| Inhibition of maize histone deacetylases by HC toxin, the host-selective toxin of Cochliobolus carbonum. G Brosch, R Ransom, T Lechner, JD Walton, P Loidl The Plant Cell 7 (11), 1941-1950, 1995 | 295 | 1995 |
| Identification of maize histone deacetylase HD2 as an acidic nucleolar phosphoprotein A Lusser, G Brosch, A Loidl, H Haas, P Loidl Science 277 (5322), 88-91, 1997 | 282 | 1997 |
| Amide analogues of trichostatin A as inhibitors of histone deacetylase and inducers of terminal cell differentiation M Jung, G Brosch, D Kölle, H Scherf, C Gerhäuser, P Loidl Journal of medicinal chemistry 42 (22), 4669-4679, 1999 | 268 | 1999 |
| Class II (IIa)-selective histone deacetylase inhibitors. 1. Synthesis and biological evaluation of novel (aryloxopropenyl) pyrrolyl hydroxyamides A Mai, S Massa, R Pezzi, S Simeoni, D Rotili, A Nebbioso, ... Journal of medicinal chemistry 48 (9), 3344-3353, 2005 | 241 | 2005 |
| Histone acetylation: facts and questions P Loidl Chromosoma 103 (7), 441-449, 1994 | 240 | 1994 |
| A plant dialect of the histone language P Loidl Trends in plant science 9 (2), 84-90, 2004 | 211 | 2004 |
| Histone acetylation: lessons from the plant kingdom A Lusser, D Kölle, P Loidl Trends in Plant Science 6 (2), 59-65, 2001 | 191 | 2001 |
| Histone modifications and chromatin dynamics: a focus on filamentous fungi G Brosch, P Loidl, S Graessle FEMS microbiology reviews 32 (3), 409-439, 2008 | 189 | 2008 |
| 3-(4-Aroyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-alkylamides as a New Class of Synthetic Histone Deacetylase Inhibitors. 1. Design, Synthesis, Biological … A Mai, S Massa, R Ragno, I Cerbara, F Jesacher, P Loidl, G Brosch Journal of Medicinal Chemistry 46 (4), 512-524, 2003 | 144 | 2003 |
| Cell growth inhibition by the Mad/Max complex through recruitment of histone deacetylase activity A Sommer, S Hilfenhaus, A Menkel, E Kremmer, C Seiser, P Loidl, ... Current Biology 7 (6), 357-365, 1997 | 131 | 1997 |
| A non-isotopic assay for histone deacetylase activity K Hoffmann, M Jung, G Brosch, P Loidl Nucleic acids research 27 (9), 2057-2058, 1999 | 128 | 1999 |
| Towards an understanding of the biological function of histone acetylation P Loidl FEBS letters 227 (2), 91-95, 1988 | 122 | 1988 |
| Analogues of trichosтatin a and trapoxin B as histone deacetylase inhibitors M Jung, K Hoffmann, G Brosch, P Loidl Bioorganic & Medicinal Chemistry Letters 7 (13), 1655-1658, 1997 | 119 | 1997 |
| Biochemical methods for analysis of histone deacetylases D Kölle, G Brosch, T Lechner, A Lusser, P Loidl Methods 15 (4), 323-331, 1998 | 114 | 1998 |
| Comparative analysis of HD2 type histone deacetylases in higher plants M Dangl, G Brosch, H Haas, P Loidl, A Lusser Planta 213 (2), 280-285, 2001 | 111 | 2001 |
| 3-(4-Aroyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides, a New Class of Synthetic Histone Deacetylase Inhibitors S Massa, A Mai, G Sbardella, M Esposito, R Ragno, P Loidl, G Brosch Journal of medicinal chemistry 44 (13), 2069-2072, 2001 | 102 | 2001 |
| Structure− activity relationships on phenylalanine-containing inhibitors of histone deacetylase: in vitro enzyme inhibition, induction of differentiation, and inhibition of … S Wittich, H Scherf, C Xie, G Brosch, P Loidl, C Gerhäuser, M Jung Journal of medicinal chemistry 45 (15), 3296-3309, 2002 | 100 | 2002 |
| 3-(4-Aroyl-1-methyl-1 H-2-pyrrolyl)-N-hydroxy-2-propenamides as a new class of synthetic histone deacetylase inhibitors. 2. Effect of pyrrole-C2 and/or-C4 substitutions on … A Mai, S Massa, I Cerbara, S Valente, R Ragno, P Bottoni, R Scatena, ... Journal of medicinal chemistry 47 (5), 1098-1109, 2004 | 94 | 2004 |
| Histone deacetylase: A key enzyme for the binding of regulatory proteins to chromatin G López-Rodas, G Brosch, EI Georgieva, R Sendra, L Franco, P Loidl FEBS letters 317 (3), 175-180, 1993 | 94 | 1993 |
| Histone deacetylases in fungi: novel members, new facts P Trojer, EM Brandtner, G Brosch, P Loidl, J Galehr, R Linzmaier, H Haas, ... Nucleic acids research 31 (14), 3971-3981, 2003 | 89 | 2003 |
