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Evolution of Constrained Gonadotropin-releasing Hormone Ligand Conformation and Receptor Selectivity

The Journal of biological chemistry, 2005-11, Vol.280 (46), p.38569-38575

2005

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Two Mutations in Extracellular Loop 2 of the Human GnRH Receptor Convert an Antagonist to an Agonist

Molecular endocrinology (Baltimore, Md.), 2002-05, Vol.16 (5), p.1079-1088

2002

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Effect of membrane mimicking environment on the conformation of a pore-forming (xSxG)6 peptide

Biopolymers, 2006, Vol.84 (3), p.317-328

2006

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A synthetic peptide forms voltage-gated porin-like ion channels in lipid bilayer membranes

Biochemical and biophysical research communications, 2005-05, Vol.330 (2), p.585-590

2005

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Aggregation and Porin-like Channel Activity of a β Sheet Peptide

Biochemistry (Easton), 2005-08, Vol.44 (30), p.10259-10270

2005

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Conversion of a Porin-like Peptide Channel into a Gramicidin-like Channel by Glycine to D-alanine Substitutions

Biophysical journal, 2006-02, Vol.90 (3), p.947-955

2006

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Immunomodulatory peptides from IgSF proteins: a review

Current protein & peptide science, 2005-04, Vol.6 (2), p.185

2005

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Pteroyl-γ-glutamate-cysteine synthesis and its application in folate receptor-mediated cancer cell targeting using folate-tethered liposomes

Analytical biochemistry, 2004-09, Vol.332 (1), p.168-177

2004

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Role of Aspartate7.32(302) of the Human Gonadotropin-Releasing Hormone Receptor in Stabilizing a High-Affinity Ligand Conformation

Molecular pharmacology, 2001-12, Vol.60 (6), p.1280-1287

2001

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Synthetic Channel-forming Peptides and Ion Selectivity

Chemical research in Chinese universities, 2006-03, Vol.22 (2), p.265-266

2006

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Conserved Amino Acid Residues that Are Important for Ligand Binding in the Type I Gonadotropin-Releasing Hormone (GnRH) Receptor Are Required for High Potency of GnRH II at the Type II GnRH Receptor

Molecular endocrinology (Baltimore, Md.), 2007-01, Vol.21 (1), p.281-292

2007

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Synthesis and Self-Alkylation of Isotope-Coded Affinity Tag Reagents

Bioconjugate chemistry, 2005-03, Vol.16 (2), p.458-464

2005

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Selection of Peptide Ligands Binding to Fibroblast Growth Factor Receptor 1

IUBMB life, 2002-08, Vol.54 (2), p.67-72

2002

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Effects of Thiol Protease Inhibitors on Cell Cycle and Proliferation of Vascular Smooth Muscle Cells in Culture

Circulation research, 1993-02, Vol.72 (2), p.413-423

1993

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Phosphoserine as a recognition determinant for glycogen synthase kinase-3: Phosphorylation of a synthetic peptide based on the G-component of protein phosphatase-1

Archives of biochemistry and biophysics, 1988-12, Vol.267 (2), p.797-802

1988

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Phosphate groups as substrate determinants for casein kinase I action

The Journal of biological chemistry, 1990-08, Vol.265 (24), p.14264-14269

1990

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Agonist activity of mammalian gonadotropin-releasing antagonists in chicken gonadotropes reflects marked differences in vertebrate gonadotropin-releasing receptors

Molecular and cellular endocrinology, 1995-02, Vol.108 (1), p.107-113

1995

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Two mutations in extracellular loop 2 of the human GnRH receptor convert an antagonist to an agonist

Molecular endocrinology (Baltimore, Md.), 2002-05, Vol.16 (5), p.1079-1088

2002

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Selective reduction of the amide carbonyl group in dipeptides by borane

