| P50 | author | Diane F. Jelinek | Q110910982 |
| P2093 | author name string | Zhenkun Lou | |
| | Tongzheng Liu | |
| | Huadong Pei | |
| | Kefei Yu | |
| | Xiaosheng Wu | |
| P2860 | cites work | Regulation of the histone H4 monomethylase PR-Set7 by CRL4(Cdt2)-mediated PCNA-dependent degradation during DNA damage | Q33733896 |
| | Selective induction of DNA repair pathways in human B cells activated by CD4+ T cells | Q33778759 |
| | 53BP1 regulates DNA resection and the choice between classical and alternative end joining during class switch recombination | Q33794964 |
| | Genomic instability, endoreduplication, and diminished Ig class-switch recombination in B cells lacking Nbs1. | Q33818028 |
| | Class switching and meiotic defects in mice lacking the E3 ubiquitin ligase RNF8 | Q33839896 |
| | Rnf8 deficiency impairs class switch recombination, spermatogenesis, and genomic integrity and predisposes for cancer | Q33839938 |
| | Histone3 lysine4 trimethylation regulated by the facilitates chromatin transcription complex is critical for DNA cleavage in class switch recombination | Q34438355 |
| | The MMSET histone methyl transferase switches global histone methylation and alters gene expression in t(4;14) multiple myeloma cells. | Q34568855 |
| | Somatic hypermutation of immunoglobulin genes: merging mechanisms for genetic diversity | Q34619789 |
| | Mechanism and regulation of class switch recombination | Q34764888 |
| | Wolf-Hirschhorn syndrome candidate 1 is involved in the cellular response to DNA damage | Q35164644 |
| | NSD2 links dimethylation of histone H3 at lysine 36 to oncogenic programming | Q35569571 |
| | H2AX is required for recombination between immunoglobulin switch regions but not for intra-switch region recombination or somatic hypermutation | Q36370913 |
| | ATM is required for efficient recombination between immunoglobulin switch regions | Q36399334 |
| | Mechanism and control of V(D)J recombination at the immunoglobulin heavy chain locus | Q36427367 |
| | DNA-PKcs and Artemis function in the end-joining phase of immunoglobulin heavy chain class switch recombination | Q36509842 |
| | 53BP1 facilitates long-range DNA end-joining during V(D)J recombination | Q36682376 |
| | Molecular mechanisms of antibody somatic hypermutation. | Q36747477 |
| | Evolution of the immunoglobulin heavy chain class switch recombination mechanism | Q36845675 |
| | The biochemistry of somatic hypermutation | Q37096080 |
| | Hijacked DNA repair proteins and unchained DNA polymerases | Q37140473 |
| | Multiple functions of MRN in end-joining pathways during isotype class switching | Q37291987 |
| | The MMSET protein is a histone methyltransferase with characteristics of a transcriptional corepressor | Q40031496 |
| | Uracil DNA glycosylase activity is dispensable for immunoglobulin class switch | Q40522938 |
| | High frequency class switching of an IgM+ B lymphoma clone CH12F3 to IgA+ cells. | Q41233018 |
| | Antibody deficiency in Wolf-Hirschhorn syndrome | Q41926268 |
| | Impact of DNA ligase IV on nonhomologous end joining pathways during class switch recombination in human cells. | Q42271523 |
| | Role of PTIP in class switch recombination and long-range chromatin interactions at the immunoglobulin heavy chain locus | Q42799741 |
| | Delineation of the role of the Mre11 complex in class switch recombination | Q47237271 |
| | WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma | Q24322575 |
| | Transcription enhances AID-mediated cytidine deamination by exposing single-stranded DNA on the nontemplate strand | Q28190690 |
| | The etiology of Wolf-Hirschhorn syndrome | Q28236976 |
| | IgH class switching and translocations use a robust non-classical end-joining pathway | Q28241679 |
| | A chromatin-wide transition to H4K20 monomethylation impairs genome integrity and programmed DNA rearrangements in the mouse | Q28289637 |
| | MMSET regulates histone H4K20 methylation and 53BP1 accumulation at DNA damage sites | Q28304648 |
| | PTIP promotes chromatin changes critical for immunoglobulin class switch recombination | Q28585503 |
| | The RNF8/RNF168 ubiquitin ligase cascade facilitates class switch recombination | Q28592784 |
| | A histone H3 lysine 36 trimethyltransferase links Nkx2-5 to Wolf-Hirschhorn syndrome | Q28593584 |
| | 53BP1 is required for class switch recombination | Q29465541 |
| | 53BP1 links DNA damage-response pathways to immunoglobulin heavy chain class-switch recombination. | Q29465548 |
| | BLM helicase-dependent and -independent roles of 53BP1 during replication stress-mediated homologous recombination. | Q30480499 |
| | The target of the NSD family of histone lysine methyltransferases depends on the nature of the substrate | Q33553524 |
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Nuclear receptor binding SET domain protein 2 | Q21988839 |
| | Transformation related protein 53 binding protein 1 | Q21992210 |
| P304 | page(s) | 756–763 | |
| P577 | publication date | 2013-01-15 | |
| P1433 | published in | Journal of Immunology | Q3521441 |
| P1476 | title | The histone methyltransferase MMSET regulates class switch recombination | |
| P478 | volume | 190 | |