Griswold DE - Search Results

1

The soluble form of E-selectin is an asymmetric monomer. Expression, purification, and characterization of the recombinant protein.

Hensley P, McDevitt PJ, Brooks I, Trill JJ, Feild JA, McNulty DE, Connor JR, Griswold DE, Kumar NV, Kopple KD, et al. Hensley P, et al. Among authors: griswold de. J Biol Chem. 1994 Sep 30;269(39):23949-58. J Biol Chem. 1994. PMID: 7523364 Free article.

2

Activation of the IL-1 gene in UV-irradiated mouse skin: association with inflammatory sequelae and pharmacologic intervention.

Griswold DE, Connor JR, Dalton BJ, Lee JC, Simon P, Hillegass L, Sieg DJ, Hanna N. Griswold DE, et al. J Invest Dermatol. 1991 Dec;97(6):1019-23. doi: 10.1111/1523-1747.ep12492422. J Invest Dermatol. 1991. PMID: 1660906 Free article.

3

Identification and initial characterization of four novel members of the interleukin-1 family.

Kumar S, McDonnell PC, Lehr R, Tierney L, Tzimas MN, Griswold DE, Capper EA, Tal-Singer R, Wells GI, Doyle ML, Young PR. Kumar S, et al. Among authors: griswold de. J Biol Chem. 2000 Apr 7;275(14):10308-14. doi: 10.1074/jbc.275.14.10308. J Biol Chem. 2000. PMID: 10744718 Free article.

4

Identification of a potent, selective non-peptide CXCR2 antagonist that inhibits interleukin-8-induced neutrophil migration.

White JR, Lee JM, Young PR, Hertzberg RP, Jurewicz AJ, Chaikin MA, Widdowson K, Foley JJ, Martin LD, Griswold DE, Sarau HM. White JR, et al. Among authors: griswold de. J Biol Chem. 1998 Apr 24;273(17):10095-8. doi: 10.1074/jbc.273.17.10095. J Biol Chem. 1998. PMID: 9553055 Free article.

5

Bicyclic N-hydroxyurea inhibitors of 5-lipoxygenase: pharmacodynamic, pharmacokinetic, and in vitro metabolic studies characterizing N-hydroxy-N-(2,3-dihydro-6-(phenylmethoxy)-3-benzofuranyl)urea.

Adams JL, Garigipati RS, Sorenson M, Schmidt SJ, Brian WR, Newton JF, Tyrrell KA, Garver E, Yodis LA, Chabot-Fletcher M, Tzimas M, Webb EF, Breton JJ, Griswold DE. Adams JL, et al. Among authors: griswold de. J Med Chem. 1996 Dec 20;39(26):5035-46. doi: 10.1021/jm960271d. J Med Chem. 1996. PMID: 8978834

6

(E)-3-[6-[[(2,6-dichlorophenyl)thio]methyl]-3-(2-phenylethoxy)-2- pyridinyl]-2-propenoic acid: a high-affinity leukotriene B4 receptor antagonist with oral antiinflammatory activity.

Daines RA, Chambers PA, Foley JJ, Griswold DE, Kingsbury WD, Martin LD, Schmidt DB, Sham KK, Sarau HM. Daines RA, et al. Among authors: griswold de. J Med Chem. 1996 Sep 13;39(19):3837-41. doi: 10.1021/jm960248s. J Med Chem. 1996. PMID: 8809171

7

Nonpeptide tachykinin receptor antagonists. II. Pharmacological and pharmacokinetic profile of SB-222200, a central nervous system penetrant, potent and selective NK-3 receptor antagonist.

Sarau HM, Griswold DE, Bush B, Potts W, Sandhu P, Lundberg D, Foley JJ, Schmidt DB, Webb EF, Martin LD, Legos JJ, Whitmore RG, Barone FC, Medhurst AD, Luttmann MA, Giardina GA, Hay DW. Sarau HM, et al. Among authors: griswold de. J Pharmacol Exp Ther. 2000 Oct;295(1):373-81. J Pharmacol Exp Ther. 2000. PMID: 10992004

8

(E)-3-[[[[6-(2-carboxyethenyl)-5-[[8-(4- methoxyphenyl)octyl]oxy]-2-pyridinyl]-methyl]thio]methyl]benzoic acid and related compounds: high affinity leukotriene B4 receptor antagonists.

Daines RA, Chambers PA, Eggleston DS, Foley JJ, Griswold DE, Haltiwanger RC, Jakas DR, Kingsbury WD, Martin LD, Pendrak I, et al. Daines RA, et al. Among authors: griswold de. J Med Chem. 1994 Sep 30;37(20):3327-36. doi: 10.1021/jm00046a017. J Med Chem. 1994. PMID: 7932560

9

(E)-3-[[[[6-(2-carboxyethenyl)-5-[[8-(4- methoxyphenyl)octyl]oxy]-2-pyridinyl]-methyl]thio]methyl]benzoic acid: a novel high-affinity leukotriene B4 receptor antagonist.

Daines RA, Chambers PA, Pendrak I, Jakas DR, Sarau HM, Foley JJ, Schmidt DB, Griswold DE, Martin LD, Tzimas MN, et al. Daines RA, et al. Among authors: griswold de. J Med Chem. 1993 Sep 3;36(18):2703-5. doi: 10.1021/jm00070a015. J Med Chem. 1993. PMID: 8410983 No abstract available.

10

1-substituted 4-aryl-5-pyridinylimidazoles: a new class of cytokine suppressive drugs with low 5-lipoxygenase and cyclooxygenase inhibitory potency.

Boehm JC, Smietana JM, Sorenson ME, Garigipati RS, Gallagher TF, Sheldrake PL, Bradbeer J, Badger AM, Laydon JT, Lee JC, Hillegass LM, Griswold DE, Breton JJ, Chabot-Fletcher MC, Adams JL. Boehm JC, et al. Among authors: griswold de. J Med Chem. 1996 Sep 27;39(20):3929-37. doi: 10.1021/jm960415o. J Med Chem. 1996. PMID: 8831759

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