Journal of organic chemistry, 1976-04, Vol.41 (7), p.1260-1261

1976

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A Continuous Spectrophotometric and Fluorometric Assay for Protein Tyrosine Phosphatase Using Phosphotyrosine-Containing Peptides

Analytical biochemistry, 1993-05, Vol.211 (1), p.7-15

1993

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Ordered multisite protein phosphorylation. Analysis of glycogen synthase kinase 3 action using model peptide substrates

The Journal of biological chemistry, 1990-04, Vol.265 (11), p.6061-6065

1990

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Amino- and guanidinoacylryanodines: basic ryanodine esters with enhanced affinity for the sarcoplasmic reticulum calcium (2+)-release channel

Journal of medicinal chemistry, 1993-05, Vol.36 (10), p.1319-1323

1993

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Cell surface specific immunoglobulin inhibits alpha factor mediated morphogenesis in Saccharomyces cerevisiae

Canadian journal of microbiology, 1987-04, Vol.33 (4), p.331

1987

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Photolabile protecting group for histidine

Journal of the American Chemical Society, 1975-01, Vol.97 (2), p.440-441

1975

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The binding of barium and calcium ions by the antibiotic beauvericin

Biochemical and biophysical research communications, 1974-04, Vol.57 (3), p.554-561

1974

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Evolution of Constrained Gonadotropin-releasing Hormone Ligand Conformation and Receptor Selectivity

Two Mutations in Extracellular Loop 2 of the Human GnRH Receptor Convert an Antagonist to an Agonist

Effect of membrane mimicking environment on the conformation of a pore-forming (xSxG)6 peptide

A synthetic peptide forms voltage-gated porin-like ion channels in lipid bilayer membranes

Aggregation and Porin-like Channel Activity of a β Sheet Peptide

Conversion of a Porin-like Peptide Channel into a Gramicidin-like Channel by Glycine to D-alanine Substitutions

Immunomodulatory peptides from IgSF proteins: a review

Pteroyl-γ-glutamate-cysteine synthesis and its application in folate receptor-mediated cancer cell targeting using folate-tethered liposomes

Role of Aspartate7.32(302) of the Human Gonadotropin-Releasing Hormone Receptor in Stabilizing a High-Affinity Ligand Conformation

Synthetic Channel-forming Peptides and Ion Selectivity

Conserved Amino Acid Residues that Are Important for Ligand Binding in the Type I Gonadotropin-Releasing Hormone (GnRH) Receptor Are Required for High Potency of GnRH II at the Type II GnRH Receptor

Synthesis and Self-Alkylation of Isotope-Coded Affinity Tag Reagents

Selection of Peptide Ligands Binding to Fibroblast Growth Factor Receptor 1

Effects of Thiol Protease Inhibitors on Cell Cycle and Proliferation of Vascular Smooth Muscle Cells in Culture

Phosphoserine as a recognition determinant for glycogen synthase kinase-3: Phosphorylation of a synthetic peptide based on the G-component of protein phosphatase-1

Phosphate groups as substrate determinants for casein kinase I action

Agonist activity of mammalian gonadotropin-releasing antagonists in chicken gonadotropes reflects marked differences in vertebrate gonadotropin-releasing receptors

Two mutations in extracellular loop 2 of the human GnRH receptor convert an antagonist to an agonist

Selective reduction of the amide carbonyl group in dipeptides by borane

A Continuous Spectrophotometric and Fluorometric Assay for Protein Tyrosine Phosphatase Using Phosphotyrosine-Containing Peptides

Ordered multisite protein phosphorylation. Analysis of glycogen synthase kinase 3 action using model peptide substrates

Amino- and guanidinoacylryanodines: basic ryanodine esters with enhanced affinity for the sarcoplasmic reticulum calcium (2+)-release channel

Cell surface specific immunoglobulin inhibits alpha factor mediated morphogenesis in Saccharomyces cerevisiae

Photolabile protecting group for histidine

The binding of barium and calcium ions by the antibiotic beauvericin

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