| scholarly article | Q13442814 |
| P2093 | author name string | Zhi-Xiang Xu | |
| Rui-Xun Zhao | |||
| Kun-Sang Chang | |||
| Anna Timanova-Atanasova | |||
| P2860 | cites work | Sequestration and inhibition of Daxx-mediated transcriptional repression by PML | Q22253162 |
| Role of SUMO-1-modified PML in nuclear body formation | Q22253970 | ||
| PML regulates p53 acetylation and premature senescence induced by oncogenic Ras | Q22254666 | ||
| Regulation of p53 activity in nuclear bodies by a specific PML isoform | Q24290520 | ||
| The growth suppressor PML represses transcription by functionally and physically interacting with histone deacetylases | Q24290948 | ||
| Regulation and localization of the Bloom syndrome protein in response to DNA damage | Q24291133 | ||
| Role of PML and PML-RARalpha in Mad-mediated transcriptional repression | Q24291380 | ||
| Stable overexpression of PML alters regulation of cell cycle progression in HeLa cells | Q24312086 | ||
| Recombinant PML adenovirus suppresses growth and tumorigenicity of human breast cancer cells by inducing G1 cell cycle arrest and apoptosis | Q24315554 | ||
| PML, a growth suppressor disrupted in acute promyelocytic leukemia | Q24324168 | ||
| The promyelocytic leukemia gene product (PML) forms stable complexes with the retinoblastoma protein | Q24324766 | ||
| The promyelocytic leukemia protein interacts with Sp1 and inhibits its transactivation of the epidermal growth factor receptor promoter | Q24522845 | ||
| A DNA damage-regulated BRCT-containing protein, TopBP1, is required for cell survival | Q24540067 | ||
| PML is critical for ND10 formation and recruits the PML-interacting protein daxx to this nuclear structure when modified by SUMO-1 | Q24670576 | ||
| Modulation of CREB binding protein function by the promyelocytic (PML) oncoprotein suggests a role for nuclear bodies in hormone signaling | Q24674185 | ||
| The function of PML in p53-dependent apoptosis | Q28140732 | ||
| Deconstructing a disease: RARalpha, its fusion partners, and their roles in the pathogenesis of acute promyelocytic leukemia | Q28143297 | ||
| The transcriptional role of PML and the nuclear body | Q28144176 | ||
| Conserved BRCT regions of TopBP1 and of the tumor suppressor BRCA1 bind strand breaks and termini of DNA | Q28145077 | ||
| BRCT domain-containing protein TopBP1 functions in DNA replication and damage response | Q28200771 | ||
| Promyelocytic leukemia protein PML inhibits Nur77-mediated transcription through specific functional interactions | Q28200940 | ||
| DNA double-strand breaks: signaling, repair and the cancer connection | Q28204231 | ||
| Regulation of Pax3 transcriptional activity by SUMO-1-modified PML | Q28204429 | ||
| PML interaction with p53 and its role in apoptosis and replicative senescence | Q28204830 | ||
| Cooperation of HECT-domain ubiquitin ligase hHYD and DNA topoisomerase II-binding protein for DNA damage response | Q28206127 | ||
| The promyelocytic leukemia protein represses A20-mediated transcription | Q28206387 | ||
| Cancer susceptibility and the functions of BRCA1 and BRCA2 | Q28217784 | ||
| Identification of three major sentrinization sites in PML | Q28284098 | ||
| PML is essential for multiple apoptotic pathways | Q28508348 | ||
| Nuclear foci of mammalian recombination proteins are located at single-stranded DNA regions formed after DNA damage | Q28610023 | ||
| Homologous recombinational repair of DNA ensures mammalian chromosome stability | Q28646561 | ||
| Brca1 controls homology-directed DNA repair | Q29614844 | ||
| DNA damage-dependent nuclear dynamics of the Mre11 complex | Q33975168 | ||
| DNA repair: spot(light)s on chromatin. | Q34218073 | ||
| The molecular control of DNA damage-induced cell death | Q34220065 | ||
| Transcriptional regulation in acute promyelocytic leukemia. | Q34435531 | ||
| SUMO: of branched proteins and nuclear bodies | Q34435551 | ||
| PML induces a novel caspase-independent death process | Q34478914 | ||
| ATM function and telomere stability | Q34535665 | ||
| Interfaces between the detection, signaling, and repair of DNA damage | Q34762844 | ||
| PML is induced by oncogenic ras and promotes premature senescence | Q35201220 | ||
| Localization of nascent RNA and CREB binding protein with the PML-containing nuclear body. | Q36062156 | ||
