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Not all of the biological activities exhibited by
2020-12-24

Not all of the biological activities exhibited by progestogens (Table 1) are mediated via binding to SRs. For example, the anti-estrogenic action of progestogens in the 2-Deoxyadenosine 5-diphosphate is due to the progestogen-bound PR suppressing ER gene expression, and consequently the ability of t
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Several large scale clinical studies have set out with
2020-12-24

Several large-scale clinical studies have set out with the common goal to further understand the cognitive impact of menopause and hormone therapies taken by women (Gleason et al., 2015, Greendale et al., 2011, Karlamangla et al., 2017, Rapp et al., 2003, Shumaker et al., 2003). Only one human study
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To further investigate mechanisms of rXCI we generated femal
2020-12-24

To further investigate mechanisms of rXCI, we generated female ESCs with a homozygous RlimKO. We found that these Melanocyte stimulating hormone release inhibiting factor undergo XCI in vivo but that XCI in vitro is strongly influenced by culture conditions, including both method of differentiation
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Targeting the MAPK pathway has attracted significant
2020-12-24

Targeting the MAPK pathway has attracted significant interest in cancer therapy. Efforts directly targeting RAS protein are believed to be very challenging in spite of the promise shown by a few RAS inhibitors in the early development stage. Clinical benefits achieved by BRAF and MEK inhibitors have
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Methods br Results First we compared A plaque number A
2020-12-24

Methods Results First, we compared Aβ plaque number, Aβ concentration, and neurobehavior functions between naive APP/PS1 and APP/PS1xEP1−/− mice. Significantly lower Aβ burden in APP/PS1xEP1−/− mice was evidenced by fewer plaques in the hippocampal area and a lower concentration of soluble Aβ42
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Conventional assays rely on a comparable transformation of t
2020-12-24

Conventional assays rely on a comparable transformation of the target analytes and the structurally similar (but not identical) proxy substrates and are commonly used to measure individual enzyme activities in (pre-treated) intact sludge flocs (Burgess and Pletschke, 2008a, Gessesse et al., 2003, Yu
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br Introduction As a serine proteinase and a
2020-12-24

Introduction As a serine proteinase and a sub-family of the chymotrypsin-like proteinase, Glutamyl endopeptidase (GE), which is mainly found in Bacillus species, specifically cleaves negatively charged amino vx 809 residues (Glu/Asp) (Yokoi et al., 2001). Madsen et al. (Madsen & Qvist, 1997) rep
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In vitro studies in NSCLC cell lines expressing
2020-12-24

In vitro studies in NSCLC cell lines expressing EGFR mutants (T790M mutation, exon 19 deletion E746-A750, L858R/T790M double mutation), demonstrated that Rociletinib potently inhibits proliferation in the mutant EGFR NSCLC SAR405838 receptor with Growth inhibition (GI50) values ranging from 7 to 32
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br Experimental Procedures br Acknowledgments
2020-12-24

Experimental Procedures Acknowledgments We thank S. Tangye and A. Swarbrick for helpful discussions and critical reading of the manuscript; K. Wood, T. Camidge, and V. Turner for technical assistance; C. Brownlee for cell sorting; the staff of the Garvan Institute Biological Testing Facility f
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Cy5 azide In addition to tissue resident stromal and myeloid
2020-12-24

In addition to tissue-resident stromal and myeloid cell populations, ILCs also readily engage in positive-feedback loops with myeloid Cy5 azide recruited from the circulation. TNF-α produced by inflammatory monocytes recruited to the lungs of mice infected with Klebsiella pneumoniae markedly increa
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In contrast to inflammatory cytokines
2020-12-24

In contrast to inflammatory cytokines, TGF-β has immunosuppressive properties yet is also important for tissue imprinting immune cell function during development [23]. Salivary gland (SG) ILCs, in addition to liver and intestinal intraepithelial ILC1, express markers denoting tissue residency and TG
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br A brief history of RBR E s RBR E
2020-12-24

A brief history of RBR E3s RBR E3s were originally defined based on sequence alignments that predicted a tripartite motif of three zinc (Zn)-binding domains: two RING domains (RING1 and RING2) connected via an in-between-RING (IBR) domain [28], [29]. The prediction together with initial observati
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Due to the high attractiveness of E and E
2020-12-24

Due to the high attractiveness of E2 and E3 ligases as drug targets, a number of drug discovery assays have been published, based on detection by fluorescence (Dudgeon et al., 2010, Krist et al., 2016, Zhang et al., 2004), 8-pCPT-2-O-Me-cAMP-AM mg (Davydov et al., 2004, Huang et al., 2005, Kenten et
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Several DA receptors heteromers with a therapeutic
2020-12-23

Several DA receptors heteromers with a therapeutic potential have been described, including D1R/D3R (Fiorentini et al., 2010), but their roles remain to be established. Moreover, most studies on receptor heteromers in addiction focused on the striatum because of its key role in the pathology and its
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Introduction Amphetamine AMPH methamphetamine MA and ethylen
2020-12-23

Introduction Amphetamine (AMPH), methamphetamine (MA), and 3,4-ethylenedioxymethamphetamine (MDMA) are widely abused psychoactive substances, with the basic chemical structure of phenylethylamine [1]. The abuse of these drugs is associated with psychostimulant, anorectic and hallucinogenic properti
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