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Acta Neuropathologica|April 24, 2013
BRAF(V600E) mutation is a negative prognosticator in pediatric gangliogliomaSonika Dahiya, Devon H Haydon, David Alvarado, et al.
Human Molecular Genetics|November 11, 2010
Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of tuberous sclerosis complexLing-Hui Zeng, Nicholas R Rensing, Bo Zhang, et al.
The Journal of Pediatrics|June 2, 2015
Racial/Ethnic Differences in Pediatric Brain Tumor Diagnoses in Patients with Neurofibromatosis Type 1Salmafatima S Abadin, Nancy L Zoellner, Melody Schaeffer, et al.
Genesis (New York, N.Y. : 2000)|April 30, 2008
Generation of a reporter mouse line expressing Akt and EGFP upon Cre-mediated recombinationLynda Elghazi, Aaron J Weiss, Aaron P Gould, et al.
Acta Neuropathologica|March 10, 2009
Histopathologic predictors of pilocytic astrocytoma event-free survivalKathleen M Tibbetts, Ryan J Emnett, Feng Gao, et al.
Journal of Neurosurgery|August 19, 2007
Colocalized cellular schwannoma and plexiform neurofibroma in the absence of neurofibromatosis. Case reportRobert J Spinner, Bernd W Scheithauer, Arie Perry, et al.
International Journal of Cancer|August 19, 2008
Frequent promoter hypermethylation and transcriptional downregulation of the NDRG2 gene at 14q11.2 in primary glioblastomaMartin Tepel, Peter Roerig, Marietta Wolter, et al.
Human Molecular Genetics|July 11, 2008
Neurofibromin regulates somatic growth through the hypothalamic-pituitary axisBalazs Hegedus, Tu-Hsueh Yeh, Da Yong Lee, et al.
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