pseudoginsenoside G(1)

Known as: pseudoginsenoside G1 
 
National Institutes of Health

Papers overview

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2014
2014
Pseudoginsenoside-F11 (PF11), an ocotillol-type ginsenoside, has been shown to possess significant neuroprotective activity… (More)
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2013
2013
PPAR γ is a nuclear hormone receptor that functions as a master regulator of adipocyte differentiation and development. Full PPAR… (More)
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2013
2013
Alzheimer's disease (AD) is a progressive neurodegenerative disease characterized by amyloid β (Aβ) deposits, elevated oxidative… (More)
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Highly Cited
2010
Highly Cited
2010
The expression of several members of the FOX gene family is known to be altered in a variety of cancers. We show that in breast… (More)
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Highly Cited
2009
Highly Cited
2009
Epigenetic silencing of secreted wingless-type (Wnt) antagonists through hypermethylation is associated with tobacco smoking and… (More)
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2009
2009
PURPOSE Antiestrogens are used to treat estrogen receptor (ER)-alpha-positive breast cancers and cause a p27-dependent G(1… (More)
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2009
2009
Three new sesquiterpene pyridine alkaloids with a beta-dihydroagarofuran sesquiterpene skeleton, celangulatin G(1), H(2) and I(3… (More)
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2003
2003
In the present study, pseudoginsenoside-F(11) (PF(11)), a saponin that existed in American ginseng, was studied on its protective… (More)
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Highly Cited
2002
Highly Cited
2002
Germline mutations of the LKB1 tumor suppressor gene lead to Peutz-Jeghers syndrome (PJS), with a predisposition to cancer. LKB1… (More)
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Highly Cited
2000
Highly Cited
2000
Induction of wild-type p53 in mouse fibroblasts causes cell cycle arrest at the G(1) phase, whereas coexpression of p53 and the… (More)
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