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Journal of Virology
|
October 24, 2000
Hepatitis C virus internal ribosome entry site (IRES) stem loop IIId contains a phylogenetically conserved GGG triplet essential for translation and IRES folding
R Jubin, N E Vantuno, J S Kieft, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 15, 1992
Detection of acute hepatitis C virus infection by ELISA using a synthetic peptide comprising a structural epitope
G J Kotwal, B M Baroudy, I K Kuramoto, et al.
Journal of Medical Virology
|
January 1, 1990
Riboprobe assay for HDV RNA: a sensitive method for the detection of the HDV genome in clinical serum samples
A Smedile, K F Bergmann, B M Baroudy, et al.
Virology
|
January 1, 1989
Biologic and molecular genetic characteristics of a unique MCF virus that is highly leukemogenic in ecotropic virus-negative mice
S K Chattopadhyay, B M Baroudy, K L Holmes, et al.
Pediatric Nephrology (Berlin, Germany)
|
February 1, 1995
Absence of hepatitis B and C viruses in pediatric idiopathic membranoproliferative glomerulonephritis
M J Nowicki, T R Welch, N Ahmad, et al.
Virology
|
March 24, 1999
Generation of transmissible hepatitis C virions from a molecular clone in chimpanzees
Z Hong, M Beaudet-Miller, R E Lanford, et al.
Journal of Virology
|
February 7, 2001
Virus-specific cofactor requirement and chimeric hepatitis C virus/GB virus B nonstructural protein 3
N Butkiewicz, N Yao, W Zhong, et al.
Journal of Medicinal Chemistry
|
October 5, 2001
Piperazine-based CCR5 antagonists as HIV-1 inhibitors. II. Discovery of 1-[(2,4-dimethyl-3-pyridinyl)carbonyl]-4- methyl-4-[3(S)-methyl-4-[1(S)-[4-(trifluoromethyl)phenyl]ethyl]-1-piperazinyl]- piperidine N1-oxide (Sch-350634), an orally bioavailable, potent CCR5 antagonist
J R Tagat, R W Steensma, S W McCombie, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 19, 2001
SCH-C (SCH 351125), an orally bioavailable, small molecule antagonist of the chemokine receptor CCR5, is a potent inhibitor of HIV-1 infection in vitro and in vivo
J M Strizki, S Xu, N E Wagner, et al.
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of 4
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Showing results (31-40 of 39) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 39 results.
Journal of Virology
|
October 24, 2000
Hepatitis C virus internal ribosome entry site (IRES) stem loop IIId contains a phylogenetically conserved GGG triplet essential for translation and IRES folding
R Jubin, N E Vantuno, J S Kieft, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 15, 1992
Detection of acute hepatitis C virus infection by ELISA using a synthetic peptide comprising a structural epitope
G J Kotwal, B M Baroudy, I K Kuramoto, et al.
Journal of Medical Virology
|
January 1, 1990
Riboprobe assay for HDV RNA: a sensitive method for the detection of the HDV genome in clinical serum samples
A Smedile, K F Bergmann, B M Baroudy, et al.
Virology
|
January 1, 1989
Biologic and molecular genetic characteristics of a unique MCF virus that is highly leukemogenic in ecotropic virus-negative mice
S K Chattopadhyay, B M Baroudy, K L Holmes, et al.
Pediatric Nephrology (Berlin, Germany)
|
February 1, 1995
Absence of hepatitis B and C viruses in pediatric idiopathic membranoproliferative glomerulonephritis
M J Nowicki, T R Welch, N Ahmad, et al.
Virology
|
March 24, 1999
Generation of transmissible hepatitis C virions from a molecular clone in chimpanzees
Z Hong, M Beaudet-Miller, R E Lanford, et al.
Journal of Virology
|
February 7, 2001
Virus-specific cofactor requirement and chimeric hepatitis C virus/GB virus B nonstructural protein 3
N Butkiewicz, N Yao, W Zhong, et al.
Journal of Medicinal Chemistry
|
October 5, 2001
Piperazine-based CCR5 antagonists as HIV-1 inhibitors. II. Discovery of 1-[(2,4-dimethyl-3-pyridinyl)carbonyl]-4- methyl-4-[3(S)-methyl-4-[1(S)-[4-(trifluoromethyl)phenyl]ethyl]-1-piperazinyl]- piperidine N1-oxide (Sch-350634), an orally bioavailable, potent CCR5 antagonist
J R Tagat, R W Steensma, S W McCombie, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 19, 2001
SCH-C (SCH 351125), an orally bioavailable, small molecule antagonist of the chemokine receptor CCR5, is a potent inhibitor of HIV-1 infection in vitro and in vivo
J M Strizki, S Xu, N E Wagner, et al.
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of 4