| Damage and replication checkpoint control in fission yeast is ensured by interactions of Crb2, a protein with BRCT motif, with Cut5 and Chk1. | Q40444140 | ||
| Deficient nonhomologous end-joining activity in cell-free extracts from Brca1-null fibroblasts. | Q40717542 | ||
| Metabolic-energy-dependent movement of PML bodies within the mammalian cell nucleus | Q40761429 | ||
| Fission yeast cut5 links nuclear chromatin and M phase regulator in the replication checkpoint control. | Q40793814 | ||
| ALT-associated PML bodies are present in viable cells and are enriched in cells in the G(2)/M phase of the cell cycle. | Q40841848 | ||
| A role for PML and the nuclear body in genomic stability | Q40905918 | ||
| Transcriptional repression by the promyelocytic leukemia protein, PML. | Q41071228 | ||
| Failure to unwind causes cancer. Genome stability | Q41110581 | ||
| Molecular genetics of Bloom's syndrome | Q41170320 | ||
| NB4, a maturation inducible cell line with t(15;17) marker isolated from a human acute promyelocytic leukemia (M3). | Q41692539 | ||
| The transcription coactivator CBP is a dynamic component of the promyelocytic leukemia nuclear body | Q42951383 | ||
| Adenovirus-mediated expression of PML suppresses growth and tumorigenicity of prostate cancer cells | Q45881890 | ||
| Modulation of Fos-mediated AP-1 transcription by the promyelocytic leukemia protein | Q47814142 | ||
| Transcriptional induction of the PML growth suppressor gene by interferons is mediated through an ISRE and a GAS element. | Q48068389 | ||
| PML NBs associate with the hMre11 complex and p53 at sites of irradiation induced DNA damage | Q64387887 | ||
| The Mre11 complex is required for repair of hairpin-capped double-strand breaks and prevention of chromosome rearrangements | Q64387924 | ||
| Telomerase-negative immortalized human cells contain a novel type of promyelocytic leukemia (PML) body | Q78257210 | ||
| P4510 | describes a project that uses | ImageQuant | Q112270642 |
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | DNA topoisomerase II binding protein 1 | Q21116531 |
| DNA damage | Q5205747 | ||
| cell biology | Q7141 | ||
| P304 | page(s) | 4247-56 | |
| P577 | publication date | 2003-06-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | PML colocalizes with and stabilizes the DNA damage response protein TopBP1 | |
| P478 | volume | 23 |
| Q39529290 | A three-dimensional colocalization RNA interference screening platform to elucidate the alternative lengthening of telomeres pathway |
| Q37624182 | Assembly of checkpoint and repair machineries at DNA damage sites |
| Q28472413 | Avicin D, a plant triterpenoid, induces cell apoptosis by recruitment of Fas and downstream signaling molecules into lipid rafts |
| Q36627909 | Candidate protein biodosimeters of human exposure to ionizing radiation. |
| Q39982335 | Cellular proteins PML and Daxx mediate an innate antiviral defense antagonized by the adenovirus E4 ORF3 protein |
| Q33953067 | Cellular senescence and protein degradation: breaking down cancer |
| Q39230416 | Components of promyelocytic leukemia nuclear bodies (ND10) act cooperatively to repress herpesvirus infection. |
| Q33759285 | DNA-SCARS: distinct nuclear structures that sustain damage-induced senescence growth arrest and inflammatory cytokine secretion |
| Q37958977 | Defective DNA-damage repair induced by nuclear lamina dysfunction is a key mediator of smooth muscle cell aging |
| Q34305439 | E2FBP1/hDril1 modulates cell growth through downregulation of promyelocytic leukemia bodies |
| Q28271191 | EDD mediates DNA damage-induced activation of CHK2 |
| Q31037336 | Functional connection between Rad51 and PML in homology-directed repair |
| Q40171594 | Identification of candidate alternative lengthening of telomeres genes by methionine restriction and RNA interference. |
| Q57817539 | Importance of Promyelocytic Leukema Protein (PML) for Kaposi's Sarcoma-Associated Herpesvirus Lytic Replication |
| Q38260450 | Importin β-dependent nuclear import of TopBP1 in ATR-Chk1 checkpoint in Xenopus egg extracts. |
| Q36392199 | Interactions between DNA viruses, ND10 and the DNA damage response |
| Q36499765 | Multiple functions of rad9 for preserving genomic integrity |
| Q37745457 | Myogenic differentiation triggers PML nuclear body loss and DAXX relocalization to chromocentres |
