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Finally not only can ERs pair with different mGluRs
2024-08-27

Finally, not only can ERs pair with different mGluRs in different GSK2194069 regions, but it is becoming increasingly clear that the same mGluRs can pair with distinct downstream signaling partners to have differential effects both within and across brain regions (Gross et al., 2016; Mannaioni et a
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imidazoline A next series of experiments explored whether ca
2024-08-26

A next series of experiments explored whether cardiac Ampkα1 imidazoline is modified in response to pressure overload imposed by TAC. As a result, 2weeks of TAC treatment significantly increased Ampkα1 protein abundance in cardiac tissue from Ampkα1+/+ mice as compared to sham treated mice (Fig. 6A
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First the complete canonical brain original RAS Angiotensino
2024-08-26

First, the complete canonical brain original RAS (Angiotensinogen, Renin, Angiotensin I, Angiotensin Converting Enzyme (ACE), Angiotensin II) has not been conclusively identified in any specific cell type within the brain [1]. Validated evidence for the presence of brain Angiotensinogen and ACE was
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Finally microRNAs miRNA seem to
2024-08-26

Finally, microRNAs (miRNA) seem to play an important role in AR signaling in BC. Some authors have described a differential 90 of miRNAs in AR-positive BCs compared to AR-negative ones. VEGF and mTOR pathways were also reported as implicated in miRNA dysregulation, suggesting a common underlying me
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Evidence shows that glial activation increases the expressio
2024-08-26

Evidence shows that glial activation increases the expression of cytokines and chemokines in Parkinson's disease, which precede the degeneration of the substance nigra (Halliday and Stevens, 2011, Tansey and Goldberg, 2010). The use of non-steroidal anti-inflammatory drugs (except aspirin) can preve
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br Special report Financial and
2024-08-26

Special report – Financial and personal benefits of early diagnosis Acknowledgments The Alzheimer’s Association acknowledges the contributions of Joseph Gaugler, Ph.D., Bryan James, Ph.D., Tricia Johnson, Ph.D., Allison Marin, Ph.D., and Jennifer Weuve, M.P.H., Sc.D., in the preparation of 201
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Imatinib was first approved for the
2024-08-26

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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This evidence suggests the strong clinical relevance of the
2024-08-26

This evidence suggests the strong clinical relevance of the identification of acquired resistance mechanisms for a proper therapeutic decision in patients with ALK-rearranged NSCLC. When the tissue is not available, the analysis of circulating tumor DNA (cfDNA) can be a valid alternative for the det
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br Conclusions br Funding br Acknowledgements and Disclosure
2024-08-26

Conclusions Funding Acknowledgements and Disclosures We would like to thank veterinarian Angelina Williams and assistants Justin Courson, Ashutosh Jnawali, Mythri Puella, Santoshi Ramachandran, and Zhihui She for support during dissections. We also thank Drs. Vallabh Das, Deborah Otteson an
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SIS3 Whereas more research is needed to identify
2024-08-26

Whereas more research is needed to identify the precise mechanism by which FIN exerts its antidyskinetic effect, the SIS3 that it can negatively modulate dopaminergic transmission is also supported by our previous findings. Indeed, we have previously shown that FIN completely reversed the behaviora
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ATX LPA signaling in cancer is
2024-08-26

ATX/LPA signaling in cancer is also well known to promote chemotherapy and radiotherapy resistance [7]. Furthermore, others have recently shown that endothelial-derived ATX activity in renal cell carcinoma promotes renal tumorgenesis and acquired resistance to sunitinib through an IL-8-mediated mech
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br Results and discussion br Conclusion In
2024-08-26

Results and discussion Conclusion In summary, a series of indazole-based derivatives were synthesized and SAR studies conducted, with view to the development of a novel Aurora kinases inhibitor. The carboxylic Rifaximin group extending from the C-3 position of the aniline and substituted grou
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Another contributor for the G M arrest in
2024-08-23

Another contributor for the G2/M arrest in A549 and H1299 cells might be p21WAF1/CIP1 which was up-regulated upon ovatodiolide treatment. p21WAF1/CIP1 is a common CDKs inhibitor which blocks Radezolid G2/M phase progression in various types of cancer cells (Kim et al., 2015, Liberio et al., 2015).
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Most of lipid lowering agents have many
2024-08-23

Most of lipid-lowering agents have many therapeutic problems with severe side effects, while dietary fibers as lipid lowering therapy are safer. Chitosan (CS) is a dietary fiber biodegradable, biocompatible and has many health benefits including wound healing, antiinflammatory, anti-cancers, immune-
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cpi 1 receptor To enhance the accuracy of SEs in eliminating
2024-08-23

To enhance the accuracy of SEs in eliminating cancer cells, the mAb recognized by specific cpi 1 receptor on tumor cells were fused with SEs. Fab C215 or C242 fused with SEA promoted apoptosis in human colon carcinoma cells via Fas (Dohlsten et al., 1994, Litton et al., 1996). SEB-incorporated exos
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