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Binding of Oligoarginine to Membrane Lipids and Heparan Sulfate: Structural and Thermodynamic Characterization of a Cell-Penetrating Peptide

Biochemistry (Easton), 2005-02, Vol.44 (7), p.2692-2702

2005

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Potent and Selective BACE-1 Peptide Inhibitors Lower Brain Aβ Levels Mediated by Brain Shuttle Transport

EBioMedicine, 2017-10, Vol.24 (C), p.76-92

2017

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Novel orally active, dibenzazepinone-based γ-secretase inhibitors

Bioorganic & medicinal chemistry letters, 2007-11, Vol.17 (21), p.5918-5923

2007

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Substituted 2-oxo-azepane derivatives are potent, orally active γ-secretase inhibitors

Bioorganic & medicinal chemistry, 2008, Vol.18 (1), p.304-308

2008

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Endothelin-Converting Enzyme-1 Inhibition and Growth of Human Glioblastoma Cells

Journal of medicinal chemistry, 2005-01, Vol.48 (2), p.483-498

2005

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riDOM, a cell penetrating peptide. Interaction with phospholipid bilayers

Biochimica et biophysica acta, 2014-03, Vol.1838 (3), p.968-977

2014

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RI-Dom, a Cell-Penetrating Peptide. Interaction with DNA and Membranes

Biophysical journal, 2014-01, Vol.106 (2), p.517a-517a

2014

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riDOM, a Cell-Penetrating Peptide. Interaction with DNA and Heparan Sulfate

The journal of physical chemistry. B, 2013-09, Vol.117 (37), p.10807-10817

2013

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Cargo Delivery into the Brain by in vivo identified Transport Peptides

Scientific reports, 2015-09, Vol.5 (1), p.14104-14104, Article 14104

2015

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SEAP expression in transiently transfected mammalian cells grown in serum-free suspension culture

Cytotechnology (Dordrecht), 2003-05, Vol.42 (1), p.47-55

2003

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Synthesis of triazole-Tethered pyrrolidine libraries: novel ECE inhibitors

Bioorganic & medicinal chemistry letters, 2002-07, Vol.12 (13), p.1727-1730

2002

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1170 EGFR-Ta:RNA: multimodal mechanism of action potentiates immune checkpoint inhibitor activity

Journal for immunotherapy of cancer, 2022-11, Vol.10 (Suppl 2), p.A1213-A1213

2022

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Protease-triggered siRNA delivery vehicles

Journal of controlled release, 2015-07, Vol.209, p.57-66

2015

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Substrate specificities of catalytic fragments of protein tyrosine phosphatases (HPTPβ, LAR, and CD45) toward phosphotyrosylpeptide substrates and thiophosphotyrosylated peptides as inhibitors

Protein science, 1993-06, Vol.2 (6), p.977-984

1993

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Structural and Thermodynamic Aspects of the Interaction between Heparan Sulfate and Analogues of Melittin

Biochemistry (Easton), 2006-03, Vol.45 (9), p.3086-3094

2006

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Allosteric FBPase inhibitors gain 10(5) times in potency when simultaneously binding two neighboring AMP sites

Bioorganic & medicinal chemistry letters, 2008-08, Vol.18 (16), p.4708-4712

2008

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Sulfonylureido thiazoles as fructose-1,6-bisphosphatase inhibitors for the treatment of Type-2 diabetes

Bioorganic & medicinal chemistry letters, 2010-01, Vol.20 (2), p.594-599

2010

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Orally active aminopyridines as inhibitors of tetrameric fructose-1,6-bisphosphatase

Bioorganic & medicinal chemistry letters, 2011-06, Vol.21 (11), p.3237-3242

2011

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Allosteric FBPase inhibitors gain 10 super(5) times in potency when simultaneously binding two neighboring AMP sites

Bioorganic & medicinal chemistry, 2008-08, Vol.18 (16), p.4708-4712

2008

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Allosteric FBPase inhibitors gain 105 times in potency when simultaneously binding two neighboring AMP sites

Bioorganic & medicinal chemistry letters, 2008-08, Vol.18 (16), p.4708-4712

2008

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Purification and characterization of active recombinant human napsin A

European journal of biochemistry, 2000-05, Vol.267 (9), p.2573-2580

2000

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Allosteric FBPase inhibitors gain 10 5 times in potency when simultaneously binding two neighboring AMP sites

Bioorganic & medicinal chemistry letters, 2008, Vol.18 (16), p.4708-4712

2008

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Chemical synthesis of o-thiophosphotyrosyl peptides

International Journal of Peptide and Protein Research, 1994-02, Vol.43 (2), p.146-153

1994

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Alternative Strategies for the Fmoc Solid‐Phase Synthesis of O 4 ‐Phospho‐L‐tyrosine‐Containing Peptides

Helvetica chimica acta, 1991-09, Vol.74 (6), p.1314-1328

1991

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Isolation and structural elucidation of a novel phosphocysteine intermediate in the LAR protein tyrosine phosphatase enzymatic pathway

Journal of the American Chemical Society, 1992-08, Vol.114 (18), p.7296-7298

1992

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Binding of Oligoarginine to Membrane Lipids and Heparan Sulfate: Structural and Thermodynamic Characterization of a Cell-Penetrating Peptide

Potent and Selective BACE-1 Peptide Inhibitors Lower Brain Aβ Levels Mediated by Brain Shuttle Transport

Novel orally active, dibenzazepinone-based γ-secretase inhibitors

Substituted 2-oxo-azepane derivatives are potent, orally active γ-secretase inhibitors

Endothelin-Converting Enzyme-1 Inhibition and Growth of Human Glioblastoma Cells

riDOM, a cell penetrating peptide. Interaction with phospholipid bilayers

RI-Dom, a Cell-Penetrating Peptide. Interaction with DNA and Membranes

riDOM, a Cell-Penetrating Peptide. Interaction with DNA and Heparan Sulfate

Cargo Delivery into the Brain by in vivo identified Transport Peptides

SEAP expression in transiently transfected mammalian cells grown in serum-free suspension culture

Synthesis of triazole-Tethered pyrrolidine libraries: novel ECE inhibitors

1170 EGFR-Ta:RNA: multimodal mechanism of action potentiates immune checkpoint inhibitor activity

Protease-triggered siRNA delivery vehicles

Substrate specificities of catalytic fragments of protein tyrosine phosphatases (HPTPβ, LAR, and CD45) toward phosphotyrosylpeptide substrates and thiophosphotyrosylated peptides as inhibitors

Structural and Thermodynamic Aspects of the Interaction between Heparan Sulfate and Analogues of Melittin

Allosteric FBPase inhibitors gain 10(5) times in potency when simultaneously binding two neighboring AMP sites

Sulfonylureido thiazoles as fructose-1,6-bisphosphatase inhibitors for the treatment of Type-2 diabetes

Orally active aminopyridines as inhibitors of tetrameric fructose-1,6-bisphosphatase

Allosteric FBPase inhibitors gain 10 super(5) times in potency when simultaneously binding two neighboring AMP sites

Allosteric FBPase inhibitors gain 105 times in potency when simultaneously binding two neighboring AMP sites

Purification and characterization of active recombinant human napsin A

Allosteric FBPase inhibitors gain 10 5 times in potency when simultaneously binding two neighboring AMP sites

Chemical synthesis of o-thiophosphotyrosyl peptides

Alternative Strategies for the Fmoc Solid‐Phase Synthesis of O 4 ‐Phospho‐L‐tyrosine‐Containing Peptides

Isolation and structural elucidation of a novel phosphocysteine intermediate in the LAR protein tyrosine phosphatase enzymatic pathway

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