about
The SCFbeta-TRCP-ubiquitin ligase complex associates specifically with phosphorylated destruction motifs in IkappaBalpha and beta-catenin and stimulates IkappaBalpha ubiquitination in vitroMxi1 inhibits the proliferation of U87 glioma cells through down-regulation of cyclin B1 gene expressionExpression of MXI1, a Myc antagonist, is regulated by Sp1 and AP2Antioncogenes and human cancer.Non-isotopic molecular cytogenetics in neuro-oncology.Alterations of BCCIP, a BRCA2 interacting protein, in astrocytomasMiR-146b-5p suppresses EGFR expression and reduces in vitro migration and invasion of glioma.Differential expression of two fibroblast growth factor-receptor genes is associated with malignant progression in human astrocytomas.Genetic alterations associated with adult diffuse astrocytic tumors.Modeling prognosis for patients with malignant astrocytic gliomas: quantifying the expression of multiple genetic markers and clinical variablesAllele loss on chromosomes 10 and 17p and epidermal growth factor receptor gene amplification in human malignant astrocytoma related to prognosis.Somatic mutation of PTEN in bladder carcinomaDeletion mapping of gliomas suggest the presence of two small regions for candidate tumor-suppressor genes in a 17-cM interval on chromosome 10q.Cancer stem cells as mediators of treatment resistance in brain tumors: status and controversies.PTEN in brain tumors.Roles of BCCIP in chromosome stability and cytokinesis.Exosomes as Tools to Suppress Primary Brain Tumor.Accumulation of allelic losses on chromosome 10 in human gliomas at recurrence.A molecular genetic model of astrocytoma histopathology.Exosomes from marrow stromal cells expressing miR-146b inhibit glioma growth.Establishment of spontaneously immortalized rat type 1 astroglial cell lines: the role of p53 in astroglial carcinogenesis.Loss of chromosome 10 in glioblastoma: relation to proliferation and angiogenesis.A genotype of the polymorphic DNA repair gene MGMT is associated with de novo glioblastoma.Mutational analysis of the PTEN gene in gliomas: molecular and pathological correlations.Astroblastoma: report of a case with ultrastructural, cell kinetic, and cytogenetic analysis.Functional and molecular analyses of 10q deletions in human gliomas.Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome.Deletion mapping of chromosome 10 in human glioma.Distinct patterns of deletion on 10p and 10q suggest involvement of multiple tumor suppressor genes in the development of astrocytic gliomas of different malignancy grades.
P2860
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P2860
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年学术文章
@wuu
1992年学术文章
@zh
1992年学术文章
@zh-cn
1992年学术文章
@zh-hans
1992年学术文章
@zh-my
1992年学术文章
@zh-sg
1992年學術文章
@yue
1992年學術文章
@zh-hant
name
Loss of heterozygosity for 10q loci in human gliomas.
@en
Loss of heterozygosity for 10q loci in human gliomas.
@nl
type
label
Loss of heterozygosity for 10q loci in human gliomas.
@en
Loss of heterozygosity for 10q loci in human gliomas.
@nl
prefLabel
Loss of heterozygosity for 10q loci in human gliomas.
@en
Loss of heterozygosity for 10q loci in human gliomas.
@nl
P2093
P356
P1476
Loss of heterozygosity for 10q loci in human gliomas.
@en
P2093
Friedman AH
Rasheed BK
P356
10.1002/GCC.2870050111
P577
1992-07-01T00:00:00Z