Naismith AL - Search Results

1

Cl- channel activity in Xenopus oocytes expressing the cystic fibrosis gene.

Bear CE, Duguay F, Naismith AL, Kartner N, Hanrahan JW, Riordan JR. Bear CE, et al. Among authors: naismith al. J Biol Chem. 1991 Oct 15;266(29):19142-5. J Biol Chem. 1991. PMID: 1717461 Free article.

2

Mislocalization of delta F508 CFTR in cystic fibrosis sweat gland.

Kartner N, Augustinas O, Jensen TJ, Naismith AL, Riordan JR. Kartner N, et al. Among authors: naismith al. Nat Genet. 1992 Aug;1(5):321-7. doi: 10.1038/ng0892-321. Nat Genet. 1992. PMID: 1284548

3

Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance.

Kartner N, Hanrahan JW, Jensen TJ, Naismith AL, Sun SZ, Ackerley CA, Reyes EF, Tsui LC, Rommens JM, Bear CE, et al. Kartner N, et al. Among authors: naismith al. Cell. 1991 Feb 22;64(4):681-91. doi: 10.1016/0092-8674(91)90498-n. Cell. 1991. PMID: 1705179

4

Study of the expression of myelin proteolipid protein (lipophilin) using a cloned complementary DNA.

Naismith AL, Hoffman-Chudzik E, Tsui LC, Riordan JR. Naismith AL, et al. Nucleic Acids Res. 1985 Oct 25;13(20):7413-25. doi: 10.1093/nar/13.20.7413. Nucleic Acids Res. 1985. PMID: 3840591 Free PMC article.

5

Novel C-terminus modifications of the Dmt-Tic motif: a new class of dipeptide analogues showing altered pharmacological profiles toward the opioid receptors.

Pagé D, Naismith A, Schmidt R, Coupal M, Labarre M, Gosselin M, Bellemare D, Payza K, Brown W. Pagé D, et al. J Med Chem. 2001 Jul 19;44(15):2387-90. doi: 10.1021/jm015532k. J Med Chem. 2001. PMID: 11448220

6

1-(Bicyclopiperazinyl)ethylindoles and 1-(homopiperazinyl)ethyl-indoles as highly selective and potent 5-HT(7) receptor ligands.

Isaac MB, Xin T, O'Brien A, St-Martin D, Naismith A, MacLean N, Wilson J, Demchyshyn L, Tehim A, Slassi A. Isaac MB, et al. Bioorg Med Chem Lett. 2002 Sep 2;12(17):2451-4. doi: 10.1016/s0960-894x(02)00438-9. Bioorg Med Chem Lett. 2002. PMID: 12161155

7

Design, synthesis and biological activity of novel dimethyl-[2-[6-substituted-indol-1-yl]-ethyl]-amine as potent, selective, and orally-bioavailable 5-HT(1D) agonists.

Isaac M, Slassi M, Xin T, Arora J, O'Brien A, Edwards L, MacLean N, Wilson J, Demschyshyn L, Labrie P, Naismith A, Maddaford S, Papac D, Harrison S, Wang H, Draper S, Tehim A. Isaac M, et al. Bioorg Med Chem Lett. 2003 Dec 15;13(24):4409-13. doi: 10.1016/j.bmcl.2003.09.025. Bioorg Med Chem Lett. 2003. PMID: 14643336

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