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Expression of metastin and a G-protein-coupled receptor (AXOR12) in epithelial ovarian cancer

European journal of cancer (1990), 2007-06, Vol.43 (9), p.1452-1459

2007

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Pharmacokinetics of tacrolimus in pediatric renal transplant recipients

Transplantation proceedings, 2001-02, Vol.33 (1-2), p.1066-1068

2001

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Development of a highly selective EP2-receptor agonist. Part 2: identification of 16-Hydroxy-17,17-trimethylene 9β-chloro PGF derivatives

Bioorganic & medicinal chemistry, 2002-04, Vol.10 (4), p.1107-1114

2002

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Study of graft-infiltrating cells in the rat small bowel allograft using low-dose FK 506

Transplantation proceedings, 1999-11, Vol.31 (7), p.2790-2791

1999

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Enantiomer separation of amino compounds by a novel chiral stationary phase derived from crown ether

Journal of Chromatography A, 1998-05, Vol.805 (1), p.85-92

1998

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Potential candidates for small bowel transplantation: from our experience and survey of home parenteral nutrition in Japan

Transplantation proceedings, 1998-09, Vol.30 (6), p.2529-2530

1998

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Novel matrix metalloproteinase inhibitors: Generation of lead compounds by the in silico fragment-based approach

Bioorganic & medicinal chemistry, 2005-07, Vol.13 (14), p.4527-4543

2005

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Clinical Characteristics Of Primary Vesicoureteral Reflux In Infants: Multicenter Retrospective Study In Japan

The Journal of urology, 2003, Vol.169 (1), p.309-312

2003

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New orally active PDE4 inhibitors with therapeutic potential

Bioorganic & medicinal chemistry, 2004-08, Vol.12 (15), p.4089-4100

2004

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Follow-up studies of anorectal malformations after posterior sagittal anorectoplasty

Journal of pediatric surgery, 2002-11, Vol.37 (11), p.1529-1533

2002

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Design and synthesis of an orally active matrix metalloproteinase inhibitor

Bioorganic & medicinal chemistry, 2006-09, Vol.14 (18), p.6383-6403

2006

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Clarification of Mechanism of Human Sputum Elastase Inhibition by a New Inhibitor, ONO-5046, Using Electrospray Ionization Mass Spectrometry

Bioorganic & medicinal chemistry letters, 2002-09, Vol.12 (17), p.2349-2353

2002

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Platelet-derived endothelial cell growth factor predicts of progression and recurrence in primary epithelial ovarian cancer

Cancer letters, 2003-10, Vol.200 (2), p.173-176

2003

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Design and Synthesis of a Highly Selective EP2-Receptor Agonist

Bioorganic & medicinal chemistry letters, 2001-08, Vol.11 (15), p.2025-2028

2001

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Orally active PDE4 inhibitors with therapeutic potential

Bioorganic & medicinal chemistry letters, 2004-03, Vol.14 (5), p.1323-1327

2004

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Antioxidants from Lespedeza homoloba. (I)

Phytochemistry (Oxford), 1999-09, Vol.52 (2), p.303-310

1999

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In Hemophilia A and Autoantibody Inhibitor Patients: The Factor VIII A2 Domain and Light Chain Are Most Immunogenic

Thrombosis research, 2001-03, Vol.101 (5), p.377-385

2001

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Increase in serotonin 5-HT1A receptors in prefrontal and temporal cortices of brains from patients with chronic schizophrenia

Life sciences (1973), 1991, Vol.48 (4), p.355-363

1991

Volltextzugriff (PDF)

Orally active PDE4 inhibitor with therapeutic potential

European journal of medicinal chemistry, 2004-07, Vol.39 (7), p.555-571

2004

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RENAL CELL CARCINOMA IN CHILDREN: EXPERIENCE AT A SINGLE INSTITUTION IN JAPAN

The Journal of urology, 1999-10, Vol.162 (4), p.1402-1405

1999

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Highly potent PDE4 inhibitors with therapeutic potential

Bioorganic & medicinal chemistry, 2004-09, Vol.12 (17), p.4645-4665

2004

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A novel class of endothelin-A receptor antagonists, (R)-2-(benzo[1,3]dioxol-5-yl)-6-isopropyloxy-2H-chromene-3-carboxylic acids (S-1255). Conformational analysis of basic structure, crucial for ETA antagonism, in solution and solid states

Bioorganic & medicinal chemistry, 2002-12, Vol.10 (12), p.3965-3972

2002

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Highly potent PDE4 inhibitors with therapeutic potential

Bioorganic & medicinal chemistry letters, 2004-01, Vol.14 (1), p.207-210

2004

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Design and synthesis of a selective EP4-receptor agonist. Part 4: Practical synthesis and biological evaluation of a novel highly selective EP4-receptor agonist

Bioorganic & medicinal chemistry, 2002-07, Vol.10 (7), p.2103-2110

2002

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Design, synthesis, and biological evaluation of new phosphodiesterase type 4 inhibitors

Bioorganic & medicinal chemistry, 2004-10, Vol.12 (19), p.5063-5078

2004

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Expression of metastin and a G-protein-coupled receptor (AXOR12) in epithelial ovarian cancer

Pharmacokinetics of tacrolimus in pediatric renal transplant recipients

Development of a highly selective EP2-receptor agonist. Part 2: identification of 16-Hydroxy-17,17-trimethylene 9β-chloro PGF derivatives

Study of graft-infiltrating cells in the rat small bowel allograft using low-dose FK 506

Enantiomer separation of amino compounds by a novel chiral stationary phase derived from crown ether

Potential candidates for small bowel transplantation: from our experience and survey of home parenteral nutrition in Japan

Novel matrix metalloproteinase inhibitors: Generation of lead compounds by the in silico fragment-based approach

Clinical Characteristics Of Primary Vesicoureteral Reflux In Infants: Multicenter Retrospective Study In Japan

New orally active PDE4 inhibitors with therapeutic potential

Follow-up studies of anorectal malformations after posterior sagittal anorectoplasty

Design and synthesis of an orally active matrix metalloproteinase inhibitor

Clarification of Mechanism of Human Sputum Elastase Inhibition by a New Inhibitor, ONO-5046, Using Electrospray Ionization Mass Spectrometry

Platelet-derived endothelial cell growth factor predicts of progression and recurrence in primary epithelial ovarian cancer

Design and Synthesis of a Highly Selective EP2-Receptor Agonist

Orally active PDE4 inhibitors with therapeutic potential

Antioxidants from Lespedeza homoloba. (I)

In Hemophilia A and Autoantibody Inhibitor Patients: The Factor VIII A2 Domain and Light Chain Are Most Immunogenic

Increase in serotonin 5-HT1A receptors in prefrontal and temporal cortices of brains from patients with chronic schizophrenia

Orally active PDE4 inhibitor with therapeutic potential

RENAL CELL CARCINOMA IN CHILDREN: EXPERIENCE AT A SINGLE INSTITUTION IN JAPAN

Highly potent PDE4 inhibitors with therapeutic potential

A novel class of endothelin-A receptor antagonists, (R)-2-(benzo[1,3]dioxol-5-yl)-6-isopropyloxy-2H-chromene-3-carboxylic acids (S-1255). Conformational analysis of basic structure, crucial for ETA antagonism, in solution and solid states

Highly potent PDE4 inhibitors with therapeutic potential

Design and synthesis of a selective EP4-receptor agonist. Part 4: Practical synthesis and biological evaluation of a novel highly selective EP4-receptor agonist

Design, synthesis, and biological evaluation of new phosphodiesterase type 4 inhibitors

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