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Annals of the New York Academy of Sciences
|
May 11, 1992
Neurotoxin-related research: from the laboratory to the clinic
L Iversen, A C Foster, R G Hill, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1990
Enantiomers of HA-966 (3-amino-1-hydroxypyrrolid-2-one) exhibit distinct central nervous system effects: (+)-HA-966 is a selective glycine/N-methyl-D-aspartate receptor antagonist, but (-)-HA-966 is a potent gamma-butyrolactone-like sedative
L Singh, A E Donald, A C Foster, et al.
Journal of Medicinal Chemistry
|
April 1, 1991
Kynurenic acid derivatives. Structure-activity relationships for excitatory amino acid antagonism and identification of potent and selective antagonists at the glycine site on the N-methyl-D-aspartate receptor
P D Leeson, R Baker, R W Carling, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 21, 1998
Displacement of insulin-like growth factors from their binding proteins as a potential treatment for stroke
S A Loddick, X J Liu, Z X Lu, et al.
The European Journal of Neuroscience
|
November 5, 2004
Evidence that exogenous and endogenous fractalkine can induce spinal nociceptive facilitation in rats
E D Milligan, V Zapata, M Chacur, et al.
Journal of Medicinal Chemistry
|
February 28, 1997
4-substituted-3-phenylquinolin-2(1H)-ones: acidic and nonacidic glycine site N-methyl-D-aspartate antagonists with in vivo activity
R W Carling, P D Leeson, K W Moore, et al.
Journal of Medicinal Chemistry
|
December 24, 1997
Effect of plasma protein binding on in vivo activity and brain penetration of glycine/NMDA receptor antagonists
M Rowley, J J Kulagowski, A P Watt, et al.
Nature
|
March 10, 2006
A photometric redshift of z = 6.39 +/- 0.12 for GRB 050904
J B Haislip, M C Nysewander, D E Reichart, et al.
Page
of 10
Search research articles
Search
Showing results (91-100 of 98) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 98 results.
Annals of the New York Academy of Sciences
|
May 11, 1992
Neurotoxin-related research: from the laboratory to the clinic
L Iversen, A C Foster, R G Hill, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1990
Enantiomers of HA-966 (3-amino-1-hydroxypyrrolid-2-one) exhibit distinct central nervous system effects: (+)-HA-966 is a selective glycine/N-methyl-D-aspartate receptor antagonist, but (-)-HA-966 is a potent gamma-butyrolactone-like sedative
L Singh, A E Donald, A C Foster, et al.
Journal of Medicinal Chemistry
|
April 1, 1991
Kynurenic acid derivatives. Structure-activity relationships for excitatory amino acid antagonism and identification of potent and selective antagonists at the glycine site on the N-methyl-D-aspartate receptor
P D Leeson, R Baker, R W Carling, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 21, 1998
Displacement of insulin-like growth factors from their binding proteins as a potential treatment for stroke
S A Loddick, X J Liu, Z X Lu, et al.
The European Journal of Neuroscience
|
November 5, 2004
Evidence that exogenous and endogenous fractalkine can induce spinal nociceptive facilitation in rats
E D Milligan, V Zapata, M Chacur, et al.
Journal of Medicinal Chemistry
|
February 28, 1997
4-substituted-3-phenylquinolin-2(1H)-ones: acidic and nonacidic glycine site N-methyl-D-aspartate antagonists with in vivo activity
R W Carling, P D Leeson, K W Moore, et al.
Journal of Medicinal Chemistry
|
December 24, 1997
Effect of plasma protein binding on in vivo activity and brain penetration of glycine/NMDA receptor antagonists
M Rowley, J J Kulagowski, A P Watt, et al.
Nature
|
March 10, 2006
A photometric redshift of z = 6.39 +/- 0.12 for GRB 050904
J B Haislip, M C Nysewander, D E Reichart, et al.
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of 10