Cullinan GJ[au] - Search Results

Year	Number of Results
1978	2
1979	1
1984	1
1987	2
1989	1
1994	1
1997	3
1998	1
2000	1
2021	0

1

Molecular determinants of tissue selectivity in estrogen receptor modulators.

Grese TA, Sluka JP, Bryant HU, Cullinan GJ, Glasebrook AL, Jones CD, Matsumoto K, Palkowitz AD, Sato M, Termine JD, Winter MA, Yang NN, Dodge JA. Grese TA, et al. Among authors: cullinan gj. Proc Natl Acad Sci U S A. 1997 Dec 9;94(25):14105-10. doi: 10.1073/pnas.94.25.14105. Proc Natl Acad Sci U S A. 1997. PMID: 9391160 Free PMC article.

2

Discovery and synthesis of [6-hydroxy-3-[4-[2-(1-piperidinyl)ethoxy]phenoxy]-2-(4-hydroxyphenyl)]b enzo[b]thiophene: a novel, highly potent, selective estrogen receptor modulator.

Palkowitz AD, Glasebrook AL, Thrasher KJ, Hauser KL, Short LL, Phillips DL, Muehl BS, Sato M, Shetler PK, Cullinan GJ, Pell TR, Bryant HU. Palkowitz AD, et al. Among authors: cullinan gj. J Med Chem. 1997 May 9;40(10):1407-16. doi: 10.1021/jm970167b. J Med Chem. 1997. PMID: 9154963

3

Hypocholesterolemic activity of raloxifene (LY139481): pharmacological characterization as a selective estrogen receptor modulator.

Kauffman RF, Bensch WR, Roudebush RE, Cole HW, Bean JS, Phillips DL, Monroe A, Cullinan GJ, Glasebrook AL, Bryant HU. Kauffman RF, et al. Among authors: cullinan gj. J Pharmacol Exp Ther. 1997 Jan;280(1):146-53. J Pharmacol Exp Ther. 1997. PMID: 8996192

4

Raloxifene (LY139481 HCI) prevents bone loss and reduces serum cholesterol without causing uterine hypertrophy in ovariectomized rats.

Black LJ, Sato M, Rowley ER, Magee DE, Bekele A, Williams DC, Cullinan GJ, Bendele R, Kauffman RF, Bensch WR, et al. Black LJ, et al. Among authors: cullinan gj. J Clin Invest. 1994 Jan;93(1):63-9. doi: 10.1172/JCI116985. J Clin Invest. 1994. PMID: 8282823 Free PMC article.

5

LY320135, a novel cannabinoid CB1 receptor antagonist, unmasks coupling of the CB1 receptor to stimulation of cAMP accumulation.

Felder CC, Joyce KE, Briley EM, Glass M, Mackie KP, Fahey KJ, Cullinan GJ, Hunden DC, Johnson DW, Chaney MO, Koppel GA, Brownstein M. Felder CC, et al. Among authors: cullinan gj. J Pharmacol Exp Ther. 1998 Jan;284(1):291-7. J Pharmacol Exp Ther. 1998. PMID: 9435190

6

Leukotriene receptor antagonists. 1. Synthesis and structure-activity relationships of alkoxyacetophenone derivatives.

Marshall WS, Goodson T, Cullinan GJ, Swanson-Bean D, Haisch KD, Rinkema LE, Fleisch JH. Marshall WS, et al. Among authors: cullinan gj. J Med Chem. 1987 Apr;30(4):682-9. doi: 10.1021/jm00387a018. J Med Chem. 1987. PMID: 3031291

7

Pharmacologic analysis of two novel inhibitors of leukotriene (slow reacting substance) release.

Fleisch JH, Haisch KD, Spaethe SM, Rinkema LE, Cullinan GJ, Schmidt MJ, Marshall WS. Fleisch JH, et al. Among authors: cullinan gj. J Pharmacol Exp Ther. 1984 Jun;229(3):681-9. J Pharmacol Exp Ther. 1984. PMID: 6202867

8

Structure-activity relationships of dimeric Catharanthus alkaloids. 2. Experimental antitumor activities of N-substituted deacetylvinblastine amide (vindesine) sulfates.

Conrad RA, Cullinan GJ, Gerzon K, Poore GA. Conrad RA, et al. Among authors: cullinan gj. J Med Chem. 1979 Apr;22(4):391-400. doi: 10.1021/jm00190a008. J Med Chem. 1979. PMID: 430477

9

New antitumor monoclonal antibody-vinca conjugates LY203725 and related compounds: design, preparation, and representative in vivo activity.

Laguzza BC, Nichols CL, Briggs SL, Cullinan GJ, Johnson DA, Starling JJ, Baker AL, Bumol TF, Corvalan JR. Laguzza BC, et al. Among authors: cullinan gj. J Med Chem. 1989 Mar;32(3):548-55. doi: 10.1021/jm00123a007. J Med Chem. 1989. PMID: 2783975

10

Antitumor activity of deacetyl vinblastine amide sulfate (vindesine) in rodents and mitotic accumulation studies in culture.

Sweeney MJ, Boder GB, Cullinan GJ, Culp HW, Daniels WD, Dyke RW, Gerzon K, McMahon RE, Nelson RL, Poore GA, Todd GC. Sweeney MJ, et al. Among authors: cullinan gj. Cancer Res. 1978 Sep;38(9):2886-91. Cancer Res. 1978. PMID: 679195 Free article. No abstract available.

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