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HIV-1 Vaccine Development: Constrained Peptide Immunogens Show Improved Binding to the Anti-HIV-1 gp41 MAb

Biochemistry (Easton), 2003-03, Vol.42 (11), p.3214-3223

2003

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Sequence dependence of protein isoprenylation

The Journal of biological chemistry, 1991-08, Vol.266 (22), p.14603-14610

1991

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The Synthesis of a Prodrug of Doxorubicin Designed to Provide Reduced Systemic Toxicity and Greater Target Efficacy

Journal of medicinal chemistry, 2001-11, Vol.44 (24), p.4216-4224

2001

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Preclinical study of influenza virus A M2 peptide conjugate vaccines in mice, ferrets, and rhesus monkeys

Vaccine, 2004-08, Vol.22 (23), p.2993-3003

2004

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Two Tarantula Peptides Inhibit Activation of Multiple Sodium Channels

Biochemistry (Easton), 2002-12, Vol.41 (50), p.14734-14747

2002

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Echistatin Is a Potent Inhibitor of Bone Resorption in Culture

The Journal of cell biology, 1990-10, Vol.111 (4), p.1713-1723

1990

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PSA-specific and non-PSA-specific conversion of a PSA-targeted peptide conjugate of doxorubicin to its active metabolites

Drug metabolism and disposition, 2001-03, Vol.29 (3), p.313

2001

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A monoclonal antibody against the platelet fibrinogen receptor contains a sequence that mimics a receptor recognition domain in fibrinogen

The Journal of biological chemistry, 1989-01, Vol.264 (1), p.259-265

1989

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Protein domains governing interactions between E2F, the retinoblastoma gene product, and human papillomavirus type 16 E7 protein

Molecular and Cellular Biology, 1993-02, Vol.13 (2), p.953-960

1993

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Substrate requirements of human rhinovirus 3C protease for peptide cleavage in vitro

The Journal of biological chemistry, 1990-06, Vol.265 (16), p.9062-9065

1990

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A peptide-doxorubicin 'prodrug' activated by prostate-specific antigen selectively kills prostate tumor cells positive for prostate-specific antigen in vivo

Nature medicine, 2000-11, Vol.6 (11), p.1248-1252

2000

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Chemical Synthesis of Echistatin, a Potent Inhibitor of Platelet Aggregation from Echis carinatus: Synthesis and Biological Activity of Selected Analogs

Proceedings of the National Academy of Sciences - PNAS, 1989-06, Vol.86 (11), p.4022-4026

1989

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Cleavage of small peptides in vitro by human rhinovirus 14 3C protease expressed in Escherichia coli

Journal of Virology, 1989-12, Vol.63 (12), p.5037-5045

1989

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The Pro Domain of β-Secretase Does Not Confer Strict Zymogen-like Properties but Does Assist Proper Folding of the Protease Domain

The Journal of biological chemistry, 2001-03, Vol.276 (13), p.10366-10373

2001

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HIV-1 protease specificity of peptide cleavage is sufficient for processing of gag and pol polyproteins

Biochemical and biophysical research communications, 1988-10, Vol.156 (1), p.297-303

1988

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Development of 1,4-benzodiazepine cholecystokinin type B antagonists

Journal of medicinal chemistry, 1993-12, Vol.36 (26), p.4276-4292

1993

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Identification of HPV-16 E7 peptides that are potent antagonists of E7 binding to the retinoblastoma suppressor protein

The Journal of biological chemistry, 1990-08, Vol.265 (22), p.12782-12785

1990

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Mutational anatomy of an HIV-1 protease variant conferring cross-resistance to protease inhibitors in clinical trials. Compensatory modulations of binding and activity

The Journal of biological chemistry, 1996-12, Vol.271 (50), p.31957-31963

1996

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Bovine liver aspartyl beta-hydroxylase. Purification and characterization

The Journal of biological chemistry, 1991-07, Vol.266 (21), p.14004-14010

1991

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Human papillomavirus type 16 E7 protein inhibits DNA binding by the retinoblastoma gene product

