Localization of common deletion regions on 1p and 19q in human gliomas and their association with histological subtype.
about
Multiplex ligation-dependent probe amplification: a diagnostic tool for simultaneous identification of different genetic markers in glial tumorsAttenuated expression of DFFB is a hallmark of oligodendrogliomas with 1p-allelic loss.Associations between polymorphisms in DNA repair genes and glioblastomaRegulation of the MDM2-P53 pathway and tumor growth by PICT1 via nucleolar RPL11.PICT-1 is a key nucleolar sensor in DNA damage response signaling that regulates apoptosis through the RPL11-MDM2-p53 pathwayBrain tumor epidemiology: consensus from the Brain Tumor Epidemiology Consortium.Delineating the cytogenomic and epigenomic landscapes of glioma stem cell linesPredictive and prognostic markers in neuro-oncology.NOTCH2 is neither rearranged nor mutated in t(1;19) positive oligodendrogliomas.Simultaneous analysis of distinct Omics data sets with integration of biological knowledge: Multiple Factor Analysis approachTumor-associated methylation of the putative tumor suppressor AJAP1 gene and association between decreased AJAP1 expression and shorter survival in patients with glioma.hHSS1: a novel secreted factor and suppressor of glioma growth located at chromosome 19q13.33.Multidimensional scaling of diffuse gliomas: application to the 2016 World Health Organization classification system with prognostically relevant molecular subtype discovery.IIp45, an insulin-like growth factor binding protein 2 (IGFBP-2) binding protein, antagonizes IGFBP-2 stimulation of glioma cell invasion.ImmunoFISH is a reliable technique for the assessment of 1p and 19q status in oligodendrogliomasThe pathobiology of glioma tumorsRecruited cells can become transformed and overtake PDGF-induced murine gliomas in vivo during tumor progressionA novel member of the WD-repeat gene family, WDR11, maps to the 10q26 region and is disrupted by a chromosome translocation in human glioblastoma cells.Isolation of the TSLL1 and TSLL2 genes, members of the tumor suppressor TSLC1 gene family encoding transmembrane proteins.Losses of chromosomal arms 1p and 19q in the diagnosis of oligodendroglioma. A study of paraffin-embedded sections.Chromogenic in situ hybridization is a reliable alternative to fluorescence in situ hybridization for diagnostic testing of 1p and 19q loss in paraffin-embedded gliomas.Histopathological-molecular genetic correlations in referral pathologist-diagnosed low-grade "oligodendroglioma".EMP3 overexpression is associated with oligodendroglial tumors retaining chromosome arms 1p and 19q.OLIG-1 and 2 gene expression and oligodendroglial tumours.Molecular pathology in adult gliomas: diagnostic, prognostic, and predictive markersOligodendroglioma: toward molecular definitions in diagnostic neuro-oncology.Molecular profile of oligodendrogliomas in young patientsSubtypes of oligodendroglioma defined by 1p,19q deletions, differ in the proportion of apoptotic cells but not in replication-licensed non-proliferating cells.The importance of 10q status in an outcomes-based comparison between 1p/19q fluorescence in situ hybridization and polymerase chain reaction-based microsatellite loss of heterozygosity analysis of oligodendrogliomas.Prognostic significance of multiple kallikreins in high-grade astrocytoma.Global analysis of H3K4me3 and H3K27me3 profiles in glioblastoma stem cells and identification of SLC17A7 as a bivalent tumor suppressor gene.PTEN is a target of chromosome 10q loss in anaplastic oligodendrogliomas and PTEN alterations are associated with poor prognosisGenetic signature of oligoastrocytomas correlates with tumor location and denotes distinct molecular subsetsDetection of 1p19q deletion by real-time comparative quantitative PCR.Molecular diagnosis of metastasizing oligodendroglioma: a case report.Glioma test array for use with formalin-fixed, paraffin-embedded tissue: array comparative genomic hybridization correlates with loss of heterozygosity and fluorescence in situ hybridization.Molecular pathogenesis of pediatric astrocytic tumors.Detection of 1p and 19q loss in oligodendroglioma by quantitative microsatellite analysis, a real-time quantitative polymerase chain reaction assay.Epigenome scans and cancer genome sequencing converge on WNK2, a kinase-independent suppressor of cell growth.Tissue microdissection and degenerate oligonucleotide primed-polymerase chain reaction (DOP-PCR) is an effective method to analyze genetic aberrations in invasive tumors
P2860
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P2860
Localization of common deletion regions on 1p and 19q in human gliomas and their association with histological subtype.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh
1999年學術文章
@zh-hant
name
Localization of common deletio ...... ion with histological subtype.
@en
Localization of common deletio ...... ion with histological subtype.
@nl
type
label
Localization of common deletio ...... ion with histological subtype.
@en
Localization of common deletio ...... ion with histological subtype.
@nl
prefLabel
Localization of common deletio ...... ion with histological subtype.
@en
Localization of common deletio ...... ion with histological subtype.
@nl
P2093
P2860
P356
P1433
P1476
Localization of common deletio ...... ion with histological subtype.
@en
P2093
Alderete B
Feuerstein BG
Jenkins RB
Mohapatra G
O'Fallon J
P2860
P2888
P304
P356
10.1038/SJ.ONC.1202759
P407
P50
P577
1999-07-01T00:00:00Z