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p as a cyclin dependent kinase inhibitor exert
2019-08-09
p21, as a cyclin-dependent kinase inhibitor, exert significant negative regulator of proliferation, and it could be transcriptional upregulated by p53 in order to impel transient 91 5msds arrest (Romanov et al., 2010). Using western blotting, we found that the protein expression of p21 upgrades firs
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(+)-MK 801 In the current study although EP agonist was the
2019-08-08
In the current study, although EP4 agonist was the most effective in relaxing corpus cavernosum, it did not affect the neuronally-mediated relaxation. On the other hand, both alprostadil and iloprost, which were less effective as direct relaxants, potentiated EFS-induced relaxation of rat corpus cav
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Chelerythrine Chloride Two nutrient sensing pathways the cAM
2019-08-08
Two nutrient-sensing pathways, the cAMP-protein kinase A (PKA) pathway and the target of rapamycin complex 1 (TORC1) pathway, are implicated in Msn2/4 regulation. Under non-stress conditions, Msn2 localizes in the cytoplasm and is inactivated by both PKA-dependent phosphorylation of the nuclear loca
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In S cerevisiae Mek a paralog of the checkpoint
2019-08-08
In S. cerevisiae, Mek1, a paralog of the checkpoint kinase Chk2, mediates cell-cycle arrest in response to meiotic defects (Bailis and Roeder, 2000, Xu et al., 1997). Mek1 is associated with meiotic chromosome axes, where its activation requires interactions with two other axis proteins, Hop1 and Re
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br Development of the double strand break repair model for
2019-08-08
Development of the double strand break repair model for meiotic recombination Meiotic recombination was first described by Frans Alfons Janssens using Fmoc-Lys(Boc)-OH calculator in the salamander Batracoseps attenuatus in 1909 [21] and then further elaborated at the genetic level in Drosophila
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Previously we had proposed three
2019-08-08
Previously we had proposed three possible models, with one being that hCrm1 fundamentally interacted more favorably or strongly with Rev-RRE complex, compared to mCrm1. We decided to test that model, which was the simplest and most straightforward, by both biochemical and genetic means. By using bac
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Within the BLA both CRF and the
2019-08-08
Within the BLA, both CRF and the CRF1 receptor have been shown to functionally regulate synaptic activity. In vivo, CRF release into the BLA originates from projections from the CeA (Roozendaal, Brunson, Holloway, McGaugh, & Baram, 2002). Central administration of both CRF and CRF1 agonists has been
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Introduction It has been well stablished the
2019-08-08
Introduction It has been well stablished the role of CRF in somatic pain regulation (Yarushkina et al., 2011, Yarushkina et al., 2016). However, the effects of CRF in pain relief are controversial and it has been described anti- and pronociceptive effects (Ji et al., 1995, Larauche et al., 2009, Ni
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br Involvement of p MAPK pathway The NF
2019-08-08
Involvement of p38 MAPK pathway The NF-κB signal transduction cascade is a major stress response signaling pathway for the COX-2 gene expression. In mice and humans, the COX-2 promoter has integrin inhibitors for many transcription factors, including NF-κB in the 5′ region of the COX-2 gene [11]
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Introduction Human cytomegalovirus CMV is a
2019-08-08
Introduction Human cytomegalovirus (CMV) is a herpesvirus which has a ubiquitous and worldwide distribution, and is the most frequent cause of congenital infection (Kenneson and Cannon, 2007). The prevalence is around 0.5–1% of all live births and is the leading cause of sensorineural hearing loss
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br Introduction Myotonic dystrophy dystrophia myotonica
2019-08-08
Introduction Myotonic dystrophy (dystrophia myotonica, DM) is an autosomal dominant disorder and the most common form of inherited muscular dystrophy in adults [1]. DM is characterised by a wide range of symptoms, including myotonia, progressive muscle loss, cataracts, cardiac conduction defects,
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br Conclusions and future perspectives It is
2019-08-08
Conclusions and future perspectives It is now evident that selective ETA or nonselective endothelin receptor antagonism provides therapeutic potentials against a variety of cardiovascular diseases such as hypertension, PAH, and diabetic microvascular dysfunction (Fig. 1). However, PAH is currentl
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br Materials and methods br Results br Discussion DUSP
2019-08-08
Materials and methods Results Discussion DUSP1 is a member of the subfamily of the Dusl specific phosphatases (DUSPs). High levels of DUSP1 observed in lung, liver and placenta, and low levels have been found in the T7 Tag Peptide and kidney. DUSP1 has been shown to be elevated in various d
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Our knowledge of DDR induced
2019-08-08
Our knowledge of DDR-induced signaling pathways is still fragmentary. In particular, we do not know which signaling effectors interact with the phosphorylated receptors and how different effectors are linked to the control of specific cellular functions. The DDRs are at the interface between RTKs an
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Based on our studies presented above atipamezole
2019-08-07
Based on our studies presented above, atipamezole can be used as a new in vitro and in vivo tool LB Broth, Miller as a pan-CYP inhibitor for CYP mediated metabolism study.
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