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pseudoginsenoside G(1)

Known as: pseudoginsenoside G1 
 
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
Pseudoginsenoside-F11 (PF11), an ocotillol-type ginsenoside, has been shown to possess significant neuroprotective activity… Expand
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2013
2013
Alzheimer's disease (AD) is a progressive neurodegenerative disease characterized by amyloid β (Aβ) deposits, elevated oxidative… Expand
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2013
2013
PPARγ is a nuclear hormone receptor that functions as a master regulator of adipocyte differentiation and development. Full PPAR… Expand
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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… Expand
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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… Expand
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Highly Cited
2009
Highly Cited
2009
Purpose: Antiestrogens are used to treat estrogen receptor (ER)-α-positive breast cancers and cause a p27-dependent G1 arrest… Expand
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Highly Cited
2004
Highly Cited
2004
CuAlO2 exhibits a unique defect structure that is dependent on the synthesis route. High-temperature solid-state and low… Expand
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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… Expand
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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… Expand
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Highly Cited
2000
Highly Cited
2000
  • F. Relaix, X. Wei, +5 authors X. Wu
  • Proceedings of the National Academy of Sciences…
  • 2000
  • Corpus ID: 25153482
Induction of wild-type p53 in mouse fibroblasts causes cell cycle arrest at the G(1) phase, whereas coexpression of p53 and the… Expand
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