| scholarly article | Q13442814 |
| P50 | author | Cheryl Arrowsmith | Q5092682 |
| Brian D Strahl | Q41544665 | ||
| Peter J. Brown | Q42713845 | ||
| Yunxiang Mu | Q55175819 | ||
| Scott B Rothbart | Q62070938 | ||
| Pavel Mader | Q92749368 | ||
| P2093 | author name string | Aiping Dong | |
| Gaofeng Cui | |||
| Georges Mer | |||
| Kevin M McBride | |||
| Stephen V Frye | |||
| Jacqueline L Norris | |||
| William P Janzen | |||
| Bradley M Dickson | |||
| Lindsey I James | |||
| Brandi M Baughman | |||
| Michael T Perfetti | |||
| P2860 | cites work | Translating the Histone Code | Q22065840 |
| MDC1 is a mediator of the mammalian DNA damage checkpoint | Q24296229 | ||
| The AAA-ATPase VCP/p97 promotes 53BP1 recruitment by removing L3MBTL1 from DNA double-strand breaks | Q24298486 | ||
| RNF8 transduces the DNA-damage signal via histone ubiquitylation and checkpoint protein assembly | Q24300428 | ||
| Tudor, MBT and chromo domains gauge the degree of lysine methylation | Q24301294 | ||
| RNF8- and RNF168-dependent degradation of KDM4A/JMJD2A triggers 53BP1 recruitment to DNA damage sites | Q24306486 | ||
| RNF168 binds and amplifies ubiquitin conjugates on damaged chromosomes to allow accumulation of repair proteins | Q24309287 | ||
| The DNA-damage response in human biology and disease | Q24606586 | ||
| Human CtIP promotes DNA end resection | Q24646062 | ||
| Structural basis for the methylation state-specific recognition of histone H4-K20 by 53BP1 and Crb2 in DNA repair | Q24669691 | ||
| Small-Molecule Ligands of Methyl-Lysine Binding Proteins | Q27667285 | ||
| Acetylation limits 53BP1 association with damaged chromatin to promote homologous recombination | Q27676128 | ||
| The language of covalent histone modifications | Q27860931 | ||
| 53BP1 regulates DSB repair using Rif1 to control 5' end resection | Q28000120 | ||
| A cell cycle-dependent regulatory circuit composed of 53BP1-RIF1 and BRCA1-CtIP controls DNA repair pathway choice | Q28000121 | ||
| 53BP1 and NFBD1/MDC1-Nbs1 function in parallel interacting pathways activating ataxia-telangiectasia mutated (ATM) in response to DNA damage | Q28236024 | ||
| A selective requirement for 53BP1 in the biological response to genomic instability induced by Brca1 deficiency | Q28256846 | ||
| The RNF8/RNF168 ubiquitin ligase cascade facilitates class switch recombination | Q28592784 | ||
| 53BP1 inhibits homologous recombination in Brca1-deficient cells by blocking resection of DNA breaks | Q29465538 | ||
| 53BP1 is required for class switch recombination | Q29465541 | ||
| 53BP1 links DNA damage-response pathways to immunoglobulin heavy chain class-switch recombination. | Q29465548 | ||
| Rif1 prevents resection of DNA breaks and promotes immunoglobulin class switching | Q29465549 | ||
| 53BP1 is a reader of the DNA-damage-induced H2A Lys 15 ubiquitin mark | Q29465773 | ||
| The tumor suppressor gene Brca1 is required for embryonic cellular proliferation in the mouse | Q29618622 | ||
| Epigenetic modifications and human disease | Q29619753 | ||
| The emerging field of dynamic lysine methylation of non-histone proteins. | Q30368231 | ||
| Identification of non-peptide malignant brain tumor (MBT) repeat antagonists by virtual screening of commercially available compounds | Q30497277 | ||
| Screening for inhibitors of low-affinity epigenetic peptide-protein interactions: an AlphaScreen-based assay for antagonists of methyl-lysine binding proteins | Q33518291 | ||
| Preparation of recombinant peptides with site- and degree-specific lysine (13)C-methylation | Q33805946 | ||
| The art of the chemical probe | Q34098693 | ||
| Setting expectations in molecular optimizations: Strengths and limitations of commonly used composite parameters | Q34369771 | ||
| Conditional mutation of Brca1 in mammary epithelial cells results in blunted ductal morphogenesis and tumour formation. | Q34503454 | ||
