scholarly article | Q13442814 |
P819 | ADS bibcode | 2013PLoSO...863032D |
P356 | DOI | 10.1371/JOURNAL.PONE.0063032 |
P932 | PMC publication ID | 3637464 |
P698 | PubMed publication ID | 23638178 |
P5875 | ResearchGate publication ID | 236604571 |
P2093 | author name string | Layne Dylla | |
Paul Jedlicka | |||
P2860 | cites work | Significance analysis of microarrays applied to the ionizing radiation response | Q24606608 |
Histone deacetylases mediate the silencing of miR-15a, miR-16, and miR-29b in chronic lymphocytic leukemia | Q24633394 | ||
Targeted deletion reveals essential and overlapping functions of the miR-17 through 92 family of miRNA clusters | Q24645192 | ||
Genetic dissection of the miR-17~92 cluster of microRNAs in Myc-induced B-cell lymphomas | Q24652219 | ||
miR-19 is a key oncogenic component of mir-17-92 | Q24652326 | ||
miR-16 family induces cell cycle arrest by regulating multiple cell cycle genes. | Q24653347 | ||
EWS-FLI1 fusion transcript structure is an independent determinant of prognosis in Ewing's sarcoma | Q27851507 | ||
c-Myc-regulated microRNAs modulate E2F1 expression | Q27861046 | ||
MiR-15 and miR-16 are direct transcriptional targets of E2F1 that limit E2F-induced proliferation by targeting cyclin E | Q28117082 | ||
The DLEU2/miR-15a/16-1 cluster controls B cell proliferation and its deletion leads to chronic lymphocytic leukemia | Q28269786 | ||
E2F1-regulated microRNAs impair TGFbeta-dependent cell-cycle arrest and apoptosis in gastric cancer | Q28271985 | ||
mir-17-92, a cluster of miRNAs in the midst of the cancer network | Q28275929 | ||
Apoptosis induction by antisense oligonucleotides against miR-17-5p and miR-20a in lung cancers overexpressing miR-17-92 | Q28294917 | ||
The myc-miR-17~92 axis blunts TGF{beta} signaling and production of multiple TGF{beta}-dependent antiangiogenic factors | Q28295428 | ||
Emerging role of miR-106b-25/miR-17-92 clusters in the control of transforming growth factor beta signaling | Q28297583 | ||
The miR-15a-miR-16-1 cluster controls prostate cancer by targeting multiple oncogenic activities | Q28297958 | ||
Oncogenic potential of the miR-106-363 cluster and its implication in human T-cell leukemia | Q28306681 | ||
Regulation of mRNA translation and stability by microRNAs | Q29547304 | ||
MicroRNA sponges: competitive inhibitors of small RNAs in mammalian cells | Q29616080 | ||
Changes in incidence and survival of Ewing sarcoma patients over the past 3 decades: Surveillance Epidemiology and End Results data. | Q31157886 | ||
Investigation of the insulin-like growth factor-1 signaling pathway in localized Ewing sarcoma: a report from the Children's Oncology Group | Q33559559 | ||
Current treatment protocols have eliminated the prognostic advantage of type 1 fusions in Ewing sarcoma: a report from the Children's Oncology Group | Q33813608 | ||
Multiple E2F-induced microRNAs prevent replicative stress in response to mitogenic signaling. | Q33877588 | ||
Overexpression of microRNAs from the miR-17-92 paralog clusters in AIDS-related non-Hodgkin's lymphomas | Q33940931 | ||
Modulation of glucose transporter 1 (GLUT1) expression levels alters mouse mammary tumor cell growth in vitro and in vivo. | Q33986152 | ||
Let-7a is a direct EWS-FLI-1 target implicated in Ewing's sarcoma development | Q33997274 | ||
miR-15a/16-1 influences BCL2 expression in keratocystic odontogenic tumors. | Q54305835 | ||
Ewing's sarcoma origin: from duel to duality | Q84386241 | ||
R1507, an anti-insulin-like growth factor-1 receptor (IGF-1R) antibody, and EWS/FLI-1 siRNA in Ewing's sarcoma: convergence at the IGF/IGFR/Akt axis | Q34055933 | ||
Identification of the miR-106b~25 microRNA cluster as a proto-oncogenic PTEN-targeting intron that cooperates with its host gene MCM7 in transformation | Q34109986 | ||
MicroRNA sponges: progress and possibilities | Q34139023 | ||
Targeted Therapy of Ewing's Sarcoma | Q34262377 | ||
Biology of EWS/ETS fusions in Ewing's family tumors | Q34405501 | ||
Genomic and clinical analysis of amplification of the 13q31 chromosomal region in alveolar rhabdomyosarcoma: a report from the Children's Oncology Group | Q34694293 | ||
The miR-106b-25 polycistron, activated by genomic amplification, functions as an oncogene by suppressing p21 and Bim | Q34979616 | ||
Inhibition of miR-33a/b in non-human primates raises plasma HDL and lowers VLDL triglycerides. | Q35606800 | ||
Mouse miRNA-709 directly regulates miRNA-15a/16-1 biogenesis at the posttranscriptional level in the nucleus: evidence for a microRNA hierarchy system | Q35796875 | ||
Discovering the first microRNA-targeted drug | Q36353486 | ||
Cisplatin sensitivity mediated by WEE1 and CHK1 is mediated by miR-155 and the miR-15 family | Q36405766 | ||
Recent advances in the molecular pathogenesis of Ewing's sarcoma | Q36562720 | ||
Locked nucleic acid holds promise in the treatment of cancer | Q37160953 | ||
Ewing sarcoma: historical perspectives, current state-of-the-art, and opportunities for targeted therapy in the future | Q37182432 | ||
