Hoo K - Search Results

1

[3H]ATPA: a high affinity ligand for GluR5 kainate receptors.

Hoo K, Legutko B, Rizkalla G, Deverill M, Hawes CR, Ellis GJ, Stensbol TB, Krogsgaard-Larsen P, Skolnick P, Bleakman D. Hoo K, et al. Neuropharmacology. 1999 Dec;38(12):1811-7. doi: 10.1016/s0028-3908(99)00133-1. Neuropharmacology. 1999. PMID: 10608276

2

LY339434, a GluR5 kainate receptor agonist.

Small B, Thomas J, Kemp M, Hoo K, Ballyk B, Deverill M, Ogden AM, Rubio A, Pedregal C, Bleakman D. Small B, et al. Among authors: hoo k. Neuropharmacology. 1998 Oct-Nov;37(10-11):1261-7. doi: 10.1016/s0028-3908(98)00122-1. Neuropharmacology. 1998. PMID: 9849663

3

Decahydroisoquinolines: novel competitive AMPA/kainate antagonists with neuroprotective effects in global cerebral ischaemia.

O'Neill MJ, Bond A, Ornstein PL, Ward MA, Hicks CA, Hoo K, Bleakman D, Lodge D. O'Neill MJ, et al. Among authors: hoo k. Neuropharmacology. 1998 Oct-Nov;37(10-11):1211-22. doi: 10.1016/s0028-3908(98)00134-8. Neuropharmacology. 1998. PMID: 9849659

4

Kainate GluR5 receptor subtype mediates the nociceptive response to formalin in the rat.

Simmons RM, Li DL, Hoo KH, Deverill M, Ornstein PL, Iyengar S. Simmons RM, et al. Among authors: hoo kh. Neuropharmacology. 1998;37(1):25-36. doi: 10.1016/s0028-3908(97)00188-3. Neuropharmacology. 1998. PMID: 9680256

5

Synthesis of willardiine and 6-azawillardiine analogs: pharmacological characterization on cloned homomeric human AMPA and kainate receptor subtypes.

Jane DE, Hoo K, Kamboj R, Deverill M, Bleakman D, Mandelzys A. Jane DE, et al. Among authors: hoo k. J Med Chem. 1997 Oct 24;40(22):3645-50. doi: 10.1021/jm9702387. J Med Chem. 1997. PMID: 9357531

6

Pharmacological characterization of a GluR6 kainate receptor in cultured hippocampal neurons.

Bleakman D, Ogden AM, Ornstein PL, Hoo K. Bleakman D, et al. Among authors: hoo k. Eur J Pharmacol. 1999 Aug 13;378(3):331-7. doi: 10.1016/s0014-2999(99)00478-1. Eur J Pharmacol. 1999. PMID: 10493110

7

A hippocampal GluR5 kainate receptor regulating inhibitory synaptic transmission.

Clarke VR, Ballyk BA, Hoo KH, Mandelzys A, Pellizzari A, Bath CP, Thomas J, Sharpe EF, Davies CH, Ornstein PL, Schoepp DD, Kamboj RK, Collingridge GL, Lodge D, Bleakman D. Clarke VR, et al. Among authors: hoo kh. Nature. 1997 Oct 9;389(6651):599-603. doi: 10.1038/39315. Nature. 1997. PMID: 9335499

8

4-Alkyl- and 4-cinnamylglutamic acid analogues are potent GluR5 kainate receptor agonists.

Pedregal C, Collado I, Escribano A, Ezquerra J, Domínguez C, Mateo AI, Rubio A, Baker SR, Goldsworthy J, Kamboj RK, Ballyk BA, Hoo K, Bleakman D. Pedregal C, et al. Among authors: hoo k. J Med Chem. 2000 May 18;43(10):1958-68. doi: 10.1021/jm9911682. J Med Chem. 2000. PMID: 10821708

9

Synthesis of a series of aryl kainic acid analogs and evaluation in cells stably expressing the kainate receptor humGluR6.

Cantrell BE, Zimmerman DM, Monn JA, Kamboj RK, Hoo KH, Tizzano JP, Pullar IA, Farrell LN, Bleakman D. Cantrell BE, et al. Among authors: hoo kh. J Med Chem. 1996 Sep 13;39(19):3617-24. doi: 10.1021/jm960155a. J Med Chem. 1996. PMID: 8809152

10

Molecular characterization of the human EAA5 (GluR7) receptor: a high-affinity kainate receptor with novel potential RNA editing sites.

Nutt SL, Hoo KH, Rampersad V, Deverill RM, Elliott CE, Fletcher EJ, Adams SL, Korczak B, Foldes RL, Kamboj RK. Nutt SL, et al. Among authors: hoo kh. Recept Channels. 1994;2(4):315-26. Recept Channels. 1994. PMID: 7719709

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