Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
BLUEPRINT to decode the epigenetic signature written in blood.
|
Nat Biotechnol
|
2012
|
3.24
|
2
|
Tumor-selective action of HDAC inhibitors involves TRAIL induction in acute myeloid leukemia cells.
|
Nat Med
|
2004
|
2.72
|
3
|
Inhibitors of histone deacetylases induce tumor-selective apoptosis through activation of the death receptor pathway.
|
Nat Med
|
2004
|
2.71
|
4
|
PML-RARalpha/RXR Alters the Epigenetic Landscape in Acute Promyelocytic Leukemia.
|
Cancer Cell
|
2010
|
2.50
|
5
|
Whole-genome bisulfite sequencing of two distinct interconvertible DNA methylomes of mouse embryonic stem cells.
|
Cell Stem Cell
|
2013
|
2.32
|
6
|
Design of selective nuclear receptor modulators: RAR and RXR as a case study.
|
Nat Rev Drug Discov
|
2007
|
1.91
|
7
|
HDAC2 blockade by nitric oxide and histone deacetylase inhibitors reveals a common target in Duchenne muscular dystrophy treatment.
|
Proc Natl Acad Sci U S A
|
2008
|
1.80
|
8
|
"Shock and kill" effects of class I-selective histone deacetylase inhibitors in combination with the glutathione synthesis inhibitor buthionine sulfoximine in cell line models for HIV-1 quiescence.
|
Retrovirology
|
2009
|
1.59
|
9
|
Estrogens and progesterone promote persistent CCND1 gene activation during G1 by inducing transcriptional derepression via c-Jun/c-Fos/estrogen receptor (progesterone receptor) complex assembly to a distal regulatory element and recruitment of cyclin D1 to its own gene promoter.
|
Mol Cell Biol
|
2004
|
1.56
|
10
|
Class II (IIa)-selective histone deacetylase inhibitors. 1. Synthesis and biological evaluation of novel (aryloxopropenyl)pyrrolyl hydroxyamides.
|
J Med Chem
|
2005
|
1.51
|
11
|
Selective class II HDAC inhibitors impair myogenesis by modulating the stability and activity of HDAC-MEF2 complexes.
|
EMBO Rep
|
2009
|
1.39
|
12
|
A genomic view of estrogen actions in human breast cancer cells by expression profiling of the hormone-responsive transcriptome.
|
J Mol Endocrinol
|
2004
|
1.35
|
13
|
Retinoids: potential in cancer prevention and therapy.
|
Expert Rev Mol Med
|
2004
|
1.25
|
14
|
Epi-drugs to fight cancer: from chemistry to cancer treatment, the road ahead.
|
Int J Biochem Cell Biol
|
2008
|
1.21
|
15
|
A dual role for Hdac1: oncosuppressor in tumorigenesis, oncogene in tumor maintenance.
|
Blood
|
2013
|
1.19
|
16
|
Histone deacetylase inhibition with valproic acid downregulates osteocalcin gene expression in human dental pulp stem cells and osteoblasts: evidence for HDAC2 involvement.
|
Stem Cells
|
2014
|
1.19
|
17
|
Trials with 'epigenetic' drugs: an update.
|
Mol Oncol
|
2012
|
1.19
|
18
|
Sirtuins and disease: the road ahead.
|
Front Pharmacol
|
2012
|
1.15
|
19
|
epigenetic multiple ligands: mixed histone/protein methyltransferase, acetyltransferase, and class III deacetylase (sirtuin) inhibitors.
|
J Med Chem
|
2008
|
1.13
|
20
|
ERG and FLI1 binding sites demarcate targets for aberrant epigenetic regulation by AML1-ETO in acute myeloid leukemia.
|
Blood
|
2012
|
1.12
|
21
|
Molecular pathways involved in neural in vitro differentiation of marrow stromal stem cells.
|
J Cell Biochem
|
2005
|
1.10
|
22
|
Nε-lysine acetylation determines dissociation from GAP junctions and lateralization of connexin 43 in normal and dystrophic heart.