| Q30475799 | ND10 components relocate to sites associated with herpes simplex virus type 1 nucleoprotein complexes during virus infection |
| Q35941485 | Nesprin-2-dependent ERK1/2 compartmentalisation regulates the DNA damage response in vascular smooth muscle cell ageing |
| Q28295561 | Noncovalent SUMO-1 binding activity of thymine DNA glycosylase (TDG) is required for its SUMO-1 modification and colocalization with the promyelocytic leukemia protein |
| Q40315900 | Nur77 forms novel nuclear structures upon DNA damage that cause transcriptional arrest |
| Q37151474 | PML nuclear body disruption impairs DNA double-strand break sensing and repair in APL. |
| Q24299467 | PML promotes MHC class II gene expression by stabilizing the class II transactivator |
| Q91807500 | PML-like subnuclear bodies, containing XRCC1, juxtaposed to DNA replication-based single-strand breaks |
| Q34337626 | PML-mediated signaling and its role in cancer stem cells |
| Q45617415 | PML-nuclear bodies accumulate DNA in response to polyomavirus BK and simian virus 40 replication |
| Q34097292 | Phosphorylation of BLM, dissociation from topoisomerase IIIalpha, and colocalization with gamma-H2AX after topoisomerase I-induced replication damage |
| Q30480527 | Promyelocytic leukemia nuclear bodies behave as DNA damage sensors whose response to DNA double-strand breaks is regulated by NBS1 and the kinases ATM, Chk2, and ATR. |
| Q35914635 | Promyelocytic leukemia nuclear bodies support a late step in DNA double-strand break repair by homologous recombination |
| Q40620245 | Promyelocytic leukemia protein 4 induces apoptosis by inhibition of survivin expression |
| Q24305398 | Promyelocytic leukemia protein interacts with werner syndrome helicase and regulates double-strand break repair in γ-irradiation-induced DNA damage responses |
| Q44719672 | Proteasome-dependent dispersal of PML nuclear bodies in response to alkylating DNA damage |
| Q34267949 | Rapid and reliable confirmation of acute promyelocytic leukemia by immunofluorescence staining with an antipromyelocytic leukemia antibody: the M. D. Anderson Cancer Center experience of 349 patients |
| Q33201426 | Recruitment of cellular recombination and repair proteins to sites of herpes simplex virus type 1 DNA replication is dependent on the composition of viral proteins within prereplicative sites and correlates with the induction of the DNA damage respo |
| Q33780662 | Relocalization of the Mre11-Rad50-Nbs1 complex by the adenovirus E4 ORF3 protein is required for viral replication |
| Q33824136 | SUMOylation of HMGA2: selective destabilization of promyelocytic leukemia protein via proteasome |
| Q40423325 | Serotype-specific reorganization of the Mre11 complex by adenoviral E4orf3 proteins |
| Q29620390 | Structure, dynamics and functions of promyelocytic leukaemia nuclear bodies |
| Q64093786 | Synthetic lethality of cytolytic HSV-1 in cancer cells with ATRX and PML deficiency |
| Q36528092 | TRAIP/RNF206 is required for recruitment of RAP80 to sites of DNA damage |
| Q21260410 | The BRCA1/2 pathway prevents hematologic cancers in addition to breast and ovarian cancers |
| Q53240738 | The acute promyelocytic leukaemia success story: curing leukaemia through targeted therapies. |
| Q26779358 | The function, regulation and therapeutic implications of the tumor suppressor protein, PML |
| Q41848711 | The functional interactome of PYHIN immune regulators reveals IFIX is a sensor of viral DNA. |
| Q33553863 | The proteins of intra-nuclear bodies: a data-driven analysis of sequence, interaction and expression |
| Q34244028 | The role of post-translational modifications in fine-tuning BLM helicase function during DNA repair |
| Q35116715 | The tumor suppressor PML specifically accumulates at RPA/Rad51-containing DNA damage repair foci but is nonessential for DNA damage-induced fibroblast senescence |
| Q48819087 | The tumor suppressor protein PML controls apoptosis induced by the HIV-1 envelope. |
| Q28261299 | TopBP1 localises to centrosomes in mitosis and to chromosome cores in meiosis |
| Q40116480 | Tyrosine kinase inhibitor, methyl 2,5-dihydromethylcinnimate, induces PML nuclear body formation and apoptosis in tumor cells |
| Q36399088 | Ubiquitin-dependent degradation of p73 is inhibited by PML. |
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