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In Vitro Antiviral Activity and Cross-Resistance Profile of PL-100, a Novel Protease Inhibitor of Human Immunodeficiency Virus Type 1

Antimicrobial Agents and Chemotherapy, 2007-11, Vol.51 (11), p.4036-4043

2007

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The Challenges of Poliovirus Eradication

Journal of human virology & retrovirology, 2016-08, Vol.3 (4)

Yelle, Jocelyn

2016

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The Urgent Need for Broad-Spectrum Antiviral Drugs

Journal of human virology & retrovirology, 2015-01, Vol.2 (1)

Yelle, Jocelyn

2015

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The 2014 Ebola Virus Outbreak in West Africa: Current Perspectives for Prevention and Treatment

Journal of human virology & retrovirology, 2014-11, Vol.1 (4)

Yelle, Jocelyn

2014

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MERS Coronavirus: Current Status

Journal of human virology & retrovirology, 2014-07, Vol.1 (3)

Yelle, Jocelyn

2014

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Lysine sulfonamides as novel HIV-protease inhibitors: Nε-Acyl aromatic α-amino acids

Bioorganic & medicinal chemistry letters, 2006-07, Vol.16 (13), p.3459-3462

2006

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Lysine derivatives as potent HIV protease inhibitors. Discovery, synthesis and structure–activity relationship studies

Bioorganic & medicinal chemistry letters, 2005-03, Vol.15 (5), p.1509-1513

2005

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Lysine sulfonamides as novel HIV-protease inhibitors: Nε-disubstituted ureas

Bioorganic & medicinal chemistry letters, 2004-08, Vol.14 (15), p.3971-3974

2004

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1,2,5,6-Tetra-O-benzyl-D-mannitol derivatives as novel HIV protease inhibitors

Bioorganic & medicinal chemistry letters, 2003-10, Vol.13 (20), p.3601-3605

2003

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Lysine sulfonamides as novel HIV-protease inhibitors: Optimization of the Nε-acyl-phenyl spacer

Bioorganic & medicinal chemistry letters, 2003-12, Vol.13 (24), p.4289-4292

2003

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Lysine sulfonamides as novel HIV-protease inhibitors: Nepsilon-acyl aromatic alpha-amino acids

Bioorganic & medicinal chemistry letters, 2006-07, Vol.16 (13), p.3459-3462

2006

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Lysine sulfonamides as novel HIV-protease inhibitors: Nepsilon-disubstituted ureas

Bioorganic & medicinal chemistry letters, 2004-08, Vol.14 (15), p.3971-3974

2004

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Lysine sulfonamides as novel HIV-protease inhibitors: optimization of the Nepsilon-acyl-phenyl spacer

Bioorganic & medicinal chemistry letters, 2003-12, Vol.13 (24), p.4289-4292

2003

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Targeting HIV-1 integrase

Expert opinion on therapeutic targets, 2001-08, Vol.5 (4), p.443-464

2001

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Characterization of mutant HIV-1 integrase carrying amino acid changes in the catalytic domain

Molecules and cells, 2000-10, Vol.10 (5), p.525-532

2000

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A Biotin-Conjugated Substrate Facilitating Analysis of HIV-1 Integrase Activity on Minigels

Analytical biochemistry, 2000-08, Vol.284 (1), p.169-172

2000

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Is antisense an appropriate nomenclature or design for oligodeoxynucleotides aimed at the inhibition of HIV-1 replication?

AAPS PharmSci, 2002-06, Vol.4 (2), p.34-44

2002

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Lipid-based delivery of combinations of antisense oligodeoxynucleotides for the in vitro inhibition of HIV-1 replication

AAPS PharmSci, 2001-01, Vol.3 (1), p.E7-91

2001

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Analysis of the DNA substrate structure and number of the processing sites on the activities of HIV-1 integrase in vitro

Molecules and cells, 2001-04, Vol.11 (2), p.231-240

2001

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ETUDE DU POUVOIR TRANSFORMANT DU CYTOMEGALOVIRUS HUMAIN

YELLE, JOCELYN

1987

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Etude de l'induction de virus endogènes dans des cultures de cellules de hamsters et de gerboises au moyen de facteurs physiques et chimiques

Yelle, Jocelyn

1981

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Low tumorigenicity of canine cells transformed by the human cytomegalovirus

Biology of the cell, 1990, Vol.70 (1-2), p.9-18

1990

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1,2,5,6-Tetra-O-benzyl-D-mannitol Derivatives as Novel HIV Protease Inhibitors

ChemInform, 2004-01, Vol.35 (3), p.no-no

2004

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Is antisense an appropriate nomenclature or design for oligodeoxynucleotides aimed at the inhibition of HIV-1 replication?

AAPS PharmSci, 2002, Vol.4 (2), p.E9-E9

2002

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A simplified procedure for the rapid identification of recombinant pAT153 plasmids in Escherichia coli HB101 cells

Analytical biochemistry, 1986-04, Vol.154 (1), p.209-212

1986

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In Vitro Antiviral Activity and Cross-Resistance Profile of PL-100, a Novel Protease Inhibitor of Human Immunodeficiency Virus Type 1

The Challenges of Poliovirus Eradication

The Urgent Need for Broad-Spectrum Antiviral Drugs

The 2014 Ebola Virus Outbreak in West Africa: Current Perspectives for Prevention and Treatment

MERS Coronavirus: Current Status

Lysine sulfonamides as novel HIV-protease inhibitors: Nε-Acyl aromatic α-amino acids

Lysine derivatives as potent HIV protease inhibitors. Discovery, synthesis and structure–activity relationship studies

Lysine sulfonamides as novel HIV-protease inhibitors: Nε-disubstituted ureas

1,2,5,6-Tetra-O-benzyl-D-mannitol derivatives as novel HIV protease inhibitors

Lysine sulfonamides as novel HIV-protease inhibitors: Optimization of the Nε-acyl-phenyl spacer

Lysine sulfonamides as novel HIV-protease inhibitors: Nepsilon-acyl aromatic alpha-amino acids

Lysine sulfonamides as novel HIV-protease inhibitors: Nepsilon-disubstituted ureas

Lysine sulfonamides as novel HIV-protease inhibitors: optimization of the Nepsilon-acyl-phenyl spacer

Targeting HIV-1 integrase

Characterization of mutant HIV-1 integrase carrying amino acid changes in the catalytic domain

A Biotin-Conjugated Substrate Facilitating Analysis of HIV-1 Integrase Activity on Minigels

Is antisense an appropriate nomenclature or design for oligodeoxynucleotides aimed at the inhibition of HIV-1 replication?

Lipid-based delivery of combinations of antisense oligodeoxynucleotides for the in vitro inhibition of HIV-1 replication

Analysis of the DNA substrate structure and number of the processing sites on the activities of HIV-1 integrase in vitro

ETUDE DU POUVOIR TRANSFORMANT DU CYTOMEGALOVIRUS HUMAIN

Etude de l'induction de virus endogènes dans des cultures de cellules de hamsters et de gerboises au moyen de facteurs physiques et chimiques

Low tumorigenicity of canine cells transformed by the human cytomegalovirus

1,2,5,6-Tetra-O-benzyl-D-mannitol Derivatives as Novel HIV Protease Inhibitors

Is antisense an appropriate nomenclature or design for oligodeoxynucleotides aimed at the inhibition of HIV-1 replication?

A simplified procedure for the rapid identification of recombinant pAT153 plasmids in Escherichia coli HB101 cells

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