Archives
- 2018-07
- 2019-04
- 2019-05
- 2019-06
- 2019-07
- 2019-08
- 2019-09
- 2019-10
- 2019-11
- 2019-12
- 2020-01
- 2020-02
- 2020-03
- 2020-04
- 2020-05
- 2020-06
- 2020-07
- 2020-08
- 2020-09
- 2020-10
- 2020-11
- 2020-12
- 2021-01
- 2021-02
- 2021-03
- 2021-04
- 2021-05
- 2021-06
- 2021-07
- 2021-08
- 2021-09
- 2021-10
- 2021-11
- 2021-12
- 2022-01
- 2022-02
- 2022-03
- 2022-04
- 2022-05
- 2022-06
- 2022-07
- 2022-08
- 2022-09
- 2022-10
- 2022-11
- 2022-12
- 2023-01
- 2023-02
- 2023-03
- 2023-04
- 2023-05
- 2023-06
- 2023-07
- 2023-08
- 2023-09
- 2023-10
- 2023-11
- 2023-12
- 2024-01
- 2024-02
- 2024-03
- 2024-04
- 2024-05
- 2024-06
- 2024-07
- 2024-08
- 2024-09
- 2024-10
- 2024-11
- 2024-12
- 2025-01
- 2025-02
- 2025-03
-
Methylpiperidino pyrazole br Competing interests br Acknowle
2020-08-04
Competing interests Acknowledgements This work was supported by a Grant-in-Aid for Scientific Research (KAKENHI) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT) (26304036), Japan. Introduction Cancer is a disease of dysregulated cell growth and metabolism-re
-
Although the activities interactions and nucleocytoplasmic t
2020-08-03
Although the activities, interactions and nucleocytoplasmic traffic of mucosal alpha genus HPV E7 oncoproteins have been well documented (McLaughlin-Drubin and Munger, 2009), much less is known about the cutaneous beta genus HPV E7 proteins. The cutaneous HPV8 E7 oncoprotein has a weaker interaction
-
br Acknowledgements br Introduction Nonmelanoma skin cancer
2020-08-03
Acknowledgements Introduction Nonmelanoma skin cancer (NMSC) is the most common cancer in fair skinned populations. Exposure to UV radiation, along with fair skin, immune status and HPV infection, are the greatest risk factors (Akgul et al., 2006a, Feltkamp et al., 2008). A link between HPV in
-
Also the prodrug to drug differential needs to be
2020-08-03
Also, the prodrug to drug differential needs to be very high. Whereas the differential of the prodrug/drug pairs for CPG2 was about 100:1, Tietze et al. have reported a series of glycosidic prodrugs that are up to million times less toxic than the drug that showed IC50 of 110fM [13]. In addition, th
-
Other membrane currents are affected as well Some
2020-08-03
Other membrane currents are affected as well. Some studies have provided evidence that sulfonylureas, in addition to blocking KATP channels, also inhibit chloride and calcium channels. GLYB has been shown to almost inhibit the current generated by Na+–K+ pumps in a concentration-dependent manner (wi
-
An impaired nitric oxide NO signaling pathway is
2020-08-03
An impaired nitric oxide (NO) signaling pathway is commonly involved in a derangement of left ventricular (LV) hemodynamics, LV remodeling, and impairment of exercise capacity in HFrEF patients.5, 6 Dysregulation of NO pathway plays a central role in a rise of pulmonary vascular tone by disturbing p
-
Despite the weak and transient nature of E E
2020-08-03
Despite the weak and transient nature of E2–E3 interactions, this binding is required for the transfer of ubiquitin to the substrate. The low affinity characteristics of this interaction may be due to the fact that E2s use the same surface to interact with E1s and E3s, and hence while binding to an
-
Muscle Ring Fingers MuRFs comprising TRIM MuRF TRIM MuRF and
2020-08-03
Muscle Ring Fingers (MuRFs) comprising TRIM63 (MuRF1), TRIM55 (MuRF2) and TRIM54 (MuRF3) are the most studied TRIMs in the heart. However, with increasing knowledge of E3 ligases and recent advancements in the field, many other TRIMs such as TRIM8, TRIM21, TRIM24, TRIM32, TRIM45, TRIM69 and TRIM72 w
-
br Experimental section br Acknowledgements This research
2020-08-03
Experimental section Acknowledgements This research was supported by the National Natural Science Foundation of China (81402795) and a Grant from the Bureau of Education of Guangzhou Municipality (1201630308). Introduction Diabetes mellitus is a serious worldwide health problem. The higher
-
PI K is a lipid kinase and generates
2020-08-03
PI3K is a lipid kinase and generates phosphatidylinositol-(3,4,5)-trisphosphate, which is a second messenger critical for the translocation of Akt to the cytoplasmic membrane. The phosphorylation of Ser473 Akt is important in the cell survival by regulating the eNOS among other targets (Dimmeler et
-
Many studies indicated that at high doses PLD
2020-07-31
Many studies indicated that, at high doses, PLD may induces apoptosis, while, at low doses, it evoked a phenomenon known as stress-induced premature senescence (SIPS), which was the result of changes in the expression of many proteins that regulate the cell cycle, cytoskeletal, and cellular architec
-
Finally the recent work to define the microcircuitry of the
2020-07-31
Finally, the recent work to define the microcircuitry of the central amygdala and the role of specific cell populations in fear conditioning can stand as a useful model for advances in preclinical alcohol research. To date, the role of the amygdala in alcohol-related behaviors, and reward-related be
-
Efforts then focused on optimizing SR to build
2020-07-31
Efforts then focused on optimizing SR19797 to build back the potency lost from replacing the hydrazone linkage (, ). Similar to the SAR observed in the hydrazone series (), movement of the -substituted phenol residue was not well tolerated. In fact, movement to the -position as in SR19886 seemed to
-
The DDRs have also been shown to be regulators of
2020-07-31
The DDRs have also been shown to be regulators of certain immunological functions. DDR1 is expressed in stimulated peripheral blood mononuclear Pravastatin sodium (Kamohara et al., 2001) and on activated T cells (Chetoui et al., 2011, Hachehouche et al., 2010, Kamohara et al., 2001). DDR1 can mediat
-
In the present study BACH downregulation did not correlate
2020-07-31
In the present study, BACH1 downregulation did not correlate with nuclear accumulation of NRF2, suggesting that these changes were triggered via an independent mechanism. BACH1 is a transcriptional repressor that is regulated by heme. Heme binding to the BACH1 C-terminal domain inhibits BACH1 DNA bi
15971 records 822/1065 page Previous Next First page 上5页 821822823824825 下5页 Last page