Recurrent chromosomal imbalances and structurally abnormal breakpoints within complex karyotypes of malignant peripheral nerve sheath tumour and malignant triton tumour: a cytogenetic and molecular cytogenetic study.
about
Intracranial malignant triton tumor in a patient with neurofibromatosis type 1: case report and review of the literature.An imprinted locus epistatically influences Nstr1 and Nstr2 to control resistance to nerve sheath tumors in a neurofibromatosis type 1 mouse model.The microenvironment-specific transformation of adult stem cells models malignant triton tumors.DNA copy number changes in high-grade malignant peripheral nerve sheath tumors by array CGH.Frequent EGFR Positivity and Overexpression in High-Grade Areas of Human MPNSTsCancer karyotypes: survival of the fittestSurvival in Malignant Peripheral Nerve Sheath Tumours: A Comparison between Sporadic and Neurofibromatosis Type 1-Associated Tumours.EGFR and erbB2 in malignant peripheral nerve sheath tumors and implications for targeted therapy.Whole-exome sequencing of breast cancer, malignant peripheral nerve sheath tumor and neurofibroma from a patient with neurofibromatosis type 1.Cytogenetic aberrations in soft tissue tumors harvested from fresh tissue submitted for surgical pathology: a single institutional experience.Molecular classification of soft tissue sarcomas and its clinical applicationsNeurogenic tumors of soft tissue.Secondary aneurysmal bone cyst following chondroblastoma of the patella.Microarray-based copy number analysis of neurofibromatosis type-1 (NF1)-associated malignant peripheral nerve sheath tumors reveals a role for Rho-GTPase pathway genes in NF1 tumorigenesis.Evaluation of copy number variation and gene expression in neurofibromatosis type-1-associated malignant peripheral nerve sheath tumours.Identification of candidate genes for devil facial tumour disease tumourigenesis.Malignant triton tumors--complete surgical resection and adjuvant radiotherapy associated with improved survival.Expression profiling of 519 kinase genes in matched malignant peripheral nerve sheath tumor/plexiform neurofibroma samples is discriminatory and identifies mitotic regulators BUB1B, PBK and NEK2 as overexpressed with transformation.Clinico-genetic aspects of a pediatric non-neurofibromatosis type 1 malignant triton tumor with loss of chromosome X.
P2860
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P2860
Recurrent chromosomal imbalances and structurally abnormal breakpoints within complex karyotypes of malignant peripheral nerve sheath tumour and malignant triton tumour: a cytogenetic and molecular cytogenetic study.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Recurrent chromosomal imbalanc ...... d molecular cytogenetic study.
@ast
Recurrent chromosomal imbalanc ...... d molecular cytogenetic study.
@en
type
label
Recurrent chromosomal imbalanc ...... d molecular cytogenetic study.
@ast
Recurrent chromosomal imbalanc ...... d molecular cytogenetic study.
@en
prefLabel
Recurrent chromosomal imbalanc ...... d molecular cytogenetic study.
@ast
Recurrent chromosomal imbalanc ...... d molecular cytogenetic study.
@en
P2093
P2860
P356
P1476
Recurrent chromosomal imbalanc ...... nd molecular cytogenetic study
@en
P2093
P2860
P304
P356
10.1136/JCP.2004.019026
P407
P577
2004-11-01T00:00:00Z