About: Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias

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About: Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias Goto Sponge NotDistinct Permalink

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scientific article published on 01 October 2005

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2005 (fr) наукова стаття, опублікована в жовтні 2005 (uk) artículu científicu espublizáu n'ochobre de 2005 (ast) scientific article published on 01 October 2005 (en)
publication date	wds:Q81362541-A5EEA91E-2D9C-4898-B5C7-8DAC460B28AB
publication date	2005-10-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q81362541-074D43B9-66D6-42EF-94BB-F322E94BD232 wds:Q81362541-080D76E0-B4E4-44E7-9F35-342012CA0B11 wds:Q81362541-1EC46685-A4CD-4B6A-AAB1-67C722400E85 wds:Q81362541-5C02911D-6FF2-44E9-A862-63F965ED59BA wds:Q81362541-9F0FDBBA-0F6A-43F5-A0D0-5A0BE9319B3D wds:Q81362541-C52C54E7-FB4E-402A-85FB-D9D1A9257063 wds:Q81362541-D2B6D87E-3FAB-46F6-8C99-D616827A96C7 wds:Q81362541-F9C48CAB-5E9D-4CA0-985B-10B857E12051
author name string	Bryan D Young Jude Fitzgibbon T Andrew Lister Debra Lillington Lan-Lan Smith Matthew L Smith Silvana Debernardi Spyros Skoulakis
rdfs:label	Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias (en) Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias (nl)
skos:prefLabel	Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias (en) Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias (nl)
name	Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias (en) Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias (nl)
author	wds:Q81362541-34930733-395A-4EDD-96E5-89030DD05B64
author	Manoj Raghavan
title	wds:Q81362541-7BE3A202-A51E-4D51-A582-14E261D5C6A1
title	Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias (en)
page(s)	wds:Q81362541-89F662A4-8F1F-401C-A98B-89F71DDC22D5
page(s)	9152-9154
instance of	wds:Q81362541-8CD34071-44A6-48F7-8D53-A503D595A67B
instance of	scholarly article
main subject	wds:Q81362541-FA23FEE2-3AEB-4A6B-9725-748F6DC8D80D
main subject	homozygosity
PubMed ID	wds:Q81362541-4C672D46-68CE-4D9F-9CFC-AF98F5926A29
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16230371
PubMed ID	16230371
published in	wds:Q81362541-4396D562-EC09-4AC9-8455-1B8F3EDB9E9F
published in	Cancer Research
issue	wds:Q81362541-4015AD7C-247E-4D22-8FB5-F6F3F8CA815A
volume	wds:Q81362541-CE919241-E6D2-4422-9922-83CCB50DEF9E
issue	20
volume	65
DOI	wds:Q81362541-5721E84C-6617-4CAE-8459-348BF8B70146
DOI	http://dx.doi.org/10.1158/0008-5472.CAN-05-2017
DOI	10.1158/0008-5472.CAN-05-2017
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q81362541
is cites work of	High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping Oncogene mutations, copy number gains and mutant allele specific imbalance (MASI) frequently occur together in tumor cells Chromosomal abnormalities and novel disease-related regions in progression from Barrett's esophagus to esophageal adenocarcinoma Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays 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? Large-scale evaluation of candidate genes identifies associations between DNA repair and genomic maintenance and development of benzene hematotoxicity Dysregulation of the C/EBPalpha differentiation pathway in human cancer Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies The application of single nucleotide polymorphism microarrays in cancer research Partial uniparental disomy: a recurrent genetic mechanism alternative to chromosomal deletion in malignant lymphoma Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia Genome-wide detection of recurring sites of uniparental disomy in follicular and transformed follicular lymphoma Structural and functional alterations of FLT3 in acute myeloid leukemia Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML Acquired copy number alterations in adult acute myeloid leukemia genomes Novel regions of acquired uniparental disomy discovered in acute myeloid leukemia Association between polymorphisms in RMI1, TOP3A, and BLM and risk of cancer, a case-control study Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms Interchromosomal crossover in human cells is associated with long gene conversion tracts Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis JAK2 V617F in myeloid disorders: molecular diagnostic techniques and their clinical utility: a paper from the 2005 William Beaumont Hospital Symposium on Molecular Pathology High hyperdiploid childhood acute lymphoblastic leukemia Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype Genetic complexity of myeloproliferative neoplasms. High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies Acquired genomic copy number aberrations and survival in adult acute myelogenous leukemia High-resolution genomic profiling of adult and pediatric core-binding factor acute myeloid leukemia reveals new recurrent genomic alterations Hidden abnormalities and novel classification of t(15;17) acute promyelocytic leukemia (APL) based on genomic alterations New lesions detected by single nucleotide polymorphism array-based chromosomal analysis have important clinical impact in acute myeloid leukemia Accurate detection of uniparental disomy and microdeletions by SNP array analysis in myelodysplastic syndromes with normal cytogenetics Pathogenesis and consequences of uniparental disomy in cancer Overexpression of wild-type or mutants forms of CEBPA alter normal human hematopoiesis. A decade of genome-wide gene expression profiling in acute myeloid leukemia: flashback and prospects Broad copy neutral-loss of heterozygosity regions and rare recurring copy number abnormalities in normal karyotype-acute myeloid leukemia genomes. Genome-wide DNA copy number analysis in pancreatic cancer using high-density single nucleotide polymorphism arrays Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies Two cell lines of t(8;21) acute myeloid leukemia with activating KIT exon 17 mutation: models for the 'second hit' hypothesis Molecular landscape of acute myeloid leukemia in younger adults and its clinical relevance Cooperating gene mutations in acute myeloid leukemia: a review of the literature. 250K single nucleotide polymorphism array karyotyping identifies acquired uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies Prevalence of copy-number neutral LOH in glioblastomas revealed by genomewide analysis of laser-microdissected tissues Association between acquired uniparental disomy and homozygous mutations and HER2/ER/PR status in breast cancer Uniparentalism in sporadic colorectal cancer is independent of imprint status, and coordinate for chromosomes 14 and 18. Genetic and molecular pathogenesis of mantle cell lymphoma: perspectives for new targeted therapeutics Genome wide analysis of DNA copy number neutral loss of heterozygosity (CNNLOH) and its relation to gene expression in esophageal squamous cell carcinoma Loss of the wild-type allele contributes to myeloid expansion and disease aggressiveness in FLT3/ITD knockin mice

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