Publications by authors named "Cheng-Xi Liu"

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  • Scientists studied tiny living things (microbes) in a special tank (bioreactor) that produces a material called polyhydroxyalkanoates (PHAs) from leftover food and sludge.
  • They found that the microbes changed a lot depending on what food they were given, and they worked better in teams to produce PHAs.
  • The researchers also discovered new types of microbes that can make PHAs from garbage, helping us understand more about how mixed-culture systems work to recycle waste.
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  • FGFR3 has varying effects in different tipos of cancers, and its specific role in pancreatic ductal adenocarcinoma (PDAC) needs more clarity.
  • Researchers used RNA interference to reduce FGFR3 levels in PDAC cell lines, confirming that its knockdown leads to decreased cell proliferation and changes in key cell cycle proteins.
  • High levels of nuclear FGFR3 in tumor tissues were linked to advanced cancer stages and poor survival rates, and it was identified as an independent poor prognostic factor for patients post-surgery.
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Objectives: To study the clinical features of intestinal polyps and the risk factors for secondary intussusception in children.

Methods: A retrospective analysis was performed for the medical data of 2 669 children with intestinal polyps. According to the presence or absence of secondary intussusception, they were divided into two groups: intussusception (=346) and non-intussusception (=2 323).

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  • The paraventricular thalamus (PVT) is a part of the brain that helps control how awake or alert we feel.
  • It gets signals from many parts of the brain and sends signals out to help manage things like sleep, attention, memory, and how we feel about pain.
  • Scientists are studying the PVT more because it might play a role in sleep problems and mood swings, and this review aims to explain more about it for future research.
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Dopamine (DA), a monoamine neurotransmitter, is synthesized and released mainly by neurons in the ventral tegmental area and the substantia nigra (SN) pars compacta of the midbrain. DA and its receptors are essential for the regulation of arousal, movement, cognition, reward, and other neurobiological behaviors. Arousal, locomotion, cognition, reward, and other neurobiological functions are all regulated by dopamine and its receptors.

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Propofol is a worldwide-used intravenous general anesthetic with ideal effects, but hedonic effects of propofol have been reported and cause addictive issue. There is little known about the neurobiological mechanism of hedonic effects of propofol. Increasing researches have shown that the dopaminergic nervous system of the ventral tegmental area (VTA) and the noradrenergic system of locus coeruleus (LC) play a crucial role in hedonic experiences, which are putative sites for mediating the hedonic effects of propofol.

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Aims: The basal forebrain (BF) plays an essential role in wakefulness and cognition. Two subtypes of BF gamma-aminobutyric acid (GABA) neurons, including somatostatin-expressing (GABA ) and parvalbumin-positive (GABA ) neurons, function differently in mediating the natural sleep-wake cycle. Since the loss of consciousness induced by general anesthesia and the natural sleep-wake cycle probably share similar mechanisms, it is important to clarify the accurate roles of these neurons in general anesthesia procedure.

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Cholinergic neurons in the basal forebrain (BF) have long been considered to be the key neurons in the regulation of cortical and behavioral arousal, and cholinergic activation in the downstream region of the BF can arouse anesthetized rats. However, whether the activation of BF cholinergic neurons can induce behavior and electroencephalogram (EEG) recovery from anesthesia is unclear. In this study, based on a transgenic mouse line expressing ChAT-IRES-Cre, we applied a fiber photometry system combined with GCaMPs expression in the BF and found that both isoflurane and propofol inhibit the activity of BF cholinergic neurons, which is closely related to the consciousness transition.

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  • * A cell lysate microarray technique called CLICK was developed using various yeast mutant strains to analyze the effects of genetic interruptions on specific proteins, particularly focusing on histone marks.
  • * The CLICK array revealed multiple regulators for the histone modification H3K4me3 and identified key enzymes Cab4p and Cab5p involved in histone acylation, showcasing the method's potential for broad applications in studying protein regulation.
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Owing to the spread of multidrug resistance (MDR) and extensive drug resistance (XDR), there is a pressing need to identify potential targets for the development of more-effective anti-M. tuberculosis (Mtb) drugs. PafA, as the sole Prokaryotic Ubiquitin-like Protein ligase in the Pup-proteasome System (PPS) of Mtb, is an attractive drug target.

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Reversible lysine acetylation is one of the most important protein posttranslational modifications that plays essential roles in both prokaryotes and eukaryotes. However, only a few lysine deacetylases (KDACs) have been identified in prokaryotes, perhaps in part due to their limited sequence homology. Herein, we developed a 'clip-chip' strategy to enable unbiased, activity-based discovery of novel KDACs in the Escherichia coli proteome.

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Protein acetylation is one of the most abundant post-translational modifications and plays critical roles in many important biological processes. Based on the recent advances in mass spectrometry technology, in bacteria, such as Escherichia coli, tremendous acetylated proteins and acetylation sites have been identified. However, only one protein deacetylase, i.

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The monitoring of genetically modified organisms (GMOs) is a primary step of GMO regulation. However, there is presently a lack of effective and high-throughput methodologies for specifically and sensitively monitoring most of the commercialized GMOs. Herein, we developed a multiplex amplification on a chip with readout on an oligo microarray (MACRO) system specifically for convenient GMO monitoring.

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Protein microarray technology is one of the most powerful tools presently available for proteomic studies. Numerous types of protein microarrays have been widely and successfully applied for both basic biological studies and clinical researches, including those designed to characterize protein-protein, protein-nucleic acid, protein-drug/small molecule and antibody-antigen interactions. In the past decade, a variety of protein microarrays have been developed, including those spotted with whole proteomes, smaller peptides, antibodies, and lectins.

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