Results 221 to 230 of about 212,008 (257)

การระบุชนิดของแบคทีเรียกรดแลคติกที่แยกได้จากน้ำพริกด้วยลำดับนิวคลีโอไทด์ของยีน 16S rRNA

2016
Thai Journal of Science and Technology, 5, 2, 160 ...
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16S rRNA sequencing in chronic dacryocystitis

Clinical and Experimental Optometry
The pathogenesis of chronic dacryocystitis (CDC) is associated with a variety of bacteria. Investigating microflora has the potential to provide a theoretical basis for preventing and treating CDC.16S rRNA sequencing is a sequence-based bacterial analysis. The application of 16S rRNA sequencing in CDC is rarely reported.A case-control study of infected
Yongxin, Zhang, Beian, Liu, Meina, Yang, Shixu, Li, Yunhao, Qu, Yingge, Ma, Lin, Ye, Jun, Mei   +7 more
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The diversity of periodontal spirochetes by 16S rRNA analysis

Oral Microbiology and Immunology, 2000
The purpose of this study was to examine the diversity of spirochetes in the subgingival pocket of multiple subjects with a range of periodontal conditions, including two healthy, one adult periodontitis, three acute necrotizing ulcerative gingivitis, eight refractory periodontitis, and one human immunodeficiency virus (HIV) periodontitis. The 16S rRNA
F E, Dewhirst, M A, Tamer, R E, Ericson, C N, Lau, V A, Levanos, S K, Boches, J L, Galvin, B J, Paster   +7 more
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The role of 16S rRNA in ribosomal binding of IF-3

Biochemistry, 1976
The binding of initiation factor IF-3 to Escherichia coli 30S ribosomal subunits has been found to be inhibited by rRNA ligands such as ethidium bromide, polyamines, and monovalent alkali metals. The order of effectiveness of the polyamines (spermine greater than spermidine greater than putrescine) and alkali metals (Li+ greater than Na+ greater than K+
C L, Pon, C, Gualerzi
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rRNA topography in ribosome. IV. The accessibility of the 5'-end region of 16S rRNA

Molecular Biology Reports, 1979
The accessibility of the 5'-end region of 16S rRNA (A8GAGUUUG15) inEscherichia coli ribosomes for complementary binding with the synthetic octanucleotide d(CAAACTCT) has been studied. Nonequilibrium gel-filtration was used to evaluate parameters of the binding of this oligonucleotide with free 16S rRNA, ribosomal subunits, and 70S ribosomes.
E A, Skripkin, A M, Kopylov, A A, Bogdanov, S V, Vinogradov, Y A, Berlin   +4 more
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Sites of contact of mRNA with 16S rRNA and 23S rRNA in the Escherichia coli ribosome

Biochemistry, 1991
The locations of close encounter between ribosomal RNA (rRNA) and messenger RNA (mRNA) were determined by photochemical cross-linking experiments that employ an artificial mRNA, 51 nucleotides long, containing 14 U residues that were randomly substituted by 1-4 4-thiouridine (s4U) residues.
P, Wollenzien, A, Expert-Bezançon, A, Favre   +2 more
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Prediction of the Recognition Sites on 16S and 23S rRNAs fromE.colifor the Formation of 16S-23S rRNA Complex

Journal of Biomolecular Structure and Dynamics, 1988
Interactions between RNA molecules have been postulated to play an important role in the assembly of ribosomes. Using the sequence analysis and the search of continuous complementary regions on 16S rRNA and 23S rRNA, the recognition sites involved in the formation of ribosome of E. coli are postulated.
T A, Thanaraj, A S, Kolaskar, M W, Pandit   +2 more
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Mouse 16S rRNA

After treating the mice with antibiotics, 16S rRNA sequencing was conducted.
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16S rRNA Targeted DGGE Fingerprinting of Microbial Communities

2008
The past decades have seen the staggering development of molecular microbial ecology as a discipline that uses the detection of so-called biomarkers to monitor microbial communities in environment samples. A variety of molecules can be used as biomarkers, including cell-wall components, proteins, lipids, DNA or RNA. Especially, the application of small
Tzeneva, V.A., Heilig, G.H.J., van Vliet, W.M., Akkermans, A.D.L., de Vos, W.M., Smidt, H.   +5 more
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16S rRNA Amplicon Sequencing for Metagenomics

2018
The 16S rRNA amplicon sequencing technique is a microbiome analysis where different samples are analyzed at the same time using multiplexing. The results can be used to evaluate microbial diversity at genus, family, order, class, and phylum levels. The resolution is normally insufficient to evaluate the species level.
Henrik Christensen, Anna Jasmine Andersson, Steffen Lynge Jørgensen, Josef Korbinian Vogt   +3 more
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