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Panobinostat (LBH589): Expanding Paradigms in HDAC Inhibi...
2025-09-29
Explore how Panobinostat (LBH589), a potent hydroxamic acid-based histone deacetylase inhibitor, drives apoptosis through innovative mechanisms beyond classical HDAC inhibition. This in-depth article uncovers new intersections between epigenetic regulation, mitochondrial signaling, and therapeutic resistance, offering insights distinct from existing literature.
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Pifithrin-α (PFTα): Unraveling p53 Inhibition in Neurodev...
2025-09-28
Explore the advanced role of Pifithrin-α as a p53 inhibitor in neurodevelopmental ferroptosis, apoptosis research, and cell cycle modulation. This in-depth article reveals unique insights into p53-dependent apoptosis inhibition and DNA damage response, setting a new benchmark for research applications.
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Trichostatin A (TSA): Unlocking HDAC Inhibition for Next-...
2025-09-27
Discover how Trichostatin A (TSA), a potent histone deacetylase inhibitor, enables precise epigenetic regulation and cell fate control in advanced cancer and organoid research. This article uniquely explores TSA's mechanistic roles and translational impact, providing scientific depth beyond existing reviews.
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Adenosine Triphosphate (ATP): Integrative Regulator in Ce...
2025-09-26
Explore the multifaceted role of Adenosine Triphosphate (ATP) as both a universal energy carrier and a dynamic extracellular signaling molecule. This article uniquely dissects ATP's integration in mitochondrial enzyme regulation, purinergic signaling, and its implications for advanced cellular metabolism research.
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Torin 1: Decoding mTOR Inhibition for ER Lipid Homeostasi...
2025-09-25
Explore how Torin 1, a potent mTOR inhibitor, uniquely elucidates the interplay between mTOR signaling, ER lipid homeostasis, and cancer cell proliferation. Gain insight into advanced experimental applications and mechanistic depth not found in prior reviews.
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BMN 673 (Talazoparib): Next-Generation PARP1/2 Inhibitor ...
2025-09-24
Explore the scientific advances of BMN 673 (Talazoparib), a potent PARP1/2 inhibitor, as a precision tool for homologous recombination deficient cancer treatment. This article uniquely dissects the synergy between PARP-DNA complex trapping, RAD51 filament dynamics, and PI3K pathway modulation, offering novel insights for translational and preclinical research.
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KU-60019: Metabolic Vulnerabilities and Radiosensitizatio...
2025-09-23
Explore how KU-60019, a selective ATM kinase inhibitor, unveils new metabolic vulnerabilities in glioma cells by promoting macropinocytosis and radiosensitization. This article highlights the mechanistic interplay between DNA damage response inhibition and cancer cell adaptation, providing advanced insights for cancer research.
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AMPK is a serine threonine protein kinase
2025-03-03
AMPK is a serine/threonine protein kinase composed of a catalytic α subunit with the activating phosphorylation site (Thr172) and two regulatory subunits, β and γ. The two AMPK variants, α1 and α2, show different cellular localization in mammalian cells. AMPKα2 is detected in nuclear and non-nuclea
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The small fishers with little or
2025-03-03
The small fishers with little or no quota who remained relied on quota leasing arrangements to continue their fishing operations. Such arrangements had relatively high transaction costs and by early 2000 it appeared that the demise of the small fisher was imminent [2]. The introduction in 2001 of t
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br Funding br Introduction l Dihydroxyphenylalanine l DOPA
2025-03-03
Funding Introduction l-3,4-Dihydroxyphenylalanine (l-DOPA) is the gold-standard treatment for the motor symptoms of Parkinson's disease (PD); however, its chronic use induces severe motor complications that eventually limit its long-term efficacy (Bastide et al., 2015). The most disabling side
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Several in vivo and in
2025-03-01
Several in vivo and in vitro studies have demonstrated changes in bioactive lipid profiles under hyperglycemic conditions and have linked these changes with increased leukocyte adhesion and vascular dysfunction during diabetes. This input has originated partly from lipidomic studies that showed elev
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br Material and methods br Results br Discussion
2025-03-01
Material and methods Results Discussion T2D is a substantial threat to global human health [31]. Obesity-associated chronic low-grade inflammation promotes insulin resistance and T2D [32]. In obese individuals, the production of numerous inflammatory molecules including IL-6 and TNF-a is up
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Songbirds are outstanding models in the
2025-03-01
Songbirds are outstanding models in the study of vocal communication (Maney and Pinaud, 2011). Following the pioneering studies of William H. Thorpe and Peter Marler on the development of song in chaffinches (Fringilla coelebs) and white-crowned sparrows (Zonotrichia leucophrys) (Marler, 2004; Thorp
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br Introduction Rhamdia quelen jundi Silurifomes Heptapterid
2025-03-01
Introduction Rhamdia quelen (jundiá, Silurifomes, Heptapteridae) is a neotropical catfish widely distributed in Central and South America (Silfvergrip, 1996). This species shows high potential for the aquaculture industry, due to an elevated growth rate, good carcass yield, and easy reproduction
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br Experimental and simulation section br Acknowledgments Fi
2025-03-01
Experimental and simulation section Acknowledgments Financial support for this work was provided by the National Natural Science Foundation of China (No. 81101688). We would like to thank NC State University High Performance Computing Center for providing us computing resources, and Dr. Lihui