Molecular Characteristics of Pediatric Ependymomas: A Systematic Review
Author:
Funder
Consejo Nacional de Ciencia y Tecnología
Fondo de Investigación en Salud, Instituto Mexicano del Seguro Social
Publisher
Springer Science and Business Media LLC
Link
http://link.springer.com/content/pdf/10.1007/s42399-019-00147-5.pdf
Reference44 articles.
1. Ammerlaan ACJ, De Bustos C, Ararou A. Localization of a putative low-penetrance ependymoma susceptibility locus to 22q11 using a chromosome 22 tiling-path genomic microarray. Genes Chromosom Cancer. 2005;43:329–38.
2. Rogers HA, Kilday JP, Mayne C. Supratentorial and spinal pediatric ependymomas display a hypermethylated phenotype which includes the loss of tumor suppressor genes involved in the control of cell growth and death. Acta Neuropathol. 2012;123:711–25.
3. Nambirajan A, Sharma MC, Gupta RK. Study of stem cell marker nestin and its correlation with vascular endothelial growth factor and microvascular density in ependymomas. Neuropathol Appl Neurobiol. 2014;40:714–25.
4. Lukashova-v. Zangen I, Kneitz S, Monoranu CM. Ependymoma gene expression profiles associated with histological subtype, proliferation, and patient survival. Acta Neuropathol. 2007;113:325–37.
5. Modena P, Buttarelli FR, Miceli R. Predictors of outcome in an AIEOP series of childhood ependymomas: a multifactorial analysis. 2012; 14: 1346–1356.
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