Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
1.
Chinese Journal of Stomatology ; (12): 168-171, 2008.
Article in Chinese | WPRIM | ID: wpr-235955

ABSTRACT

<p><b>OBJECTIVE</b>To apply the bioinformatics tools for analyzing the differentially expressed genes in oral submucous fibrosis (OSF) to obtain the implied biological significance.</p><p><b>METHODS</b>By using DAVID and Onto-express bioinformatic tools, 865 differentially expressed genes in OSF were analyzed and the analysis of chromosome location, gene ontology (GO) and genetic-association diseases were performed.</p><p><b>RESULTS</b>A majority of the differentially expressed genes were located on chromosome 1,2,5,6,7,11,12 (P < 0.01). GO classification of the differentially expressed genes identified the biological process subgroups, including genes involved in immune response, defense response and so on. The cellular component subgroups were associated with extracellular matrix, cytoskeleton and membrane, molecular function subgroups related to protein binding, extracellular matrix structural constituent and signal transducer activity. The diseases genetically associated with these genes included infection, immune and cardiovascular diseases.</p><p><b>CONCLUSIONS</b>Bioinformatics can provide the quick and parallel analysis of massive data got from gene microarrays and enable the function classification of the differentially expressed genes, which provides new ideas on the research of pathogenesis and epidemiology of OSF.</p>


Subject(s)
Humans , Computational Biology , Methods , Gene Expression Profiling , Oligonucleotide Array Sequence Analysis , Oral Submucous Fibrosis , Genetics , Software
2.
Journal of Central South University(Medical Sciences) ; (12): 796-799, 2007.
Article in Chinese | WPRIM | ID: wpr-813797

ABSTRACT

OBJECTIVE@#To culture human gingival epithelia in vitro, and to construct the tissue engineered gingiva with the acellular dermal matrix (ADM).@*METHODS@#Human gingival epithelia were isolated from the gingival tissue, and the cells were cultured and seeded onto the surface of ADM. After 7 days of submerged incubation, an air-liquid interface culture was performed for 7, 14, and 21 days. The complex constructed above was taken for histological examination.@*RESULTS@#Human gingival epithelia could proliferate well on the surface of ADM, and form multilayer structure. But the superficial epithelium was partially keratinized.@*CONCLUSION@#Tissue engineered gingiva may be constructed with human gingival epithelia and ADM in vitro.


Subject(s)
Humans , Acellular Dermis , Cells, Cultured , Connective Tissue , Epithelial Cells , Cell Biology , Gingiva , Cell Biology , Skin, Artificial , Tissue Engineering , Methods
SELECTION OF CITATIONS
SEARCH DETAIL