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Dopaminergic signaling involves a delicate
2020-08-04
Dopaminergic signaling involves a delicate balance between DA release and re-uptake by the pre-synaptic nerve terminal. Normally, neuronal activation promotes vesicular release of DA into the synapse. DAT removes DA from the synapse and VMAT-2 transports cytoplasmic DA into vesicles for storage, and
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The current study provides evidence for a previously unknown
2020-08-04
The current study provides evidence for a previously unknown role for DHODH as a growth/survival factor in KRAS mutant tumors. While many aspects of the link between DHODH inhibition and survival of KRAS mutant Iberin remain to be established, de novo pyrimidine biosynthesis appears to be a crucial
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SKI II sale Propranolol initially discovered in is first
2020-08-03
Propranolol, initially discovered in 1964, is first and most widely studied as a non-selective beta-blocker. Propranolol through β-adrenergic receptor blockade has reduced heart rate and blood pressure and have anti-arrhythmogenic and anti-ischemic effects, and been proposed as an effective strategy
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The genetic basis of resistance to dieldrin
2020-08-03
The genetic basis of resistance to dieldrin has been described for several insect species as a mutation in the transmembrane domain II of the GABA-Cl or rdl (resistance to dieldrin) gene (ffrench-Constant et al., 2004; Bass et al., 2004; Du et al., 2005). A mutation in the GABA-Cl gene was found at
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Over the last years it has
2020-08-03
Over the last 5 years, it has become clear that proper regulation of apoptosis is dependent on appropriate ubiquitylation of various cellular components (Vucic, Dixit, & Wertz, 2011). Here, we have focused on IAP proteins that contain a RING domain, but other E3 ligases such as MDM2, which is the pr
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Terazosin In addition studies using multiple
2020-08-03
In addition, studies using multiple behavioral and molecular analyses are required to better understand the mechanisms by which EWSR1 regulates Terazosin and motor neuron functions. It is with great anticipation that future studies will further scrutinize and unravel new functions of EWSR1, which c
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The cellular sources of inflammatory
2020-08-03
The cellular sources of inflammatory cytokines enhanced in chronic renal failure patients are mainly neutrophils and monocytes [10]. Although the distinct mechanisms for the induction of leukocyte apoptosis remain uncertain, oxidant stress has been suggested as a major triggering factor. Our results
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The CRF receptors are listed in Table
2020-07-31
The CRF2 receptors are listed in Table 1A and B. The corresponding Class II cytokines are organized by families in Table 2, and are diagrammatically paired with their receptors in Fig. 1. All the receptors except TF appear to function as heterodimers (see below). Although this review will focus on
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Neuropeptide Y 13-36 (porcine) In some of our studies we exa
2020-07-31
In some of our studies we examined the occurrence of ERβ and SHBG and a possible colocalization between them. Fig. 5 shows that there is no big difference in the occurence of ERβ after short time (A) as well as long time (B) treatment with E2. We can find the receptor at the cell membrane as well as
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br Materials and methods br Results
2020-07-31
Materials and methods Results Discussion Schistosome cercarial elastase secreted from the acetabular glands of cercariae is recognized to play a critical role in mammalian host skin penetration upon infection. The present study extends the understanding of biochemical and immunological prop
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The two major families of
2020-07-31
The two major cck 1303 synthesis of E3 ubiquitin ligases (see Glossary) that coordinate cell division are SCFs (SKP1–CUL1–Fbox proteins), which were initially recognized for regulating interphase and are now known to control many stages of the cell cycle, and anaphase-promoting complex/cyclosome (AP
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The potential off target activity of against other ATP
2020-07-31
The potential off-target activity of against other ATP-dependent enzymes, such as kinases, was also investigated. Encouragingly, there was no significant inhibition of ATP binding to 97 human kinases, when was evaluated at 10μM within a DiscoveRx scanEDGE® kinome screen (, ). All together, these da
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The roles of ginsenoside in E
2020-07-31
The roles of ginsenoside in E1 and 26S proteasome inhibition are shown in Table 2. The nitro substitute on the furan ring may be important for PYR-41 inhibition of the E1 enzyme (Yang et al., 2007). The macrocycle core and aliphatic tail of Largazole are responsible for inhibiting E1 activity (Unger
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DNA PK plays an essential role in protecting
2020-07-31
DNA-PK plays an essential role in protecting genome stability during the events of double-strand break (DSB), and considered crucial component in NHEJ repair pathway. Where, in such pathway, DNA-PKcs is recruited at the site of DSB by the Ku protein, which in turn recruits and phosphorylates a nucle
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HOBt Tamoxifen was approved by the US Food and Drug Administ
2020-07-31
Tamoxifen was approved by the US Food and Drug Administration in 1977 (Del Re et al., 2012) and it has been used as an agent of choice in the treatment of hormone responsive breast tumors for over four decades. Furthermore, this drug is prescribed as a chemo-preventive agent for high-risk women who
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