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Items: 6

1.

Statistical modeling of the hormetic dose zone and the toxic potency completes the quantitative description of hormetic dose responses.

Belz RG, Piepho HP.

Environ Toxicol Chem. 2015 May;34(5):1169-77. doi: 10.1002/etc.2857. Epub 2015 Apr 7.

PMID:
25523646
2.

Drastic reduction of the slow gate of human muscle chloride channel (ClC-1) by mutation C277S.

Accardi A, Ferrera L, Pusch M.

J Physiol. 2001 Aug 1;534(Pt 3):745-52.

3.

Further structure-activity relationships in the series of tropanyl esters endowed with potent antinociceptive activity.

Scapecchi S, Giorgi A, Bellucci C, Dei S, Ghelardini C, Manetti D, Romanelli MN, Teodori E.

Farmaco. 1998 Dec 30;53(12):764-72.

PMID:
10230057
4.

In vivo and in vitro peroxisome proliferation properties of selected clofibrate analogues in the rat. Structure-activity relationships.

Esbenshade TA, Kamanna VS, Newman HA, Tortorella V, Witiak DT, Feller DR.

Biochem Pharmacol. 1990 Sep 15;40(6):1263-74.

PMID:
2403380
5.

Stereospecificity of the chloride ion channel: the action of chiral clofibric acid analogues.

Bettoni G, Loiodice F, Tortorella V, Conte-Camerino D, Mambrini M, Ferrannini E, Bryant SH.

J Med Chem. 1987 Aug;30(8):1267-70.

PMID:
2441051
6.

Dissociation of hypolipidemic and antiplatelet actions from adverse myotonic effects of clofibric acid related enantiomers.

Feller DR, Kamanna VS, Newman HA, Romstedt KJ, Witiak DT, Bettoni G, Bryant SH, Conte-Camerino D, Loiodice F, Tortorella V.

J Med Chem. 1987 Aug;30(8):1265-7.

PMID:
2441050

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