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Results: 1-7 |
Results: 7
High frequency of mitochondrial DNA mutations in glioblastoma multiforme identified by direct sequence comparison to blood samples
Authors: Kirches, E Krause, G Warich-Kirches, M Weis, S Schneider, T Meyer-Puttlitz, B Mawrin, C Dietzmann, K
Citation: E. Kirches et al., High frequency of mitochondrial DNA mutations in glioblastoma multiforme identified by direct sequence comparison to blood samples, INT J CANC, 93(4), 2001, pp. 534-538
Alterations of the tumor suppressor genes CDKN2A (p16(INK4a)), p14(ARF), CDKN2B (p15(INK4b)), and CDKN2C (p18(INK4c)) in atypical and anaplastic meningiomas
Authors: Bostrom, J Meyer-Puttlitz, B Wolter, M Blaschke, B Weber, RG Lichter, P Ichimura, K Collins, VP Reifenberger, G
Citation: J. Bostrom et al., Alterations of the tumor suppressor genes CDKN2A (p16(INK4a)), p14(ARF), CDKN2B (p15(INK4b)), and CDKN2C (p18(INK4c)) in atypical and anaplastic meningiomas, AM J PATH, 159(2), 2001, pp. 661-669
Analysis of the TSC2 gene in human medulloblastoma
Authors: Przkora, R Meyer-Puttlitz, B Schmitt, O Berthold, F Nothen, M Krauss, J Tonn, JC von Deimling, A Wiestler, OD Pietsch, T
Citation: R. Przkora et al., Analysis of the TSC2 gene in human medulloblastoma, ACT NEUROP, 102(4), 2001, pp. 380-384
Characteristic chromosomal imbalances in primary central nervous system lymphomas of the diffuse large B-cell type
Authors: Weber, T Weber, RG Kaulich, K Actor, B Meyer-Puttlitz, B Lampel, S Buschges, R Weigel, R Deckert-Schluter, M Schmiedek, P Reifenberger, G Lichter, P
Citation: T. Weber et al., Characteristic chromosomal imbalances in primary central nervous system lymphomas of the diffuse large B-cell type, BRAIN PATH, 10(1), 2000, pp. 73-84
Comprehensive allelotype and genetic analysis of 466 human nervous system tumors
Authors: von Deimling, A Fimmers, R Schmidt, MC Bender, B Fassbender, F Nagel, J Jahnke, R Kaskel, P Duerr, EM Koopmann, J Maintz, D Steinbeck, S Wick, W Platten, M Muller, DJ Przkora, R Waha, A Blumcke, B Wellenreuther, R Meyer-Puttlitz, B Schmidt, O Mollenhauer, J Poustka, A Stangl, AP Lenartz, D von Ammon, K Henson, JW Schramm, J Louis, DN Wiestler, OD
Citation: A. Von Deimling et al., Comprehensive allelotype and genetic analysis of 466 human nervous system tumors, J NE EXP NE, 59(6), 2000, pp. 544-558
Analysis of the MEN1 gene in sporadic pituitary adenomas
Authors: Schmidt, MC Henke, RT Stangl, AP Meyer-Puttlitz, B Stoffel-Wagner, B Schramm, J von Deimling, A
Citation: Mc. Schmidt et al., Analysis of the MEN1 gene in sporadic pituitary adenomas, J PATHOLOGY, 188(2), 1999, pp. 168-173
Molecular genetic analysis of ependymal tumors - NF2 mutations and chromosome 22q loss occur preferentially in intramedullary spinal ependymomas
Authors: Ebert, C von Haken, M Meyer-Puttlitz, B Wiestler, OD Reifenberger, G Pietsch, T von Deimling, A
Citation: C. Ebert et al., Molecular genetic analysis of ependymal tumors - NF2 mutations and chromosome 22q loss occur preferentially in intramedullary spinal ependymomas, AM J PATH, 155(2), 1999, pp. 627-632
Risultati: 1-7 |