scholarly article | Q13442814 |
P2093 | author name string | Michael J Nemeth | |
Elizabeth A Griffiths | |||
Benjamin E Paluch | |||
Abdul R Naqash | |||
Zachary Brumberger | |||
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Tools and landscapes of epigenetics | Q84441692 | ||
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Hydroxymethylation of DNA influences nucleosomal conformation and stability in vitro | Q85645100 | ||
Further insights into the SAR of α-substituted cyclopropylamine derivatives as inhibitors of histone demethylase KDM1A | Q86522060 | ||
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Phase 2 trial of oral vorinostat (suberoylanilide hydroxamic acid, SAHA) for refractory cutaneous T-cell lymphoma (CTCL) | Q24681480 | ||
DNMT3A Mutations in Acute Myeloid Leukemia | Q27559610 | ||
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Biochemical, structural, and biological evaluation of tranylcypromine derivatives as inhibitors of histone demethylases LSD1 and LSD2 | Q27660798 | ||
Adding a Lysine Mimic in the Design of Potent Inhibitors of Histone Lysine Methyltransferases | Q27661108 | ||
Structurally designed trans-2-phenylcyclopropylamine derivatives potently inhibit histone demethylase LSD1/KDM1 | Q27662593 | ||
Suppression of inflammation by a synthetic histone mimic | Q27665789 | ||
Quantitative High-Throughput Screening Identifies 8-Hydroxyquinolines as Cell-Active Histone Demethylase Inhibitors | Q27666155 | ||
Structural basis for CARM1 inhibition by indole and pyrazole inhibitors | Q27666983 | ||
Inhibition of Histone Demethylases by 4-Carboxy-2,2′-Bipyridyl Compounds | Q27667281 | ||
Small-Molecule Ligands of Methyl-Lysine Binding Proteins | Q27667285 | ||
A Small Molecule Binding to the Coactivator CREB-Binding Protein Blocks Apoptosis in Cardiomyocytes | Q27667526 | ||
Discovery and characterization of small molecule inhibitors of the BET family bromodomains | Q27667834 | ||
Structural basis of substrate methylation and inhibition of SMYD2 | Q27670959 | ||
Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemia | Q27674674 | ||
Contribution of histone N-terminal tails to the structure and stability of nucleosomes | Q27680641 | ||
Synthesis, biological activity and mechanistic insights of 1-substituted cyclopropylamine derivatives: a novel class of irreversible inhibitors of histone demethylase KDM1A | Q27694826 | ||
TET2 mutation is an independent favorable prognostic factor in myelodysplastic syndromes (MDSs). | Q27851480 | ||
Recurrent DNMT3A mutations in patients with myelodysplastic syndromes | Q27851629 | ||
An inhibitor of mutant IDH1 delays growth and promotes differentiation of glioma cells. | Q27852141 | ||
The language of covalent histone modifications | Q27860931 | ||
Histone demethylation by a family of JmjC domain-containing proteins | Q27939224 | ||
Targeted mutation of the DNA methyltransferase gene results in embryonic lethality | Q28131773 | ||
Genetic control of wing disc development in Drosophila | Q28139220 | ||
A gene hypermethylation profile of human cancer | Q28213253 | ||
Lysine-specific demethylase 1 is strongly expressed in poorly differentiated neuroblastoma: implications for therapy | Q28235397 | ||
Histone deacetylases and cancer | Q28240447 | ||
Discovery and optimization of small-molecule ligands for the CBP/p300 bromodomains | Q28242369 | ||
BET bromodomain inhibition as a therapeutic strategy to target c-Myc | Q28247024 | ||
DNA hydroxymethylation profiling reveals that WT1 mutations result in loss of TET2 function in acute myeloid leukemia | Q28253465 | ||
Decitabine and vorinostat cooperate to sensitize colon carcinoma cells to Fas ligand-induced apoptosis in vitro and tumor suppression in vivo | Q28263221 | ||
An essential role for CoREST in nucleosomal histone 3 lysine 4 demethylation | Q28265681 | ||
Selective killing of mixed lineage leukemia cells by a potent small-molecule DOT1L inhibitor. | Q33716402 | ||
