Acute myeloid leukemia with complex karyotypes and abnormal chromosome 21: Amplification discloses overexpression of APP, ETS2, and ERG genes. - Wikidata - awgldk - TriplyDB

Acute myeloid leukemia with complex karyotypes and abnormal chromosome 21: Amplification discloses overexpression of APP, ETS2, and ERG genes.

Acute myeloid leukemia with complex karyotypes and abnormal chromosome 21: Amplification discloses overexpression of APP, ETS2, and ERG genes.

http://www.wikidata.org/entity/Q37095280

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Caryoscope: an Open Source Java application for viewing microarray data in a genomic context Regulation of endothelial homeostasis, vascular development and angiogenesis by the transcription factor ERG Stem Cell Modeling of Core Binding Factor Acute Myeloid Leukemia The associations between Parkinson's disease and cancer: the plot thickens Molecular mechanisms of ETS transcription factor-mediated tumorigenesis Favorable prognostic impact of NPM1 mutations in older patients with cytogenetically normal de novo acute myeloid leukemia and associated gene- and microRNA-expression signatures: a Cancer and Leukemia Group B study.TET2 mutations improve the new European LeukemiaNet risk classification of acute myeloid leukemia: a Cancer and Leukemia Group B study.Clinical outcome of de novo acute myeloid leukaemia patients with normal cytogenetics is affected by molecular genetic alterations: a concise review ETS2 and ERG promote megakaryopoiesis and synergize with alterations in GATA-1 to immortalize hematopoietic progenitor cells Autism as early neurodevelopmental disorder: evidence for an sAPPα-mediated anabolic pathway Frequent overexpression of ETS-related gene-1 (ERG1) in prostate cancer transcriptome.Gene-resolution analysis of DNA copy number variation using oligonucleotide expression microarrays.Quantitative comparison of microarray experiments with published leukemia related gene expression signatures.Identification of a 20-gene expression-based risk score as a predictor of clinical outcome in chronic lymphocytic leukemia patients.E-26 Transformation-specific Related Gene Expression and Outcomes in Cytogenetically Normal Acute Myeloid Leukemia: A Meta-analysis.Cancer and neurodegeneration: between the devil and the deep blue sea.IDH1 and IDH2 gene mutations identify novel molecular subsets within de novo cytogenetically normal acute myeloid leukemia: a Cancer and Leukemia Group B study.Prognostic gene mutations and distinct gene- and microRNA-expression signatures in acute myeloid leukemia with a sole trisomy 8.Ets-1 global gene expression profile reveals associations with metabolism and oxidative stress in ovarian and breast cancers Genetic determinants at the interface of cancer and neurodegenerative disease.BAALC and ERG expression levels are associated with outcome and distinct gene and microRNA expression profiles in older patients with de novo cytogenetically normal acute myeloid leukemia: a Cancer and Leukemia Group B study.Complex genomic alterations and gene expression in acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21.ERG induces epigenetic activation of Tudor domain-containing protein 1 (TDRD1) in ERG rearrangement-positive prostate cancer.The Prognostic Relevance of BAALC and ERG Expression Levels in Cytogenetically Normal Pediatric Acute Myeloid Leukemia.Rapid diagnosis of aneuploidy using segmental duplication quantitative fluorescent PCR.The nuclear receptor transcriptional coregulator RIP140.Expression and role of RIP140/NRIP1 in chronic lymphocytic leukemia.Early lineage priming by trisomy of Erg leads to myeloproliferation in a Down syndrome model.Clinical relevance of mutations and gene-expression changes in adult acute myeloid leukemia with normal cytogenetics: are we ready for a prognostically prioritized molecular classification?Genome-wide assessment of recurrent genomic imbalances in canine leukemia identifies evolutionarily conserved regions for subtype differentiation.Evaluation of multiplex ligation dependent probe amplification (MLPA) for identification of acute lymphoblastic leukemia with an intrachromosomal amplification of chromosome 21 (iAMP21) in a Brazilian population.Genome-wide DNA methylation profiling of chronic lymphocytic leukemia allows identification of epigenetically repressed molecular pathways with clinical impact.Cytogenetic, molecular genetic, and clinical characteristics of acute myeloid leukemia with a complex karyotype.Detection of DNA copy number alterations in cancer by array comparative genomic hybridization.Mithramycin is a gene-selective Sp1 inhibitor that identifies a biological intersection between cancer and neurodegeneration.Insights into the manifestations, outcomes, and mechanisms of leukemogenesis in Down syndrome Molecular prognostic markers for adult acute myeloid leukemia with normal cytogenetics.Epigenetics in acute myeloid leukemia.The role of the proto-oncogene ETS2 in acute megakaryocytic leukemia biology and therapy Ets transcription factors in intestinal morphogenesis, homeostasis and disease.

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Acute myeloid leukemia with complex karyotypes and abnormal chromosome 21: Amplification discloses overexpression of APP, ETS2, and ERG genes.

http://www.wikidata.org/entity/Q37095280

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article científic

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bilimsel makale

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scientific article published on 08 March 2004

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Acute myeloid leukemia with co ...... n of APP, ETS2, and ERG genes.

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Acute myeloid leukemia with co ...... n of APP, ETS2, and ERG genes.

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Acute myeloid leukemia with co ...... n of APP, ETS2, and ERG genes.

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PNAS.0400272101

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Proceedings of the National Academy of Sciences of the United States of America

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Acute myeloid leukemia with co ...... n of APP, ETS2, and ERG genes.

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Amy S Ruppert

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Claudia D Baldus

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Herbert Auer

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Martin Guimond

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Michael A Caligiuri

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Nehad Mohamed

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Ramana V Davuluri

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Sandya Liyanarachchi

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Stephan M Tanner

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P2860

Model-based analysis of oligonucleotide arrays: expression index computation and outlier detection

The DNA sequence of human chromosome 21

Pretreatment cytogenetic abnormalities are predictive of induction success, cumulative incidence of relapse, and overall survival in adult patients with de novo acute myeloid leukemia: results from Cancer and Leukemia Group B (CALGB 8461)

An RNA-binding protein gene, TLS/FUS, is fused to ERG in human myeloid leukemia with t(16;21) chromosomal translocation

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.

The role of chromosome translocations in leukemogenesis.

Assembly of microarrays for genome-wide measurement of DNA copy number.

Regulation of amyloid precursor protein expression and secretion via activation of ERK1/2 by hepatocyte growth factor in HEK293 cells transfected with APP751.

The biological role of the Alzheimer amyloid precursor protein in epithelial cells.

New mechanisms of AML1 gene alteration in hematological malignancies.

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10.1073/PNAS.0400272101

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11

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101

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Sandya Liyanarachchi

Clara D. Bloomfield

Albert de la Chapelle

Krzysztof Mrózek

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2004-03-08T00:00:00Z

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