|
Proc Natl Acad Sci U S A
|
2011
|
1.09
|
23
|
Comparative genome-wide DNA methylation analysis of colorectal tumor and matched normal tissues.
|
Epigenetics
|
2012
|
1.08
|
24
|
Epigenetic silencing of peroxisome proliferator-activated receptor γ is a biomarker for colorectal cancer progression and adverse patients' outcome.
|
PLoS One
|
2010
|
1.08
|
25
|
Bispyridinium dienes: histone deacetylase inhibitors with selective activities.
|
J Med Chem
|
2007
|
1.08
|
26
|
Specific activity of class II histone deacetylases in human breast cancer cells.
|
Mol Cancer Res
|
2008
|
1.07
|
27
|
Molecular identification of ERalpha-positive breast cancer cells by the expression profile of an intrinsic set of estrogen regulated genes.
|
J Cell Physiol
|
2004
|
1.06
|
28
|
Chromatin accessibility, p300, and histone acetylation define PML-RARα and AML1-ETO binding sites in acute myeloid leukemia.
|
Blood
|
2012
|
1.02
|
29
|
Small-molecule inhibitors of histone acetyltransferase activity: identification and biological properties.
|
J Med Chem
|
2006
|
1.02
|
30
|
HDAC-class II specific inhibition involves HDAC proteasome-dependent degradation mediated by RANBP2.
|
Biochim Biophys Acta
|
2008
|
1.02
|
31
|
Comparative gene expression profiling reveals partially overlapping but distinct genomic actions of different antiestrogens in human breast cancer cells.
|
J Cell Biochem
|
2006
|
0.98
|
32
|
HDACs class II-selective inhibition alters nuclear receptor-dependent differentiation.
|
J Mol Endocrinol
|
2010
|
0.98
|
33
|
Synthesis and biological validation of novel synthetic histone/protein methyltransferase inhibitors.
|
ChemMedChem
|
2007
|
0.97
|
34
|
Study of 1,4-dihydropyridine structural scaffold: discovery of novel sirtuin activators and inhibitors.
|
J Med Chem
|
2009
|
0.97
|
35
|
Identification of two new synthetic histone deacetylase inhibitors that modulate globin gene expression in erythroid cells from healthy donors and patients with thalassemia.
|
Mol Pharmacol
|
2007
|
0.97
|
36
|
Context-selective death of acute myeloid leukemia cells triggered by the novel hybrid retinoid-HDAC inhibitor MC2392.
|
Cancer Res
|
2014
|
0.96
|
37
|
Discovery of salermide-related sirtuin inhibitors: binding mode studies and antiproliferative effects in cancer cells including cancer stem cells.
|
J Med Chem
|
2012
|
0.96
|
38
|
Synthesis and biological characterization of the histone deacetylase inhibitor largazole and C7- modified analogues.
|
J Med Chem
|
2010
|
0.96
|
39
|
Histone deacetylase inhibitors promote apoptosis and senescence in human mesenchymal stem cells.
|
Stem Cells Dev
|
2009
|
0.95
|
40
|
Identification of PR-SET7 and EZH2 selective inhibitors inducing cell death in human leukemia U937 cells.
|
Biochimie
|
2012
|
0.94
|
41
|
Simplification of the tetracyclic SIRT1-selective inhibitor MC2141: coumarin- and pyrimidine-based SIRT1/2 inhibitors with different selectivity profile.
|
Bioorg Med Chem
|
2011
|
0.92
|
42
|
Competitive or noncompetitive, that's the question: research toward histone deacetylase inhibitors.
|
Mol Cancer Ther
|
2008
|
0.91
|
43
|
Evaluation of histone deacetylases as drug targets in Huntington's disease models. Study of HDACs in brain tissues from R6/2 and CAG140 knock-in HD mouse models and human patients and in a neuronal HD cell model.
|
PLoS Curr
|
2010
|
0.91
|
44
|
Pan-histone demethylase inhibitors simultaneously targeting Jumonji C and lysine-specific demethylases display high anticancer activities.
|
J Med Chem
|
2013
|
0.91
|
45
|
Histone acetyltransferase inhibitors and preclinical studies.
