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SK-7041

 
National Institutes of Health

Papers overview

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2013
2013
Purpose This preclinical study is to determine whether the capacity of histone deacetylase (HDAC) inhibitors to enhance radiation… Expand
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Highly Cited
2009
Highly Cited
2009
  • H. Noh, Eunseo Oh, +4 authors H. Lee
  • American journal of physiology. Renal physiology
  • 2009
  • Corpus ID: 9235437
Excessive accumulation of extracellular matrix (ECM) in the kidneys and epithelial-to-mesenchymal transition (EMT) of renal… Expand
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2008
2008
Activation of the JAK/STAT pathway appears common in AML, occurring in up to 70% of AML patients. Therefore, JAK/STAT signal… Expand
2007
2007
Although STI571 still plays a key role in the treatment of chronic myeloid leukemia, emergence of resistance to STI571 is a major… Expand
2007
2007
Histone acetyltransferase (HAT) and histone deacetylase (HDAC) activities determine the acetylation status of histones, which… Expand
Highly Cited
2006
Highly Cited
2006
Background— A number of distinct stress signaling pathways in myocardium cause cardiac hypertrophy and heart failure. Class II… Expand
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2006
2006
A novel hybrid synthetic histone deacetylase inhibitor, SK-7041, was synthesized from hydroaxamic acid of trichostatin A (TSA… Expand
2006
2006
  • Keun-Wook Lee, Jee Hyun Kim, +10 authors Y. Bang
  • Anticancer research
  • 2006
  • Corpus ID: 521109
BACKGROUND A class of synthetic histone deacetylase (HDAC) inhibitors, which are hybrids of trichostatin A and MS-275 were… Expand
2005
2005
Histone acetyltransferase (HAT) and histone deacetylase (HDAC) activities determine the acetylation status of histones, and have… Expand
Highly Cited
2004
Highly Cited
2004
We have developed previously a class of synthetic hybrid histone deacetylase (HDAC) inhibitors, which were built from hydroxamic… Expand
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