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The Biochemical Journal
|
November 15, 1988
Solubilization of a tamoxifen-binding protein. Assessment of its molecular mass
A Fargin, J C Faye, M le Maire, et al.
The Journal of Biological Chemistry
|
September 5, 1989
Effector coupling mechanisms of the cloned 5-HT1A receptor
A Fargin, J R Raymond, J W Regan, et al.
Biochemical Pharmacology
|
August 1, 1990
The anti-proliferative properties of 4-benzylphenoxy ethanamine derivatives are mediated by the anti-estrogen binding site (ABS), whereas the anti-estrogenic effects of trifluopromazine are not
M Poirot, M Garnier, F Bayard, et al.
Chemico-Biological Interactions
|
January 1, 1988
Further evidence for a biological role of anti-estrogen-binding sites in mediating the growth inhibitory action of diphenylmethane derivatives
A Fargin, F Bayard, J C Faye, et al.
Nature
|
September 22, 1988
The genomic clone G-21 which resembles a beta-adrenergic receptor sequence encodes the 5-HT1A receptor
A Fargin, J R Raymond, M J Lohse, et al.
Molecular Pharmacology
|
July 1, 1989
Identification of the ligand-binding subunit of the human 5-hydroxytryptamine1A receptor with N-(p-azido-m-[125I] iodophenethyl)spiperone, a high affinity radioiodinated photoaffinity probe
J R Raymond, A Fargin, M J Lohse, et al.
Cellular Signalling
|
January 1, 1991
Dual coupling of the cloned 5-HT1A receptor to both adenylyl cyclase and phospholipase C is mediated via the same Gi protein
A Fargin, K Yamamoto, S Cotecchia, et al.
The Journal of Biological Chemistry
|
December 25, 1989
The human 5-HT1A receptor expressed in HeLa cells stimulates sodium-dependent phosphate uptake via protein kinase C
J R Raymond, A Fargin, J P Middleton, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 18 results.
The Biochemical Journal
|
November 15, 1988
Solubilization of a tamoxifen-binding protein. Assessment of its molecular mass
A Fargin, J C Faye, M le Maire, et al.
The Journal of Biological Chemistry
|
September 5, 1989
Effector coupling mechanisms of the cloned 5-HT1A receptor
A Fargin, J R Raymond, J W Regan, et al.
Biochemical Pharmacology
|
August 1, 1990
The anti-proliferative properties of 4-benzylphenoxy ethanamine derivatives are mediated by the anti-estrogen binding site (ABS), whereas the anti-estrogenic effects of trifluopromazine are not
M Poirot, M Garnier, F Bayard, et al.
Chemico-Biological Interactions
|
January 1, 1988
Further evidence for a biological role of anti-estrogen-binding sites in mediating the growth inhibitory action of diphenylmethane derivatives
A Fargin, F Bayard, J C Faye, et al.
Nature
|
September 22, 1988
The genomic clone G-21 which resembles a beta-adrenergic receptor sequence encodes the 5-HT1A receptor
A Fargin, J R Raymond, M J Lohse, et al.
Molecular Pharmacology
|
July 1, 1989
Identification of the ligand-binding subunit of the human 5-hydroxytryptamine1A receptor with N-(p-azido-m-[125I] iodophenethyl)spiperone, a high affinity radioiodinated photoaffinity probe
J R Raymond, A Fargin, M J Lohse, et al.
Cellular Signalling
|
January 1, 1991
Dual coupling of the cloned 5-HT1A receptor to both adenylyl cyclase and phospholipase C is mediated via the same Gi protein
A Fargin, K Yamamoto, S Cotecchia, et al.
The Journal of Biological Chemistry
|
December 25, 1989
The human 5-HT1A receptor expressed in HeLa cells stimulates sodium-dependent phosphate uptake via protein kinase C
J R Raymond, A Fargin, J P Middleton, et al.
Page
of 2