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Suivi de polypectomies colorectales Étude d’une cohorte en région Bretagne

Oncologie (Paris, France), 2009-02, Vol.11 (2), p.95-100

2009

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L’Hémoccult occulte

Oncologie (Paris, France), 2006-10, Vol.8 (8), p.708-709

Bader, J.-P.

2006

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Inhibitors of HIV Nucleocapsid Protein Zinc Fingers as Candidates for the Treatment of AIDS

Science (American Association for the Advancement of Science), 1995-11, Vol.270 (5239), p.1194-1197

1995

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Natural Product-Based Anti-HIV Drug Discovery and Development Facilitated by the NCI Developmental Therapeutics Program

Journal of natural products (Washington, D.C.), 2001-02, Vol.64 (2), p.265-277

2001

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Inhibition of multiple phases of human immunodeficiency virus type 1 replication by a dithiane compound that attacks the conserved zinc fingers of retroviral nucleocapsid proteins

Antimicrobial Agents and Chemotherapy, 1997-02, Vol.41 (2), p.419-426

1997

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Polémiques ?

Oncologie (Paris, France), 1999, Vol.1 (6), p.273-275

BADER, J.-P

1999

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Unique Anti-Human Immunodeficiency Virus Activities of the Nonnucleoside Reverse Transcriptase Inhibitors Calanolide A, Costatolide, and Dihydrocostatolide

Antimicrobial Agents and Chemotherapy, 1999-08, Vol.43 (8), p.1827-1834

1999

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Structure-activity and cross-resistance evaluations of a series of human immunodeficiency virus type-1-specific compounds related to oxathiin carboxanilide

Antimicrobial Agents and Chemotherapy, 1995-12, Vol.39 (12), p.2718-2727

1995

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Effect of Omeprazole and Ranitidine on Ulcer Healing and Relapse Rates in Patients with Benign Gastric Ulcer

The New England journal of medicine, 1989-01, Vol.320 (2), p.69-75

1989

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Biological and biochemical anti-HIV activity of the benzothiadiazine class of nonnucleoside reverse transcriptase inhibitors

Antiviral research, 1994-09, Vol.25 (1), p.43-56

1994

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Diarylsulfones, a new chemical class of nonnucleoside antiviral inhibitors of human immunodeficiency virus type 1 reverse transcriptase

Antimicrobial Agents and Chemotherapy, 1993-04, Vol.37 (4), p.754-760

1993

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Oxathiin Carboxanilide, a Potent Inhibitor of Human Immunodeficiency Virus Reproduction

Proceedings of the National Academy of Sciences - PNAS, 1991-08, Vol.88 (15), p.6740-6744

1991

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Clinical efficacy of pantoprazole compared with ranitidine

Alimentary pharmacology & therapeutics, 1994, Vol.8 (s1), p.47-52

1994

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Efficacy, pharmacokinetics, and in vivo antiviral activity of UC781, a highly potent, orally bioavailable nonnucleoside reverse transcriptase inhibitor of HIV type 1

AIDS research and human retroviruses, 1997-06, Vol.13 (9), p.789-796

1997

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Novel sulfonated and phosphonated analogs of distamycin which inhibit the replication of HIV

Antiviral Research, 1995-08, Vol.27 (4), p.335-354

1995

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Azodicarbonamide inhibits HIV-1 replication by targeting the nucleocapsid protein

Nature medicine, 1997-03, Vol.3 (3), p.341-345

1997

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Sulfonic acid dyes : inhibition of the human immunodeficiency virus and mechanism of action

Journal of acquired immune deficiency syndromes (1988), 1992, Vol.5 (8), p.771-781

1992

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2′-Fluoro-2′,3′-Dideoxyarabinosyladenine (F-ddA): Activity against Drug-Resistant Human Immunodeficiency Virus Strains and Clades A-E

Antiviral chemistry & chemotherapy, 1997-04, Vol.8 (2), p.107-111

1997

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Thank you to M. Souques and K. Zummer

La Presse médicale (1983), 2000-05, Vol.29 (18), p.1001-1002

Bader, J P

2000

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Pourquoi individualiser la cancérologie digestive?

