Nf1 mutation expands an EGFR-dependent peripheral nerve progenitor that confers neurofibroma tumorigenic potential.
about
A RASopathy gene commonly mutated in cancer: the neurofibromatosis type 1 tumour suppressorNeuroblastoma cell lines contain pluripotent tumor initiating cells that are susceptible to a targeted oncolytic virusCancer stem cell-like cells derived from malignant peripheral nerve sheath tumors.MAF mediates crosstalk between Ras-MAPK and mTOR signaling in NF1.Cancer stem cells: a stride towards cancer cure?In vivo regulation of TGF-β by R-Ras2 revealed through loss of the RasGAP protein NF1.Cells of origin in the embryonic nerve roots for NF1-associated plexiform neurofibromaSerum biomarkers for neurofibromatosis type 1 and early detection of malignant peripheral nerve-sheath tumors.Neurofibromin deficiency-associated transcriptional dysregulation suggests a novel therapy for tibial pseudoarthrosis in NF1.Integrative genomic analyses of neurofibromatosis tumours identify SOX9 as a biomarker and survival geneRunx1 contributes to neurofibromatosis type 1 neurofibroma formation.Transgenic mice overexpressing neuregulin-1 model neurofibroma-malignant peripheral nerve sheath tumor progression and implicate specific chromosomal copy number variations in tumorigenesisInsertional Mutagenesis Identifies a STAT3/Arid1b/β-catenin Pathway Driving Neurofibroma Initiation.Transient brown adipocyte-like cells derive from peripheral nerve progenitors in response to bone morphogenetic protein 2.The protein kinase A regulatory subunit R1A (Prkar1a) plays critical roles in peripheral nerve development.Ossifying fibroma tumor stem cells are maintained by epigenetic regulation of a TSP1/TGF-β/SMAD3 autocrine loop.Genomic amplification and high expression of EGFR are key targetable oncogenic events in malignant peripheral nerve sheath tumor.An inflammatory gene signature distinguishes neurofibroma Schwann cells and macrophages from cells in the normal peripheral nervous systemRac1 controls Schwann cell myelination through cAMP and NF2/merlin.EGFR-Stat3 signalling in nerve glial cells modifies neurofibroma initiation.The role of stem cells in benign tumors.Back to the future: proceedings from the 2010 NF Conference.What's new in neurofibromatosis? Proceedings from the 2009 NF Conference: new frontiers
P2860
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P2860
Nf1 mutation expands an EGFR-dependent peripheral nerve progenitor that confers neurofibroma tumorigenic potential.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Nf1 mutation expands an EGFR-d ...... fibroma tumorigenic potential.
@ast
Nf1 mutation expands an EGFR-d ...... fibroma tumorigenic potential.
@en
type
label
Nf1 mutation expands an EGFR-d ...... fibroma tumorigenic potential.
@ast
Nf1 mutation expands an EGFR-d ...... fibroma tumorigenic potential.
@en
prefLabel
Nf1 mutation expands an EGFR-d ...... fibroma tumorigenic potential.
@ast
Nf1 mutation expands an EGFR-d ...... fibroma tumorigenic potential.
@en
P2093
P2860
P1433
P1476
Nf1 mutation expands an EGFR-d ...... ofibroma tumorigenic potential
@en
P2093
Gunnar Johansson
Hartmut Geiger
Jianqiang Wu
Jon P Williams
Jose A Cancelas
Nancy Ratner
Punam Malik
Shyra C Miller
Tilat A Rizvi
Wenling Li
P2860
P304
P356
10.1016/J.STEM.2008.10.003
P407
P577
2008-12-01T00:00:00Z