Whole-genome analysis of 5-hydroxymethylcytosine and 5-methylcytosine at base resolution in the human brain. | Q33741993 | ||
Inhibition of BRD4 attenuates tumor cell self-renewal and suppresses stem cell signaling in MYC driven medulloblastoma. | Q33756997 | ||
Rethinking how DNA methylation patterns are maintained | Q33763852 | ||
Early aberrant DNA methylation events in a mouse model of acute myeloid leukemia | Q33772607 | ||
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IDH1 and IDH2 gene mutations identify novel molecular subsets within de novo cytogenetically normal acute myeloid leukemia: a Cancer and Leukemia Group B study | Q33897586 | ||
Mechanisms of resistance to decitabine in the myelodysplastic syndrome. | Q33999539 | ||
Protein lysine methyltransferase G9a inhibitors: design, synthesis, and structure activity relationships of 2,4-diamino-7-aminoalkoxy-quinazolines | Q34059822 | ||
CpG island clusters and pro-epigenetic selection for CpGs in protein-coding exons of HOX and other transcription factors | Q34100309 | ||
Dnmt3a and Dnmt1 functionally cooperate during de novo methylation of DNA. | Q34154656 | ||
Differential methylation in CN-AML preferentially targets non-CGI regions and is dictated by DNMT3A mutational status and associated with predominant hypomethylation of HOX genes | Q34183388 | ||
Dnmt3a is essential for hematopoietic stem cell differentiation | Q34237926 | ||
Loss of 5-hydroxymethylcytosine is an epigenetic hallmark of melanoma | Q34299814 | ||
Base-pair resolution DNA methylation sequencing reveals profoundly divergent epigenetic landscapes in acute myeloid leukemia | Q34318280 | ||
The Dnmt1 DNA-(cytosine-C5)-methyltransferase methylates DNA processively with high preference for hemimethylated target sites | Q34344734 | ||
Clinical development of demethylating agents in hematology | Q34395179 | ||
Selective small molecules blocking HIV-1 Tat and coactivator PCAF association | Q34396565 | ||
Identification of pre-leukaemic haematopoietic stem cells in acute leukaemia | Q34403931 | ||
Preleukemic mutations in human acute myeloid leukemia affect epigenetic regulators and persist in remission | Q34405195 | ||
DNA methylation signatures identify biologically distinct subtypes in acute myeloid leukemia. | Q34433577 | ||
Assessing the underlying pattern of human germline mutations: lessons from the factor IX gene | Q34474779 | ||
Structure-guided optimization of small molecules inhibiting human immunodeficiency virus 1 Tat association with the human coactivator p300/CREB binding protein-associated factor | Q34620638 | ||
Sumoylated human histone H4 prevents chromatin compaction by inhibiting long-range internucleosomal interactions | Q34634124 | ||
The novel, small-molecule DNA methylation inhibitor SGI-110 as an ovarian cancer chemosensitizer. | Q34717933 | ||
DNA methylation and chromatin - unraveling the tangled web. | Q34770498 | ||
Modulating T-cell immunity to tumours: new strategies for monitoring T-cell responses | Q34791108 | ||
The rate of hydrolytic deamination of 5-methylcytosine in double-stranded DNA | Q34811750 | ||
The quantitative separation of purines, pyrimidines, and nucleosides by paper chromatography. | Q34854256 | ||
Small-molecule ligands of methyl-lysine binding proteins: optimization of selectivity for L3MBTL3. | Q34990803 | ||
A selective inhibitor and probe of the cellular functions of Jumonji C domain-containing histone demethylases | Q35097231 | ||
Phase 1 study of epigenetic priming with decitabine prior to standard induction chemotherapy for patients with AML. | Q35164242 | ||
Evaluation of azacitidine and entinostat as sensitization agents to cytotoxic chemotherapy in preclinical models of non-small cell lung cancer | Q35238397 | ||
Decitabine priming enhances the antileukemic effects of exportin 1 (XPO1) selective inhibitor selinexor in acute myeloid leukemia | Q35533613 | ||
