Results 121 to 130 of about 9,592 (218)
Genetically Engineered T-Cells for Malignant Glioma: Overcoming the Barriers to Effective Immunotherapy. [PDF]
, 2018 Malignant gliomas carry a dismal prognosis. Conventional treatment using chemo- and radiotherapy has limited efficacy with adverse events. Therapy with genetically engineered T-cells, such as chimeric antigen receptor (CAR) T-cells, may represent a ...Almeida, Neil D, Chuntova, Pavlina, Downey, Kira M, Hegde, Bindu, Okada, Hideho +4 morecore Progenetix: 12 years of oncogenomic data curation [PDF]
, 2017 DNA copy number aberrations (CNAs) can be found in the majority of cancer genomes and are crucial for understanding the potential mechanisms underlying tumor initiation and progression.Ai, Ni, Baudis, Michael, Cai, Haoyang, Gupta, Saumya, Kumar, Nitin, Rath, Prisni +5 morecore Clinico–Pathological Features of Diffuse Midline Glioma, H3 K27-Altered in Adults: A Comprehensive Review of the Literature with an Additional Single-Institution Case Series
DiagnosticsBackground: Diffuse midline glioma (DMG), H3 K27-altered, is a WHO grade 4 malignant glioma located at midline structures, including the thalamus, brainstem and spinal cord.Giuseppe Broggi, Serena Salzano, Maria Failla, Giuseppe Maria Vincenzo Barbagallo, Francesco Certo, Magda Zanelli, Andrea Palicelli, Maurizio Zizzo, Nektarios Koufopoulos, Gaetano Magro, Rosario Caltabiano +10 moredoaj +1 more sourceDIFFUSE INTRINSIC PONTINE GLIOMA (DIPG) [PDF]
Neuro-Oncology, 2012 M. Zaghloul, S. Ahmed, E. Eldebaway, A. Mousa, A. Amin, N. Elkhateeb, M. Sabry, H. Ogiwara, N. Morota, A. Sufit, A. Donson, D. Birks, P. Patel, N. Foreman, M. Handler, M. Massimino, V. Biassoni, L. Gandola, E. Schiavello, E. Pecori, P. Potepan, F. Bach, G. O. Janssens, M. H. Jansen, S. J. Lauwers, P. J. Nowak, F. R. Oldenburger, E. Bouffet, F. Saran, K. K. van Ulzen, E. J. van Lindert, J. H. Schieving, T. Boterberg, G. J. Kaspers, P. N. Span, J. H. Kaanders, C. E. Gidding, D. Hargrave, S. Bailey, A. Howman, B. Pizer, D. Harris, D. Jones, P. Kearns, S. Picton, F. Saran, K. Wheatley, M. Gibson, A. Glaser, D. Connolly, D. Hargrave, A. Kawamura, T. Nagashima, K. Yamamoto, J. Sakata, R. Lober, M. Freret, P. Fisher, M. Edwards, K. Yeom, M. Monje, M. Jansen, E. S. Aliaga, E. Van Der Hoeven, D. Van Vuurden, M. Heymans, C. Gidding, E. De Bont, R. Reddingius, C. Peeters-Scholte, A. S. van Meeteren, R. Gooskens, B. Granzen, G. Paardekoper, G. Janssens, D. Noske, F. Barkhof, W. P. Vandertop, G. Kaspers, A. Saratsis, S. Yadavilli, J. Nazarian, M. Monje, M. Freret, S. Mitra, S. Mallick, J. Kim, P. Beachy, L. Nobre, F. Vasconcelos, F. Lima, D. Mattos, N. Kuiven, G. Lima, J. Silveira, M. Sevilha, M. A. Lima, S. Ferman, P. Leblond, A. Lansiaux, X. Rialland, J.-C. Gentet, B. Geoerger, D. Frappaz, I. Aerts, V. Bernier-Chastagner, R. Shah, W. Zaky, J. Grimm, S. Bluml, K. Wong, G. Dhall, V. Caretti, P. Schellen, T. Lagerweij, M. Bugiani, A. Navis, P. Wesseling, W. P. Vandertop, D. P. Noske, G. Kaspers, T. Wurdinger, H. Lee, D. Ziegler, K. Schroeder, E. Huang, N. Berlow, R. Patel, O. Becher, I. Taylor, X.-g. Mao, M. Hutt, M. Weingart, U. Kahlert, J. Maciacyk, G. Nikkhah, C. Eberhart, E. Raabe, K. Barton, K. Misuraca, K. Misuraca, O. Becher, Z. Zhou, L. Rotman, S. Ho, M. Souweidane, M. Hutt, K. J. Lim, K. Warren, H. Chang, C. Eberhart, E. Raabe, D. Lightner, S. Haque, M. Souweidane, Y. Khakoo, I. Dunkel, S. Gilheeney, K. Kramer, D. Lyden, S. Wolden, J. Greenfield, K. De Braganca, H. Ting-Rong, L. Muh-Li, C. Kai-Ping, W. Tai-Tong, C. Hsin-Hung, R. Kebudi, F. B. Cakir, F. Y. Agaoglu, O. Gorgun, Y. Dizdar, I. Ayan, E. Darendeliler, M. Zapotocky, M. Churackova, B. Malinova, R. Kodet, M. Kyncl, M. Tichy, J. Stary, D. Sumerauer, J. Minturn, H.-K. Shu, M. Fisher, R. Patti, A. Janss, J. Allen, P. Phillips, J. Belasco, K. Taylor, M. Baudis, A. von Beuren, M. Fouladi, C. Jones +195 moreopenaire +1 more sourceDiencephalic syndrome in child with NF-1 and hypothalamic
tumour [PDF]
, 2018 We describe a 20 month old boy with neuro-fibromatosis type 1 (NF-1) who presented with diencephalic syndrome due to a large hypothalamic tumour and developed massive necrosis after chemotherapy associated with severe encephalopathy.Didcock, Liz, Howarth, Simon P.S., Pilotto, Chiara, Thomas, Adam, Thomas, Shery, Walker, David A. +5 morecore Role of SOX family of transcription factors in central nervous system tumors [PDF]
, 2014 SOX genes are developmental regulators with functions in the instruction of cell fate and maintenance of
progenitor’s identity during embryogenesis. They play additional roles during tissue homeostasis and regeneration
in adults particularly in the ...Acanda-de-la-Rocha, A.M. (Arlet María), Alonso-Roldán, M.M. (Marta María), Matheu, A. (Ander), Sampron, N. (Nicolas) +3 morecore
