studies have shown that ω-3 PUFA incorporation into the lipid raft can affect the distribution and function of protein in the lipid raft by altering raft composition [25], [26], [27]. For example, DHA treatment excluded phospholipase D (PLD) from lipid raft toward non-lipid raft, resulting
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Brain biopsy was performed from
2025-02-13
Brain biopsy was performed from the white matter lesion around the posterior horn of the right lateral ventricle, and revealed inflammatory demyelination, such as myelin loss with relative preservation of axons, astrocytosis immnolabeled by diosmin hesperidin against glial fibrillary acidic protein
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Our initial approach to identify hits was two pronged and
2025-02-13
Our initial approach to identify hits was two-pronged and included a high-throughput screening (HTS) campaign of the OSI Danshen component library as well as a virtual screening (VS) campaign, utilizing a publically available crystal structure of ACK1 (PDB code: ). A tolerance for protein flexibilit
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On the basis of the above
2025-02-13
On the basis of the above information, we designed a new series of benzothiazole–piperazine derivatives (–) that have the aforementioned structural requirements (). Benzothiazole is an important ring system in the drug discovery studies of AD. There are several benzothiazole compounds that show pote
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The first suggestions that the
2025-02-13
The first suggestions that the cleaved intracellular domain of APP, AICD, might transit to the nucleus and hence selectively regulate gene transcription arose from analogies with the Notch receptor signalling system where similar intra-membrane proteolysis occurs [84], [85] and it was later confirme
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The link between HPV infection
2025-02-13
The link between HPV infection and neoplasia has been well established. HPV encodes two oncogenes (E6 and E7) that drive 4-iodo-SAHA progression by controlling the functions of tumor suppressor proteins p53 and Rb [7]. HPV is associated with more than 99% of cervical CESC cases [8]. CESC remains a m
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Aurora B is also very important
2025-02-13
Aurora-B is also very important in proper cytokinesis. In the absence of Aurora-B mediated phosphorylation of Ser72 in vimentin, the two daughter cells remain attached to each other through bridges of cytoplasm; cytokinesis fails [31]. Other Aurora-B dependent proteins that are important for cytokin
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Aurora kinases are a conserved family of
2025-02-13
Aurora kinases are a conserved family of serine/threonine kinases that are important for the transition through mitosis and amplification and overexpression of Aurora kinases have been implicated in 99026 australia and transformation. Aurora B is located at the centromere and controls aspects of ki
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br Material and methods br Results br
2025-02-13
Material and methods Results Discussion Although we were not able to detect 12/15-LOX mRNA in the lungs of 12/15-LOX knockout mice substantial amounts of 15-HETE could be detected in BALF. In fact, significant synthesis of 15-HETE in 12/15-LOX mice have been already reported [17]. The redun
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ATM dependent initiation of radiation induced G M
2025-02-13
ATM-dependent initiation of radiation-induced G2/M checkpoint arrest is well established [11], [34], [35]. However, the ATR pathway may also be involved [36], [37]. Brown and Baltimore generated Cre/lox-conditional cell lines or SphK1 activity inhibitor with a kinase inactive allele of ATR (ATRkd)
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The downstream targets of ATR
2025-02-13
The downstream targets of ATR involved in mediating human telomerase recruitment have not yet been identified. Under stalled fork conditions, activated ATR is able to phosphorylate and activate ATM (Stiff et al., 2006, and Figures 4C and 4D); whether this PF-670462 of ATM participates in a positive
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br Materials and methods br Results
2025-02-12
Materials and methods Results Discussion Pulmonary fibrosis is a progressive and chronic lung disease and its typical features include inos inhibitor proliferation, epithelial injury, chronic interstitial inflammation, increased extracellular matrix (ECM) production, and collapse of alveol
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