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br A brief introduction to DUBs The reversal
2019-09-02

A brief introduction to DUBs The reversal of ubiquitin conjugation of targeted proteins relies on deubiquitinating A 77636 hydrochloride and (DUBs), which catalytically cleave single Ub or poly-ubiquitin chains from proteins. The human genome encodes approximately 100 potential DUBs which can be
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br Methods br Results br Discussion Preclinical data indicat
2019-09-02

Methods Results Discussion Preclinical data indicate that nepicastat modulates sympathetic drive to the GSK2126458 mass with a mild pressor effect in various animal models of hypertension (Stanney et al., 1998). However in this clinical study, the doses of nepicastat employed did not signif
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br The modulation of ER from SERMs to TSECs
2019-09-02

The modulation of ERα: from SERMs to TSECs Continued efforts to provide women with efficacious menopausal therapies have generated interest in the development of selective rac inhibitor receptor modulators (SERMs). Similar to estrogens, SERMs have been shown to bind to ERs with high affinity, de
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Hepatocyte proliferation is accompanied by changing gene exp
2019-09-02

Hepatocyte proliferation is accompanied by changing gene expression [1,2]. as two of the three estrogen receptors are transcription factors: Estrogen Receptor alpha (ERα) and ERβ [[3], [4], [5]]. The most potent ligand estradiol, binds to ERα/ERβ and exerts changing cognate gene transcription [5]. O
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In different body organs a number of
2019-09-02

In different body organs, a number of biological functions are generally mediated by binding of the extracellular substances to the particular transmembrane receptors, which results in subsequent signal stimulation by intracellular signaling cascades. These cascades function over the complex network
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mk-801 clinical Molecular imaging that provides a non invasi
2019-09-02

Molecular imaging that provides a non-invasive means to visualize and measure a biological process of interest at the molecular and cellular level in living subjects has emerged as a promising approach for in vivo detection of enzyme activity in recent decades [6]. In mk-801 clinical to anatomical
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In the current study we
2019-09-02

In the current study, we have elucidated an intrinsic mechanism by which PD-1 signaling maintains Foxp3 in Tbet+iTreg and iTreg cells. The data presented here demonstrate that PD-1 can inhibit a functional nuclear pool of active asparaginyl endopeptidase (AEP), an endo-lysosomal protease previously
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AEBSF pathway DDR although normally expressed in cells with
2019-09-02

DDR2, although normally expressed in AEBSF pathway with mesenchymal features, has also been reported to enhance EMT. In A549 lung cancer cells, TGFβ1 increases the expression of type I collagen and DDR2. Knocking-down COL1A1 or DDR2 with siRNA is sufficient to inhibit EMT and cell migration induced
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br Introduction br Sphingolipid metabolism Sphingolipids are
2019-09-02

Introduction Sphingolipid metabolism Sphingolipids, are fundamental constituents of all eukaryotic membranes and their metabolism is carried out by a broad array of anabolic and abscisic acid with ceramide as their hub (for a review, (Hannun and Obeid, 2018)). Ceramide can be formed by multipl
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DDR upregulation in patients with kidney diseases such as
2019-09-02

DDR1 upregulation in patients with kidney diseases such as lupus nephritis and Goodpasture\'s syndrome [8] as well as in animal models of kidney injury [7], [8], [18] suggests that DDR1 plays an important role in kidney disease. Studies in various mouse models of kidney injury indicate that DDR1 del
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br Introduction Lung cancer is the leading
2019-09-02

Introduction Lung cancer is the leading cause of cancer-related death worldwide, accounting for more than 1.5 million deaths in 2012. Non–small-cell lung cancers represent approximately 85% of lung neoplasms; among these, squamous cell carcinomas (SCC) account for approximately 30% of cases. The
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br Results br Discussion Taking advantage
2019-08-30

Results Discussion Taking advantage of the highly specific protein–protein interactions among cognate pkc inhibitors that mediate SUMO conjugation to substrates, we have developed a novel strategy for achieving inhibition of SUMO conjugation in vivo based on disruption of SUMO E1–E2 interactio
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br Experimental br Results and discussion Fig shows schemati
2019-08-30

Experimental Results and discussion Fig. 2 shows schematically the fundamentals of the developed HRP-P4-(P4)-anti-P4-Protein-G-MBs/SPCE immunosensor. Oriented immobilization of anti-P4 was accomplished onto Protein G-MBs due to the Protein G binding ability with the Fc region of many mammals i
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Amyloid β-Peptide (1-42) br Conclusion This patient was hype
2019-08-30

Conclusion This patient was hypercoaguable as evidenced by a lower extremity DVT, pulmonary emboli, and a splenic infarct. Excluding acute CMV infectious mononucleosis, she had no disorders predisposing to splenic infarcts.4, 5 In this case, CMV infectious mononucleosis was accompanied by CMV lun
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Chk is dramatically induce by the IL family of
2019-08-30

Chk is dramatically induce by the IL-4 family of cytokines and equally dramatically inhibited by IFN-γ, a regulation that appears to be specific for human monocytes. In primary human T cells, Chk is not normally present, but it can be induced by potent activators of T Pimozide such as PHA or IL-2 (
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