| p53 Binding protein 53BP1 is required for DNA damage responses and tumor suppression in mice | Q34784963 | ||
| Small-molecule ligands of methyl-lysine binding proteins: optimization of selectivity for L3MBTL3. | Q34990803 | ||
| Regulation of DNA end joining, resection, and immunoglobulin class switch recombination by 53BP1. | Q35125130 | ||
| CtIP-dependent DNA resection is required for DNA damage checkpoint maintenance but not initiation. | Q36062092 | ||
| Dynamic assembly and sustained retention of 53BP1 at the sites of DNA damage are controlled by Mdc1/NFBD1 | Q36320732 | ||
| Discovery of a chemical probe for the L3MBTL3 methyllysine reader domain | Q36625174 | ||
| Role for 53BP1 Tudor domain recognition of p53 dimethylated at lysine 382 in DNA damage signaling | Q37000240 | ||
| BRCA1 and BRCA2: different roles in a common pathway of genome protection | Q37149848 | ||
| Epigenetic modifications as therapeutic targets | Q37800011 | ||
| BRCA mutations in the management of breast cancer: the state of the art | Q37801266 | ||
| gamma-H2AX dephosphorylation by protein phosphatase 2A facilitates DNA double-strand break repair | Q40347113 | ||
| Amino-terminal phosphorylation of activation-induced cytidine deaminase suppresses c-myc/IgH translocation | Q42582794 | ||
| Role of ATM and the damage response mediator proteins 53BP1 and MDC1 in the maintenance of G(2)/M checkpoint arrest | Q42738049 | ||
| Potential role for 53BP1 in DNA end-joining repair through direct interaction with DNA. | Q44489693 | ||
| Using halogen bonds to address the protein backbone: a systematic evaluation | Q47301557 | ||
| Ligand binding efficiency: trends, physical basis, and implications | Q80992297 | ||
| P433 | issue | 4 | |
| P304 | page(s) | 1072-1081 | |
| P577 | publication date | 2015-01-28 | |
| P1433 | published in | ACS Chemical Biology | Q165583 |
| P1476 | title | Identification of a fragment-like small molecule ligand for the methyl-lysine binding protein, 53BP1. | |
| P478 | volume | 10 |
| Q30378316 | A cellular chemical probe targeting the chromodomains of Polycomb repressive complex 1 |
| Q39423291 | Chemical modulators for epigenome reader domains as emerging epigenetic therapies for cancer and inflammation |
| Q38878310 | Chemical probes for methyl lysine reader domains |
| Q36371775 | Developing Spindlin1 small-molecule inhibitors by using protein microarrays |
| Q48273323 | Discovery of Peptidomimetic Ligands of EED as Allosteric Inhibitors of PRC2. |
| Q36135192 | Identification and Structure-Activity Relationship Studies of Small-Molecule Inhibitors of the Methyllysine Reader Protein Spindlin1. |
| Q36914593 | Identification of a small-molecule ligand of the epigenetic reader protein Spindlin1 via a versatile screening platform. |
| Q99548779 | Inhibition of DNA Repair in Cancer Therapy: Toward a Multi-Target Approach |
| Q47419320 | Phosphorylation promotes activation-induced cytidine deaminase activity at the Myc oncogene |
| Q93119673 | Rational Adaptation of L3MBTL1 Inhibitors to Create Small-Molecule Cbx7 Antagonists |
| Q52767723 | Replication-Coupled Dilution of H4K20me2 Guides 53BP1 to Pre-replicative Chromatin. |
| Q38434032 | Selective Inhibition of CBX6: A Methyllysine Reader Protein in the Polycomb Family |
| Q89511226 | Small Molecules Targeting the Specific Domains of Histone-Mark Readers in Cancer Therapy |
| Q38826160 | Structural aspects of small-molecule inhibition of methyllysine reader proteins |
| Q38749422 | Structure-Activity Relationships and Kinetic Studies of Peptidic Antagonists of CBX Chromodomains |
| Q90468310 | Targeting non-bromodomain chromatin readers |
| Q48379350 | Unlocking the potential of chemical probes for methyl-lysine reader proteins |
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