Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies - Wikidata - awgldk - TriplyDB

Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

http://www.wikidata.org/entity/Q33788643

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SNPs Array Karyotyping in Non-Hodgkin Lymphoma Detectable clonal mosaicism from birth to old age and its relationship to cancer Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency.Array CGH in human leukemia: from somatics to genetics.Copy-neutral loss of heterozygosity is prevalent and a late event in the pathogenesis of FLT3/ITD AML Genome wide analysis of DNA copy number neutral loss of heterozygosity (CNNLOH) and its relation to gene expression in esophageal squamous cell carcinoma Single-nucleotide polymorphism array-based karyotyping of acute promyelocytic leukemia.Translocation (8;21) acute myeloid leukemia presenting as severe aplastic anemia.Loss of wild-type Jak2 allele enhances myeloid cell expansion and accelerates myelofibrosis in Jak2V617F knock-in mice Mitotic recombination in patients with ichthyosis causes reversion of dominant mutations in KRT10 The Biology and Targeting of FLT3 in Pediatric Leukemia.Copy number alteration and uniparental disomy analysis categorizes Japanese papillary thyroid carcinomas into distinct groups.Genome-wide single nucleotide polymorphism array analysis reveals recurrent genomic alterations associated with histopathologic features in intrahepatic cholangiocarcinoma.Germline DNA copy number aberrations identified as potential prognostic factors for breast cancer recurrence.Genome-wide analysis of recurrent copy-number alterations and copy-neutral loss of heterozygosity in head and neck squamous cell carcinoma.Parent-specific copy number in paired tumor-normal studies using circular binary segmentation Cross-laboratory validation of the OncoScan® FFPE Assay, a multiplex tool for whole genome tumour profiling.Temporal dissection of tumorigenesis in primary cancers Rapid high-resolution mapping of balanced chromosomal rearrangements on tiling CGH arrays.Loss of the wild-type allele contributes to myeloid expansion and disease aggressiveness in FLT3/ITD knockin mice.Double inv(3)(q21q26.2) in acute myeloid leukemia is resulted from an acquired copy neutral loss of heterozygosity of chromosome 3q and associated with disease progression.Generation of KCL040 clinical grade human embryonic stem cell line.Patterns of somatic uniparental disomy identify novel tumor suppressor genes in colorectal cancer.Genomic array as compared to karyotyping in myelodysplastic syndromes in a prospective clinical trial.The Molecular Karyotype of 25 Clinical-Grade Human Embryonic Stem Cell Lines.Epigenetic modification of the repair donor regulates targeted gene correction.Acquired copy-neutral loss of heterozygosity of chromosome 1p as a molecular event associated with marrow fibrosis in MPL-mutated myeloproliferative neoplasms Development and validation of a comprehensive genomic diagnostic tool for myeloid malignancies.Genetic-pathologic characterization of myeloproliferative neoplasms.Germline large genomic alterations on 7q in patients with multiple primary cancers.Detection of copy number alterations in acute myeloid leukemia and myelodysplastic syndromes.Targeted gene therapies: tools, applications, optimization Molecular diagnosis of leukemia.Cancer cytogenetics: methodology revisited.Single-nucleotide polymorphism-array improves detection rate of genomic alterations in core-binding factor leukemia.Different characteristics identified by single nucleotide polymorphism array analysis in leukemia suggest the need for different application strategies depending on disease category.Immunophenotypic, cytogenetic, and mutational characterization of cell lines derived from myelodysplastic syndrome patients after progression to acute myeloid leukemia.The role of CDKN2A/B deletions in pediatric acute lymphoblastic leukemia.Combination of Complement-Dependent Cytotoxicity and Relative Fluorescent Quantification of HLA Length Polymorphisms Facilitates the Detection of a Loss of Heterozygosity Chromosome 17p Homodisomy Is Associated With Better Outcome in 1p19q Non-Codeleted and IDH-Mutated Gliomas.

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P2860

Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

http://www.wikidata.org/entity/Q33788643

description

2010 nî lūn-bûn

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2010 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունվարին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

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Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

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Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

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Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

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Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

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Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

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Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

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Christine O'Keefe

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Jaroslaw P Maciejewski

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Michael A McDevitt

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P2860

Long homozygous chromosomal segments in reference families from the centre d'Etude du polymorphisme humain

Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers

Runs of homozygosity in European populations

Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML

Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays

Mechanisms leading to uniparental disomy and their clinical consequences

Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia

A gain-of-function mutation of JAK2 in myeloproliferative disorders

Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics.

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