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Brain Pathology, ISSN 1015-6305, 10/2008, Volume 18, Issue 4, pp. 517 - 519
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 03/2006, Volume 26, Issue 13, pp. 3390 - 3395
Schwanncell-axon interaction is the hallmark feature of peripheral nerves, yet the intracellular signals underlying this interaction are unknown. Schwann cells... 
Axon | FRET | Live-cell imaging | NF2 | Rac | Schwann cell | MERLIN | ACTIVATION | MEMBRANE | KINASE | PROLIFERATION | NEUROSCIENCES | NF2 TUMOR-SUPPRESSOR | GTPASES | live-cell imaging | GROWTH | axon | GENE-PRODUCT | Time Factors | Humans | Cells, Cultured | Axons - metabolism | Cell Communication | rac GTP-Binding Proteins - metabolism | Metabolic Clearance Rate | Schwann Cells - metabolism | Neurofibromin 2 - metabolism | Brief Communications
Journal Article
Journal of Neuro-Oncology, ISSN 0167-594X, 2/2009, Volume 91, Issue 3, pp. 265 - 270
Journal Article
Neurology, ISSN 0028-3878, 06/2003, Volume 60, Issue 12, pp. 1968 - 1974
Journal Article
2007, AD-a473 383.
Schwannomatosis is a recently recognized third major type of neurofibromatosis. Our preliminary studies of the NF2 gene in tumors from schwannomatosis patients... 
suppressors | coding | pathogenesis | mutations | diagnosis(medicine) | genes | vaccines | molecules | resources | locus | neoplasms
Government Document
Neurobiology of disease, ISSN 0969-9961, 2/2008, Volume 29, Issue 2, pp. 278 - 292
Meningiomas, common tumors arising from arachnoidal cells of the meninges, may occur sporadically, or in association with the inherited disorder,... 
meningioma | senescence | actin cytoskeleton | merlin | RNA interference | arachnoidal | NF2 | α-catenin | neurofibromatosis 2 | contact inhibition
Journal Article
2006, AD-a460 470.
Background: Schwannomatosis is a recently recognized third major type of neurofibromatosis. Our preliminary studies of the NF2 gene in tumors from... 
suppressors | coding | pathogenesis | mutations | diagnosis(medicine) | genes | vaccines | molecules | resources | locus | neoplasms
Government Document
Human Mutation, ISSN 1059-7794, 01/2007, Volume 28, Issue 1, pp. 1 - 12
The NF2 tumor suppressor gene on chromosome 22 is a member of the protein 4.1 family of cytoskeletal elements. A number of single‐ and multiple‐tumor... 
meningioma | neurofibromatosis | NF2 | schwannoma | tumor suppressor gene | Neurofibromatosis | Meningioma | Schwannoma | Tumor suppressor gene | Molecular Diagnostic Techniques - methods | Phenotype | Genes, Tumor Suppressor - physiology | Humans | Genotype | Cytogenetic Analysis | Mutation | Genes, Neurofibromatosis 2 | Polymorphism, Genetic
Journal Article
Brain Pathology, ISSN 1015-6305, 10/2008, Volume 18, Issue 4, pp. 517 - 519
The INI1/SMARCB1 protein product (INI1), a component of a transcription complex, was recently implicated in the pathogenesis of schwannomas in two members of a... 
SMARCB1 | expression | Schwannomatosis | NF2 | Schwannoma | INI1
Journal Article