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BET bromodomain inhibitors br ACh and ER tests hereafter Spa
2024-12-21
ACh and ER tests hereafter Spasm provocation tests have self-limitations to document coronary artery spasm during daily life. In the past reports, ST elevation was reproducible in some patients with variant BET bromodomain inhibitors by the administration of ACh or ER. However, we now employ the
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NLX a k a F or befiradol
2024-12-21
NLX-112 (a.k.a. F13640 or befiradol), exhibits nanomolar affinity at 5-HT1A receptors, and, in FITC, Fluorescein isothiocyanate to the 5-HT1A receptor agonists listed above, it presents exceptional selectivity and high efficacy at these receptors (Colpaert et al., 2002, Newman-Tancredi et al., 2017
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prime cap br Autophagy in cancer br
2024-12-21
Autophagy in cancer Phytochemicals as a valuable source of autophagy modulation agents Epidemiological studies demonstrated that there is a strong association between diet and human cancer mortality so that daily consumption of phytochemicals declines the incidence of different types of cancer
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Although several different membrane estrogen receptors have
2024-12-20
Although several different membrane estrogen receptors have been reported (Qiu et al., 2008; Revankar et al., 2005), a large percentage of membrane-initiated steroid hormone signaling appears to be performed by a subpopulation of the same receptors that act in the nucleus. Specifically, estrogen rec
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br In vivo visualization of aromatase with positron emission
2024-12-20
In vivo visualization of aromatase with positron emission tomography (PET) Positron emission tomography (PET) utilizes the high Rink Amide Resin photons formed during the annihilation of positrons to detect the changes in the amount and localization of injected radiopharmaceuticals in the living
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Angiotensin Fragment 1-7 acetate As aforementioned this stud
2024-12-20
As aforementioned, this study aimed to design, synthesize and investigate aromatase inhibitory and anti-breast cancer activities of N,N′-disubstituted thiourea derivatives. Based on the attractive phenotypic molecule 1, the synthetic N,N′-disubstituted thioureas have been designed including monothio
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Furthermore we also found that the basic
2024-12-20
Furthermore, we also found that the basic level of ROS was markedly lower in mtDNA-reduced SW480 SC-514 than that in the parent cells. Endogenous ROS is most notably produced at the sites of complex I and complex III [5], it might be plausible that the decreased quantity of ROS observed in mtDNA-re
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It is reported that calpain plays
2024-12-20
It is reported that calpain-2 plays a critical role in BDNF-induced signaling and memory formation, and knockdown of calpain-2, but not calpain-1, completely suppresses BDNF-induced pathway activation and protein translation (Briz et al., 2013). BDNF prevents neuronal apoptosis or death (Ferrer et
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NK 252 mg The alamarBlue test revealed that recombinant apel
2024-12-20
The alamarBlue test revealed that recombinant apelin led to an increase in basal and IGF1- and FHS-induced ovarian cell proliferation. Apelin increased ERK1/2 and Akt protein expression, but cell proliferation returned to control levels in the presence of kinase inhibitors. This suggests that the pr
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How do increased levels of
2024-12-20
How do increased levels of ammonia as observed in clinical HE constrain synaptic plasticity? Numerous studies have investigated the modulation of signal transduction pathways activated in LTP or LTD irrespective of being necessary or sufficient for changes in synaptic efficacy (Wen et al., 2013). Y
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Clinical observations of individuals with a decrease in LOX
2024-12-20
Clinical observations of individuals with a decrease in 12-LOX Sweroside receptor are consistent with 12-LOX potentiating platelet activation and thrombus formation [40]. However, the relative contribution of 12-LOX to these complex disorders cannot be fully elucidated in the absence of a biochemica
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Cyclopamine synthesis Liao and van Linden et
2024-12-20
Liao [47] and van Linden et al. [48] divided the gap between the N-terminal and C-terminal lobes into a front cleft or pocket, a gate area, and a back cleft. The back pocket corresponds to the gate area and the back cleft. The front cleft includes the Gly-rich loop, the hinge, the linker connecting
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Various compounds have been designed to inhibit aldose reduc
2024-12-20
Various compounds have been designed to inhibit aldose reductase (AR) [12]. These compounds can be classified into two main categories, the first category comprises those containing a carboxylic a66 moiety, for example, 3-thiazolidineacetic acid derivative, which has been reported to be a potent AR
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br Conflict of interest br Introduction The Piezo proteins P
2024-12-20
Conflict of interest Introduction The Piezo proteins, Piezo1/FAM38A and Piezo2/FAM38B, are multi-pass transmembrane proteins that have been identified as mechanically-activated (MA) homomultimeric, pore-forming ion channels [1,2]. Piezo1 is broadly expressed with its highest expression in blad
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APPL is highly expressed in pancreatic cells but its
2024-12-20
APPL1 is highly expressed in pancreatic β cells, but its levels are significantly decreased in several mouse models of obesity and diabetes, including HFD-induced obese mice and db/db mice [6], [73], suggesting that the dysregulation of APPL1 may be associated with malfunction of the pancreas in obe
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