Acta endoscopica, 1981-11, Vol.11 (6), p.459-461

Bader, J. -P.

1981

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A Diarylsulphone Non-Nucleoside Reverse Transcriptase Inhibitor with a Unique Sensitivity Profile to Drug-Resistant Virus Isolates

Antiviral chemistry & chemotherapy, 1996-10, Vol.7 (5), p.243-252

1996

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Cerebral hemodynamics and processing speed during category learning

Neuroreport, 2004-05, Vol.15 (7), p.1195-1198

2004

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Inhibition of human immunodeficiency virus replication by the sulfonated stilbene dye resobene

Antiviral research, 1996-12, Vol.33 (1), p.41-53

1996

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Characteristics of a group of nonnucleoside reverse transcriptase inhibitors with structural diversity and potent anti-human immunodeficiency virus activity

Leukemia, 1995-10, Vol.9, p.S75-S85

1995

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PrgE: an OB-fold protein from plasmid pCF10 with striking differences to prototypical bacterial SSBs

Life science alliance, 2024-08, Vol.7 (8), p.e202402693

2024

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Suivi de polypectomies colorectales Étude d’une cohorte en région Bretagne

L’Hémoccult occulte

Inhibitors of HIV Nucleocapsid Protein Zinc Fingers as Candidates for the Treatment of AIDS

Natural Product-Based Anti-HIV Drug Discovery and Development Facilitated by the NCI Developmental Therapeutics Program

Inhibition of multiple phases of human immunodeficiency virus type 1 replication by a dithiane compound that attacks the conserved zinc fingers of retroviral nucleocapsid proteins

Polémiques ?

Unique Anti-Human Immunodeficiency Virus Activities of the Nonnucleoside Reverse Transcriptase Inhibitors Calanolide A, Costatolide, and Dihydrocostatolide

Structure-activity and cross-resistance evaluations of a series of human immunodeficiency virus type-1-specific compounds related to oxathiin carboxanilide

Effect of Omeprazole and Ranitidine on Ulcer Healing and Relapse Rates in Patients with Benign Gastric Ulcer

Biological and biochemical anti-HIV activity of the benzothiadiazine class of nonnucleoside reverse transcriptase inhibitors

Diarylsulfones, a new chemical class of nonnucleoside antiviral inhibitors of human immunodeficiency virus type 1 reverse transcriptase

Oxathiin Carboxanilide, a Potent Inhibitor of Human Immunodeficiency Virus Reproduction

Clinical efficacy of pantoprazole compared with ranitidine

Efficacy, pharmacokinetics, and in vivo antiviral activity of UC781, a highly potent, orally bioavailable nonnucleoside reverse transcriptase inhibitor of HIV type 1

Novel sulfonated and phosphonated analogs of distamycin which inhibit the replication of HIV

Azodicarbonamide inhibits HIV-1 replication by targeting the nucleocapsid protein

Sulfonic acid dyes : inhibition of the human immunodeficiency virus and mechanism of action

2′-Fluoro-2′,3′-Dideoxyarabinosyladenine (F-ddA): Activity against Drug-Resistant Human Immunodeficiency Virus Strains and Clades A-E

Thank you to M. Souques and K. Zummer

Pourquoi individualiser la cancérologie digestive?

A Diarylsulphone Non-Nucleoside Reverse Transcriptase Inhibitor with a Unique Sensitivity Profile to Drug-Resistant Virus Isolates

Cerebral hemodynamics and processing speed during category learning

Inhibition of human immunodeficiency virus replication by the sulfonated stilbene dye resobene

Characteristics of a group of nonnucleoside reverse transcriptase inhibitors with structural diversity and potent anti-human immunodeficiency virus activity

PrgE: an OB-fold protein from plasmid pCF10 with striking differences to prototypical bacterial SSBs

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