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Sperm total motility and hyperactivated motility are
2024-02-26
Sperm total motility and hyperactivated motility are mediated by PLD-dependent endothelin receptor antagonist polymerization [20]. Reduction of PIP2 synthesis inhibited actin polymerization and motility, and increasing PIP2 synthesis enhanced these activities. Furthermore, sperm demonstrating low m
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Here we show that the co activation of RTKs and
2024-02-26
Here, we show that the co-activation of RTKs and non-RTKs is a common trait in treatment-naïve EGFR-mutation-positive NSCLC Iloperidone and patients, with AXL and CDCP1 being commonly over-expressed. The combination of gefitinib or osimertinib with the Src/FAK/Janus kinase 2 (JAK2) inhibitor TPX-00
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Although the LB domains of mGlu receptors
2024-02-26
Although the LB2 domains of mGlu receptors have not been shown to form an extensive interface during activation, they do draw closer to each other, as demonstrated in crystal structures (Kunishima et al., 2000, Muto et al., 2007, Tsuchiya et al., 2002) and by FRET analysis (Doumazane et al., 2013, V
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Our previous studies and others have identified
2024-02-26
Our previous studies and others have identified that the inhalational anesthetic isoflurane induces neuronal apoptosis via [Ca2+]i overload through the opening of synaptic voltage-dependent calcium channels (VDCCs) and the excessive Ca2+ release from the endoplasmic reticulum (Zhao et al., 2011; Zha
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The reception of antiangiogenic treatment in neuro
2024-02-23
The reception of antiangiogenic treatment in neuro-oncology has yet to achieve the wide success rapidly accomplished for other malignancies. In 1984, mutated receptor tyrosine kinase became a culprit for aberrant tumorigenesis signal, providing a target for monoclonal Calcein AM (mAbs) and small-mo
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Infections inflammation and corneal transplant can
2024-02-23
Infections, inflammation, and corneal transplant can all cause corneal neovascularization via upregulation of inflammatory cytokines, which attract myeloid (R)-PFI 2 hydrochloride into the cornea. These myeloid cells establish a cycle of cytokine secretion and further myeloid cell recruitment in th
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First the complete canonical brain original RAS
2024-02-23
First, the complete canonical brain original RAS (Angiotensinogen, Renin, Angiotensin I, Angiotensin Converting Enzyme (ACE), Angiotensin II) has not been conclusively identified in any specific cell type within the brain [1]. Validated evidence for the presence of brain Angiotensinogen and ACE was
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Finally microRNAs miRNA seem to play an important role in
2024-02-23
Finally, microRNAs (miRNA) seem to play an important role in AR signaling in BC. Some authors have described a differential Tirofiban hydrochloride monohydrate of miRNAs in AR-positive BCs compared to AR-negative ones. VEGF and mTOR pathways were also reported as implicated in miRNA dysregulation,
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br Introduction Quenchbody Q body immunoassay
2024-02-23
Introduction Quenchbody (Q-body) immunoassay is a novel biosensing technology that uses the quenching of fluorescence by intrinsic tryptophan (Trp) residues in antibody variable regions when dye(s) are conjugated to an antibody or antibody fragments in appropriate position, and de-quenching while
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Phenacetin The evidence points toward a role for LO
2024-02-23
The evidence points toward a role for 12/15-LO activity in WAT in modulating chronic local inflammation and subsequent systemic metabolic decline in the obese state. However, little is known as to the role of 12- and 15-LOs in BAT. Indeed, in addition to WAT, platelet- and leukocyte-type 12-LO are e
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br Depletion of serum amino acids Currently the only antican
2024-02-23
Depletion of serum amino acids Currently, the only anticancer agents that directly target amino 63 7 metabolism are bacterial l-asparaginases (from Escherichia coli and Erwinia chrysanthemi), which are FDA-approved for treatment of pediatric and adult ALL. A potential complication of using bacte
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All desired compounds with a
2024-02-23
All desired compounds with a carboxylic INCB3344 substituent at N1 position of the quinoxalinone scaffold and a variety of aromatic substituents at C3 position were obtained by the syntheses starting from methoxy-substituted 3-chloro-quinoxalin-2(1)-ones () prepared as previously. As shown in , com
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In addition to the above mentioned synaptic mechanisms the s
2024-02-23
In addition to the above-mentioned synaptic mechanisms, the serotonergic system also has a critical role in the antidepressant effects of mGlu2/3 receptor antagonists. Indeed, we previously reported that mGlu2/3 receptor antagonists increased the firing rate of serotonin neurons in the dorsal raphe
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BVT 2733 In order to get a better understanding of this
2024-02-23
In order to get a better understanding of this synergy, we tested the effect of preliminary incubation of BVT 2733 with non-stimulating concentrations of gonadotropins or FSK before subsequent stimulation by FSK or gonadotropins alone, also at sub-stimulating concentrations. We observed that human L
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We have expressed the ECDs of the
2024-02-23
We have expressed the ECDs of the human α1, β1, γ and ɛ AChR subunits in the past using the methylotropic yeast Pichia pastoris as soluble glycosylated proteins [15], [16]. Further work with the γ subunit ECD revealed a marked improvement of the solubility and yield following the mutation of hydroph
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