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The Journal of Experimental Medicine
|
January 6, 1997
Follicular dendritic cells specifically express the long CR2/CD21 isoform
Y J Liu, J Xu, O de Bouteiller, et al.
Immunological Reviews
|
October 1, 1991
Diversity of cytokine synthesis and function of mouse CD4+ T cells
T R Mosmann, J H Schumacher, N F Street, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
October 25, 2000
IL-18 receptors, their role in ligand binding and function: anti-IL-1RAcPL antibody, a potent antagonist of IL-18
R Debets, J C Timans, T Churakowa, et al.
Journal of Medicinal Chemistry
|
October 29, 1993
3-Nitro-3,4-dihydro-2(1H)-quinolones. Excitatory amino acid antagonists acting at glycine-site NMDA and (RS)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors
R W Carling, P D Leeson, K W Moore, et al.
Science (New York, N.Y.)
|
November 25, 1994
Lymphotactin: a cytokine that represents a new class of chemokine
G S Kelner, J Kennedy, K B Bacon, et al.
The Journal of Experimental Medicine
|
June 16, 1997
Altered immune responses in interleukin 10 transgenic mice
A Hagenbaugh, S Sharma, S M Dubinett, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 15, 1991
Isolation and expression of human cytokine synthesis inhibitory factor cDNA clones: homology to Epstein-Barr virus open reading frame BCRFI
P Vieira, R de Waal-Malefyt, M N Dang, 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.
Journal of Medicinal Chemistry
|
July 20, 1999
1-(3-Cyanobenzylpiperidin-4-yl)-5-methyl-4-phenyl-1, 3-dihydroimidazol-2-one: a selective high-affinity antagonist for the human dopamine D(4) receptor with excellent selectivity over ion channels
R W Carling, K W Moore, C R Moyes, 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.
Page
of 8
Search research articles
Search
Showing results (61-70 of 72) with videos related to
Sort By:
Page
of 8
The Journal of Experimental Medicine
|
January 6, 1997
Follicular dendritic cells specifically express the long CR2/CD21 isoform
Y J Liu, J Xu, O de Bouteiller, et al.
Immunological Reviews
|
October 1, 1991
Diversity of cytokine synthesis and function of mouse CD4+ T cells
T R Mosmann, J H Schumacher, N F Street, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
October 25, 2000
IL-18 receptors, their role in ligand binding and function: anti-IL-1RAcPL antibody, a potent antagonist of IL-18
R Debets, J C Timans, T Churakowa, et al.
Journal of Medicinal Chemistry
|
October 29, 1993
3-Nitro-3,4-dihydro-2(1H)-quinolones. Excitatory amino acid antagonists acting at glycine-site NMDA and (RS)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors
R W Carling, P D Leeson, K W Moore, et al.
Science (New York, N.Y.)
|
November 25, 1994
Lymphotactin: a cytokine that represents a new class of chemokine
G S Kelner, J Kennedy, K B Bacon, et al.
The Journal of Experimental Medicine
|
June 16, 1997
Altered immune responses in interleukin 10 transgenic mice
A Hagenbaugh, S Sharma, S M Dubinett, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 15, 1991
Isolation and expression of human cytokine synthesis inhibitory factor cDNA clones: homology to Epstein-Barr virus open reading frame BCRFI
P Vieira, R de Waal-Malefyt, M N Dang, 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.
Journal of Medicinal Chemistry
|
July 20, 1999
1-(3-Cyanobenzylpiperidin-4-yl)-5-methyl-4-phenyl-1, 3-dihydroimidazol-2-one: a selective high-affinity antagonist for the human dopamine D(4) receptor with excellent selectivity over ion channels
R W Carling, K W Moore, C R Moyes, 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.
Page
of 8