[1]
K. Hayash, PCR-SSCP: A simple and sensitive method for detection of mutations in the genomic DNA. J. PCR Methods Appl. 1 (1991) 34-39.
DOI: 10.1101/gr.1.1.34
Google Scholar
[2]
Schwieger F, Tebbe C C, Effect of field inoculation with sigorhizobium meliloti L33 on the composition of bacterial communities in rhizospheres of a target plant (Medicago sativa) and a non- target Plant (chenopodium album)- Linking of 16S rRNA gene based single-strand conformation polymorphism community profiles to the diversity of cultivated bacteria,J. Applied Environmental Microbiology, 66 (2000).
DOI: 10.1128/aem.66.8.3556-3565.2000
Google Scholar
[3]
Stach JEM, S. Bathe, J P. Clapp, PCR-SSCP comparison of 16S rRNA sequence diversity in soil DNA obtained using different isolation and purification methods. J. FEMS Microbiol Ecol. 36 (2000) 139-151.
DOI: 10.1111/j.1574-6941.2001.tb00834.x
Google Scholar
[4]
Yang Likuan, Zhou Guimin, Xie Ling, Discussion about the use of single-strand conformation polymorphism technology to identify a variety of Candida. J, Chinese Journal of Laboratory Medicine, 21 (1999) 167-170.
Google Scholar
[5]
Li Hongmin, Wu Xueqiong, Zhuang Junxian, Rapid identification of M. tuberculosis-complex by PCR-SSCP, J. Microbiology, 27 (2000) 202-204.
Google Scholar
[6]
Li Lei, Zhang Kui, Detection of bacterial 16SrRNA gene by nested PCR, J. Chinese Journal of Coal Industry Medicine, 12 (2002) 1226-1227.
Google Scholar
[7]
MyranW, FluitA D, JanV, Rapid identification of bacteria by PCR-single-strand conformation poly-morphis, J. J Clin Microbiol, 32 (1996) 3002-3007.
Google Scholar
[8]
KumarM, Shukla PK, Single-strand conformation polymorphism of large subunit of ribosomal RNA is best suited to diagnosing fungal infections and differentiating fungi at species level. J. Diagnostic Microbiology and Infections Disease, 56 (2006).
DOI: 10.1016/j.diagmicrobio.2006.03.003
Google Scholar
[9]
Liu Yunxi, Zhao Zhongtang, Gao Yuan, Zhang Jinglan, Yang Zhanqing, Application of PCR/SSCP in genotyping of R. tsutsugamushi, J. Chinese Journal of Public Health, 20 (2004) 400-402.
Google Scholar
[10]
Lee D- H, Zo Y G, Kim S J, Nonradioactive method to study genetic profiles of natural bacterial communities by PCR-single-strand-conformation polymorphism. J. Appl Environ Microbiol. 62 (1996) 3112-3120.
DOI: 10.1128/aem.62.9.3112-3120.1996
Google Scholar
[11]
Delbès C, Moletta R, Godon J-J, Bacterial and archaeal 16S rDNA and 16S rRNA dynamics during an acetate crisis in an anaerobic digestor ecosystem, J. FEMS Microbiol Ecol, 35 (2001) 16-26.
DOI: 10.1016/s0168-6496(00)00107-0
Google Scholar
[12]
Zumstein E, Moletta R, Godon J-J, Examination of two years of community dynamics in an anaerobic bioreactor using fluorescence polymerase chain reaction (PCR) single-strand conformation polymorphism analysis. J. Environ Microbiol, 2 (2000) 69-78.
DOI: 10.1046/j.1462-2920.2000.00072.x
Google Scholar
[13]
Li Jian, Study on Kidney syndrome hemorrhagic fever epidemiology in Shandong, D, (2007).
Google Scholar