Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
1990-8-21
pubmed:abstractText
We have synthesized 32P-labeled hybridization probes from a hyperdivergent region (nucleotides 51 to 392) of the rotavirus gene encoding the VP7 glycoprotein by using the polymerase chain reaction method. Both RNA (after an initial reverse transcription step) and cloned cDNA from human rotavirus serotypes 1 through 4 could be used as templates to amplify this region. High-stringency hybridization of each of the four probes to rotavirus RNAs dotted on nylon membranes allowed the specific detection of corresponding sequences and thus permitted identification of the serotype of the strains dotted. The procedure was useful when applied to rotaviruses isolated from field studies.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/2164610-2536391, http://linkedlifedata.com/resource/pubmed/commentcorrection/2164610-2541169, http://linkedlifedata.com/resource/pubmed/commentcorrection/2164610-2823458, http://linkedlifedata.com/resource/pubmed/commentcorrection/2164610-2833626, http://linkedlifedata.com/resource/pubmed/commentcorrection/2164610-2842373, http://linkedlifedata.com/resource/pubmed/commentcorrection/2164610-2999980, http://linkedlifedata.com/resource/pubmed/commentcorrection/2164610-3023533, http://linkedlifedata.com/resource/pubmed/commentcorrection/2164610-3033013, http://linkedlifedata.com/resource/pubmed/commentcorrection/2164610-3033090, http://linkedlifedata.com/resource/pubmed/commentcorrection/2164610-3038948, http://linkedlifedata.com/resource/pubmed/commentcorrection/2164610-6198242, http://linkedlifedata.com/resource/pubmed/commentcorrection/2164610-6292446
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0022-538X
pubmed:author
pubmed:issnType
Print
pubmed:volume
64
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4021-4
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:2164610-Antigens, Viral, pubmed-meshheading:2164610-Base Sequence, pubmed-meshheading:2164610-Blotting, Northern, pubmed-meshheading:2164610-Capsid, pubmed-meshheading:2164610-Capsid Proteins, pubmed-meshheading:2164610-DNA, Viral, pubmed-meshheading:2164610-Feces, pubmed-meshheading:2164610-Genes, Viral, pubmed-meshheading:2164610-Humans, pubmed-meshheading:2164610-Infant, Newborn, pubmed-meshheading:2164610-Molecular Sequence Data, pubmed-meshheading:2164610-Nucleic Acid Hybridization, pubmed-meshheading:2164610-Oligonucleotide Probes, pubmed-meshheading:2164610-Phosphorus Radioisotopes, pubmed-meshheading:2164610-Polymerase Chain Reaction, pubmed-meshheading:2164610-RNA, Viral, pubmed-meshheading:2164610-Rotavirus, pubmed-meshheading:2164610-Serotyping, pubmed-meshheading:2164610-Viral Structural Proteins, pubmed-meshheading:2164610-Viral Vaccines
pubmed:year
1990
pubmed:articleTitle
Identification of human rotavirus serotype by hybridization to polymerase chain reaction-generated probes derived from a hyperdivergent region of the gene encoding outer capsid protein VP7.
pubmed:affiliation
Laboratory of Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892.
pubmed:publicationType
Journal Article