Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay. - Wikidata - awgldk - TriplyDB

Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay.

Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay.

http://www.wikidata.org/entity/Q35868591

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A mouse model of paralytic myelitis caused by enterovirus D68.Clinical Characterization of Children Presenting to the Hospital with Enterovirus D68 Infection During the 2014 Outbreak in St. Louis Challenges in the Etiology and Diagnosis of Acute Febrile Illness in Children in Low- and Middle-Income Countries.Surveillance for enterovirus D68 in colorado children reveals continued circulation.The emergence of enterovirus D68 in England in autumn 2014 and the necessity for reinforcing enterovirus respiratory screening.Genome Sequence of Enterovirus D68 from St. Louis, Missouri, USA, 2016.A new real-time RT-PCR targeting VP4-VP2 to detect and quantify enterovirus D68 in respiratory samples.Clinical Features of Acute Flaccid Myelitis Temporally Associated with an Enterovirus D68 Outbreak: Results of a Nationwide Survey of Acute Flaccid Paralysis in Japan, August-December 2015.Adult case of acute flaccid paralysis with enterovirus D68 detected in the CSF.Enterovirus D68 Surveillance, St. Louis, Missouri, USA, 2016

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Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay.

http://www.wikidata.org/entity/Q35868591

description

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Journal of Clinical Microbiology

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Gregory A Storch

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Kristine M Wylie

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Maria Cannella

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Richard S Buller

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Todd N Wylie

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P2860

MUSCLE: multiple sequence alignment with high accuracy and high throughput

Basic local alignment search tool

BEDTools: a flexible suite of utilities for comparing genomic features.

NCBI BLAST: a better web interface

A diverse group of previously unrecognized human rhinoviruses are common causes of respiratory illnesses in infants.

A new method to compute K-mer frequencies and its application to annotate large repetitive plant genomes.

Typing of human enteroviruses by partial sequencing of VP1.

Rapid and sensitive routine detection of all members of the genus enterovirus in different clinical specimens by real-time PCR

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DNA analysis by fluorescence quenching detection.

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2641-2647

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10.1128/JCM.00923-15

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