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Comparison of the pharmacological properties of rat Na(V)1.8 with rat Na(V)1.2a and human Na(V)1.5 voltage-gated sodium channel subtypes using a membrane potential sensitive dye and FLIPR. [electronic resource] by
- Vickery, R G
- Amagasu, S M
- Chang, R
- Mai, N
- Kaufman, E
- Martin, J
- Hembrador, J
- O'Keefe, M D
- Gee, C
- Marquess, D
- Smith, J A M
Producer: 20041007
In:
Receptors & channels vol. 10
Availability: No items available.
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Evidence for a multivalent interaction of symmetrical, N-linked, lidocaine dimers with voltage-gated Na+ channels. [electronic resource] by
- Smith, J A M
- Amagasu, S M
- Hembrador, J
- Axt, S
- Chang, R
- Church, T
- Gee, C
- Jacobsen, J R
- Jenkins, T
- Kaufman, E
- Mai, N
- Vickery, R G
Producer: 20060419
In:
Molecular pharmacology vol. 69
Availability: No items available.
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18.
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The 5-HT4 receptor agonist, tegaserod, is a potent 5-HT2B receptor antagonist in vitro and in vivo. [electronic resource] by
- Beattie, D T
- Smith, J A M
- Marquess, D
- Vickery, R G
- Armstrong, S R
- Pulido-Rios, T
- McCullough, J L
- Sandlund, C
- Richardson, C
- Mai, N
- Humphrey, P P A
Producer: 20050428
In:
British journal of pharmacology vol. 143
Availability: No items available.
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