Lysine-specific demethylase 1 (LSD1) is highly expressed in ER-negative breast cancers and a biomarker predicting aggressive biology | Q28269080 | ||
Regulation of LSD1 histone demethylase activity by its associated factors | Q28270391 | ||
Androgen receptor coactivators lysine-specific histone demethylase 1 and four and a half LIM domain protein 2 predict risk of prostate cancer recurrence | Q28277232 | ||
Defining an epigenetic code | Q28281451 | ||
The epigenomics of cancer | Q28289975 | ||
The CpG dinucleotide and human genetic disease | Q28296311 | ||
Decitabine improves patient outcomes in myelodysplastic syndromes: results of a phase III randomized study | Q28301602 | ||
A comparison of azacitidine and decitabine activities in acute myeloid leukemia cell lines | Q28472733 | ||
Role of Tet proteins in 5mC to 5hmC conversion, ES-cell self-renewal and inner cell mass specification | Q28504641 | ||
Enzymatic properties of recombinant Dnmt3a DNA methyltransferase from mouse: the enzyme modifies DNA in a non-processive manner and also methylates non-CpG [correction of non-CpA] sites | Q28506872 | ||
Cloning and characterization of a family of novel mammalian DNA (cytosine-5) methyltransferases | Q28507226 | ||
Carboplatin with Decitabine Therapy, in Recurrent Platinum Resistant Ovarian Cancer, Alters Circulating miRNAs Concentrations: A Pilot Study | Q28550381 | ||
The behaviour of 5-hydroxymethylcytosine in bisulfite sequencing | Q28749183 | ||
Perceptions of epigenetics | Q29547310 | ||
Methylation of lysine 4 on histone H3: intricacy of writing and reading a single epigenetic mark | Q29614516 | ||
JmjC-domain-containing proteins and histone demethylation | Q29614517 | ||
Histone H4-K16 acetylation controls chromatin structure and protein interactions | Q29614521 | ||
Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer | Q29615066 | ||
Leukemic IDH1 and IDH2 mutations result in a hypermethylation phenotype, disrupt TET2 function, and impair hematopoietic differentiation | Q29615366 | ||
DNA methylation and human disease | Q29615417 | ||
Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia | Q29615735 | ||
Epigenetic protein families: a new frontier for drug discovery | Q29616621 | ||
Epigenetics: a landscape takes shape | Q29616623 | ||
DNA methylation: roles in mammalian development | Q29616796 | ||
Targeting MYC dependence in cancer by inhibiting BET bromodomains | Q29617196 | ||
Gene silencing in cancer in association with promoter hypermethylation | Q29617274 | ||
Linking DNA methylation and histone modification: patterns and paradigms | Q29617801 | ||
Chromatin modification and epigenetic reprogramming in mammalian development | Q29617802 | ||
Cytosine methylation and the ecology of intragenomic parasites | Q29618264 | ||
Mutation in TET2 in myeloid cancers | Q29619292 | ||
Charting histone modifications and the functional organization of mammalian genomes | Q29620707 | ||
Impairment of prostate cancer cell growth by a selective and reversible lysine-specific demethylase 1 inhibitor | Q30414643 | ||
Reversal of H3K9me2 by a small-molecule inhibitor for the G9a histone methyltransferase | Q33272939 | ||
trans-2-Phenylcyclopropylamine is a mechanism-based inactivator of the histone demethylase LSD1. | Q33279148 | ||
Treatment of resistant metastatic melanoma using sequential epigenetic therapy (decitabine and panobinostat) combined with chemotherapy (temozolomide). | Q33416734 | ||
Panobinostat plus bortezomib and dexamethasone versus placebo plus bortezomib and dexamethasone in patients with relapsed or relapsed and refractory multiple myeloma: a multicentre, randomised, double-blind phase 3 trial | Q33417762 | ||
Quantitative DNA methylation predicts survival in adult acute myeloid leukemia | Q33515724 | ||
Comparative analysis of small molecules and histone substrate analogues as LSD1 lysine demethylase inhibitors | Q33530669 | ||
