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Cholecystokinin-2/gastrin antagonists: 5-hydroxy-5-aryl-pyrrol-2-ones as anti-inflammatory analgesics for the treatment of inflammatory bowel disease

MedChemComm, 2017-03, Vol.8 (3), p.680-685

2017

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Cholecystokinin-1 receptor antagonists: 5-hydroxy-5-aryl-pyrrol-2-ones as anticancer agents

MedChemComm, 2016-01, Vol.7 (6), p.1138-1145

2016

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Analgesic Effects of 5-Alkyloxy-4-amino-2(5H)-furanones as Cholecystokinin-2 Antagonists

Archiv der Pharmazie (Weinheim), 2016-06, Vol.349 (6), p.456-465

2016

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Cholecystokinin-2/gastrin antagonists: 5-hydroxy-5-aryl-pyrrol-2-ones as anti-inflammatory analgesics for the treatment of inflammatory bowel diseaseThe authors declare no competing interests.Electronic supplementary information (ESI) available. See DOI: 10.1039/c6md00707d

2017-03

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Cholecystokinin-2/gastrin antagonists: 5-hydroxy-5-aryl-pyrrol-2-ones as anti-inflammatory analgesics for the treatment of inflammatory bowel disease† †The authors declare no competing interests. ‡ ‡Electronic supplementary information (ESI) available. See DOI: 10.1039/c6md00707d

MedChemComm, 2017-02, Vol.8 (3), p.680-685

2017

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Cholecystokinin-1 receptor antagonists: 5-hydroxy-5-aryl-pyrrol-2-ones as anticancer agentsConflict of interest: The study was sponsored by PNB Vesper Life Sciences.Electronic supplementary information (ESI) available. See DOI: 10.1039/c6md00052e

2016-06

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Werden und Lernen des Menschen: Lebenssinn und Lebensgestaltung in anthropologisch-paedagogischer Sicht

Lattmann, Urs P

1986

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Synthesis and evaluation of N-(3-oxo-2,3-dihydro-1H-pyrazol-4-yl)-1H-indole-carboxamides as cholecystokinin antagonists

Journal of pharmacy and pharmacology, 2006-03, Vol.58 (3), p.393-401

2006

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Synthesis of Substituted 3-Anilino-5-phenyl-1,3-dihydro- 2H-1,4-benzodiazepine-2-ones and their Evaluation as Cholecystokinin-Ligands

Archiv der Pharmazie (Weinheim), 2006-04, Vol.339 (4), p.163-173

2006

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Der Stellenwert der dynamischen Posturographie (Equitest®) bei gutachterlichen Beurteilungen

Laryngo- rhino- otologie, 2004-10, Vol.83 (10), p.669-679

2004

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Cholecystokinin antagonists (part 1): Antinociceptive, anxiolytic and antidepressant effects of N-(5-methyl-3-oxo-1,2-diphenyl-2,3-dihydro-1H-pyrazol-4-yl)-N'-phenylureas and carboxamides

Drug discoveries & therapeutics, 2008-06, Vol.2 (3), p.156-167

2008

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Irreversible Cholecystokinin-1 Receptor Antagonists PNB-028/81: N-isobutyl-5-hydroxy-5-aryl-pyrrol-2-ones as Experimental Therapeutic Agents against Colon and Pancreatic Cancer

Cancer Science & Research, 2018-09, Vol.1 (3), p.1-10

2018

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Novel 5-HT7 Ligands as Antidepressants: Automated Synthesis of NSubstituted- N-[1-Methyl-3-(4-Methylpiperidin-1-yl)propyl]-Arylsulfonamides

Letters in drug design & discovery, 2006-02, Vol.3 (1), p.49-54

2006

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Anti-depressant and anti-nociceptive effects of 1,4-benzodiazepine-2-ones based cholecystokinin (CCK(2)) antagonists

Drug discoveries & therapeutics, 2007-08, Vol.1 (1), p.45-56

2007

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Home versus hospital deliveries: follow up study of matched pairs for procedures and outcome

BMJ, 1996-11, Vol.313 (7068), p.1313-1318

International edition, 1996

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The value of dynamic posturography (Equitest) in preparing an expert's report

Laryngo- rhino- otologie, 2004-10, Vol.83 (10), p.669-679

2004

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Synthesis and evaluation of N-(5-methyl-3-oxo-1,2- diphenyl-2,3-dihydro-1H-pyrazol-4-yl)-N'-phenylureas as cholecystokinin antagonists

Arzneimittel-Forschung, 2005-01, Vol.55 (5), p.251-258

2005

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Professional education in the health care professions. Task and position of the professional schools

Krankenpflege. Soins infirmiers, 1982-05 (5), p.34

Lattmann, U P

1982

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Staff vaccination with a new subunit influenza vaccine

Schweizerische medizinische Wochenschrift, 1978-01, Vol.108 (2), p.47

1978

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Reformen in der Lehrerbildung : Beispiele aus dem Kanton Aargau

