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br ACh and ER tests hereafter Spasm provocation
2024-07-20
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 thapsigargin by the administration of ACh or ER. However, we now employ the ER and ACh spa
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br In patients with spina bifida and spinal
2024-07-20
In patients with spina bifida and spinal cord injury, fecal incontinence is a serious issue that can impair activities of daily living and patient self-esteem. To address this Malone et al. first described the Antegrade Continence Enema (ACE) procedure in 1990 [1], which achieves continence by al
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Recent studies have demonstrated significant cross talk betw
2024-07-20
Recent studies have demonstrated significant cross-talk between XRCC1 (a key player in mts assay kit excision repair (BER) and single strand break repair) and DDR [30], [31], [32]. ATM and DNA-PKcs are known to be involved in the phosphorylation of XRCC1 to promote BER [30], [31]. We have recently
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block builder strain TLX may promote survival and prevent ap
2024-07-20
TLX may promote survival and prevent apoptosis in NB block builder strain [12]. Here, we ask whether the survival-promoting effects of TLX are mediated by Apoptosis Signal-regulating Kinase-1 (ASK1, MAP3K5). ASK1 is a member of the Mitogen-Activated Protein (MAP) kinase family and it preferentially
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Apoptosis a major process of programmed cell
2024-07-20
Apoptosis, a major process of programmed cell death, and in response to many chemopreventive agents (Jeyamohan et al., 2016). In general, two major signaling pathways control apoptosis, namely, a pathway mediated by cell death receptor and a pathway mediated by mitochondrion, and possible drug targe
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The functions of HMGN protein are modulated by various post
2024-07-20
The functions of HMGN1 protein are modulated by various post-translational modifications, including phosphorylation , , , acetylation , and glycosylation . Phosphorylation in HMGN1 may influence its binding affinity to DNA or nucleosome-associated proteins and affect the sub-cellular localization an
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Complementing the effects of ARB and
2024-07-20
Complementing the effects of ARB and ACEI on HDL capacity to elicit cholesterol efflux, HDL of ARB- and ACEI-treated groups significantly lessened macrophage production of superoxide (Fig 2). As with efflux, there was no difference in this effect between the ARB and ACEI groups. These data are inter
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Recent retrospective cohort studies have supported these pre
2024-07-20
Recent retrospective cohort studies have supported these preclinical findings in animals indicating the correlation of AR activation with the induction of (+)- Corydaline synthesis carcinogenesis. First, men with prostate cancer who underwent androgen deprivation therapy were shown to have a signifi
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In order to postulate its binding
2024-07-19
In order to postulate its binding mode in APN, Letrozole 13v was docked into the active site of APN (PDB code: 2DQM) using Sybyl_X 1.3. As illustrated in Fig. 5A, the catalytic zinc ion of APN was chelated by the hydroxamate moiety of 13v, and the S1, S1′ and S2′ pockets of APN were occupied by the
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An issue related to research without biomarkers is that
2024-07-19
An issue related to research without biomarkers is that many studies will ascertain some but not all biomarker groups in study participants. Because tau PET is relatively new, incomplete biomarker information will occur in studies that use imaging for amyloid and neurodegenerative biomarker characte
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The AHR potentially enhances IDO
2024-07-19
The AHR potentially enhances IDO-expression, possibly via crosstalk with several inflammatory signaling pathways (shown by now for IL6 and ‘signal transducer and activator of transcription’ (STAT) 3, and for NFκB, toll like receptor-pathways) [56,59,60]. IDO metabolizes Trp to kynurenines, which are
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PKA signalling in the http www apexbt com media diy
2024-07-19
PKA signalling in the nucleus was thought to be due to the translocation of the catalytic subunit upon activation from the Caspase-1, human recombinant proteinase to the nucleus via diffusion [72]. However, a new understanding has emerged, as both the regulatory and catalytic subunits have been iden
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The subdivision of HT receptors
2024-07-19
The subdivision of 5-HT receptors started in the 1950s by Gaddum and colleagues, when they realised that in the guinea pig ileum, the effects of 5-HT could be blocked in part by morphine (M), and in part by dibenzyline (D). Gaddum and Picarelli proposed two receptor classes, 5-HT M and 5-HT D (1957)
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The relatively high concentration of HT
2024-07-19
The relatively high concentration of 5-HT used in this study (100 µM) is consistent with the concentrations used in other published ex vivo studies (Ropert and Guy, 1991, Passani et al., 1994, Shen and Andrade, 1998). In our paradigm 5-HT was focally applied at the surface of the slice via a fast pe
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br Materials and methods br Results br Discussion This study
2024-07-19
Materials and methods Results Discussion This study demonstrates that treatment with a selective adenosine kinase inhibitor ABT-702, thereby enhancing extracellular adenosine, can provide partial protection from age-related hearing loss in C57BL/6J mice. Chronic treatment with ABT-702, comm
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