DNA methylation predicts survival and response to therapy in patients with myelodysplastic syndromes | Q33628772 | ||
Decitabine immunosensitizes human gliomas to NY-ESO-1 specific T lymphocyte targeting through the Fas/Fas ligand pathway | Q35589288 | ||
Characterization of in vitro and in vivo hypomethylating effects of decitabine in acute myeloid leukemia by a rapid, specific and sensitive LC-MS/MS method | Q35781849 | ||
Transient low doses of DNA-demethylating agents exert durable antitumor effects on hematological and epithelial tumor cells | Q35851931 | ||
Role of androgen receptor and associated lysine-demethylase coregulators, LSD1 and JMJD2A, in localized and advanced human bladder cancer. | Q35860815 | ||
Vaccination with an NY-ESO-1 peptide of HLA class I/II specificities induces integrated humoral and T cell responses in ovarian cancer | Q35921697 | ||
Tet family proteins and 5-hydroxymethylcytosine in development and disease | Q35944741 | ||
A potential role for epigenetic modulatory drugs in the enhancement of cancer/germ-line antigen vaccine efficacy | Q35968482 | ||
CBP30, a selective CBP/p300 bromodomain inhibitor, suppresses human Th17 responses | Q36008355 | ||
The Pathogenesis of Mixed-Lineage Leukemia | Q36052947 | ||
Specific molecular signatures predict decitabine response in chronic myelomonocytic leukemia. | Q36179524 | ||
Clonal inheritance of the pattern of DNA methylation in mouse cells | Q36274408 | ||
Detection of mutant TET2 in myeloid malignancies other than myeloproliferative neoplasms: CMML, MDS, MDS/MPN and AML. | Q36303442 | ||
Combination therapy with DNA methyltransferase inhibitors in hematologic malignancies | Q36338031 | ||
DNA methylation and gene expression: endogenous retroviral genome becomes infectious after molecular cloning. | Q36383610 | ||
Harnessing Noxa demethylation to overcome Bortezomib resistance in mantle cell lymphoma | Q36413767 | ||
Inhibition of the LSD1 (KDM1A) demethylase reactivates the all-trans-retinoic acid differentiation pathway in acute myeloid leukemia | Q36515569 | ||
Highly effective combination of LSD1 (KDM1A) antagonist and pan-histone deacetylase inhibitor against human AML cells | Q36539785 | ||
Accumulation and loss of asymmetric non-CpG methylation during male germ-cell development | Q36559178 | ||
Discovery of a chemical probe for the L3MBTL3 methyllysine reader domain | Q36625174 | ||
Genomic impact of transient low-dose decitabine treatment on primary AML cells | Q36654140 | ||
Perceiving the epigenetic landscape through histone readers. | Q36821309 | ||
Small-molecule inhibition of BRD4 as a new potent approach to eliminate leukemic stem- and progenitor cells in acute myeloid leukemia AML. | Q36926120 | ||
Non-CpG methylation is prevalent in embryonic stem cells and may be mediated by DNA methyltransferase 3a. | Q36967574 | ||
Transcriptional plasticity promotes primary and acquired resistance to BET inhibition | Q37038076 | ||
DNA methyltransferase and histone deacetylase inhibitors in the treatment of myelodysplastic syndromes | Q37052250 | ||
Aberrant DNA methylation is a dominant mechanism in MDS progression to AML. | Q37086937 | ||
Chemical mechanisms of histone lysine and arginine modifications | Q37097824 | ||
Mechanism-based epigenetic chemosensitization therapy of diffuse large B-cell lymphoma | Q37164915 | ||
Finding the fifth base: genome-wide sequencing of cytosine methylation. | Q37253268 | ||
Efficacy of BET bromodomain inhibition in Kras-mutant non-small cell lung cancer | Q37338486 | ||
Two DNA methyltransferases from murine erythroleukemia cells: purification, sequence specificity, and mode of interaction with DNA. | Q37348708 | ||
Early epigenetic changes and DNA damage do not predict clinical response in an overlapping schedule of 5-azacytidine and entinostat in patients with myeloid malignancies. | Q37372837 | ||
Alterations of immune response of Non-Small Cell Lung Cancer with Azacytidine | Q37420192 | ||
