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1.
Journal of Medical Informatics ; (12): 30-32, 2018.
Artículo en Chino | WPRIM | ID: wpr-700728

RESUMEN

In order to improve the access and control of core data in medical information security,the paper builds a virtual isolation private cloud storage architecture in hospital,including virtualized reconstruction,metadata model application based on hierarchical model,access to remote clients design and application based on virtual isolation and so on,providing a reliable method for the isolation and intercommunication between the intranet and extranet.

2.
Journal of Zhejiang University. Medical sciences ; (6): 257-263, 2010.
Artículo en Chino | WPRIM | ID: wpr-259206

RESUMEN

<p><b>OBJECTIVE</b>To construct COL1A1-targeted short hairpin RNA (shRNA) vector with pSilencer 4.1-CMV neo siRNA expression vector and to evaluate its effect on proliferation and migration of gastric cancer BGC-823 cells in vitro.</p><p><b>METHODS</b>Three COL1A1-shRNA plasmids (COL1A1-shRNA-1, COL1A1-shRNA-2, COL1A1-shRNA-3), targeting different sites of COL1A1 gene, were constructed using pSilencer 4.1-CMV neo siRNA expression vector and transfected into gastric cancer BGC-823 cells. Real time quantitative RT-PCR and Western blot were performed to detect expression levels of COL1A1. MTT and Transwell migration assays were employed to evaluate the effects of COL1A1 gene silence on cell proliferation and migration.</p><p><b>RESULT</b>Three recombinant plasmids targeting COL1A1 were constructed successfully. The expressions of COL1A1 in BGC-823 cells, including mRNA and protein levels, were significantly inhibited by the COL1A1-shRNA transfectants, which resulted in a clear reduction of cell proliferation and migration capacity.</p><p><b>CONCLUSION</b>The COL1A1-shRNA can effectively knock down gene expression and inhibit proliferation and migration of gastric cancer BGC-823 cells.</p>


Asunto(s)
Humanos , Línea Celular Tumoral , Proliferación Celular , Colágeno Tipo I , Genética , Metabolismo , Vectores Genéticos , Plásmidos , Genética , ARN Mensajero , Genética , ARN Interferente Pequeño , Genética , Neoplasias Gástricas , Patología , Transfección , Transformación Bacteriana
3.
Journal of Zhejiang University. Medical sciences ; (6): 465-469, 2007.
Artículo en Chino | WPRIM | ID: wpr-271501

RESUMEN

<p><b>OBJECTIVE</b>To screen metronidazole (MTZ) -resistance associated gene fragments of Helicobacter pylori (H.pylori) by suppression subtractive hybridization(SSH).</p><p><b>METHODS</b>The suppression subtractive hybridization (SSH) was used to screen the different DNA fragments between MTZ-resistant and -susceptible clinical strains of H.pylori. The resistant strains specific gene fragments were obtained by SSH and identified by dot blotting.</p><p><b>RESULT</b>Among the 120 subtractive colonies which were randomly chosen, 37 DNA fragments were different (>or=2 times) in DNA-copy numbers between resistant and susceptible strains and 17 of them were significantly different (>or=3 times). These 17 DNA fragments were sequenced subsequently. Ten of them were new sequences and the other 7 were duplicated sequences. These sequences represented respectively: depeptide ABC transporter periplasmic dipeptide-binding protein (dppA), permease protein (dppB), et al.</p><p><b>CONCLUSION</b>Gene fragments specific to MTZ-resistant H. pylori strains were obtained by SSH and these genes may associated with MTZ-resistance of H.pylori.</p>


Asunto(s)
Humanos , Antiinfecciosos , Farmacología , Clonación Molecular , ADN Bacteriano , Química , Genética , Farmacorresistencia Bacteriana , Genética , Helicobacter pylori , Genética , Metronidazol , Farmacología , Hibridación de Ácido Nucleico , Métodos , Análisis de Secuencia de ADN
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