Publications by authors named "Jian-ming Xing"

The aim of the present study was to assess the atypical imaging manifestations of branchial cleft cysts (BCCs) confirmed by pathology. Computerized tomography (CT) or magnetic resonance imaging (MRI) of 17 BCC cases were reviewed. The imaging features, including laterality, location, border, attenuation and internal architecture, were evaluated.

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Through introduction of the methodological mechanism and comparison with classic randomized controlled trial, the status and the applicability of the expertise-based randomized controlled trials in clinic are explored, and its characteristics in acupuncture clinical application are analyzed. It is held that expertise-based randomized controlled trial is more suitable for the acupuncture clinical research, especially for acupuncture practice which emphasizes manipulations and different schools.

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Objective: To develop a rapid, sensitive and specific real time reverse transcription PCR for detecting and identifying human metapneumovirus.

Methods: The Hmpv-L gene of human metapneumovirus was chosen as target gene, the primers and TaqMan probe were designed, and the PCR reaction was optimized systematically. The total RNA was extracted from respiratory specimens, and reverse transcription was performed through random primer.

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Objective: To develop a new platform for genotyping human papillomavirus(HPV) and to investigate its effect in clinical application.

Methods: By combining L1 consensus PCR and multiplex hybridization using a Luminex xMAP system-based suspension array, we developed a rapid high-throughput assay,the HPV DNA suspension array (HPV-SA), capable of simultaneously typing 30 HPVs, including 18 high-risk HPV genotypes and 12 low-risk HPV genotypes. 810 clinical specimens were used to investigate the effect of HPV-SA.

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Aim: To develop a new, rapid and accurate reverse dot blot (RDB) method for the detection of intestinal pathogens in fecal samples.

Methods: The 12 intestinal pathogens tested were Salmonella spp., Brucella spp.

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Article Synopsis
  • * A double PCR method successfully amplified the target genes, and the microarray showed high sensitivity (10^3 cfu/ml), accurately identifying bacteria in stool samples of 81 patients, with a 39.5% positive detection rate.
  • * The results indicated that the method is reliable and efficient, making it suitable for quick diagnostics in clinical settings and epidemiological studies.
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