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Malaria Journal
|
May 21, 2024
Considerations for first field trials of low-threshold gene drive for malaria vector control
John B Connolly, Austin Burt, George Christophides, et al.
Scientific Reports
|
June 30, 2021
An increasing role of pyrethroid-resistant Anopheles funestus in malaria transmission in the Lake Zone, Tanzania
Nancy S Matowo, Jackline Martin, Manisha A Kulkarni, et al.
Basic & Clinical Pharmacology & Toxicology
|
September 28, 2004
In vitro optimization of structure activity relationships of analogues of A-331440 combining radioligand receptor binding assays and micronucleus assays of potential antiobesity histamine H3 receptor antagonists
Arthur A Hancock, Marilyn S Diehl, Ramin Faghih, et al.
Annals of Internal Medicine
|
June 1, 1982
In-vitro studies of interactions between tampons and Staphylococcus aureus
C V Broome, P S Hayes, G W Ajello, et al.
Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]
|
April 1, 2004
Cognition enhancing effects of novel H(3) receptor (H(3)R) antagonists in several animal models
G B Fox, J B Pan, A M Lewis, et al.
Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]
|
June 2, 2005
Achievement of behavioral efficacy and improved potency in new heterocyclic analogs of benzofuran H3 antagonists
M Cowart, R Faghih, G Gfesser, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
September 15, 2007
An 80-amino acid deletion in the third intracellular loop of a naturally occurring human histamine H3 isoform confers pharmacological differences and constitutive activity
Gerold Bongers, Kathleen M Krueger, Thomas R Miller, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 27, 2004
Structure-activity relationships of non-imidazole H(3) receptor ligands. Part 3: 5-Substituted 3-phenyl-1,2,4-oxadiazoles as potent antagonists
Gregory A Gfesser, Henry Zhang, Jurgen Dinges, et al.
Journal of Medicinal Chemistry
|
August 8, 2008
The alkaloid conessine and analogues as potent histamine H3 receptor antagonists
Chen Zhao, Minghua Sun, Youssef L Bennani, et al.
Journal of Medicinal Chemistry
|
April 26, 2000
Structure-activity studies for a novel series of tricyclic substituted hexahydrobenz[e]isoindole alpha(1A) adrenoceptor antagonists as potential agents for the symptomatic treatment of benign prostatic hyperplasia (BPH)
M D Meyer, R J Altenbach, F Z Basha, et al.
Page
of 56
Search research articles
Search
Showing results (501-510 of 557) with videos related to
Sort By:
Page
of 56
Malaria Journal
|
May 21, 2024
Considerations for first field trials of low-threshold gene drive for malaria vector control
John B Connolly, Austin Burt, George Christophides, et al.
Scientific Reports
|
June 30, 2021
An increasing role of pyrethroid-resistant Anopheles funestus in malaria transmission in the Lake Zone, Tanzania
Nancy S Matowo, Jackline Martin, Manisha A Kulkarni, et al.
Basic & Clinical Pharmacology & Toxicology
|
September 28, 2004
In vitro optimization of structure activity relationships of analogues of A-331440 combining radioligand receptor binding assays and micronucleus assays of potential antiobesity histamine H3 receptor antagonists
Arthur A Hancock, Marilyn S Diehl, Ramin Faghih, et al.
Annals of Internal Medicine
|
June 1, 1982
In-vitro studies of interactions between tampons and Staphylococcus aureus
C V Broome, P S Hayes, G W Ajello, et al.
Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]
|
April 1, 2004
Cognition enhancing effects of novel H(3) receptor (H(3)R) antagonists in several animal models
G B Fox, J B Pan, A M Lewis, et al.
Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]
|
June 2, 2005
Achievement of behavioral efficacy and improved potency in new heterocyclic analogs of benzofuran H3 antagonists
M Cowart, R Faghih, G Gfesser, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
September 15, 2007
An 80-amino acid deletion in the third intracellular loop of a naturally occurring human histamine H3 isoform confers pharmacological differences and constitutive activity
Gerold Bongers, Kathleen M Krueger, Thomas R Miller, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 27, 2004
Structure-activity relationships of non-imidazole H(3) receptor ligands. Part 3: 5-Substituted 3-phenyl-1,2,4-oxadiazoles as potent antagonists
Gregory A Gfesser, Henry Zhang, Jurgen Dinges, et al.
Journal of Medicinal Chemistry
|
August 8, 2008
The alkaloid conessine and analogues as potent histamine H3 receptor antagonists
Chen Zhao, Minghua Sun, Youssef L Bennani, et al.
Journal of Medicinal Chemistry
|
April 26, 2000
Structure-activity studies for a novel series of tricyclic substituted hexahydrobenz[e]isoindole alpha(1A) adrenoceptor antagonists as potential agents for the symptomatic treatment of benign prostatic hyperplasia (BPH)
M D Meyer, R J Altenbach, F Z Basha, et al.
Page
of 56