|
Expert Opin Ther Pat
|
2009
|
0.90
|
46
|
Cannabinoid receptor 1 influences chromatin remodeling in mouse spermatids by affecting content of transition protein 2 mRNA and histone displacement.
|
Endocrinology
|
2010
|
0.90
|
47
|
Identification of long chain alkylidenemalonates as novel small molecule modulators of histone acetyltransferases.
|
Bioorg Med Chem Lett
|
2008
|
0.89
|
48
|
Endocannabinoid control of sperm motility: the role of epididymus.
|
Gen Comp Endocrinol
|
2007
|
0.89
|
49
|
Distinct signaling pathways mediate stimulation of cell cycle progression and prevention of apoptotic cell death by estrogen in rat pituitary tumor PR1 cells.
|
Mol Biol Cell
|
2003
|
0.88
|
50
|
Piroxicam and cisplatin in a mouse model of peritoneal mesothelioma.
|
Clin Cancer Res
|
2006
|
0.88
|
51
|
Death receptor pathway activation and increase of ROS production by the triple epigenetic inhibitor UVI5008.
|
Mol Cancer Ther
|
2011
|
0.88
|
52
|
New pyrrole-based histone deacetylase inhibitors: binding mode, enzyme- and cell-based investigations.
|
Int J Biochem Cell Biol
|
2008
|
0.87
|
53
|
Histone deacetylase inhibitors: recent insights from basic to clinical knowledge & patenting of anti-cancer actions.
|
Recent Pat Anticancer Drug Discov
|
2011
|
0.87
|
54
|
Carbamate prodrug concept for hydroxamate HDAC inhibitors.
|
ChemMedChem
|
2011
|
0.86
|
55
|
Identification of tri- and tetracyclic pyrimidinediones as sirtuin inhibitors.
|
ChemMedChem
|
2010
|
0.86
|
56
|
A gradient of 2-arachidonoylglycerol regulates mouse epididymal sperm cell start-up.
|
Biol Reprod
|
2009
|
0.86
|
57
|
Growth factor-antagonized rexinoid apoptosis involves permissive PPARgamma/RXR heterodimers to activate the intrinsic death pathway by NO.
|
Cancer Cell
|
2009
|
0.85
|
58
|
Synthesis of benzamides related to anacardic acid and their histone acetyltransferase (HAT) inhibitory activities.
|
ChemMedChem
|
2008
|
0.85
|
59
|
Regulation of interleukin-8 gene at a distinct site of its promoter by CCAAT enhancer-binding protein homologous protein in prostaglandin E2-treated human T cells.
|
J Biol Chem
|
2008
|
0.85
|
60
|
Histone deacetylase inhibitors: a patent review (2009 - 2011).
|
Expert Opin Ther Pat
|
2012
|
0.85
|
61
|
Low 17beta-estradiol levels in CNR1 knock-out mice affect spermatid chromatin remodeling by interfering with chromatin reorganization.
|
Biol Reprod
|
2013
|
0.85
|
62
|
Molecular pathways: the complexity of the epigenome in cancer and recent clinical advances.
|
Clin Cancer Res
|
2012
|
0.84
|
63
|
Impact of histone deacetylase inhibitors SAHA and MS-275 on DNA repair pathways in human mesenchymal stem cells.
|
J Cell Physiol
|
2010
|
0.84
|
64
|
Feijoa sellowiana derived natural Flavone exerts anti-cancer action displaying HDAC inhibitory activities.
|
Int J Biochem Cell Biol
|
2007
|
0.83
|
65
|
Identification of microRNA expression patterns in cutaneous and uveal melanoma cell lines.
|
Tumori
|
2014
|
0.83
|
66
|
HDAC modulation and cell death in the clinic.
|
Exp Cell Res
|
2012
|
0.83
|
67
|
Synthesis and biological properties of novel, uracil-containing histone deacetylase inhibitors.
|
J Med Chem
|
2006
|
0.83
|
68
|
1,3,4-Oxadiazole-containing histone deacetylase inhibitors: anticancer activities in cancer cells.
|
J Med Chem
|
2014
|
0.82
|
69
|
Relationship between genome and epigenome--challenges and requirements for future research.
