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153 related items for PubMed ID: 27699950
1. Improving qPCR methodology for detection of foaming bacteria by analysis of broad-spectrum primers and a highly specific probe for quantification of Nocardia spp. in activated sludge. Asvapathanagul P, Olson BH. J Appl Microbiol; 2017 Jan; 122(1):97-105. PubMed ID: 27699950 [Abstract] [Full Text] [Related]
2. Group-specific small-subunit rRNA hybridization probes to characterize filamentous foaming in activated sludge systems. de los Reyes FL, Ritter W, Raskin L. Appl Environ Microbiol; 1997 Mar; 63(3):1107-17. PubMed ID: 9055425 [Abstract] [Full Text] [Related]
4. Primer and probe sets for group-specific quantification of the genera Nitrosomonas and Nitrosospira using real-time PCR. Lim J, Do H, Shin SG, Hwang S. Biotechnol Bioeng; 2008 Apr 15; 99(6):1374-83. PubMed ID: 18023051 [Abstract] [Full Text] [Related]
5. Dispelling the "Nocardia amarae" myth: a phylogenetic and phenotypic study of mycolic acid-containing actinomycetes isolated from activated sludge foam. Stainsby FM, Soddel J, Seviour R, Upton J, Goodfellow M. Water Sci Technol; 2002 Apr 15; 46(1-2):81-90. PubMed ID: 12216692 [Abstract] [Full Text] [Related]
6. Dual color fluorescence in situ hybridization (FISH) assays for detecting Mycobacterium tuberculosis and Mycobacterium avium complexes and related pathogens in cultures. Shah J, Weltman H, Narciso P, Murphy C, Poruri A, Baliga S, Sharon L, York M, Cunningham G, Miller S, Caviedes L, Gilman R, Desmond E, Ramasamy R. PLoS One; 2017 Apr 15; 12(4):e0174989. PubMed ID: 28399124 [Abstract] [Full Text] [Related]
7. Molecular detection of Nocardia: development and application of a real-time PCR assay in sputum and bronchoalveolar lavage fluid samples. Wang S, Wang P, Liu J, Yang C, Li T, Yang J, Gu L, Wei M. Eur J Clin Microbiol Infect Dis; 2023 Jul 15; 42(7):865-872. PubMed ID: 37156981 [Abstract] [Full Text] [Related]
9. A Duplex Digital PCR Assay for Simultaneous Quantification of the Enterococcus spp. and the Human Fecal-associated HF183 Marker in Waters. Cao Y, Raith MR, Griffith JF. J Vis Exp; 2016 Mar 09; (109):. PubMed ID: 27023488 [Abstract] [Full Text] [Related]
10. The opportunistic pathogen Nocardia farcinica is a foam-producing bacterium in activated sludge plants. Stratton HM, Seviour RJ, Soddell JA, Blackall LL, Muir D. Lett Appl Microbiol; 1996 May 09; 22(5):342-6. PubMed ID: 8672272 [Abstract] [Full Text] [Related]
11. In situ hybridization for the differentiation of Actinomyces and Nocardia in tissue sections. Isotalo PA, Qian X, Hayden RT, Roberts GD, Lloyd RV. Diagn Mol Pathol; 2009 Sep 09; 18(3):183-8. PubMed ID: 19704264 [Abstract] [Full Text] [Related]
14. Evaluation of genetic markers from the 16S rRNA gene V2 region for use in quantitative detection of selected Bacteroidales species and human fecal waste by qPCR. Haugland RA, Varma M, Sivaganesan M, Kelty C, Peed L, Shanks OC. Syst Appl Microbiol; 2010 Oct 09; 33(6):348-57. PubMed ID: 20655680 [Abstract] [Full Text] [Related]
16. Rapid identification of clinically relevant Nocardia species to genus level by 16S rRNA gene PCR. Laurent FJ, Provost F, Boiron P. J Clin Microbiol; 1999 Jan 09; 37(1):99-102. PubMed ID: 9854071 [Abstract] [Full Text] [Related]
17. Development of a real-time PCR for detection of the oyster pathogen Nocardia crassostreae based on its homogeneous 16S-23S rRNA intergenic spacer region. Carrasco N, Roozenburg I, Voorbergen-Laarman M, Itoh N, Engelsma MY. J Invertebr Pathol; 2013 Oct 09; 114(2):120-7. PubMed ID: 23876658 [Abstract] [Full Text] [Related]