UB Paderborn / Katalog / Suche / in CDI

Feasibility and safety of a three-dimensional anatomic map–guided transseptal puncture for left-sided catheter ablation procedures

Europace (London, England), 2023-03, Vol.25 (3), p.1126-1134

2023

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3D mapping for the identification of the fossa ovalis in left atrial ablation procedures: a pilot study of a first step towards an electroanatomic-guided transseptal puncture

Europace (London, England), 2020-05, Vol.22 (5), p.732-738

2020

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Pressure-Guided Cryoballoon Isolation of the Pulmonary Veins for the Treatment of Paroxysmal Atrial Fibrillation

Journal of cardiovascular electrophysiology, 2010-02, Vol.21 (2), p.120-125

2010

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Cryoballoon Pulmonary Vein Isolation Guided by Transesophageal Echocardiography: Novel Aspects on an Emerging Ablation Technique

Journal of cardiovascular electrophysiology, 2009-11, Vol.20 (11), p.1197-1202

2009

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ABP688, a novel selective and high affinity ligand for the labeling of mGlu5 receptors: Identification, in vitro pharmacology, pharmacokinetic and biodistribution studies

Bioorganic & medicinal chemistry, 2007-01, Vol.15 (2), p.903-914

2007

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Metabotropic Glutamate Receptors: Novel Targets for Drug Development

Journal of medicinal chemistry, 1995-04, Vol.38 (9), p.1417-1426

1995

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SIB-1757 and SIB-1893: selective, noncompetitive antagonists of metabotropic glutamate receptor type 5

The Journal of pharmacology and experimental therapeutics, 1999-07, Vol.290 (1), p.170

1999

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5-Phosphonomethylquinoxalinediones as competitive NMDA receptor antagonists with a preference for the human 1A/2A, rather than 1A/2B receptor composition

Bioorganic & medicinal chemistry letters, 2002-04, Vol.12 (7), p.1099-1102

2002

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2-Methyl-6-(phenylethynyl)-pyridine (MPEP), a potent, selective and systemically active mGlu5 receptor antagonist

Neuropharmacology, 1999-10, Vol.38 (10), p.1493-1503

1999

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6-Amino quinazolinedione sulfonamides as orally active competitive AMPA receptor antagonists

Bioorganic & medicinal chemistry letters, 2012-01, Vol.22 (2), p.996-999

2012

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Differentiation of Glycine Antagonist Sites ofN-Methyl-d-aspartate Receptor Subtypes

The Journal of biological chemistry, 1998-05, Vol.273 (18), p.11158-11163

1998

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Differentiation of glycine antagonist sites of N-methyl-D-aspartate receptor subtypes. Preferential interaction of CGP 61594 with NR1/2B receptors

The Journal of biological chemistry, 1998-05, Vol.273 (18), p.11158-11163

1998

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5-aminomethylquinoxaline-2,3-diones, Part III: Arylamide derivatives as highly potent and selective glycine-site NMDA receptor antagonists

Bioorganic & medicinal chemistry letters, 1998-03, Vol.8 (5), p.493-498

1998

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5-aminomethylquinoxaline-2,3-diones. Part II: N-aryl derivatives as novel NMDA/glycine and AMPA antagonists

Bioorganic & medicinal chemistry letters, 1998-01, Vol.8 (1), p.71-74

1998

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[ 3H]CGP 61594, the first photoaffinity ligand for the glycine site of NMDA receptors

Neuropharmacology, 1999-02, Vol.38 (2), p.233-242

1999

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Synthesis and binding properties of 2-amino-5-phosphono-3-pentenoic acid photoaffinity ligands as probes for the glutamate recognition site of the NMDA receptor

Journal of medicinal chemistry, 1993-11, Vol.36 (23), p.3721-3726

1993

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Die Cardenolide der Samen von Mansonia altissima A. Chev. : die Struktur von Mansonin und Strophothevosid

Allgeier, Hans

1967

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Photoaffinity labeling of the NMDA receptor

European journal of pharmacology, 1993-07, Vol.246 (2), p.179-180

1993

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[2 + 4]cycloaddition of thiophosgene with anthracenes

Tetrahedron letters, 1976, Vol.17 (3), p.215-218

1976

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ChemInform Abstract: 5-Phosphonomethylquinoxalinediones as Competitive NMDA Receptor Antagonists with a Preference for the Human 1A/2A, Rather than 1A/2B Receptor Composition

