Mallee JJ - Search Results

1

Identification and pharmacological characterization of domains involved in binding of CGRP receptor antagonists to the calcitonin-like receptor.

Salvatore CA, Mallee JJ, Bell IM, Zartman CB, Williams TM, Koblan KS, Kane SA. Salvatore CA, et al. Among authors: mallee jj. Biochemistry. 2006 Feb 14;45(6):1881-7. doi: 10.1021/bi052044w. Biochemistry. 2006. PMID: 16460034

2

Receptor activity-modifying protein 1 determines the species selectivity of non-peptide CGRP receptor antagonists.

Mallee JJ, Salvatore CA, LeBourdelles B, Oliver KR, Longmore J, Koblan KS, Kane SA. Mallee JJ, et al. J Biol Chem. 2002 Apr 19;277(16):14294-8. doi: 10.1074/jbc.M109661200. Epub 2002 Feb 14. J Biol Chem. 2002. PMID: 11847213 Free article.

3

Identification of a novel RAMP-independent CGRP receptor antagonist.

Zartman CB, Bell IM, Gallicchio SN, Graham SL, Kane SA, Mallee JJ, Rutledge RZ, Salvatore CA, Vacca JP, Williams TM. Zartman CB, et al. Among authors: mallee jj. Bioorg Med Chem Lett. 2011 Nov 15;21(22):6705-8. doi: 10.1016/j.bmcl.2011.09.056. Epub 2011 Sep 21. Bioorg Med Chem Lett. 2011. PMID: 21982500

4

Effects of inhibition of alpha-CGRP receptors on cardiac and peripheral vascular dynamics in conscious dogs with chronic heart failure.

Shen YT, Mallee JJ, Handt LK, Gilberto DB, Lynch JJ Jr, Hargreaves RJ, Koblan KS, Gould RJ, Kane SA. Shen YT, et al. Among authors: mallee jj. J Cardiovasc Pharmacol. 2003 Nov;42(5):656-61. doi: 10.1097/00005344-200311000-00012. J Cardiovasc Pharmacol. 2003. PMID: 14576515

5

Cloning, characterization and central nervous system distribution of receptor activity modifying proteins in the rat.

Oliver KR, Kane SA, Salvatore CA, Mallee JJ, Kinsey AM, Koblan KS, Keyvan-Fouladi N, Heavens RP, Wainwright A, Jacobson M, Dickerson IM, Hill RG. Oliver KR, et al. Among authors: mallee jj. Eur J Neurosci. 2001 Aug;14(4):618-28. doi: 10.1046/j.0953-816x.2001.01688.x. Eur J Neurosci. 2001. PMID: 11556887

6

Identification and characterization of novel mammalian neuropeptide FF-like peptides that attenuate morphine-induced antinociception.

Liu Q, Guan XM, Martin WJ, McDonald TP, Clements MK, Jiang Q, Zeng Z, Jacobson M, Williams DL Jr, Yu H, Bomford D, Figueroa D, Mallee J, Wang R, Evans J, Gould R, Austin CP. Liu Q, et al. J Biol Chem. 2001 Oct 5;276(40):36961-9. doi: 10.1074/jbc.M105308200. Epub 2001 Jul 31. J Biol Chem. 2001. PMID: 11481330 Free article.

7

The structural organization of the human Na+/myo-inositol cotransporter (SLC5A3) gene and characterization of the promoter.

Mallee JJ, Atta MG, Lorica V, Rim JS, Kwon HM, Lucente AD, Wang Y, Berry GT. Mallee JJ, et al. Genomics. 1997 Dec 15;46(3):459-65. doi: 10.1006/geno.1997.5055. Genomics. 1997. PMID: 9441750 Free article.

8

Multiple comparison of primary structure of the osmoregulatory Na+/myo-inositol cotransporter from bovine, human, and canine species.

Mallee JJ, Parella T, Kwon HM, Berry GT. Mallee JJ, et al. Mamm Genome. 1996 Mar;7(3):252. doi: 10.1007/s003359900076. Mamm Genome. 1996. PMID: 8833264 No abstract available.

9

The human osmoregulatory Na+/myo-inositol cotransporter gene (SLC5A3): molecular cloning and localization to chromosome 21.

Berry GT, Mallee JJ, Kwon HM, Rim JS, Mulla WR, Muenke M, Spinner NB. Berry GT, et al. Among authors: mallee jj. Genomics. 1995 Jan 20;25(2):507-13. doi: 10.1016/0888-7543(95)80052-n. Genomics. 1995. PMID: 7789985 Free article.

10

The 21q22.1 STS marker, VN02 (EST00541 cDNA), is part of the 3' sequence of the human Na+/myo-inositol cotransporter (SLC5A3) gene.

Berry GT, Mallee JJ, Blouin JL, Antonarakis SE. Berry GT, et al. Among authors: mallee jj. Cytogenet Cell Genet. 1996;73(1-2):77-8. doi: 10.1159/000134311. Cytogenet Cell Genet. 1996. PMID: 8646889

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