Rapid detection of all known ebolavirus species by reverse transcription-loop-mediated isothermal amplification (RT-LAMP)

Journal of Virological Methods

Volumn 246, Issue , 2017, Pages 8-14

  Oloniniyi, Olamide K ^a   Kurosaki, Yohei ^a   Miyamoto, Hiroko ^b   Takada, Ayato ^b   Yasuda, Jiro ^a  

^a NAGASAKI UNIVERSITY   (Japan)

^b HOKKAIDO UNIVERSITY   (Japan)

Author keywords

Diagnosis; Ebola virus disease; Ebolavirus; RT LAMP

Indexed keywords

ARTICLE; BUNDIBUGYO EBOLAVIRUS; CONSENSUS SEQUENCE; CONTROLLED STUDY; DENGUE VIRUS; DIAGNOSTIC TEST ACCURACY STUDY; EBOLAVIRUS; GENE AMPLIFICATION; IN VITRO STUDY; LASSA VIRUS; LIMIT OF DETECTION; MARBURGVIRUS; NONHUMAN; NUCLEOTIDE SEQUENCE; RESTON EBOLAVIRUS; REVERSE TRANSCRIPTION LOOP MEDIATED ISOTHERMAL AMPLIFICATION; SENSITIVITY ANALYSIS; SENSITIVITY AND SPECIFICITY; SUDAN EBOLAVIRUS; TAI FOREST EBOLAVIRUS; VIRUS DETECTION; ZAIRE EBOLAVIRUS; CLASSIFICATION; DEVICES; EBOLA HEMORRHAGIC FEVER; GENETICS; HUMAN; ISOLATION AND PURIFICATION; NUCLEIC ACID AMPLIFICATION; POINT OF CARE SYSTEM; PROCEDURES; REVERSE TRANSCRIPTION; TEMPERATURE;

PRIMER DNA; VIRUS RNA;

DENGUE VIRUS; DNA PRIMERS; EBOLAVIRUS; HEMORRHAGIC FEVER, EBOLA; HUMANS; LASSA VIRUS; LIMIT OF DETECTION; MARBURGVIRUS; NUCLEIC ACID AMPLIFICATION TECHNIQUES; POINT-OF-CARE SYSTEMS; REVERSE TRANSCRIPTION; RNA, VIRAL; SENSITIVITY AND SPECIFICITY; TEMPERATURE;

EID: 85018485320     PISSN: 01660934     EISSN: 18790984     Source Type: Journal    
DOI: 10.1016/j.jviromet.2017.03.011     Document Type: Article

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