Multiplatform molecular analyses refine classification of gliomas arising in patients with neurofibromatosis type 1

Gliomas arising in the setting of neurofibromatosis type 1 (NF1) are heterogeneous, occurring from childhood through adulthood, can be histologically low-grade or high-grade, and follow an indolent or aggressive clinical course. Comprehensive profiling of genetic alterations beyond NF1 inactivation...

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Detalles Bibliográficos
Autores principales: Lucas, Calixto-Hope G., Sloan, Emily A., Gupta, Rohit, Wu, Jasper, Pratt, Drew, Vasudevan, Harish N., Ravindranathan, Ajay, Barreto, Jairo, Williams, Erik A., Shai, Anny, Whipple, Nicholas S., Bruggers, Carol S., Maher, Ossama, Nabors, Burt, Rodriguez, Michael, Samuel, David, Brown, Melandee, Carmichael, Jason, Lu, Rufei, Mirchia, Kanish, Sullivan, Daniel V., Pekmezci, Melike, Tihan, Tarik, Bollen, Andrew W., Perry, Arie, Banerjee, Anuradha, Mueller, Sabine, Gupta, Nalin, Hervey-Jumper, Shawn L., Oberheim Bush, Nancy Ann, Daras, Mariza, Taylor, Jennie W., Butowski, Nicholas A., de Groot, John, Clarke, Jennifer L., Raleigh, David R., Costello, Joseph F., Phillips, Joanna J., Reddy, Alyssa T., Chang, Susan M., Berger, Mitchel S., Solomon, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468105/
https://www.ncbi.nlm.nih.gov/pubmed/35945463
http://dx.doi.org/10.1007/s00401-022-02478-5

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