A (CA)n dinucleotide repeat assay for evaluating loss of allelic heterozygosity in small and archival human brain tumor specimens.
about
Molecular genetic analysis of ependymal tumors. NF2 mutations and chromosome 22q loss occur preferentially in intramedullary spinal ependymomasAnalysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma.Survey of somatic mutations in tuberous sclerosis complex (TSC) hamartomas suggests different genetic mechanisms for pathogenesis of TSC lesionsHuman keratinocytes that express hTERT and also bypass a p16(INK4a)-enforced mechanism that limits life span become immortal yet retain normal growth and differentiation characteristicsPatients with high-grade gliomas harboring deletions of chromosomes 9p and 10q benefit from temozolomide treatment.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 subsetsMalignant transformation of neurofibromas in neurofibromatosis 1 is associated with CDKN2A/p16 inactivationGlioma test array for use with formalin-fixed, paraffin-embedded tissue: array comparative genomic hybridization correlates with loss of heterozygosity and fluorescence in situ hybridization.NF2 gene analysis distinguishes hemangiopericytoma from meningioma.DNA aberrations in the epithelial cell component of adamantinoma of long bones.Loss of heterozygosity studies revisited: prior quantification of the amplifiable DNA content of archival samples improves efficiency and reliabilityPCR-based microsatellite polymorphisms in the detection of loss of heterozygosity in fresh and archival tumour tissue.Clonal analysis in recurrent astrocytic, oligoastrocytic and oligodendroglial tumors implicates IDH1- mutation as common tumor initiating event.Chromosome 5 allelic losses are early events in tumours of the papilla of Vater and occur at sites similar to those of gastric cancerLoss of heterozygosity at the mannose 6-phosphate insulin-like growth factor 2 receptor gene correlates with poor differentiation in early breast carcinomas.Rapid detection of allele loss in colorectal tumours using microsatellites and fluorescent DNA technology.Expression of mitogen-activated protein kinase phosphatase-1 in the early phases of human epithelial carcinogenesisMultiple polymorphisms, but no mutations, in the WAF1/CIP1 gene in human brain tumours.7q31-32 allelic loss is a frequent finding in splenic marginal zone lymphoma
P2860
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P2860
A (CA)n dinucleotide repeat assay for evaluating loss of allelic heterozygosity in small and archival human brain tumor specimens.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
A (CA)n dinucleotide repeat as ...... l human brain tumor specimens.
@en
type
label
A (CA)n dinucleotide repeat as ...... l human brain tumor specimens.
@en
prefLabel
A (CA)n dinucleotide repeat as ...... l human brain tumor specimens.
@en
P2860
P1476
A (CA)n dinucleotide repeat as ...... al human brain tumor specimens
@en
P2093
B R Seizinger
P2860
P304
P407
P577
1992-10-01T00:00:00Z