ChemInform, 2002-08, Vol.33 (31), p.no-no

2002

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Profiling of trans-azetidine-2,4-dicarboxylic acid at the human metabotropic glutamate receptors mGlu1b,-2, -4a and -5a

European journal of pharmacology. Molecular pharmacology section, 1995-02, Vol.288 (3), p.389-392

1995

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Macro rings. XLVII. Syntheses and spectral properties of heteroannularly disubstituted [2.2]paracyclophanes

Journal of the American Chemical Society, 1975-06, Vol.97 (13), p.3782-3789

1975

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Profiling of trans-azetidine-2,4-dicarboxylic acid at the human metabotropic glutamate receptors mGlu 1b, - 2, - 4a and - 5a

European journal of pharmacology. Molecular pharmacology section, 1995, Vol.288 (3), p.389-392

1995

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Adjuvant Procarbazine, Lomustine, and Vincristine Chemotherapy in Newly Diagnosed Anaplastic Oligodendroglioma: Long-Term Follow-Up of EORTC Brain Tumor Group Study 26951

Journal of clinical oncology, 2013-01, Vol.31 (3), p.344-350

2013

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Feasibility and safety of a three-dimensional anatomic map–guided transseptal puncture for left-sided catheter ablation procedures

3D mapping for the identification of the fossa ovalis in left atrial ablation procedures: a pilot study of a first step towards an electroanatomic-guided transseptal puncture

Pressure-Guided Cryoballoon Isolation of the Pulmonary Veins for the Treatment of Paroxysmal Atrial Fibrillation

Cryoballoon Pulmonary Vein Isolation Guided by Transesophageal Echocardiography: Novel Aspects on an Emerging Ablation Technique

ABP688, a novel selective and high affinity ligand for the labeling of mGlu5 receptors: Identification, in vitro pharmacology, pharmacokinetic and biodistribution studies

Metabotropic Glutamate Receptors: Novel Targets for Drug Development

SIB-1757 and SIB-1893: selective, noncompetitive antagonists of metabotropic glutamate receptor type 5

5-Phosphonomethylquinoxalinediones as competitive NMDA receptor antagonists with a preference for the human 1A/2A, rather than 1A/2B receptor composition

2-Methyl-6-(phenylethynyl)-pyridine (MPEP), a potent, selective and systemically active mGlu5 receptor antagonist

6-Amino quinazolinedione sulfonamides as orally active competitive AMPA receptor antagonists

Differentiation of Glycine Antagonist Sites ofN-Methyl-d-aspartate Receptor Subtypes

Differentiation of glycine antagonist sites of N-methyl-D-aspartate receptor subtypes. Preferential interaction of CGP 61594 with NR1/2B receptors

5-aminomethylquinoxaline-2,3-diones, Part III: Arylamide derivatives as highly potent and selective glycine-site NMDA receptor antagonists

5-aminomethylquinoxaline-2,3-diones. Part II: N-aryl derivatives as novel NMDA/glycine and AMPA antagonists

[ 3H]CGP 61594, the first photoaffinity ligand for the glycine site of NMDA receptors

Synthesis and binding properties of 2-amino-5-phosphono-3-pentenoic acid photoaffinity ligands as probes for the glutamate recognition site of the NMDA receptor

Die Cardenolide der Samen von Mansonia altissima A. Chev. : die Struktur von Mansonin und Strophothevosid

Photoaffinity labeling of the NMDA receptor

[2 + 4]cycloaddition of thiophosgene with anthracenes

ChemInform Abstract: 5-Phosphonomethylquinoxalinediones as Competitive NMDA Receptor Antagonists with a Preference for the Human 1A/2A, Rather than 1A/2B Receptor Composition

Profiling of trans-azetidine-2,4-dicarboxylic acid at the human metabotropic glutamate receptors mGlu1b,-2, -4a and -5a

Macro rings. XLVII. Syntheses and spectral properties of heteroannularly disubstituted [2.2]paracyclophanes

Profiling of trans-azetidine-2,4-dicarboxylic acid at the human metabotropic glutamate receptors mGlu 1b, - 2, - 4a and - 5a

Adjuvant Procarbazine, Lomustine, and Vincristine Chemotherapy in Newly Diagnosed Anaplastic Oligodendroglioma: Long-Term Follow-Up of EORTC Brain Tumor Group Study 26951

Adjuvant Procarbazine, Lomustine, and Vincristine Improves Progression-Free Survival but Not Overall Survival in Newly Diagnosed Anaplastic Oligodendrogliomas and Oligoastrocytomas: A Randomized European Organisation for Research and Treatment of Cancer Phase III Trial

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