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geranylgeraniol

Known as: 2,6,10,14-Hexadecatetraen-1-ol, 3,7,11,15-tetramethyl- 
 
National Institutes of Health

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Highly Cited
2006
Highly Cited
2006
The mevalonate pathway produces cholesterol and nonsterol isoprenoids, such as geranylgeraniol. In the brain, a fraction of… Expand
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Highly Cited
2006
Highly Cited
2006
We recently developed a genome‐length hepatitis C virus (HCV) RNA replication system (OR6) with luciferase as a reporter. The OR6… Expand
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Highly Cited
2005
Highly Cited
2005
ABSTRACT We examined the antibacterial activities against Staphylococcus aureus of three diterpenes, namely, geranylgeraniol… Expand
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Highly Cited
2003
Highly Cited
2003
The endoplasmic reticulum enzyme 3-hydroxy-3-methylglutaryl-CoA reductase produces mevalonate, which is converted to sterols and… Expand
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Highly Cited
2000
Highly Cited
2000
We examined the effects of four 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors (pravastatin, simvastatin… Expand
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Highly Cited
1999
Highly Cited
1999
Nitrogen-containing bisphosphonates were shown to cause macrophage apoptosis by inhibiting enzymes in the biosynthetic pathway… Expand
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Review
1999
Review
1999
Compounds derived from the isoprenoid/cholesterol biosynthetic pathway have recently been shown to have novel biological… Expand
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Highly Cited
1999
Highly Cited
1999
Recently, advances have been made in understanding the molecular mechanisms by which bisphosphonate drugs inhibit bone resorption… Expand
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Highly Cited
1998
Highly Cited
1998
We have previously shown that, among various isoprenoids, farnesol and geranylgeraniol specifically induced actin fiber… Expand
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Highly Cited
1997
Highly Cited
1997
We examined the effect of fluvastatin, the first entirely synthetic 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor… Expand
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