Emerging roles of microRNAs as molecular switches in the integrated circuit of the cancer cell. | Q37272418 | ||
Gene expression profile of ewing sarcoma cell lines differing in their EWS-FLI1 fusion type. | Q38320073 | ||
MiR-30a-5p connects EWS-FLI1 and CD99, two major therapeutic targets in Ewing tumor | Q38321646 | ||
A novel oncogenic mechanism in Ewing sarcoma involving IGF pathway targeting by EWS/Fli1-regulated microRNAs | Q38334606 | ||
Hsa-mir-145 is the top EWS-FLI1-repressed microRNA involved in a positive feedback loop in Ewing's sarcoma | Q38338166 | ||
miR-106a–mediated Malignant Transformation of Cells Induced by Anti-benzo[a]pyrene-trans-7,8-diol-9,10-epoxide | Q38340387 | ||
A TARBP2-dependent miRNA expression profile underlies cancer stem cell properties and provides candidate therapeutic reagents in Ewing sarcoma | Q39331421 | ||
WEE1 accumulation and deregulation of S-phase proteins mediate MLN4924 potent inhibitory effect on Ewing sarcoma cells | Q39340936 | ||
Vector-based miR-15a/16-1 plasmid inhibits colon cancer growth in vivo | Q39350883 | ||
Involvement of microRNA-93, a new regulator of PTEN/Akt signaling pathway, in regulation of chemotherapeutic drug cisplatin chemosensitivity in ovarian cancer cells | Q39371337 | ||
miR-106a is frequently upregulated in gastric cancer and inhibits the extrinsic apoptotic pathway by targeting FAS. | Q39376733 | ||
Nucleolin protein interacts with microprocessor complex to affect biogenesis of microRNAs 15a and 16. | Q39448784 | ||
miR-34a predicts survival of Ewing's sarcoma patients and directly influences cell chemo-sensitivity and malignancy | Q39465507 | ||
EWS/FLI-1 oncoprotein subtypes impose different requirements for transformation and metastatic activity in a murine model | Q40142173 | ||
The microRNA miR-92 increases proliferation of myeloid cells and by targeting p63 modulates the abundance of its isoforms. | Q45927530 | ||
Efficient in vivo microRNA targeting of liver metastasis | Q46584676 | ||
Synthetic lethality between Rb, p53 and Dicer or miR-17-92 in retinal progenitors suppresses retinoblastoma formation | Q47302451 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | e63032 | |
P577 | publication date | 2013-04-26 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Growth-promoting role of the miR-106a~363 cluster in Ewing sarcoma | |
P478 | volume | 8 |
Q35121814 | A microRNA signature associated with early recurrence in breast cancer |
Q46036353 | Biomarker significance of plasma and tumor miR-21, miR-221, and miR-106a in osteosarcoma. |
Q52647082 | Circulating microRNAs from the miR-106a-363 cluster on chromosome X as novel diagnostic biomarkers for breast cancer. |
Q38325485 | Competing endogenous RNA interplay in cancer: mechanism, methodology, and perspectives |
Q64238834 | Comprehensive Investigation of miRNome Identifies Novel Candidate miRNA-mRNA Interactions Implicated in T-Cell Acute Lymphoblastic Leukemia |
Q48343656 | Development of Novel Therapeutic Agents by Inhibition of Oncogenic MicroRNAs |
Q30818838 | Inhibition of microRNA 128 promotes excitability of cultured cortical neuronal networks |
Q64267571 | Interferon-induced IFIT5 promotes epithelial-to-mesenchymal transition leading to renal cancer invasion |
Q39117246 | MiR-106a targets Mcl-1 to suppress cisplatin resistance of ovarian cancer A2780 cells |
Q36380991 | MiR-193b, downregulated in Ewing Sarcoma, targets the ErbB4 oncogene to inhibit anchorage-independent growth. |
Q39519803 | MiRNA expression profiling in human gliomas: upregulated miR-363 increases cell survival and proliferation |
Q100512506 | MicroRNA determinants of neuroendocrine differentiation in metastatic castration-resistant prostate cancer |
Q38296481 | MicroRNA expression and its clinical implications in Ewing's sarcoma |
Q39112720 | MicroRNA-106a induces multidrug resistance in gastric cancer by targeting RUNX3. |
Q38854767 | MicroRNA-23a enhances migration and invasion through PTEN in osteosarcoma |
Q35619546 | Prospects for Therapeutic Targeting of MicroRNAs in Human Immunological Diseases |
Q35598357 | Retracted: MiR-506 Suppresses Tumor Proliferation and Invasion by Targeting FOXQ1 in Nasopharyngeal Carcinoma |
Q92713862 | Signatures of circulating microRNA in four sarcoma subtypes |
Q36299692 | Simultaneous inhibition of multiple oncogenic miRNAs by a multi-potent microRNA sponge |
Q26748969 | The Three Paralogous MicroRNA Clusters in Development and Disease, miR-17-92, miR-106a-363, and miR-106b-25 |
Q38289575 | The role of miR-17-92 in the miRegulatory landscape of Ewing sarcoma |
Q26782649 | Twenty Years on: What Do We Really Know about Ewing Sarcoma and What Is the Path Forward? |
Q26800124 | What Do We Know about the Role of miRNAs in Pediatric Sarcoma? |
Q38584497 | ceRNA in cancer: possible functions and clinical implications. |
Q61760942 | miRNA-Targeted Therapies in the Most Prevalent Pediatric Solid Tumors |