|
BMC Genomics
|
2014
|
0.82
|
70
|
Nuclear size as estrogen-responsive chromatin quality parameter of mouse spermatozoa.
|
Gen Comp Endocrinol
|
2013
|
0.82
|
71
|
Coexpression of Helicobacter pylori's proteins CagA and HspB induces cell proliferation in AGS gastric epithelial cells, independently from the bacterial infection.
|
Cancer Res
|
2003
|
0.82
|
72
|
Laccase treatment impairs bisphenol A-induced cancer cell proliferation affecting estrogen receptor alpha-dependent rapid signals.
|
IUBMB Life
|
2008
|
0.82
|
73
|
Epigenetic drugs against cancer: an evolving landscape.
|
Arch Toxicol
|
2014
|
0.81
|
74
|
Altered folate receptor 2 expression in uraemic patients on haemodialysis: implications for folate resistance.
|
Nephrol Dial Transplant
|
2013
|
0.81
|
75
|
Modulation of the activity of histone acetyltransferases by long chain alkylidenemalonates (LoCAMs).
|
Bioorg Med Chem
|
2011
|
0.81
|
76
|
Antioxidant, antimicrobial and anti-proliferative activities of Solanum tuberosum L. var. Vitelotte.
|
Food Chem Toxicol
|
2013
|
0.81
|
77
|
TNF-related apoptosis-inducing ligand: signalling of a 'smart' molecule.
|
Int J Biochem Cell Biol
|
2007
|
0.81
|
78
|
Molecular analysis of the effects of Piroxicam and Cisplatin on mesothelioma cells growth and viability.
|
J Transl Med
|
2008
|
0.81
|
79
|
MePR: a novel human mesenchymal progenitor model with characteristics of pluripotency.
|
Stem Cells Dev
|
2013
|
0.81
|
80
|
Characterization of sirtuin inhibitors in nematodes expressing a muscular dystrophy protein reveals muscle cell and behavioral protection by specific sirtinol analogues.
|
J Med Chem
|
2010
|
0.81
|
81
|
New anacardic acid-inspired benzamides: histone lysine acetyltransferase activators.
|
ChemMedChem
|
2010
|
0.81
|
82
|
Epigenetic profiling of the antitumor natural product psammaplin A and its analogues.
|
Bioorg Med Chem
|
2010
|
0.80
|
83
|
ARHGEF3 controls HDACi-induced differentiation via RhoA-dependent pathways in acute myeloid leukemias.
|
Epigenetics
|
2015
|
0.80
|
84
|
Benzodeazaoxaflavins as sirtuin inhibitors with antiproliferative properties in cancer stem cells.
|
J Med Chem
|
2012
|
0.80
|
85
|
Novel pyrrole-containing histone deacetylase inhibitors endowed with cytodifferentiation activity.
|
Int J Biochem Cell Biol
|
2007
|
0.80
|
86
|
Functions, aberrations, and advances for chromatin modulation in cancer.
|
Cancer Treat Res
|
2014
|
0.80
|
87
|
Quinoline-based p300 histone acetyltransferase inhibitors with pro-apoptotic activity in human leukemia U937 cells.
|
ChemMedChem
|
2014
|
0.80
|
88
|
Identification of 4-hydroxyquinolines inhibitors of p300/CBP histone acetyltransferases.
|
Bioorg Med Chem Lett
|
2008
|
0.80
|
89
|
Indole-derived psammaplin A analogues as epigenetic modulators with multiple inhibitory activities.
|
J Med Chem
|
2012
|
0.80
|
90
|
Highlighting chromosome loops in DNA-picked chromatin (DPC).
|
Epigenetics
|
2011
|
0.79
|
91
|
New synthetic approach to paullones and characterization of their SIRT1 inhibitory activity.
|
Org Biomol Chem
|
2012
|
0.79
|
92
|
Molecular analysis of the apoptotic effects of BPA in acute myeloid leukemia cells.
|
J Transl Med
|
2009
|
0.79
|
93
|
Targeting epigenetic networks with polypharmacology: a new avenue to tackle cancer.
