Capacity of nine thermostable DNA polymerases To mediate DNA amplification in the presence of PCR-inhibiting samples
about
Helix-hairpin-helix motifs confer salt resistance and processivity on chimeric DNA polymerasesAnalysis of single nucleic acid molecules in micro- and nano-fluidicsEffects of amplification facilitators on diagnostic PCR in the presence of blood, feces, and meatCurrent and developing technologies for monitoring agents of bioterrorism and biowarfare.Differential susceptibility of PCR reactions to inhibitors: an important and unrecognised phenomenon.Variants of a Thermus aquaticus DNA polymerase with increased selectivity for applications in allele- and methylation-specific amplification.PCR performance of a thermostable heterodimeric archaeal DNA polymerase.Challenges in the culture-independent analysis of oral and respiratory samples from intubated patients.Development of procedures for direct extraction of Cryptosporidium DNA from water concentrates and for relief of PCR inhibitorsMolecular diagnosis of Chlamydia pneumoniae infection.Molecular breeding of polymerases for resistance to environmental inhibitors.Toward standardization of diagnostic PCR testing of fecal samples: lessons from the detection of salmonellae in pigsIncorporation of real-time PCR into routine public health surveillance of culture negative bacterial meningitis in São Paulo, Brazil.Purification and characterization of PCR-inhibitory components in blood cells.Identification and characterization of immunoglobulin G in blood as a major inhibitor of diagnostic PCR.Inhibitory effects of collagen on the PCR for detection of Clostridium perfringensDevelopment of a combined selection and enrichment PCR procedure for Clostridium botulinum Types B, E, and F and its use to determine prevalence in fecal samples from slaughtered pigsSpecimen processing and concentration of Chlamydia trachomatis added can influence false-negative rates in the LCx assay but not in the APTIMA Combo 2 assay when testing for inhibitorsEvaluation of inhibitor-resistant real-time PCR methods for diagnostics in clinical and environmental samples.Quantitation of human immunodeficiency virus type 1 in breast milk.Real-time PCR analysis of enteric pathogens from fecal samples of irritable bowel syndrome subjectsQuantitative detection of Corynebacterium casei in cheese by real-time PCRSpecific capture and detection of Staphylococcus aureus with high-affinity modified aptamers to cell surface components.Evaluation of the use of PCR and reverse transcriptase PCR for detection of pathogenic bacteria in biosolids from anaerobic digestors and aerobic composters.Real-time detection and identification of Chlamydophila species in veterinary specimens by using SYBR green-based PCR assaysRapid and specific detection of Salmonella spp. in animal feed samples by PCR after culture enrichment.Duplex real-time PCR assay for rapid detection of ampicillin-resistant Enterococcus faecium.High-risk human papilloma virus in archival tissues of oral pathosis and normal oral mucosa.Plasma components affect accuracy of circulating cancer-related microRNA quantitationComparative evaluation of commercially available manual and automated nucleic acid extraction methods for rotavirus RNA detection in stoolsTransparent DNA/RNA Co-extraction Workflow Protocol Suitable for Inhibitor-Rich Environmental Samples That Focuses on Complete DNA Removal for Transcriptomic Analyses.Sensitive PCR-based quantitation of cell-free circulating microRNAsRapid quantification of Yersinia enterocolitica in pork samples by a novel sample preparation method, flotation, prior to real-time PCR.Human malaria diagnosis using a single-step direct-PCR based on the Plasmodium cytochrome oxidase III gene.qPCR, dPCR, NGS - A journey.Purification of crime scene DNA extracts using centrifugal filter devicesA novel, multi-parallel, real-time polymerase chain reaction approach for eight gastrointestinal parasites provides improved diagnostic capabilities to resource-limited at-risk populationsMutants of Taq DNA polymerase resistant to PCR inhibitors allow DNA amplification from whole blood and crude soil samples.Direct cell lysis for single-cell gene expression profilingA low complexity rapid molecular method for detection of Clostridium difficile in stool.
P2860
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P2860
Capacity of nine thermostable DNA polymerases To mediate DNA amplification in the presence of PCR-inhibiting samples
description
1998 nî lūn-bûn
@nan
1998 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Capacity of nine thermostable ...... ence of PCR-inhibiting samples
@ast
Capacity of nine thermostable ...... ence of PCR-inhibiting samples
@en
type
label
Capacity of nine thermostable ...... ence of PCR-inhibiting samples
@ast
Capacity of nine thermostable ...... ence of PCR-inhibiting samples
@en
prefLabel
Capacity of nine thermostable ...... ence of PCR-inhibiting samples
@ast
Capacity of nine thermostable ...... ence of PCR-inhibiting samples
@en
P2860
P1476
Capacity of nine thermostable ...... ence of PCR-inhibiting samples
@en
P2093
P Râdström
W Abu Al-Soud
P2860
P304
P407
P577
1998-10-01T00:00:00Z