Neurofibromatosis type 1 - a model for nervous system tumour formation?
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Treating brain tumors with PDE4 inhibitorsNf1+/- mast cells induce neurofibroma like phenotypes through secreted TGF-beta signalingAbrogating drug resistance in malignant peripheral nerve sheath tumors by disrupting hyaluronan-CD44 interactions with small hyaluronan oligosaccharides.Identification of novel therapeutic targets in the PI3K/AKT/mTOR pathway in hepatocellular carcinoma using targeted next generation sequencing.Cells of origin in the embryonic nerve roots for NF1-associated plexiform neurofibromaThe cyclic AMP pathway is a sex-specific modifier of glioma risk in type I neurofibromatosis patients.Tumorigenic cells are common in mouse MPNSTs but their frequency depends upon tumor genotype and assay conditions.Targeting brain tumor cAMP: the case for sex-specific therapeutics3-D imaging mass spectrometry of protein distributions in mouse Neurofibromatosis 1 (NF1)-associated optic glioma.Modelling oncogenic Ras/Raf signalling in the mouse.Hijacking the ERK signaling pathway: Mycobacterium leprae shuns MEK to drive the proliferation of infected Schwann cells.CXCR4/CXCL12 mediate autocrine cell- cycle progression in NF1-associated malignant peripheral nerve sheath tumors.The loss of Nf1 transiently promotes self-renewal but not tumorigenesis by neural crest stem cells.Intersections at the crossroads: Neurofibromatosis type 1, cAMP, sex, and glioma risk.NF1 loss disrupts Schwann cell-axonal interactions: a novel role for semaphorin 4F.Chemokine signaling in cancer: one hump or two?Microarray analyses reveal regional astrocyte heterogeneity with implications for neurofibromatosis type 1 (NF1)-regulated glial proliferation.Inactivation of NF1 in CNS causes increased glial progenitor proliferation and optic glioma formation.Monitoring of plexiform neurofibroma in children and adolescents with neurofibromatosis type 1 by [(18) F]FDG-PET imaging. Is it of value in asymptomatic patients?Cancer of the Peripheral Nerve in Neurofibromatosis Type 1.Isolated Neurofibroma of the Sigmoid Colon: a Case Report and Review of the Literature.Oligodendrocyte progenitor cell numbers and migration are regulated by the zebrafish orthologs of the NF1 tumor suppressor geneGenomic imbalance of HMMR/RHAMM regulates the sensitivity and response of malignant peripheral nerve sheath tumour cells to aurora kinase inhibition.CXCL12 alone is insufficient for gliomagenesis in Nf1 mutant mice.The tumor suppressor neurofibromin confers sensitivity to apoptosis by Ras-dependent and Ras-independent pathways.Overexpression of PDGFRA cooperates with loss of NF1 and p53 to accelerate the molecular pathogenesis of malignant peripheral nerve sheath tumors.An isolated neurofibromal polyp of the colon.BCRP expression in schwannoma, plexiform neurofibroma and MPNST.
P2860
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P2860
Neurofibromatosis type 1 - a model for nervous system tumour formation?
description
2005 nî lūn-bûn
@nan
2005 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Neurofibromatosis type 1 - a model for nervous system tumour formation?
@ast
Neurofibromatosis type 1 - a model for nervous system tumour formation?
@en
Neurofibromatosis type 1 - a model for nervous system tumour formation?
@nl
type
label
Neurofibromatosis type 1 - a model for nervous system tumour formation?
@ast
Neurofibromatosis type 1 - a model for nervous system tumour formation?
@en
Neurofibromatosis type 1 - a model for nervous system tumour formation?
@nl
prefLabel
Neurofibromatosis type 1 - a model for nervous system tumour formation?
@ast
Neurofibromatosis type 1 - a model for nervous system tumour formation?
@en
Neurofibromatosis type 1 - a model for nervous system tumour formation?
@nl
P2860
P356
P1476
Neurofibromatosis type 1 - a model for nervous system tumour formation?
@en
P2093
Joshua B Rubin
P2860
P2888
P304
P356
10.1038/NRC1653
P407
P577
2005-07-01T00:00:00Z
P5875
P6179
1048373737