Bildungspolitik, 1977, Vol.61/197562/1976, p.191

Lattmann, Urs P

1977

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The Role of Extracellular Vesicles in Melanoma Progression

Cancers, 2022-06, Vol.14 (13), p.3086

2022

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Behandlung von Bauchaortenaneurysmen in der Schweiz

Swiss medical forum, 2024-02

2024

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The Caenorhabditis elegans homolog of the Evi1 proto-oncogene, egl-43, coordinates G1 cell cycle arrest with pro-invasive gene expression during anchor cell invasion

PLoS genetics, 2020-03, Vol.16 (3), p.e1008470-e1008470

2020

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A DNA replication-independent function of pre-replication complex genes during cell invasion in C. elegans

PLoS biology, 2022-02, Vol.20 (2), p.e3001317-e3001317

2022

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Role of the amino terminal RHAU-specific motif in the recognition and resolution of guanine quadruplex-RNA by the DEAH-box RNA helicase RHAU

Nucleic acids research, 2010-10, Vol.38 (18), p.6219-6233

2010

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Cholecystokinin-2/gastrin antagonists: 5-hydroxy-5-aryl-pyrrol-2-ones as anti-inflammatory analgesics for the treatment of inflammatory bowel disease

Cholecystokinin-1 receptor antagonists: 5-hydroxy-5-aryl-pyrrol-2-ones as anticancer agents

Analgesic Effects of 5-Alkyloxy-4-amino-2(5H)-furanones as Cholecystokinin-2 Antagonists

Cholecystokinin-2/gastrin antagonists: 5-hydroxy-5-aryl-pyrrol-2-ones as anti-inflammatory analgesics for the treatment of inflammatory bowel diseaseThe authors declare no competing interests.Electronic supplementary information (ESI) available. See DOI: 10.1039/c6md00707d

Cholecystokinin-2/gastrin antagonists: 5-hydroxy-5-aryl-pyrrol-2-ones as anti-inflammatory analgesics for the treatment of inflammatory bowel disease† †The authors declare no competing interests. ‡ ‡Electronic supplementary information (ESI) available. See DOI: 10.1039/c6md00707d

Cholecystokinin-1 receptor antagonists: 5-hydroxy-5-aryl-pyrrol-2-ones as anticancer agentsConflict of interest: The study was sponsored by PNB Vesper Life Sciences.Electronic supplementary information (ESI) available. See DOI: 10.1039/c6md00052e

Werden und Lernen des Menschen: Lebenssinn und Lebensgestaltung in anthropologisch-paedagogischer Sicht

Synthesis and evaluation of N-(3-oxo-2,3-dihydro-1H-pyrazol-4-yl)-1H-indole-carboxamides as cholecystokinin antagonists

Synthesis of Substituted 3-Anilino-5-phenyl-1,3-dihydro- 2H-1,4-benzodiazepine-2-ones and their Evaluation as Cholecystokinin-Ligands

Der Stellenwert der dynamischen Posturographie (Equitest®) bei gutachterlichen Beurteilungen

Cholecystokinin antagonists (part 1): Antinociceptive, anxiolytic and antidepressant effects of N-(5-methyl-3-oxo-1,2-diphenyl-2,3-dihydro-1H-pyrazol-4-yl)-N'-phenylureas and carboxamides

Irreversible Cholecystokinin-1 Receptor Antagonists PNB-028/81: N-isobutyl-5-hydroxy-5-aryl-pyrrol-2-ones as Experimental Therapeutic Agents against Colon and Pancreatic Cancer

Novel 5-HT7 Ligands as Antidepressants: Automated Synthesis of NSubstituted- N-[1-Methyl-3-(4-Methylpiperidin-1-yl)propyl]-Arylsulfonamides

Anti-depressant and anti-nociceptive effects of 1,4-benzodiazepine-2-ones based cholecystokinin (CCK(2)) antagonists

Home versus hospital deliveries: follow up study of matched pairs for procedures and outcome

The value of dynamic posturography (Equitest) in preparing an expert's report

Synthesis and evaluation of N-(5-methyl-3-oxo-1,2- diphenyl-2,3-dihydro-1H-pyrazol-4-yl)-N'-phenylureas as cholecystokinin antagonists

Professional education in the health care professions. Task and position of the professional schools

Staff vaccination with a new subunit influenza vaccine

Reformen in der Lehrerbildung : Beispiele aus dem Kanton Aargau

The Role of Extracellular Vesicles in Melanoma Progression

Behandlung von Bauchaortenaneurysmen in der Schweiz

The Caenorhabditis elegans homolog of the Evi1 proto-oncogene, egl-43, coordinates G1 cell cycle arrest with pro-invasive gene expression during anchor cell invasion

A DNA replication-independent function of pre-replication complex genes during cell invasion in C. elegans

Role of the amino terminal RHAU-specific motif in the recognition and resolution of guanine quadruplex-RNA by the DEAH-box RNA helicase RHAU

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