Modified enzyme immunoassay to detect hepatitis C virus antibodies in oral fluid

1996 ◽  
Vol 15 (11) ◽  
pp. 882-884 ◽  
Author(s):  
P. G. McIntyre ◽  
J. Laszlo ◽  
K. Appleyard ◽  
G. R. Ogden
1991 ◽  
Vol 13 ◽  
pp. S35
Author(s):  
A. Hatzidaki ◽  
A. Katsoulidou ◽  
V. Miriagou ◽  
L. Pani ◽  
S. Voudiklari ◽  
...  

1998 ◽  
Vol 36 (5) ◽  
pp. 1461-1463 ◽  
Author(s):  
S. Le Pogam ◽  
F. Dubois ◽  
R. Christen ◽  
C. Raby ◽  
A. Cavicchini ◽  
...  

Two methods for genotyping hepatitis C virus (DNA enzyme immunoassay [DEIA] and line probe assay [Inno-LiPA HCV I and II]) were compared on 120 samples and of these 87% were assigned to the same subtype by both assays. There were 15 subtyping discrepancies which involved 5% of type 1 isolates and 90% of type 2 isolates. Amplified products from the core and 5′ untranslated regions (UTR) were sequenced to resolve conflicts. Type 1 discordant samples had a guanosine at position −99 in the 5′ UTR, a characteristic of genotype 1b, and a core region typical of subtype 1a. The eight isolates classified as 2a/2c by LiPA and as subtype 2c by DEIA belonged to type 2.


1992 ◽  
Vol 13 (3) ◽  
pp. 393-410 ◽  
Author(s):  
John Todd ◽  
John Kink ◽  
David Leahy ◽  
Barbara Preisel-Simmons ◽  
Sharon Laska ◽  
...  

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