Analysis of genetic alterations in patients affected with neurofibromatosis type 2 and its associated tumors.
作者： Caisa Marie Hansson
DOI:
关键词:
摘要: Neurofibromatosis type 2 (NF2) is an autosomal dominant disorder with the clinical hallmark of bilateral vestibular schwannomas (VS). Patients affected by a severe NF2 phenotype also presents ...
参考文章(159)
Peter McIntyre, Ruth Jepson, Stephen Leeder, Les Irwig, The outcome of childhood Haemophilus influenzae meningitis. A population based study. The Medical Journal of Australia. ,vol. 159, pp. 766- 772 ,(1993) , 10.5694/J.1326-5377.1993.TB141344.X
J. Gusella, D. Pinney, C. Gonzalez-Agosti, W. Hobbs, V. Ramesh, R. Beauchamp, L. Xu, The merlin tumor suppressor localizes preferentially in membrane ruffles. Oncogene. ,vol. 13, pp. 1239- 1247 ,(1996)
Daniel Pinkel, Richard Segraves, Damir Sudar, Steven Clark, Ian Poole, David Kowbel, Colin Collins, Wen-Lin Kuo, Chira Chen, Ye Zhai, Shanaz H. Dairkee, Britt-marie Ljung, Joe W. Gray, Donna G. Albertson, High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays Nature Genetics. ,vol. 20, pp. 207- 211 ,(1998) , 10.1038/2524
Ruth Wellenreuther, John M. Tew, Andreas Waha, Anil G. Menon, Jeffrey J. Larson, Ronald E. Warnick, Peter Kaskel, Andreas von Deimling, Matthias Simon, Allelic Losses on Chromosomes 14, 10, and 1 in Atypical and Malignant Meningiomas: A Genetic Model of Meningioma Progression Cancer Research. ,vol. 55, pp. 4696- 4701 ,(1995)
Warburton D, De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints. American Journal of Human Genetics. ,vol. 49, pp. 995- 1013 ,(1991)
Lucien Jules Rubinstein, Dorothy S. Russell, Pathology of tumours of the nervous system ,(1977)
S. Rangaratnam, A. A. Andermann, M. MacCollin, D. Parry, G. A. Rouleau, B. D. Hall, F. Y. Han, P. Short, P. Propping, V. Michels, K. Kitamura, V. M. Riccardi, J. M. Bradburn, J. O. Claudio, N. Chretien, R. Weksberg, C. M. Phelan, M. H. Ruttledge, Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. American Journal of Human Genetics. ,vol. 59, pp. 331- 342 ,(1996)
Christoph Lengauer, Kenneth W. Kinzler, Bert Vogelstein, Genetic instabilities in human cancers Nature. ,vol. 396, pp. 643- 649 ,(1998) , 10.1038/25292
Timothy Bestor, Andrew Laudano, Robert Mattaliano, Vernon Ingram, Cloning and sequencing of a cDNA encoding DNA methyltransferase of mouse cells: The carboxyl-terminal domain of the mammalian enzymes is related to bacterial restriction methyltransferases☆ Journal of Molecular Biology. ,vol. 203, pp. 971- 983 ,(1988) , 10.1016/0022-2836(88)90122-2
J. F. Gusella, R. Wellenreuther, A. Von Deimling, O. D. Wiestler, Vijaya Ramesh, D. N. Louis, J. Schramm, A. G. Menon, J. A. Kraus, D. Lenartz, Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma. American Journal of Pathology. ,vol. 146, pp. 827- 832 ,(1995)