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TUMOR MODELS (IN VIVO/IN VITRO)

Autor: E. Brognaro, S. Chang, J. Cha, K. Choi, C. Choi, J. DePetro, C. Binding, M. Blough, J. Kelly, S. Lawn, J. Chan, S. Weiss, G. Cairncross, A. Eisenbeis, R. Goldbrunner, M. Timmer, K. Gabrusiewicz, N. Cortes-Santiago, X. Fan, M. B. Hossain, B. Kaminska, A. Heimberger, G. Rao, W. K. A. Yung, F. Marini, J. Fueyo, C. Gomez-Manzano, B. Halle, E. Marcusson, C. Aaberg-Jessen, S. S. Jensen, M. Meyer, M. K. Schulz, C. Andersen, null Bjarne, W. Kristensen, R. Hashizume, Y. Ihara, T. Ozawa, A. Parsa, J. Clarke, N. Butowski, M. Prados, A. Perry, M. McDermott, D. James, R. Jensen, D. Gillespie, T. Martens, M. Zamykal, M. Westphal, K. Lamszus, E. Monsalves, S. Jalali, T. Tateno, S. Ezzat, G. Zadeh, M. K. Nedergaard, K. Kristoffersen, H. S. Poulsen, M.-T. Stockhausen, U. Lassen, A. Kjaer, F. Ohka, A. Natsume, H. Zong, C. Liu, A. Hatanaka, K. Katsushima, K. Shinjo, T. Wakabayashi, Y. Kondo, K. Picotte, L. Li, B. Westerhuis, H. Zhao, S. Plotkin, M. James, M. Kalamarides, W.-n. Zhao, J. Kim, A. Stemmer-Rachamimov, S. Haggarty, J. Gusella, V. Ramesh, F. Nunes, T. Doucette, Y. Yang, G. Fuller, A. Rao, N. O. Schmidt, N. Humke, H. Meissner, F.-J. Mueller, O. Schnell, I. Jaehnert, V. Albrecht, P. Fu, J.-C. Tonn, C. Schichor, G. Shackleford, K. Swanson, X.-H. Shi, M. D'Apuzzo, I. Gonzalez-Gomez, R. Sposto, R. Seeger, A. Erdreich-Epstein, R. Moats, R. W. Sirianni, J. M. Heffernan, D. J. Overstreet, L. Sleire, B. S. Skeie, I. A. Netland, J. Heggdal, P.-H. Pedersen, P. O. Enger, C. Stiles, Y. Sun, S. Mehta, C. Taylor, J. Alberta, T. Sundstrom, I. Wendelbo, I. Daphu, E. Hodneland, A. Lundervold, H. Immervoll, K. O. Skaftnesmo, M. Babic, P. Jendelova, E. Sykova, M. Lund-Johansen, R. Bjerkvig, F. Thorsen, M. Synowitz, M.-C. Ku, S. A. Wolf, D. Respondek, V. Matyash, A. Pohlmann, S. Waiczies, H. Waiczies, T. Niendorf, R. Glass, H. Kettenmann, N. Thompson, D. Elder, K. Hopkins, V. Iyer, N. Cohen, J. Tavare, B. Fite, L. M. Mahakian, J. W. Seo, S. Qin, V. Harrison, P. N. Harter, S. Johnson, E. Ingham, C. Caskey, T. Meade, K. W. Ferrara, B. R. Tschida, A. R. Lowy, C. A. Marek, T. Ringstrom, T. J. Beadnell, S. M. Wiesner, D. A. Largaespada, C. Wenger, P. C. Miranda, A. Mekonnen, R. Salvador, P. Basser, J. Yoon, H. Shin

Publikováno v: Neuro-Oncology. 15:iii235-iii241

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1e29a6ed7d359d2f6d79c8b774ad2a7
https://doi.org/10.1093/neuonc/not193

Exon trapping and sequence-based methods of gene finding in transcript mapping of human 4p 16.3

Autor: James F. Gusella, Mabel P. Duyao, Marcy E. MacDonald, Glenn Barnes, Hans Lehrach, Matthew J. Gusella, Jianmin Chen, Ingrid Pribill, Deanna Church, Gillian P. Bates, Christine Ambrose, Sarah Baxendale, Alan Buckler

Publikováno v: Somatic Cell and Molecular Genetics. 23:413-427

We have applied exon amplification, GRAIL2 exon prediction and EST database searching to a 2 Mb segment of chromosome 4p16.3. Experimental and computational methods of identifying exons were comparable in efficiency and apparent false positive rate,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5ed180e9f88df1334c752f327681304
https://doi.org/10.1007/bf02673751

DNA diagnosis of neurofibromatosis 2. Altered coding sequence of the merlin tumor suppressor in an extended pedigree

Autor: M, MacCollin, T, Mohney, J, Trofatter, W, Wertelecki, V, Ramesh, J, Gusella

Publikováno v: JAMA: The Journal of the American Medical Association. 270:2316-2320

To define the DNA mutation causing neurofibromatosis 2 (NF2), a severe genetic disorder involving the development of multiple nervous system tumors in adulthood, in a large, well-studied NF2 pedigree previously used to chromosomally map and to isolat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f65fe3c27216292ec816dcc97858bea
https://doi.org/10.1001/jama.270.19.2316

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