LG 100268

Known as: LG-100268, LG100268 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1995-2016
024619952016

Papers overview

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2007
2007
PURPOSE To test whether a novel rexinoid, LG100268, prevents the development of preinvasive and invasive estrogen receptor… (More)
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2002
2002
The selective estrogen receptor modulator arzoxifene and the rexinoid LG 100268 were active not only as single agents for… (More)
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Highly Cited
2002
Highly Cited
2002
It has been shown that the novel synthetic triterpenoid CDDO inhibits proliferation and induces differentiation and apoptosis in… (More)
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2002
2002
Ligands that specifically target retinoid-X receptors (RXRs) are emerging as potentially powerful therapies for cancer, diabetes… (More)
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2000
2000
Ovarian granulosa cells synthesize estrogens from androgens, which are catalyzed by aromatase cytochrome P450 (P450arom… (More)
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2000
2000
Hyperlipidemia may complicate the use of HIV protease inhibitors (PIs) in AIDS therapy. To determine the cause of hyperlipidemia… (More)
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Highly Cited
1999
Highly Cited
1999
The present study examined the expression and role of the thiazolidinedione (TZD)-activated transcription factor, peroxisome… (More)
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1999
1999
Aims/hypothesis. Although retinoid X receptor (RXR) and peroxisome proliferator activated receptor-γ (PPARγ) agonists have… (More)
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Highly Cited
1995
Highly Cited
1995
Structural modifications of the retinoid X receptor (RXR) selective compound 4-[1-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2… (More)
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1995
1995
T-cell hybridomas, thymocytes, and T cells can be induced to undergo apoptotic cell death by activation through the T-cell… (More)
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