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Showing results (51-60 of 66) with videos related to

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Medicinal Chemistry (Shariqah (United Arab Emirates))|June 22, 2006
Synthesis and biological evaluation of 2-, 3-, and 4-acylaminocinnamyl-N-hydroxyamides as novel synthetic HDAC inhibitorsA Mai, S Massa, R Pezzi, et al.
The Journal of Biological Chemistry|October 15, 1992
Specificity of Zea mays histone deacetylase is regulated by phosphorylationG Brosch, E I Georgieva, G López-Rodas, et al.
Biochimica Et Biophysica Acta|September 5, 1996
A comparative study of histone deacetylases of plant, fungal and vertebrate cellsT Lechner, A Lusser, G Brosch, et al.
FEBS Letters|January 13, 1992
Enzymes involved in the dynamic equilibrium of core histone acetylation of Physarum polycephalumG López-Rodas, G Brosch, G Golderer, et al.
FEBS Letters|June 22, 2001
Histone deacetylases in replicative senescence: evidence for a senescence-specific form of HDAC-2M Wagner, G Brosch, W Zwerschke, et al.
Current Biology : CB|June 1, 1997
Cell growth inhibition by the Mad/Max complex through recruitment of histone deacetylase activityA Sommer, S Hilfenhaus, A Menkel, et al.
Biochemistry|May 29, 1999
Different types of maize histone deacetylases are distinguished by a highly complex substrate and site specificityD Kölle, G Brosch, T Lechner, et al.
FEBS Letters|February 15, 1993
Histone deacetylase. A key enzyme for the binding of regulatory proteins to chromatinG López-Rodas, G Brosch, E I Georgieva, et al.
Oncogene|August 3, 2010
Cell cycle-dependent acetylation of Rb2/p130 in NIH3T3 cellsF Schwarze, J Meraner, M Lechner, et al.
Journal of Medicinal Chemistry|June 19, 2001
3-(4-aroyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides, a new class of synthetic histone deacetylase inhibitorsS Massa, A Mai, G Sbardella, et al.
Pageof 7

Showing results (51-60 of 66) with videos related to

Sort By:
Pageof 7
Medicinal Chemistry (Shariqah (United Arab Emirates))|June 22, 2006
Synthesis and biological evaluation of 2-, 3-, and 4-acylaminocinnamyl-N-hydroxyamides as novel synthetic HDAC inhibitorsA Mai, S Massa, R Pezzi, et al.
The Journal of Biological Chemistry|October 15, 1992
Specificity of Zea mays histone deacetylase is regulated by phosphorylationG Brosch, E I Georgieva, G López-Rodas, et al.
Biochimica Et Biophysica Acta|September 5, 1996
A comparative study of histone deacetylases of plant, fungal and vertebrate cellsT Lechner, A Lusser, G Brosch, et al.
FEBS Letters|January 13, 1992
Enzymes involved in the dynamic equilibrium of core histone acetylation of Physarum polycephalumG López-Rodas, G Brosch, G Golderer, et al.
FEBS Letters|June 22, 2001
Histone deacetylases in replicative senescence: evidence for a senescence-specific form of HDAC-2M Wagner, G Brosch, W Zwerschke, et al.
Current Biology : CB|June 1, 1997
Cell growth inhibition by the Mad/Max complex through recruitment of histone deacetylase activityA Sommer, S Hilfenhaus, A Menkel, et al.
Biochemistry|May 29, 1999
Different types of maize histone deacetylases are distinguished by a highly complex substrate and site specificityD Kölle, G Brosch, T Lechner, et al.
FEBS Letters|February 15, 1993
Histone deacetylase. A key enzyme for the binding of regulatory proteins to chromatinG López-Rodas, G Brosch, E I Georgieva, et al.
Oncogene|August 3, 2010
Cell cycle-dependent acetylation of Rb2/p130 in NIH3T3 cellsF Schwarze, J Meraner, M Lechner, et al.
Journal of Medicinal Chemistry|June 19, 2001
3-(4-aroyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides, a new class of synthetic histone deacetylase inhibitorsS Massa, A Mai, G Sbardella, et al.
Pageof 7