Molecular and Cellular Biology, 1992-05, Vol.12 (5), p.1905-1914

1992

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The significance of monoisotopic and carbon-13 isobars for the identification of a 19-component dodecapeptide library by positive ion electrospray Fourier transform ion cyclotron resonance mass spectrometry

Rapid communications in mass spectrometry, 2000-01, Vol.14 (15), p.1368-1376

2000

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Aspartyl β -hydroxylase: In vitro Hydroxylation of a Synthetic Peptide Based on the Structure of the First Growth Factor-Like Domain of Human Factor IX

Proceedings of the National Academy of Sciences - PNAS, 1989-05, Vol.86 (10), p.3609-3613

1989

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Proton NMR assignments and secondary structure of the snake venom protein echistatin

Biochemistry (Easton), 1991-12, Vol.30 (50), p.11625-11636

1991

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Thermodynamics of Peptide Inhibitor Binding to HIV-1 gp41

Biochemistry (Easton), 2001-05, Vol.40 (19), p.5633-5641

2001

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Progress towards the development of a HIV-1 gp41-directed vaccine

Current HIV research, 2004-04, Vol.2 (2), p.193-204

2004

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HIV-1 Vaccine Development: Constrained Peptide Immunogens Show Improved Binding to the Anti-HIV-1 gp41 MAb

Sequence dependence of protein isoprenylation

The Synthesis of a Prodrug of Doxorubicin Designed to Provide Reduced Systemic Toxicity and Greater Target Efficacy

Preclinical study of influenza virus A M2 peptide conjugate vaccines in mice, ferrets, and rhesus monkeys

Two Tarantula Peptides Inhibit Activation of Multiple Sodium Channels

Echistatin Is a Potent Inhibitor of Bone Resorption in Culture

PSA-specific and non-PSA-specific conversion of a PSA-targeted peptide conjugate of doxorubicin to its active metabolites

A monoclonal antibody against the platelet fibrinogen receptor contains a sequence that mimics a receptor recognition domain in fibrinogen

Protein domains governing interactions between E2F, the retinoblastoma gene product, and human papillomavirus type 16 E7 protein

Substrate requirements of human rhinovirus 3C protease for peptide cleavage in vitro

A peptide-doxorubicin 'prodrug' activated by prostate-specific antigen selectively kills prostate tumor cells positive for prostate-specific antigen in vivo

Chemical Synthesis of Echistatin, a Potent Inhibitor of Platelet Aggregation from Echis carinatus: Synthesis and Biological Activity of Selected Analogs

Cleavage of small peptides in vitro by human rhinovirus 14 3C protease expressed in Escherichia coli

The Pro Domain of β-Secretase Does Not Confer Strict Zymogen-like Properties but Does Assist Proper Folding of the Protease Domain

HIV-1 protease specificity of peptide cleavage is sufficient for processing of gag and pol polyproteins

Development of 1,4-benzodiazepine cholecystokinin type B antagonists

Identification of HPV-16 E7 peptides that are potent antagonists of E7 binding to the retinoblastoma suppressor protein

Mutational anatomy of an HIV-1 protease variant conferring cross-resistance to protease inhibitors in clinical trials. Compensatory modulations of binding and activity

Bovine liver aspartyl beta-hydroxylase. Purification and characterization

Human papillomavirus type 16 E7 protein inhibits DNA binding by the retinoblastoma gene product

The significance of monoisotopic and carbon-13 isobars for the identification of a 19-component dodecapeptide library by positive ion electrospray Fourier transform ion cyclotron resonance mass spectrometry

Aspartyl β -hydroxylase: In vitro Hydroxylation of a Synthetic Peptide Based on the Structure of the First Growth Factor-Like Domain of Human Factor IX

Proton NMR assignments and secondary structure of the snake venom protein echistatin

Thermodynamics of Peptide Inhibitor Binding to HIV-1 gp41

Progress towards the development of a HIV-1 gp41-directed vaccine

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