Effect of probe-site mismatches on detection of virulent Newcastle disease viruses using a fusion-gene real-time reverse transcription polymerase chain reaction test.
about
International Biological Engagement Programs Facilitate Newcastle Disease Epidemiological StudiesNewcastle disease: a review of field recognition and current methods of laboratory detectionBroad detection of diverse H5 and H7 hemagglutinin genes of avian influenza viruses by real-time reverse transcription-PCR using primer and probe sets containing mixed bases.Characterization of class I Newcastle disease virus isolates from Hong Kong live bird markets and detection using real-time reverse transcription-PCR.Avian paramyxovirus serotype-1: a review of disease distribution, clinical symptoms, and laboratory diagnosticsA robust and cost-effective approach to sequence and analyze complete genomes of small RNA viruses.Application of real-time reverse transcription polymerase chain reaction to the detection the matrix, H5 and H7 genes of avian influenza viruses in field samples from South Korea.Biological and phylogenetic characterization of pigeon paramyxovirus serotype 1 circulating in wild North American pigeons and doves.Real-time PCR-based pathotyping of Newcastle disease virus by use of TaqMan minor groove binder probes.Evaluation of TaqMan qPCR System Integrating Two Identically Labelled Hydrolysis Probes in Single AssayDetection of Newcastle disease virus minor genetic variants by modified single-stranded conformational polymorphism analysis.Natural Infections With Pigeon Paramyxovirus Serotype 1: Pathologic Changes in Eurasian Collared-Doves ( Streptopelia decaocto) and Rock Pigeons ( Columba livia) in the United States.Phylogenetic and biological characterization of Newcastle disease virus isolates from Pakistan.Recent sequence variation in probe binding site affected detection of respiratory syncytial virus group B by real-time RT-PCR.Phylogenetic assessment reveals continuous evolution and circulation of pigeon-derived virulent avian avulaviruses 1 in Eastern Europe, Asia, and Africa.Assessment of Preparation of Samples Under the Field Conditions and a Portable Real-Time RT-PCR Assay for the Rapid On-Site Detection of Newcastle Disease Virus.Opinion of the Scientific Panel on Animal Health and Welfare (AHAW) to review Newcastle disease focussing on vaccination worldwide in order to determine its optimal use for disease control purposesWhole-genome sequencing of genotype VI Newcastle disease viruses from formalin-fixed paraffin-embedded tissues from wild pigeons reveals continuous evolution and previously unrecognized genetic diversity in the U.S.Analytical validation of a real-time reverse transcription polymerase chain reaction test for Pan-American lineage H7 subtype Avian influenza viruses.
P2860
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P2860
Effect of probe-site mismatches on detection of virulent Newcastle disease viruses using a fusion-gene real-time reverse transcription polymerase chain reaction test.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年學術文章
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2006年學術文章
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name
Effect of probe-site mismatche ...... olymerase chain reaction test.
@en
Effect of probe-site mismatche ...... olymerase chain reaction test.
@nl
type
label
Effect of probe-site mismatche ...... olymerase chain reaction test.
@en
Effect of probe-site mismatche ...... olymerase chain reaction test.
@nl
prefLabel
Effect of probe-site mismatche ...... olymerase chain reaction test.
@en
Effect of probe-site mismatche ...... olymerase chain reaction test.
@nl
P2093
P2860
P1476
Effect of probe-site mismatche ...... olymerase chain reaction test.
@en
P2093
Claudio L Afonso
David L Suarez
P2860
P304
P356
10.1177/104063870601800601
P577
2006-11-01T00:00:00Z