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Formulation and Stability of Cytokine Therapeutics

Journal of pharmaceutical sciences, 2015-02, Vol.104 (2), p.307-326

2015

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Lone Pair−Aromatic Interactions: To Stabilize or Not to Stabilize

Accounts of chemical research, 2007-03, Vol.40 (3), p.197-205

2007

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Injectable Biodegradable Silica Depot: Two Months of Sustained Release of the Blood Glucose Lowering Peptide, Pramlintide

Pharmaceutics, 2022-03, Vol.14 (3), p.553

2022

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Avoiding the Pitfalls of siRNA Delivery to the Retinal Pigment Epithelium with Physiologically Relevant Cell Models

Pharmaceutics, 2020-07, Vol.12 (7), p.667

2020

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Release of functional dexamethasone by intracellular enzymes: A modular peptide-based strategy for ocular drug delivery

Journal of controlled release, 2020-11, Vol.327, p.584-594

2020

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Expression without boundaries: Cell-free protein synthesis in pharmaceutical research

International journal of pharmaceutics, 2013-01, Vol.440 (1), p.39-47

2013

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NH...O, OH...O, and CH...O hydrogen bonds in protein-ligand complexes: Strong and weak interactions in molecular recognition

Proteins, structure, function, and bioinformatics, 2004-02, Vol.54 (2), p.247-259

2004

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Differentially cleaving peptides as a strategy for controlled drug release in human retinal pigment epithelial cells

Journal of controlled release, 2017-04, Vol.251, p.37-48

2017

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Novel biodegradable polyesteramide microspheres for controlled drug delivery in Ophthalmology

Journal of controlled release, 2015-08, Vol.211, p.105-117

2015

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Structure-based drug design: Synthesis, crystal structure, biological evaluation and docking studies of mono- and bis-benzo[b]oxepines as non-steroidal estrogens

Bioorganic & medicinal chemistry, 2003-11, Vol.11 (23), p.5025-5033

2003

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Water−Nucleobase “Stacking”: H−π and Lone Pair−π Interactions in the Atomic Resolution Crystal Structure of an RNA Pseudoknot

Journal of the American Chemical Society, 2003-07, Vol.125 (30), p.8998-8999

2003

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High-throughput in vitro drug release and pharmacokinetic simulation as a tool for drug delivery system development: Application to intravitreal ocular administration

International journal of pharmaceutics, 2014-12, Vol.477 (1-2), p.469-475

2014

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Codon optimization and factorial screening for enhanced soluble expression of human ciliary neurotrophic factor in Escherichia coli

BMC biotechnology, 2014-11, Vol.14 (1), p.92-92, Article 92

2014

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2‘-Fluoroarabino- and Arabinonucleic Acid Show Different Conformations, Resulting in Deviating RNA Affinities and Processing of Their Heteroduplexes with RNA by RNase H

Biochemistry (Easton), 2006-04, Vol.45 (13), p.4141-4152

2006

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NH…O, OH…O, and CH…O hydrogen bonds in protein–ligand complexes: Strong and weak interactions in molecular recognition

Proteins, structure, function, and bioinformatics, 2004-02, Vol.54 (2), p.247-259

2004

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A convenient synthesis and hepatoprotective activity of imidazo[1,2-c]pyrimido[5,4-e]pyrimidine, tetraazaacenaphthene and tetraazaphenalene from cyclic ketene aminals through tandem addition-cyclization reactions

Bioorganic & medicinal chemistry, 2002-05, Vol.10 (5), p.1275-1280

2002

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Asymmetric Usage of Antagonist Charged Residues Drives Interleukin-5 Receptor Recruitment but Is Insufficient for Receptor Activation

Biochemistry (Easton), 2006-01, Vol.45 (4), p.1106-1115

2006

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Recruitment pharmacophore for interleukin 5 receptor α antagonism

Biopolymers, 2007, Vol.88 (1), p.83-93

2007

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Recruitment pharmacophore for interleukin 5 receptor a antagonism

Biopolymers, 2007-01, Vol.88 (1), p.83-93

2007

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Structure and Function of the Ribosomal Frameshifting Pseudoknot RNA from Beet Western Yellow Virus

Helvetica chimica acta, 2003-05, Vol.86 (5), p.1709-1727

2003

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A Convenient Synthesis and Hepatoprotective Activity of Imidazo[1,2- c ]pyrimido[5,4- e ]pyrimidine, Tetraazaacenaphthene and Tetraazaphenalene from Cyclic Ketene Aminals Through Tandem Addition-Cyclization Reactions ‡ ‡CDRI communication number 5986

