about
Organization and chromosomal localization of the human platelet-derived endothelial cell growth factor gene.Brain tumors: Special characters for research and bankingA noncoding RNA gene on chromosome 10p15.3 may function upstream of hTERT.Neuronal aneuploidy in health and disease: a cytomic approach to understand the molecular individuality of neurons.Chromosome arm 6q loss is the most common recurrent autosomal alteration detected in primary pediatric ependymoma.Endocrine aspects of the diagnosis and treatment of primary brain tumours.Increased expression of the immune modulatory molecule PD-L1 (CD274) in anaplastic meningiomaGenetic profile of gliosarcomasPatterns of epidermal growth factor receptor amplification in malignant gliomasComparative genomic hybridization analysis of astrocytomas: prognostic and diagnostic implications.MTS1/p16/CDKN2 lesions in primary glioblastoma multiforme.Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1pComparative genomic hybridization of human malignant gliomas reveals multiple amplification sites and nonrandom chromosomal gains and lossesPurine and pyrimidine metabolism in human gliomas: relation to chromosomal aberrations.High glycolysis in gliomas despite low hexokinase transcription and activity correlated to chromosome 10 lossComparative genomic hybridization detects many recurrent imbalances in central nervous system primitive neuroectodermal tumours in children.hTR repressor-related gene on human chromosome 10p15.1.Molecular structure of double-minute chromosomes bearing amplified copies of the epidermal growth factor receptor gene in gliomas.Cell cycle activation and aneuploid neurons in Alzheimer's disease.Somatic structural variation and cancer.Microsatellite analysis of loss of heterozygosity on chromosomes 9q, 11p and 17p in medulloblastomas.Investigation of genetic alterations associated with the grade of astrocytic tumor by comparative genomic hybridization.Loss of chromosome 10 is an independent prognostic factor in high-grade gliomas.Extrachromosomal driver mutations in glioblastoma and low-grade glioma.Double minute amplification of mutant PDGF receptor α in a mouse glioma model.Double minute chromosomes in glioblastoma multiforme are revealed by precise reconstruction of oncogenic amplicons.Analysis of the Max-binding protein MNT in human medulloblastomas.Astroblastoma: report of a case with ultrastructural, cell kinetic, and cytogenetic analysis.Intracranial ependymomas: a review.High-throughput molecular profiling of high-grade astrocytomas: the utility of fluorescence in situ hybridization on tissue microarrays (TMA-FISH).Numerical aberrations of chromosomes 1, 2, and 7 in astrocytomas studied by interphase cytogenetics.Molecular genetic alterations on chromosomes 11 and 22 in ependymomas.Early proliferation enhancement by monosomy 10 and intratumor heterogeneity in malignant human gliomas as revealed by smear preparations from biopsies.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Cytogenetics of human brain tumors.
@en
Cytogenetics of human brain tumors.
@nl
type
label
Cytogenetics of human brain tumors.
@en
Cytogenetics of human brain tumors.
@nl
prefLabel
Cytogenetics of human brain tumors.
@en
Cytogenetics of human brain tumors.
@nl
P1476
Cytogenetics of human brain tumors.
@en
P2093
P304
P356
10.1016/0165-4608(90)90024-5
P577
1990-07-01T00:00:00Z