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American Journal of Medical Genetics|October 1, 1991
Oculodentodigital dysplasia syndrome associated with abnormal cerebral white matterD H Gutmann, E H Zackai, D M McDonald-McGinn, et al.Genes, Chromosomes & Cancer|May 1, 1994
Loss of neurofibromin in adrenal gland tumors from patients with neurofibromatosis type ID H Gutmann, J L Cole, W J Stone, et al.The Journal of Cell Biology|September 7, 2000
CD44 enhances neuregulin signaling by Schwann cellsL S Sherman, T A Rizvi, S Karyala, et al.Human Molecular Genetics|December 26, 2001
Heterozygosity for the neurofibromatosis 1 (NF1) tumor suppressor results in abnormalities in cell attachment, spreading and motility in astrocytesD H Gutmann, Y L Wu, N M Hedrick, et al.American Journal of Medical Genetics|May 1, 1991
Congenital nystagmus in a (46,XX/45,X) mosaic woman from a family with X-linked congenital nystagmusD H Gutmann, M L Brooks, B S Emanuel, et al.Annals of Neurology|August 1, 1997
Reduced TSC2 RNA and protein in sporadic astrocytomas and ependymomasR Wienecke, A Guha, J C Maize, et al.Investigative Ophthalmology & Visual Science|August 1, 1993
Detection of melanocytes from uveal melanoma in peripheral blood using the polymerase chain reactionK Tobal, L S Sherman, A J Foss, et al.Neurology|October 25, 2006
The role of surgical biopsy in the diagnosis of glioma in individuals with neurofibromatosis-1J R Leonard, A Perry, J B Rubin, et al.Acta Neuropathologica|February 9, 2000
Expression of the tuberous sclerosis complex gene products, hamartin and tuberin, in central nervous system tissuesD H Gutmann, Y Zhang, M J Hasbani, et al.Journal of Neuropathology and Experimental Neurology|September 27, 2000
Loss of neurofibromin is associated with activation of RAS/MAPK and PI3-K/AKT signaling in a neurofibromatosis 1 astrocytomaN Lau, M M Feldkamp, L Roncari, et al.Pageof 14