Pathogenesis and consequences of uniparental disomy in cancer.
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Defects in spliceosomal machinery: a new pathway of leukaemogenesisMutant allele-specific imbalance modulates prognostic impact of KRAS mutations in colorectal adenocarcinoma and is associated with worse overall survivalCopy number alteration and uniparental disomy analysis categorizes Japanese papillary thyroid carcinomas into distinct groups.SNP array analysis reveals novel genomic abnormalities including copy neutral loss of heterozygosity in anaplastic oligodendrogliomas.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.Copy-neutral loss of heterozygosity and chromosome gains and losses are frequent in gastrointestinal stromal tumors.Acquisition of meiotic DNA repair regulators maintain genome stability in glioblastoma.Copy number of the Adenomatous Polyposis Coli gene is not always neutral in sporadic colorectal cancers with loss of heterozygosity for the geneCD45-deficient severe combined immunodeficiency caused by uniparental disomy.Patterns of somatic uniparental disomy identify novel tumor suppressor genes in colorectal cancer.The Molecular Karyotype of 25 Clinical-Grade Human Embryonic Stem Cell Lines.β Thalassemia major due to acquired uniparental disomy in a previously healthy adolescent.Functional genomic analysis of chromosomal aberrations in a compendium of 8000 cancer genomes.The genetic tumor background is an important determinant for heterogeneous MYCN-amplified neuroblastoma.Genetic-pathologic characterization of myeloproliferative neoplasms.Unexpected frequency of genomic alterations in histologically normal colonic tissue from colon cancer patients.The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesis.Homology-directed repair of DNA nicks via pathways distinct from canonical double-strand break repair.Whole genome profiling and other high throughput technologies in lymphoid neoplasms--current contributions and future hopes.Back to biology: new insights on inheritance in myeloproliferative disorders.Different characteristics identified by single nucleotide polymorphism array analysis in leukemia suggest the need for different application strategies depending on disease category.A genome-wide single-nucleotide polymorphism-array can improve the prognostic stratification of the core binding factor acute myeloid leukemia.Acquired uniparental disomy of chromosome 9p in hematologic malignancies.Genome-wide acquired uniparental disomy as well as chromosomal gains and losses in an uterine epithelioid leiomyoma.Pediatric T-cell acute lymphoblastic leukemia.Additional genomic aberrations identified by single nucleotide polymorphism array-based karyotyping in an acute myeloid leukemia case with isolated del(20q) abnormalityRing chromosome 5 in acute myeloid leukemia defined by whole-genome single nucleotide polymorphism array.Metaphase cytogenetics and single nucleotide polymorphism arrays in myeloid malignancies.Single nucleotide polymorphisms of mucosa-associated lymphoid tissue 1 in oral carcinoma cells and gingival fibroblasts.From cryptic chromosomal lesions to pathologically relevant genes: integration of SNP-array with gene expression profiling in myelodysplastic syndrome with normal karyotype.Single nucleotide polymorphism array-based karyotyping in acute myeloid leukemia or myelodysplastic syndrome with trisomy 8 as the sole chromosomal abnormality.Mutant allele specific imbalance in oncogenes with copy number alterations: Occurrence, mechanisms, and potential clinical implications.The 11q-Gain/Loss Aberration Occurs Recurrently in MYC-Negative Burkitt-like Lymphoma With 11q Aberration, as Well as MYC-Positive Burkitt Lymphoma and MYC-Positive High-Grade B-Cell Lymphoma, NOS.Genetic and molecular characterization of myelodysplastic syndromes and related myeloid neoplasms.Characterizing Genetic Transitions of Copy Number Alterations and Allelic Imbalances in Oral Tongue Carcinoma Metastasis.Genomic aberrations of myeloproliferative and myelodysplastic/myeloproliferative neoplasms in chronic phase and during disease progression.Positive Caricature Transcriptomic Effects Associated with Broad Genomic Aberrations in Colorectal CancerGermlineCBLmutation associated with a noonan-like syndrome with primary lymphedema and teratoma associated with acquired uniparental isodisomy of chromosome 11q23
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Pathogenesis and consequences of uniparental disomy in cancer.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 25 April 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Pathogenesis and consequences of uniparental disomy in cancer.
@en
Pathogenesis and consequences of uniparental disomy in cancer.
@nl
type
label
Pathogenesis and consequences of uniparental disomy in cancer.
@en
Pathogenesis and consequences of uniparental disomy in cancer.
@nl
prefLabel
Pathogenesis and consequences of uniparental disomy in cancer.
@en
Pathogenesis and consequences of uniparental disomy in cancer.
@nl
P2860
P1476
Pathogenesis and consequences of uniparental disomy in cancer.
@en
P2093
Hideki Makishima
Jaroslaw P Maciejewski
P2860
P304
P356
10.1158/1078-0432.CCR-10-2900
P407
P577
2011-04-25T00:00:00Z