Multiple displacement amplification as a pre-polymerase chain reaction (pre-PCR) to process difficult to amplify samples and low copy number sequences from natural environments.
about
Further evidence supporting a role for gs signal transduction in severe malaria pathogenesisPopulation genetic analysis of Plasmodium falciparum parasites using a customized Illumina GoldenGate genotyping assayPicodroplet partitioned whole genome amplification of low biomass samples preserves genomic diversity for metagenomic analysisEnvironmental whole-genome amplification to access microbial populations in contaminated sediments.Unexpected diversity in populations of the many-celled magnetotactic prokaryote.Production of in vitro amplified DNA pseudolibraries and high-throughput cDNA target amplification.Sequence specific detection of DNA using nicking endonuclease signal amplification (NESA).Concurrent genotyping of Helicobacter pylori virulence genes and human cytokine SNP sites using whole genome amplified DNA derived from minute amounts of gastric biopsy specimen DNA.Lack of association of interferon regulatory factor 1 with severe malaria in affected child-parental trio studies across three African populationsTwo decades of describing the unseen majority of aquatic microbial diversity.Amplification by PCR artificially reduces the proportion of the rare biosphere in microbial communities.Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibility.Testing the reproducibility of multiple displacement amplification on genomes of clonal endosymbiont populations.Isothermal multiple displacement amplification: a methodical approach enhancing molecular routine diagnostics of microcarcinomas and small biopsies.Use of PCR-DGGE Based Molecular Methods to Analyse Microbial Community Diversity and Stability during the Thermophilic Stages of an ATAD Wastewater Sludge Treatment Process as an Aid to Performance Monitoring.New perspectives on microbial community distortion after whole-genome amplification.Performance assessment of a novel two-step multiple displacement amplification-PCR assay for detection of Mycobacterium tuberculosis complex in sputum specimens.Candidate human genetic polymorphisms and severe malaria in a Tanzanian population.Retrieval of entire genes from environmental DNA by inverse PCR with pre-amplification of target genes using primers containing locked nucleic acids.The genetic risk of acute seizures in African children with falciparum malariaSomething from (almost) nothing: the impact of multiple displacement amplification on microbial ecology.Common variation in the ABO glycosyltransferase is associated with susceptibility to severe Plasmodium falciparum malaria.Association of the GNAS locus with severe malaria.Positive selection of a CD36 nonsense variant in sub-Saharan Africa, but no association with severe malaria phenotypesSerotonin gene variants are unlikely to play a significant role in the pathogenesis of the sudden infant death syndrome.Nucleic acids as viability markers for bacteria detection using molecular tools.Fc gamma receptor IIa-H131R polymorphism and malaria susceptibility in sympatric ethnic groups, Fulani and Dogon of MaliAssessment of REPLI-g Multiple Displacement Whole Genome Amplification (WGA) Techniques for Metagenomic Applications.Searching for Helicobacter pylori and Chlamydia pneumoniae in primary endodontic infections.Intriguing Interaction of Bacteriophage-Host Association: An Understanding in the Era of OmicsTumor necrosis factor and lymphotoxin-alpha polymorphisms and severe malaria in African populations.TLR9 polymorphisms in African populations: no association with severe malaria, but evidence of cis-variants acting on gene expression.Variation in the ICAM1 gene is not associated with severe malaria phenotypes.Whole-genome amplification (WGA) of marine photosynthetic eukaryote populations.Microbial characterization of a subzero, hypersaline methane seep in the Canadian High Arctic.Whole-community genome amplification (WCGA) leads to compositional bias in methane-oxidizing communities as assessed by pmoA-based microarray analyses and QPCR.Isolation of a thioesterase gene from the metagenome of a mountain peak, Apharwat, in the northwestern Himalayas.Multiple displacement amplification compromises quantitative analysis of metagenomes
P2860
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P2860
Multiple displacement amplification as a pre-polymerase chain reaction (pre-PCR) to process difficult to amplify samples and low copy number sequences from natural environments.
description
2005 nî lūn-bûn
@nan
2005 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Multiple displacement amplific ...... ces from natural environments.
@ast
Multiple displacement amplific ...... ces from natural environments.
@en
type
label
Multiple displacement amplific ...... ces from natural environments.
@ast
Multiple displacement amplific ...... ces from natural environments.
@en
prefLabel
Multiple displacement amplific ...... ces from natural environments.
@ast
Multiple displacement amplific ...... ces from natural environments.
@en
P2860
P1476
Multiple displacement amplific ...... nces from natural environments
@en
P2093
Cesareo Saiz-Jimenez
P2860
P304
P356
10.1111/J.1462-2920.2005.00779.X
P577
2005-07-01T00:00:00Z