BET bromodomain protein inhibition is a therapeutic option for medulloblastoma. | Q37420196 | ||
The activation of human gene MAGE-1 in tumor cells is correlated with genome-wide demethylation. | Q37491118 | ||
Superior sulcus tumors with vertebral body involvement: a multimodality approach | Q37493211 | ||
Histone acetyltransferase inhibitors and preclinical studies | Q37497374 | ||
Histone acetyl transferases as emerging drug targets. | Q37540911 | ||
Covalent bond formation between a DNA-cytosine methyltransferase and DNA containing 5-azacytosine | Q37576837 | ||
Epigenetic potentiation of NY-ESO-1 vaccine therapy in human ovarian cancer | Q37585487 | ||
Protein methyltransferases as a target class for drug discovery | Q37590090 | ||
Hydroxymethylation at gene regulatory regions directs stem/early progenitor cell commitment during erythropoiesis | Q37686349 | ||
Prolonged administration of azacitidine with or without entinostat for myelodysplastic syndrome and acute myeloid leukemia with myelodysplasia-related changes: results of the US Leukemia Intergroup trial E1905. | Q37702336 | ||
Therapy with azanucleosides for myelodysplastic syndromes | Q37765469 | ||
5-Hydroxymethylcytosine, the sixth base of the genome | Q37891924 | ||
Epigenetic reprogramming in mouse pre-implantation development and primordial germ cells | Q37965513 | ||
Molecular mechanisms and potential functions of histone demethylases | Q37999690 | ||
Protein arginine methyltransferases and cancer | Q38067063 | ||
X-Inactivation, Imprinting, and Long Noncoding RNAs in Health and Disease | Q38090112 | ||
Histone lysine demethylases as targets for anticancer therapy | Q38162717 | ||
New themes in the biological functions of 5-methylcytosine and 5-hydroxymethylcytosine. | Q38289020 | ||
BET inhibitor resistance emerges from leukaemia stem cells | Q38835493 | ||
Guadecitabine (SGI-110) priming sensitizes hepatocellular carcinoma cells to oxaliplatin | Q38854734 | ||
Immunomodulatory action of SGI-110, a hypomethylating agent, in acute myeloid leukemia cells and xenografts. | Q38952962 | ||
BET bromodomain inhibition of MYC-amplified medulloblastoma. | Q39050679 | ||
Nonpeptidic propargylamines as inhibitors of lysine specific demethylase 1 (LSD1) with cellular activity | Q39099941 | ||
Immunomodulatory activity of SGI-110, a 5-aza-2'-deoxycytidine-containing demethylating dinucleotide. | Q39247530 | ||
Identification of additional IDH mutations associated with oncometabolite R(-)-2-hydroxyglutarate production | Q39458545 | ||
MAGE-A1, MAGE-A3, and NY-ESO-1 can be upregulated on neuroblastoma cells to facilitate cytotoxic T lymphocyte-mediated tumor cell killing | Q39533432 | ||
Enantioselective synthesis of tranylcypromine analogues as lysine demethylase (LSD1) inhibitors. | Q39580033 | ||
Synthesis and biological activity of optically active NCL-1, a lysine-specific demethylase 1 selective inhibitor | Q39608783 | ||
The DNA demethylating agent 5-aza-2'-deoxycytidine induces expression of NY-ESO-1 and other cancer/testis antigens in myeloid leukemia cells | Q39716492 | ||
Overexpression of LSD1 contributes to human carcinogenesis through chromatin regulation in various cancers | Q39723644 | ||
Identification of cell-active lysine specific demethylase 1-selective inhibitors | Q39768788 | ||
Preference of DNA methyltransferases for CpG islands in mouse embryonic stem cells | Q39968046 | ||
DNA methylation inhibitor 5-Aza-2'-deoxycytidine induces reversible genome-wide DNA damage that is distinctly influenced by DNA methyltransferases 1 and 3B. | Q40054309 | ||
P433 | issue | 4 | |
P921 | main subject | epigenetics | Q26939 |
P304 | page(s) | 285-295 | |
P577 | publication date | 2016-02-26 | |
P1433 | published in | Blood Reviews | Q15724415 |
P1476 | title | Epigenetics: A primer for clinicians | |
P478 | volume | 30 |
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