Search research articles
Contact Us
Filters
Showing results (341-350 of 852) with videos related to
Page
of 86
Sort By:
Gene
|
October 16, 2010
Differential gene expression activity among species-specific polypyrimidine/polypurine motifs in mu opioid receptor gene promoters
Chung-Youl Choe, Jinping Dong, Ping-Yee Law, et al.
Journal of Neurochemistry
|
May 1, 1981
Demonstration and characterization of opiate inhibition of the striatal adenylate cyclase
P Y Law, J Wu, J E Koehler, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1976
beta-endorphin is a potent analgesic agent
H H Loh, L F Tseng, E Wei, et al.
Biochemical and Biophysical Research Communications
|
January 15, 1988
Different molecular weight forms of opioid receptors revealed by polyclonal antibodies
S Roy, Y X Zhu, N M Lee, et al.
Biochemical and Biophysical Research Communications
|
April 17, 1995
Complementary DNA cloning of a mu-opioid receptor from rat peritoneal macrophages
M Sedqi, S Roy, S Ramakrishnan, et al.
European Journal of Pharmacology
|
November 21, 1980
Opiate and peptide interaction: effect of enkephalins on morphine analgesia
N M Lee, L Leybin, J K Chang, et al.
Nature
|
December 6, 1984
Dynorphin(1-13) improves survival in cats with focal cerebral ischaemia
D S Baskin, Y Hosobuchi, H H Loh, et al.
Journal of Chromatography
|
February 28, 1973
Estimation of morphine by polyamide mini thin-layer chromatography
H H Loh, I K Ho, T M Cho, et al.
Neurobiology
|
January 1, 1974
Rotation cultures from different regions of embryonic chick brain. II. Presence of stereospecific opiate binding and responses to narcotics
G R Peterson, P H Fischer, H H Loh, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 25, 2005
In vivo activation of a mutant mu-opioid receptor by naltrexone produces a potent analgesic effect but no tolerance: role of mu-receptor activation and delta-receptor blockade in morphine tolerance
Sabita Roy, Xiaohong Guo, Jennifer Kelschenbach, et al.
Page
of 86
Search research articles
Search
Showing results (341-350 of 852) with videos related to
Sort By:
Page
of 86
Gene
|
October 16, 2010
Differential gene expression activity among species-specific polypyrimidine/polypurine motifs in mu opioid receptor gene promoters
Chung-Youl Choe, Jinping Dong, Ping-Yee Law, et al.
Journal of Neurochemistry
|
May 1, 1981
Demonstration and characterization of opiate inhibition of the striatal adenylate cyclase
P Y Law, J Wu, J E Koehler, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1976
beta-endorphin is a potent analgesic agent
H H Loh, L F Tseng, E Wei, et al.
Biochemical and Biophysical Research Communications
|
January 15, 1988
Different molecular weight forms of opioid receptors revealed by polyclonal antibodies
S Roy, Y X Zhu, N M Lee, et al.
Biochemical and Biophysical Research Communications
|
April 17, 1995
Complementary DNA cloning of a mu-opioid receptor from rat peritoneal macrophages
M Sedqi, S Roy, S Ramakrishnan, et al.
European Journal of Pharmacology
|
November 21, 1980
Opiate and peptide interaction: effect of enkephalins on morphine analgesia
N M Lee, L Leybin, J K Chang, et al.
Nature
|
December 6, 1984
Dynorphin(1-13) improves survival in cats with focal cerebral ischaemia
D S Baskin, Y Hosobuchi, H H Loh, et al.
Journal of Chromatography
|
February 28, 1973
Estimation of morphine by polyamide mini thin-layer chromatography
H H Loh, I K Ho, T M Cho, et al.
Neurobiology
|
January 1, 1974
Rotation cultures from different regions of embryonic chick brain. II. Presence of stereospecific opiate binding and responses to narcotics
G R Peterson, P H Fischer, H H Loh, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 25, 2005
In vivo activation of a mutant mu-opioid receptor by naltrexone produces a potent analgesic effect but no tolerance: role of mu-receptor activation and delta-receptor blockade in morphine tolerance
Sabita Roy, Xiaohong Guo, Jennifer Kelschenbach, et al.
Page
of 86