期刊文献+

口腔修复工艺专业实习模式探索 被引量:5

Practice training mode in the Department of Dental Laboratory Center
下载PDF
导出
摘要 口腔修复工艺学是口腔修复学的重要分支,是以口腔临床医学、材料学、美学等多学科为基础,以制作加工各类修复体为目标的一门学科。实践操作能力的养成是培养口腔技师的特色与核心环节,为培养优秀的口腔技师,我们通过制定完善的实习计划,建立规范化的操作技能培训,取得较好的教学效果。 Dental technology in an important part of prosthodontics.The key point and characteristic of dental technician training are to cultivate the hands-on ability of the trainees.To achieve the goal of cultivating quali-fied dental technicians,we developed a complete teaching curriculum and established a set of standards of operations and achieved very good results.
出处 《牙体牙髓牙周病学杂志》 CAS 2015年第3期184-185,152,共3页 Chinese Journal of Conservative Dentistry
关键词 口腔修复工艺学 实习教学 dental technology practice teaching
  • 相关文献

参考文献13

  • 1Gasc AM, Giammarinaro P, Richter S, et al. Organization a- round the dnaA gene of Streptococcus pneumoniae [ Jl. Microbi- ol, 1998, 144:433-439.
  • 2Seol JH, Woo SK, Jung EM, et al. Protease Do is essential for survival of Escherichia coli at high temperature : Its identity with the htrA gene product [ J ]. Biochem Biophys Res Commun, 199l, 176:730 -736.
  • 3Ponting CP. Evidence for PDZ domains in bacteria, yeast, and plants [J]. Protein Sci, 1997, 6(2) : 464 -468.
  • 4Gray CW, Ward RV, Karran E, et al. Characterization of hu- man HtrA2, a novel serine protease involved in the nlanlnlalian cellular stress response [J]. Eur J Biochem, 2000, 267(18) : 5699 - 5710.
  • 5Spiess C, Beil A, Ehrmann M, et al. A temperature-dependent switch from chaperone to protease in a widely conserved heat shock protein [J]. Cell, 1999, 97(3) : 339 -347.
  • 6Wonderling LD, Wilkinson B J, Bayles DO. The htrA (degP) gene of Listeria monocytogenes 10403S is essential for optimal growth understrcss conditions [ J ]. Appl Environ Microbiol, 2004, 70(4) : 1935 - 1943.
  • 7Poquet IV, Saint E, Seznec N, et al. HtrA is the unique surfacehousekeeping protease in Lactococcus lactis and is required for natural protein processing [ J ]. Mol Microbiol, 2000, 35 ( 5 ) : 1042 - 1051.
  • 8Diaz ML, Russell RR. HtrA protease and processing of extracel- lular proteins of Streptococcus mutans [ J ]. FEMS Microbiol Lett, 2001, 204( 1 ) : 23 -28.
  • 9杨江华,郭夕源,王光平,李明霞,刘兴容.不同龋敏感儿童口腔变异链球菌临床分离株与HtrA关系的研究[J].重庆医学,2013,42(24):2834-2836. 被引量:4
  • 10Robinson WG, Old LA, Shah DS, et al. Chromosomal inser- tions and deletions in Streptococcus mutans [ J ]. Caries Res, 2003, 37(2) : 148 -156.

二级参考文献12

  • 1黄远帅,许颂霄,朱旦,阳强,刘明芳,陈淑惠,张雪梅,尹一兵.HtrA基因缺陷对肺炎链球菌毒力影响的研究[J].第四军医大学学报,2006,27(17):1542-1546. 被引量:3
  • 2Carletto Korber FP, Cornejo LS, Gimenez MG. Early ac- quisition of streptococcus mutans for children[J]. Acta Odontol Latinoam, 2005,18 ( 2 ) : 69-74.
  • 3Berkowitz RJ. Mutans streptococci:acquisition and trans- mission[J]. Pediatr Dent,2006,28(2) : 106-109.
  • 4Aguilera Galaviz LA, Aceves Medina Mdel C, Estrada Garcia IC. Detection of potentially cariogenic strains of streptococcus mutans using the polymerase chain reaction[J]. J Clin Pediatr Dent,2002,27(1) :47-51.
  • 5Ajdic D, McShan WM, McLaughlin RE, et al. Genome se- quence of Streptococcus mutans UA159, a cariogenic dental pathogen[J]. Proc Natl Acad Sei USA,2002,99(22):14434- 14439.
  • 6Gilbert P, McBain A,Sreenivasan P. Common therapeutic approaches for the control of oral hiofilms : microbiological safety and efficacy [J]. Clin Microhiol Infect, 2007, 13 (Suppl 4) :S17-24.
  • 7Truong TL, Menard C, Mouton C, et al. Identification of mutans and other oral streptococci by random amplified polymorphic DNA analysis[J]. J Med microbiol, 2000,49 (1) :63-71.
  • 8Fujiwara T, Hoshino T,Ooshima T,et al. Differential and quantitative analyses of mRNA expression of glueosyl- transferases from Streptococcus mutans TM8148 [J]. J Dent Res,2002,81(2):109-113.
  • 9Mattos-Graner RO, Napimoga MH, Fukushima K, et al. Comparative analysis of GTF isozyme production and di- versity in isolates of Streptococcus mutans with different biofilm growth phenotypes[J]. J Clin Microbiol, 2004,42 (10) : 4586-4592.
  • 10曹元书,刘兴容.不同龋敏感儿童变形链球菌临床分离株产酸、耐酸能力的实验研究[J].实用口腔医学杂志,2009,25(1):103-106. 被引量:11

共引文献3

同被引文献47

引证文献5

二级引证文献30

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部