353 related articles for article (PubMed ID: 10386377)
21. A modified pulsed-field gel electrophoresis (PFGE) protocol for subtyping previously non-PFGE typeable isolates of Clostridium difficile polymerase chain reaction ribotype 001.
Gal M; Northey G; Brazier JS
J Hosp Infect; 2005 Nov; 61(3):231-6. PubMed ID: 16002184
[TBL] [Abstract][Full Text] [Related]
22. PCR amplification of species specific sequences of 16S rDNA and 16S-23S rDNA intergenic spacer region for identification of Streptococcus phocae.
Hassan AA; Vossen A; Lämmler C; Siebert U; Fernández-Garayzábal JF
Microbiol Res; 2008; 163(2):132-5. PubMed ID: 16793248
[TBL] [Abstract][Full Text] [Related]
23. PCR-mediated detection of the chemolithotrophic bacterium Thiobacillus cuprinus using 23S rDNA- and 16S/23S intergenic spacer region-targeted oligonucleotide primers.
Moreira D; Amils R
FEMS Microbiol Lett; 1996 Sep; 142(2-3):289-93. PubMed ID: 8810512
[TBL] [Abstract][Full Text] [Related]
24. Identification of Lactobacillus isolates from the gastrointestinal tract, silage, and yoghurt by 16S-23S rRNA gene intergenic spacer region sequence comparisons.
Tannock GW; Tilsala-Timisjarvi A; Rodtong S; Ng J; Munro K; Alatossava T
Appl Environ Microbiol; 1999 Sep; 65(9):4264-7. PubMed ID: 10473450
[TBL] [Abstract][Full Text] [Related]
25. Molecular characterization of Serratia marcescens strains by RFLP and sequencing of PCR-amplified 16S rDNA and 16S-23S rDNA intergenic spacer.
Zhu H; Zhou WY; Xu M; Shen YL; Wei DZ
Lett Appl Microbiol; 2007 Aug; 45(2):174-8. PubMed ID: 17651214
[TBL] [Abstract][Full Text] [Related]
26. Analysis of Clostridium difficile isolates from nosocomial outbreaks at three hospitals in diverse areas of Japan.
Kato H; Kato N; Watanabe K; Yamamoto T; Suzuki K; Ishigo S; Kunihiro S; Nakamura I; Killgore GE; Nakamura S
J Clin Microbiol; 2001 Apr; 39(4):1391-5. PubMed ID: 11283061
[TBL] [Abstract][Full Text] [Related]
27. Identification of Pseudomonas aeruginosa on the basis of polymerase chain reaction-amplified ribosomal DNA spacer polymorphisms.
Kur J; Burkiewicz A; Zablocka A; Gospodarek E
Acta Microbiol Pol; 1995; 44(2):111-7. PubMed ID: 8906931
[TBL] [Abstract][Full Text] [Related]
28. Method for rapid identification and differentiation of the species of the Mycobacterium chelonae complex based on 16S-23S rRNA gene internal transcribed spacer PCR-restriction analysis.
Khan IU; Selvaraju SB; Yadav JS
J Clin Microbiol; 2005 Sep; 43(9):4466-72. PubMed ID: 16145093
[TBL] [Abstract][Full Text] [Related]
29. Use of 16S-23S rRNA spacer-region (SR)-PCR for identification of intestinal clostridia.
Song Y; Liu C; Molitoris D; Tomzynski TJ; Mc Teague M; Read E; Finegold SM
Syst Appl Microbiol; 2002 Dec; 25(4):528-35. PubMed ID: 12583713
[TBL] [Abstract][Full Text] [Related]
30. Comparison of repetitive extragenic palindromic sequence-based PCR with PCR ribotyping and pulsed-field gel electrophoresis in studying the clonality of Clostridium difficile.
Pasanen T; Kotila SM; Horsma J; Virolainen A; Jalava J; Ibrahem S; Antikainen J; Mero S; Tarkka E; Vaara M; Tissari P
Clin Microbiol Infect; 2011 Feb; 17(2):166-75. PubMed ID: 20331683
[TBL] [Abstract][Full Text] [Related]
31. Long PCR-RFLP of 16S-ITS-23S rRNA genes: a high-resolution molecular tool for bacterial genotyping.
Zeng YH; Koblížek M; Li YX; Liu YP; Feng FY; Ji JD; Jian JC; Wu ZH
J Appl Microbiol; 2013 Feb; 114(2):433-47. PubMed ID: 23126629
[TBL] [Abstract][Full Text] [Related]
32. Typing of Clostridium difficile by polymerase chain reaction with an arbitrary primer.
Wilks M; Tabaqchali S
J Hosp Infect; 1994 Nov; 28(3):231-4. PubMed ID: 7852736
[TBL] [Abstract][Full Text] [Related]
33. Sequence and phylogenetic analysis of the gene for surface layer protein, slpA, from 14 PCR ribotypes of Clostridium difficile.
Ní Eidhin D; Ryan AW; Doyle RM; Walsh JB; Kelleher D
J Med Microbiol; 2006 Jan; 55(Pt 1):69-83. PubMed ID: 16388033
[TBL] [Abstract][Full Text] [Related]
34. Comparison of conventional ribotyping and PCR-RFLP ribotyping for the analysis of endemic strains of Neisseria meningitidis isolated in a local community over 7 years.
Verdú ME; Coll P; Fontanals D; March F; Pons I; Van Esso D; Prats G
FEMS Microbiol Lett; 1999 Oct; 179(2):247-53. PubMed ID: 10518723
[TBL] [Abstract][Full Text] [Related]
35. Heteroduplex structures in 16S-23S rRNA intergenic transcribed spacer PCR products reveal ribosomal interoperonic polymorphisms within single Frankia strains.
Gtari M; Brusetti L; Cherif A; Boudabous A; Daffonchio D
J Appl Microbiol; 2007 Oct; 103(4):1031-40. PubMed ID: 17897207
[TBL] [Abstract][Full Text] [Related]
36. Accurate identification of desired clones from 16S-23S rDNA spacer libraries using single PCR.
González-Escalona N; Jaykus LA; DePaola A
Anal Biochem; 2007 Jan; 360(1):146-7. PubMed ID: 17113024
[No Abstract] [Full Text] [Related]
37. Current application and future perspectives of molecular typing methods to study Clostridium difficile infections.
Knetsch CW; Lawley TD; Hensgens MP; Corver J; Wilcox MW; Kuijper EJ
Euro Surveill; 2013 Jan; 18(4):20381. PubMed ID: 23369393
[TBL] [Abstract][Full Text] [Related]
38. Restriction Endonuclease Analysis Typing of Clostridium difficile Isolates.
Sambol SP; Johnson S; Gerding DN
Methods Mol Biol; 2016; 1476():1-13. PubMed ID: 27507329
[TBL] [Abstract][Full Text] [Related]
39. DNA sequence heterogeneity in the three copies of the long 16S-23S rDNA spacer of Enterococcus faecalis isolates.
Gürtler V; YuJun R; Pearson SR; Bates SM; Mayall BC
Microbiology (Reading); 1999 Jul; 145 ( Pt 7)():1785-1796. PubMed ID: 10439418
[TBL] [Abstract][Full Text] [Related]
40. Typing and subtyping of Clostridium difficile isolates by using multiple-locus variable-number tandem-repeat analysis.
van den Berg RJ; Schaap I; Templeton KE; Klaassen CH; Kuijper EJ
J Clin Microbiol; 2007 Mar; 45(3):1024-8. PubMed ID: 17166961
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]