scholarly article | Q13442814 |
P50 | author | Peter J F Snijders | Q90768556 |
Pieter E Postmus | Q56826661 | ||
Chris J L M Meijer | Q90379336 | ||
P2093 | author name string | Arie P Otte | |
Egbert F Smit | |||
Folkert J van Kemenade | |||
Thomas G Sutedja | |||
Richard G A B Sewalt | |||
Frank M Raaphorst | |||
Roderick H J Breuer | |||
P2860 | cites work | The Drosophila Polycomb Group proteins ESC and E(Z) are present in a complex containing the histone-binding protein p55 and the histone deacetylase RPD3 | Q24290657 |
RING1 is associated with the polycomb group protein complex and acts as a transcriptional repressor | Q24312810 | ||
Interference with the expression of a novel human polycomb protein, hPc2, results in cellular transformation and apoptosis | Q24315842 | ||
Interaction of mouse polycomb-group (Pc-G) proteins Enx1 and Enx2 with Eed: indication for separate Pc-G complexes | Q24522505 | ||
Selective interactions between vertebrate polycomb homologs and the SUV39H1 histone lysine methyltransferase suggest that histone H3-K9 methylation contributes to chromosomal targeting of Polycomb group proteins | Q24537616 | ||
Control of the replicative life span of human fibroblasts by p16 and the polycomb protein Bmi-1 | Q24540711 | ||
The polycomb group protein EED interacts with YY1, and both proteins induce neural tissue in Xenopus embryos | Q24548361 | ||
RING1 interacts with multiple Polycomb-group proteins and displays tumorigenic activity | Q24554805 | ||
Identification and characterization of interactions between the vertebrate polycomb-group protein BMI1 and human homologs of polyhomeotic | Q24646581 | ||
EZH2 is a marker of aggressive breast cancer and promotes neoplastic transformation of breast epithelial cells | Q24672969 | ||
Role of histone H3 lysine 27 methylation in Polycomb-group silencing | Q28131795 | ||
Transcriptional repression mediated by the human polycomb-group protein EED involves histone deacetylation | Q28139187 | ||
HPC3 is a new human polycomb orthologue that interacts and associates with RING1 and Bmi1 and has transcriptional repression properties | Q28145079 | ||
Cancer statistics, 2001 | Q28189339 | ||
Ring1A is a transcriptional repressor that interacts with the Polycomb-M33 protein and is expressed at rhombomere boundaries in the mouse hindbrain. | Q28587211 | ||
The polycomb group protein EZH2 is involved in progression of prostate cancer | Q29614514 | ||
Drosophila enhancer of Zeste/ESC complexes have a histone H3 methyltransferase activity that marks chromosomal Polycomb sites | Q29615395 | ||
The oncogene and Polycomb-group gene bmi-1 regulates cell proliferation and senescence through the ink4a locus | Q29619815 | ||
Polycomb silencing and the maintenance of stable chromatin states. | Q33642295 | ||
Cell memory and cancer--the story of the trithorax and Polycomb group genes | Q33870428 | ||
Molecular and genetic aspects of lung cancer | Q33891465 | ||
Distinct BMI-1 and EZH2 expression patterns in thymocytes and mature T cells suggest a role for Polycomb genes in human T cell differentiation | Q33945892 | ||
A Drosophila ESC-E(Z) protein complex is distinct from other polycomb group complexes and contains covalently modified ESC | Q33963183 | ||
The Bmi-1 oncogene induces telomerase activity and immortalizes human mammary epithelial cells | Q34144912 | ||
Mutation analysis of the mel-18 gene that shows decreased expression in human breast cancer cell lines | Q34146131 | ||
EZH2 is downstream of the pRB-E2F pathway, essential for proliferation and amplified in cancer | Q34268216 | ||
Identification of Bmi1-interacting proteins as constituents of a multimeric mammalian polycomb complex | Q34414481 | ||
Fluorescence bronchoscopy for early detection of lung cancer: a clinical perspective | Q34419269 | ||
Polycomb-group genes as regulators of mammalian lymphopoiesis | Q34460698 | ||
RAE28, BMI1, and M33 are members of heterogeneous multimeric mammalian Polycomb group complexes | Q34466512 | ||
Polycomb repression: from cellular memory to cellular proliferation and cancer. | Q34646680 | ||
Characteristic genetic alterations in lung cancer | Q34988579 | ||
Role of the RB tumor suppressor in cancer. | Q35076045 | ||
Polycomb group genes as epigenetic regulators of normal and leukemic hemopoiesis | Q35169776 | ||
Bmi-1 collaborates with c-Myc in tumorigenesis by inhibiting c-Myc-induced apoptosis via INK4a/ARF. | Q35208164 | ||
Gene repression by Polycomb group protein complexes: a distinct complex for every occasion? | Q35555950 | ||
Coexpression of BMI-1 and EZH2 polycomb group genes in Reed-Sternberg cells of Hodgkin's disease | Q35829466 | ||
The bmi-1 oncoprotein is differentially expressed in non-small cell lung cancer and correlates with INK4A-ARF locus expression | Q36622224 | ||
The Bmi-1 oncoprotein is overexpressed in human colorectal cancer and correlates with the reduced p16INK4a/p14ARF proteins | Q38518363 | ||
Site-specific expression of polycomb-group genes encoding the HPC-HPH/PRC1 complex in clinically defined primary nodal and cutaneous large B-cell lymphomas | Q38584864 | ||
Unique polycomb gene expression pattern in Hodgkin's lymphoma and Hodgkin's lymphoma-derived cell lines | Q38704458 | ||
The Polycomb group protein EZH2 is upregulated in proliferating, cultured human mantle cell lymphoma | Q40813288 | ||
Poorly differentiated breast carcinoma is associated with increased expression of the human polycomb group EZH2 gene | Q41602005 | ||
Functional analysis of mouse Polycomb group genes | Q41714824 | ||
Polycomb group proteins ESC and E(Z) are present in multiple distinct complexes that undergo dynamic changes during development | Q47071351 | ||
Distinct expression patterns of polycomb oncoproteins and their binding partners during the germinal center reaction | Q47299700 | ||
Evidence for at least three alternative mechanisms targeting the p16INK4A/cyclin D/Rb pathway in penile carcinoma, one of which is mediated by high-risk human papillomavirus | Q47653493 | ||
Cutting edge: polycomb gene expression patterns reflect distinct B cell differentiation stages in human germinal centers. | Q52172389 | ||
Coexpression of BMI-1 and EZH2 polycomb-group proteins is associated with cycling cells and degree of malignancy in B-cell non-Hodgkin lymphoma. | Q53398447 | ||
Comprehensive gene expression analysis of prostate cancer reveals distinct transcriptional programs associated with metastatic disease | Q57908314 | ||
Perturbation of B and T cell development and predisposition to lymphomagenesis in EμBmi1 transgenic mice require the Bmi1 RING finger | Q58451225 | ||
P433 | issue | 6 | |
P921 | main subject | carcinogenesis | Q1637543 |
P304 | page(s) | 736-743 | |
P577 | publication date | 2004-11-01 | |
P1433 | published in | Neoplasia | Q2962042 |
P1476 | title | Increased expression of the EZH2 polycomb group gene in BMI-1-positive neoplastic cells during bronchial carcinogenesis | |
P478 | volume | 6 |