Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Development and application of a capsid VP1 (region D) based reverse transcription PCR assay for genotyping of genogroup I and II noroviruses.

Journal of virological methods - 15 Mar 2004

Vinjé Jan, Hamidjaja Raditijo A, Sobsey Mark D

Abstract excerpt

Noroviruses (NoV), previously called "Norwalk-like viruses", have emerged as the single most important cause of acute gastroenteritis worldwide. Most diagnostic reverse transcription-polymerase chain reaction (RT-PCR) assays target the viral RNA-dependent RNA polymerase; however, the major capsid protein (VP1) is the reference genomic region for establishing genotypes. In this study, we analyzed complete NoV VP1...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Base Sequence
Share to Capsid
Share to Capsid Proteins

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to DNA Primers

Share to Norovirus

Share to Phylogeny

Share to Reverse Transcriptase Polymerase Chain Reaction

Share to RNA, Viral

Source

Identifiers

PMID: 14738976
DOI: 10.1016/j.jviromet.2003.11.001

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Development and application of a capsid VP1 (region D) based reverse transcription PCR assay for genotyping of genogroup I and II noroviruses.PMID 14738976Read ↗

Single-step RT-PCR assay for dual genotyping of GI and GII norovirus strains.Semantic proximity Read ↗

Evaluation of real-time RT-PCR assays for detection and quantification of norovirus genogroups I and II.Semantic proximity Read ↗

Detection of waterborne norovirus genogroup I strains using an improved real time RT-PCR assay.Semantic proximity Read ↗

Genomic diversity and comparative phylogenomic analysis of genus Norovirus.Semantic proximity Read ↗

Development of enhanced primer sets for detection of norovirus.Semantic proximity Read ↗

Clinical and molecular epidemiology of norovirus infection in childhood diarrhea in China.Semantic proximity Read ↗

Environmental detection of genogroup I, II, and IV noroviruses by using a generic real-time reverse transcription-PCR assay.Semantic proximity Read ↗

Molecular Identification and Genetic Analysis of Norovirus Genogroups I and II in Water Environments: Comparative Analysis of Different Reverse Transcription-PCR AssaysSemantic proximity Read ↗

Use of TaqMan Real-Time Reverse Transcription-PCR for Rapid Detection, Quantification, and Typing of NorovirusSemantic proximity Read ↗

Evaluation of Various Real-Time Reverse Transcription Quantitative PCR Assays for Norovirus DetectionSemantic proximity Read ↗

Prevalence and genetic diversity of norovirus in outpatient children with acute diarrhea in Shanghai, China.Semantic proximity Read ↗

Molecular detection and genotyping of noroviruses.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.