|
Epigenomics
|
2010
|
0.79
|
94
|
The class I-specific HDAC inhibitor MS-275 modulates the differentiation potential of mouse embryonic stem cells.
|
Biol Open
|
2013
|
0.78
|
95
|
Novel N-hydroxybenzamide-based HDAC inhibitors with branched CAP group.
|
Bioorg Med Chem Lett
|
2009
|
0.78
|
96
|
miRNA-mediated deregulation in leukemia.
|
Front Genet
|
2012
|
0.78
|
97
|
Regulation of nuclear receptor and cofactor expression in breast cancer cell lines.
|
Eur J Endocrinol
|
2003
|
0.78
|
98
|
tert-Butylcarbamate-containing histone deacetylase inhibitors: apoptosis induction, cytodifferentiation, and antiproliferative activities in cancer cells.
|
ChemMedChem
|
2013
|
0.78
|
99
|
The Jumonji family: past, present and future of histone demethylases in cancer.
|
Biomol Concepts
|
2014
|
0.78
|
100
|
SIRT1 inhibition affects angiogenic properties of human MSCs.
|
Biomed Res Int
|
2014
|
0.77
|
101
|
Carprofen analogues as sirtuin inhibitors: enzyme and cellular studies.
|
ChemMedChem
|
2012
|
0.77
|
102
|
TRAIL: at the center of drugable anti-tumor pathways.
|
Cell Cycle
|
2005
|
0.77
|
103
|
Analysis of chromatin-nuclear receptor interactions by laser-chromatin immunoprecipitation.
|
Methods Mol Biol
|
2014
|
0.77
|
104
|
Time for epigenetics.
|
Int J Biochem Cell Biol
|
2008
|
0.76
|
105
|
Total synthesis of the proposed structures of the DNA methyl transferase inhibitors peyssonenynes, and structural revision of peyssonenyne B.
|
Org Biomol Chem
|
2011
|
0.76
|
106
|
Synthetic approaches to DNMT inhibitor SGI-1027 and effects on the U937 leukemia cell line.
|
Bioorg Med Chem Lett
|
2013
|
0.76
|
107
|
Histone deacetylase inhibitors: clinical implications for hematological malignancies.
|
Clin Epigenetics
|
2010
|
0.76
|
108
|
Design, synthesis, and biological evaluation of 2-aminobenzanilide derivatives as potent and selective HDAC inhibitors.
|
ChemMedChem
|
2012
|
0.76
|
109
|
Pyrrole-based hydroxamates and 2-aminoanilides: histone deacetylase inhibition and cellular activities.
|
ChemMedChem
|
2009
|
0.76
|
110
|
Up-regulation of miR-146b and down-regulation of miR-200b contribute to the cytotoxic effect of histone deacetylase inhibitors on ras-transformed thyroid cells.
|
J Clin Endocrinol Metab
|
2013
|
0.76
|
111
|
Novel uracil-based 2-aminoanilide and 2-aminoanilide-like derivatives: histone deacetylase inhibition and in-cell activities.
|
Bioorg Med Chem Lett
|
2008
|
0.76
|
112
|
Genetic mutations in epigenetic modifiers as therapeutic targets in acute myeloid leukemia.
|
Expert Opin Ther Targets
|
2015
|
0.75
|
113
|
Epigenetic multiple modulators.
|
Curr Top Med Chem
|
2011
|
0.75
|
114
|
Cancer therapy: new drugs are emerging based on molecular targeting but still many challenges.
|
Int J Biochem Cell Biol
|
2007
|
0.75
|
115
|
A DNA methyltransferase modulator inspired by peyssonenyne natural product structures.
|
ChemMedChem
|
2012
|
0.75
|
116
|
Design, synthesis and biological evaluation of novel compounds with conjugated structure as anti-tumor agents.
|
Bioorg Med Chem
|
2008
|
0.75
|
117
|
Novel cinnamyl hydroxyamides and 2-aminoanilides as histone deacetylase inhibitors: apoptotic induction and cytodifferentiation activity.
|
ChemMedChem
|
2011
|
0.75
|