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1.
Military Medical Sciences ; (12): 635-637, 2017.
Article in Chinese | WPRIM | ID: wpr-664506

ABSTRACT

Objective To construct a scenario database for high altitude military medical comprehensive exercises to enhance the training efficiency.Methods Related documents were used as guidelines for construction.Information technologies were used as construction support.The hierarchical model was used as a technical framework.JAVA,Linux,Oracle and Tomcat were used as development tools.Results First,the foundation of the system was elaborated regarding of guiding ideology,construction principles and standards.Second,the architectural design of the system was stated around the functional framework,technical framework and information framework.Third,the implementation of the system was outlined in terms of development tools and function modules.Conclusion The scenario database can provide standard data resources for related simulation training systems and perfect scenario support for high altitude health service training,which can contribute to the training reform and the improvement of training quality.

2.
Chinese Medical Journal ; (24): 2691-2694, 2009.
Article in English | WPRIM | ID: wpr-307836

ABSTRACT

<p><b>BACKGROUND</b>Mutations in the transforming growth factor beta I (TGFBI) gene cause several types of autosomal-dominant corneal dystrophies. We investigated the role of this gene in a Chinese family affected by granular corneal dystrophy (GCD).</p><p><b>METHODS</b>Family history and phenotypic data were recorded. The diagnosis of GCD was made on the basis of clinical evaluation. The genomic DNA was extracted from peripheral blood leukocytes. All the exons and flanking intron-exon boundary sequences of TGFbetaI were amplified by polymerase chain reaction (PCR) and screened for mutation by direct DNA sequencing.</p><p><b>RESULTS</b>A heterozygous C to T transition at nucleotide c.1663 (CGG to TGG R555W) of TGFbetaI gene was present in two affected members but was absent in the rest of the family members.</p><p><b>CONCLUSION</b>A recurrent pathogenic R555W of TGFbetaI gene mutation is identified, which appears to be the predominant mutations causing GCD in different populations.</p>


Subject(s)
Adult , Female , Humans , Middle Aged , Corneal Dystrophies, Hereditary , Genetics , Mutation , Transforming Growth Factor beta1 , Genetics
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