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The Journal of Biological Chemistry
|
October 19, 2005
Molecular characterization of the gerbil C5a receptor and identification of a transmembrane domain V amino acid that is crucial for small molecule antagonist interaction
Stephen M Waters, Robbin M Brodbeck, Jeremy Steflik, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
August 30, 2008
Identification and characterization of NDT 9513727 [N,N-bis(1,3-benzodioxol-5-ylmethyl)-1-butyl-2,4-diphenyl-1H-imidazole-5-methanamine], a novel, orally bioavailable C5a receptor inverse agonist
Robbin M Brodbeck, Daniel N Cortright, Andrzej P Kieltyka, et al.
BMC Psychiatry
|
November 25, 2016
Psychotherapy integration under scrutiny: investigating the impact of integrating emotion-focused components into a CBT-based approach: a study protocol of a randomized controlled trial
Anna Babl, Martin Grosse Holtforth, Sara Heer, et al.
Plos Pathogens
|
January 5, 2016
Papillomavirus-Associated Tumor Formation Critically Depends on c-Fos Expression Induced by Viral Protein E2 and Bromodomain Protein Brd4
Maria Delcuratolo, Jasmin Fertey, Markus Schneider, et al.
JMIR Research Protocols
|
November 30, 2022
A Web-Based Self-help Intervention for Coping With the Loss of a Partner: Protocol for Randomized Controlled Trials in 3 Countries
Jeannette Brodbeck, Sofia Jacinto, Afonso Gouveia, et al.
JMIR Research Protocols
|
September 8, 2020
LEAVES (optimizing the mentaL health and resiliencE of older Adults that haVe lost thEir spouSe via blended, online therapy): Proposal for an Online Service Development and Evaluation
Lex van Velsen, Miriam Cabrita, Harm Op den Akker, et al.
Journal of Medicinal Chemistry
|
April 23, 2021
From High-Throughput Screening to Target Validation: Benzo[<i>d</i>]isothiazoles as Potent and Selective Agonists of Human Transient Receptor Potential Cation Channel Subfamily M Member 5 Possessing In Vivo Gastrointestinal Prokinetic Activity in Rodents
Alessio Barilli, Laura Aldegheri, Federica Bianchi, et al.
Journal of Medicinal Chemistry
|
January 28, 2016
New 4-Functionalized Glutamate Analogues Are Selective Agonists at Metabotropic Glutamate Receptor Subtype 2 or Selective Agonists at Metabotropic Glutamate Receptor Group III
Tri H V Huynh, Mette N Erichsen, Amélie S Tora, et al.
JMIR Formative Research
|
March 10, 2022
RWD-Cockpit: Application for Quality Assessment of Real-world Data
Lmar Marie Babrak, Erand Smakaj, Teyfik Agac, et al.
Bioorganic & Medicinal Chemistry
|
November 19, 2022
The discovery of (1R, 3R)-1-(3-chloro-5-fluorophenyl)-3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-6-carbonitrile, a potent and selective agonist of human transient receptor potential cation channel subfamily m member 5 (TRPM5) and evaluation of as a potential gastrointestinal prokinetic agent
M Sabat, L F Raveglia, L Aldegheri, et al.
Page
of 50
Search research articles
Search
Showing results (431-440 of 493) with videos related to
Sort By:
Page
of 50
The Journal of Biological Chemistry
|
October 19, 2005
Molecular characterization of the gerbil C5a receptor and identification of a transmembrane domain V amino acid that is crucial for small molecule antagonist interaction
Stephen M Waters, Robbin M Brodbeck, Jeremy Steflik, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
August 30, 2008
Identification and characterization of NDT 9513727 [N,N-bis(1,3-benzodioxol-5-ylmethyl)-1-butyl-2,4-diphenyl-1H-imidazole-5-methanamine], a novel, orally bioavailable C5a receptor inverse agonist
Robbin M Brodbeck, Daniel N Cortright, Andrzej P Kieltyka, et al.
BMC Psychiatry
|
November 25, 2016
Psychotherapy integration under scrutiny: investigating the impact of integrating emotion-focused components into a CBT-based approach: a study protocol of a randomized controlled trial
Anna Babl, Martin Grosse Holtforth, Sara Heer, et al.
Plos Pathogens
|
January 5, 2016
Papillomavirus-Associated Tumor Formation Critically Depends on c-Fos Expression Induced by Viral Protein E2 and Bromodomain Protein Brd4
Maria Delcuratolo, Jasmin Fertey, Markus Schneider, et al.
JMIR Research Protocols
|
November 30, 2022
A Web-Based Self-help Intervention for Coping With the Loss of a Partner: Protocol for Randomized Controlled Trials in 3 Countries
Jeannette Brodbeck, Sofia Jacinto, Afonso Gouveia, et al.
JMIR Research Protocols
|
September 8, 2020
LEAVES (optimizing the mentaL health and resiliencE of older Adults that haVe lost thEir spouSe via blended, online therapy): Proposal for an Online Service Development and Evaluation
Lex van Velsen, Miriam Cabrita, Harm Op den Akker, et al.
Journal of Medicinal Chemistry
|
April 23, 2021
From High-Throughput Screening to Target Validation: Benzo[<i>d</i>]isothiazoles as Potent and Selective Agonists of Human Transient Receptor Potential Cation Channel Subfamily M Member 5 Possessing In Vivo Gastrointestinal Prokinetic Activity in Rodents
Alessio Barilli, Laura Aldegheri, Federica Bianchi, et al.
Journal of Medicinal Chemistry
|
January 28, 2016
New 4-Functionalized Glutamate Analogues Are Selective Agonists at Metabotropic Glutamate Receptor Subtype 2 or Selective Agonists at Metabotropic Glutamate Receptor Group III
Tri H V Huynh, Mette N Erichsen, Amélie S Tora, et al.
JMIR Formative Research
|
March 10, 2022
RWD-Cockpit: Application for Quality Assessment of Real-world Data
Lmar Marie Babrak, Erand Smakaj, Teyfik Agac, et al.
Bioorganic & Medicinal Chemistry
|
November 19, 2022
The discovery of (1R, 3R)-1-(3-chloro-5-fluorophenyl)-3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-6-carbonitrile, a potent and selective agonist of human transient receptor potential cation channel subfamily m member 5 (TRPM5) and evaluation of as a potential gastrointestinal prokinetic agent
M Sabat, L F Raveglia, L Aldegheri, et al.
Page
of 50