Publications by authors named "Chun-Mei Ji"

Article Synopsis
  • * High levels of RNPC1 correlate with advanced cancer stages and contribute to mitotic issues and chromosomal instability in gastric cancer cells.
  • * Targeting RNPC1 and its interaction with AURKB may offer new strategies for diagnosis and treatment of gastric cancer.
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Increasing evidence emphasizes the protective role of Eph receptors in synaptic function in the pathological development of Alzheimer's disease (AD); however, their roles in the regulation of hippocampal astrocytes remain largely unknown. Here, we directly investigated the function of astroglial EphB2 on synaptic plasticity in APP/PS1 mice. Using cell isolation and transgene technologies, we first isolated hippocampal astrocytes and evaluated the expression levels of ephrinB ligands and EphB receptors.

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The prevalence of food allergies is increasing worldwide. To understand the regional specificities of food allergies and develop effective therapeutic interventions, extensive regional epidemiological studies are necessary. While data regarding incidence, prevalence, regional variation, and treatment in food allergies are available for western countries, such studies may not be available in many Asian countries.

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Platanus acerifolia pollen is considered an important source of airborne allergens in numerous cities. Pla a 1 is a major allergen from P. acerifolia pollen.

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Platanus acerifolia (P. acerifolia) is an important cause of pollinosis in cities. The use of allergen extracts on patients with allergic diseases is the most commonly applied method to attempt to treat pollinosis.

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Astrocytes and apolipoprotein E (apoE) play critical roles in cognitive function, not only under physiological conditions but also in some pathological situations, particularly in the pathological progression of Alzheimer's disease (AD). The regulatory mechanisms underlying the effect of apoE, derived from astrocytes, on cognitive deficits during AD pathology development are unclear. In this study, we generated amyloid precursor protein/apoE knockout (APP/apoE) and APP/glial fibrillary acidic protein (GFAP)-apoE mice (the AD mice model used in this study was based on the APP-familial Alzheimer disease overexpression) to investigate the role of apoE, derived from astrocytes, in AD pathology and cognitive function.

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Background: Chronic spontaneous urticaria (CSU) is defined by itchy hives, angioedema, or both for at least 6 weeks. Omalizumab, an anti-IgE antibody that affects mast cell and basophil function, is a promising new treatment option. As of now, however, the efficacy and safety of different doses of omalizumab used in clinical trials for CSU have not been systematically analyzed and summarized.

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Background: Mutations in the dual oxidase maturation factor 2 (DUOXA2) and thyroid peroxidase (TPO) genes have been reported to cause goitrous congenital hypothyroidism (GCH). The aim of this study was to determine the genetic basis of GCH in affected children.

Methods: Thirty children with GCH were enrolled for molecular analysis of the DUOXA2 and TPO genes.

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Objective: To investigate well-controlled congenital hypothyroidism on the markers associated with early kidney injury and oxidative DNA damage.

Methods: Twenty-three children with euthyroid congenital hypothyroidism aged 3-6 years and 19 age- and gender-matched controls were enrolled. Serum levels of albumin, C-reactive protein, cysteine C, globulin, pre-albumin, and total protein were detected.

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In the title mol-ecule, C(30)H(52)O(4), the three six-membered rings are in chair conformations, the cyclo-pentane ring is in an envelope form and the tetra-hydro-furan ring has a conformation inter-mediate between half-chair and sofa. In the crystal, mol-ecules are linked by inter-molecular O-H⋯O hydrogen bonds into helical chains along [100]. Two intra-molecular O-H⋯O hydrogen bonds are also present.

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Article Synopsis
  • The study investigates the link between specific genetic variations of the mannose-binding protein (MBP) and the risk of developing pulmonary tuberculosis (TB) among patients and healthy individuals.
  • Researchers analyzed genetic mutations in the MBP gene from 125 TB cases and 198 controls, using a case-control design and advanced statistical techniques to assess risk factors.
  • Results indicated that certain MBP mutations (especially MBP-52) were more common in TB patients, suggesting a potential genetic susceptibility to the disease.
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Article Synopsis
  • The study examined how variations in the NRAMP1 gene are linked to the risk of pulmonary tuberculosis (TB) among Han individuals in Northern China.
  • Researchers used a case-control method with 124 pairs of TB patients and healthy controls, employing genetic testing techniques to analyze specific NRAMP1 polymorphisms (3'UTR and INT4).
  • The results indicated that the 3'UTR TGTG+/del genotype increased TB susceptibility, while no significant link was found with the INT4 polymorphism, although it did affect the disease's characteristics.
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