Bioorganic & medicinal chemistry, 2002-05, Vol.10 (5), p.1275-1280

2002

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A dimeric layered structure of a 4-oxo-4,5-dihydro-1 H -pyrazolo[3,4- d ]pyrimidine compound

Acta crystallographica. Section C, Crystal structure communications, 2002-06, Vol.58 (6), p.o325-o327

2002

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A dimeric layered structure of a 4-oxo-4,5-dihydro-1H-pyrazolo[3,4-d]pyrimidine compound

Acta crystallographica. Section C, Crystal structure communications, 2002-06, Vol.58 (Pt 6), p.o325-o327

2002

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A dimeric layered structure of a 4-oxo-4,5-dihydro-1H-pyrazolo[3,4-d]pyrimidine compound

Acta crystallographica. Section C, Crystal structure communications, 2002-06, Vol.58 (6), p.o325-o327

2002

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A dimeric layered structure of a 4-oxo-4,5-dihydropyrazolo[3,4-d]pyrimidine compound

Acta crystallographica. Section C, Crystal structure communications, 2002-06, Vol.58, p.o325-o327

2002

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Formulation and Stability of Cytokine Therapeutics

Lone Pair−Aromatic Interactions: To Stabilize or Not to Stabilize

Injectable Biodegradable Silica Depot: Two Months of Sustained Release of the Blood Glucose Lowering Peptide, Pramlintide

Avoiding the Pitfalls of siRNA Delivery to the Retinal Pigment Epithelium with Physiologically Relevant Cell Models

Release of functional dexamethasone by intracellular enzymes: A modular peptide-based strategy for ocular drug delivery

Expression without boundaries: Cell-free protein synthesis in pharmaceutical research

NH...O, OH...O, and CH...O hydrogen bonds in protein-ligand complexes: Strong and weak interactions in molecular recognition

Differentially cleaving peptides as a strategy for controlled drug release in human retinal pigment epithelial cells

Novel biodegradable polyesteramide microspheres for controlled drug delivery in Ophthalmology

Structure-based drug design: Synthesis, crystal structure, biological evaluation and docking studies of mono- and bis-benzo[b]oxepines as non-steroidal estrogens

Water−Nucleobase “Stacking”: H−π and Lone Pair−π Interactions in the Atomic Resolution Crystal Structure of an RNA Pseudoknot

High-throughput in vitro drug release and pharmacokinetic simulation as a tool for drug delivery system development: Application to intravitreal ocular administration

Codon optimization and factorial screening for enhanced soluble expression of human ciliary neurotrophic factor in Escherichia coli

2‘-Fluoroarabino- and Arabinonucleic Acid Show Different Conformations, Resulting in Deviating RNA Affinities and Processing of Their Heteroduplexes with RNA by RNase H

NH…O, OH…O, and CH…O hydrogen bonds in protein–ligand complexes: Strong and weak interactions in molecular recognition

A convenient synthesis and hepatoprotective activity of imidazo[1,2-c]pyrimido[5,4-e]pyrimidine, tetraazaacenaphthene and tetraazaphenalene from cyclic ketene aminals through tandem addition-cyclization reactions

Asymmetric Usage of Antagonist Charged Residues Drives Interleukin-5 Receptor Recruitment but Is Insufficient for Receptor Activation

Recruitment pharmacophore for interleukin 5 receptor α antagonism

Recruitment pharmacophore for interleukin 5 receptor a antagonism

Structure and Function of the Ribosomal Frameshifting Pseudoknot RNA from Beet Western Yellow Virus

A Convenient Synthesis and Hepatoprotective Activity of Imidazo[1,2- c ]pyrimido[5,4- e ]pyrimidine, Tetraazaacenaphthene and Tetraazaphenalene from Cyclic Ketene Aminals Through Tandem Addition-Cyclization Reactions ‡ ‡CDRI communication number 5986

A dimeric layered structure of a 4-oxo-4,5-dihydro-1 H -pyrazolo[3,4- d ]pyrimidine compound

A dimeric layered structure of a 4-oxo-4,5-dihydro-1H-pyrazolo[3,4-d]pyrimidine compound

A dimeric layered structure of a 4-oxo-4,5-dihydro-1H-pyrazolo[3,4-d]pyrimidine compound

A dimeric layered structure of a 4-oxo-4,5-dihydropyrazolo[3,4-d]pyrimidine compound

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