Výsledky vyhledávání - "Christina, Blume"

Recurrent fusions in PLAGL1 define a distinct subset of pediatric-type supratentorial neuroepithelial tumors

Autor: Konstantin Okonechnikov, Christina Blume, Mariëtte E.G. Kranendonk, Stephanie Bunkowski, Dominik Sturm, Matija Snuderl, David R Ghasemi, Damian Stichel, Philipp Sievers, David T.W. Jones, Richard Grundy, Christian Mawrin, Ofelia Cruz, Andreas von Deimling, David W. Ellison, Tuyu Zheng, Daniel Schrimpf, Mark R. Gilbert, Lenka Krskova, Pascale Varlet, Hildegard Dohmen, Till Acker, Henning B. Boldt, Sophie C Henneken, Kenneth Aldape, Stefan Rutkowski, Mariona Suñol, Andrey Korshunov, Stefan M. Pfister, Julia Benzel, David Capper, Wolf Mueller, Ulrich Schüller, Sebastian Brandner, Patrick N. Harter, Zied Abdullaev, Celso Pouget, Rudi Beschorner, Kendra K Maaß, Viktoria Ruf, Pieter Wesseling, Mélanie Pagès, Nada Jabado, Terri S. Armstrong, Patricia Kohlhof-Meinecke, Martin Sill, Marcel Kool, Koichi Ichimura, Felix Sahm, Guido Reifenberger, Kristian W. Pajtler, Wolfgang Wick, David E. Reuss, Leonille Schweizer, Christine Stadelmann, Cinzia Lavarino, Ales Vicha, Michal Zapotocky, Noreen Akhtar

Publikováno v: Acta Neuropathologica
Acta Neuropathologica, 142(5), 827-839. Springer Verlag
ACTA NEUROPATHOLOGICA
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
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Sievers, P, Henneken, S C, Blume, C, Sill, M, Schrimpf, D, Stichel, D, Okonechnikov, K, Reuss, D E, Benzel, J, Maaß, K K, Kool, M, Sturm, D, Zheng, T, Ghasemi, D R, Kohlhof-Meinecke, P, Cruz, O, Suñol, M, Lavarino, C, Ruf, V, Boldt, H B, Pagès, M L, Pouget, C, Schweizer, L, Kranendonk, M E G, Akhtar, N, Bunkowski, S, Stadelmann, C, Schüller, U, Mueller, W C, Dohmen, H, Acker, T, Harter, P N, Mawrin, C, Beschorner, R, Brandner, S, Snuderl, M, Abdullaev, Z, Aldape, K, Gilbert, M R, Armstrong, T S, Ellison, D W, Capper, D, Ichimura, K, Reifenberger, G, Grundy, R G, Jabado, N, Krskova, L, Zapotocky, M, Vicha, A, Varlet, P, Wesseling, P, Rutkowski, S, Korshunov, A, Wick, W, Pfister, S M, Jones, D T W, von Deimling, A, Pajtler, K W & Sahm, F 2021, ' Recurrent fusions in PLAGL1 define a distinct subset of pediatric-type supratentorial neuroepithelial tumors ', Acta Neuropathologica, vol. 142, no. 5, pp. 827-839 . https://doi.org/10.1007/s00401-021-02356-6
Sievers, P, Henneken, S C, Blume, C, Sill, M, Schrimpf, D, Stichel, D, Okonechnikov, K, Reuss, D E, Benzel, J, Maaß, K K, Kool, M, Sturm, D, Zheng, T, Ghasemi, D R, Kohlhof-Meinecke, P, Cruz, O, Suñol, M, Lavarino, C, Ruf, V, Boldt, H B, Pagès, M, Pouget, C, Schweizer, L, Kranendonk, M E G, Akhtar, N, Bunkowski, S, Stadelmann, C, Schüller, U, Mueller, W C, Dohmen, H, Acker, T, Harter, P N, Mawrin, C, Beschorner, R, Brandner, S, Snuderl, M, Abdullaev, Z, Aldape, K, Gilbert, M R, Armstrong, T S, Ellison, D W, Capper, D, Ichimura, K, Reifenberger, G, Grundy, R G, Jabado, N, Krskova, L, Zapotocky, M, Vicha, A, Varlet, P, Wesseling, P, Rutkowski, S, Korshunov, A, Wick, W, Pfister, S M, Jones, D T W, von Deimling, A, Pajtler, K W & Sahm, F 2021, ' Recurrent fusions in PLAGL1 define a distinct subset of pediatric-type supratentorial neuroepithelial tumors ', Acta Neuropathologica, vol. 142, no. 5, pp. 827-839 . https://doi.org/10.1007/s00401-021-02356-6

Ependymomas encompass a heterogeneous group of central nervous system (CNS) neoplasms that occur along the entire neuroaxis. In recent years, extensive (epi-)genomic profiling efforts have identified several molecular groups of ependymoma that are ch

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Glioneuronal tumor with ATRX alteration, kinase fusion and anaplastic features (GTAKA):a molecularly distinct brain tumor type with recurrent NTRK gene fusions

Autor: Henri Bogumil, Martin Sill, Daniel Schrimpf, Britta Ismer, Christina Blume, Ramin Rahmanzade, Felix Hinz, Asan Cherkezov, Rouzbeh Banan, Dennis Friedel, David E. Reuss, Florian Selt, Jonas Ecker, Till Milde, Kristian W. Pajtler, Jens Schittenhelm, Jürgen Hench, Stephan Frank, Henning B. Boldt, Bjarne Winther Kristensen, David Scheie, Linea C. Melchior, Viola Olesen, Astrid Sehested, Daniel R. Boué, Zied Abdullaev, Laveniya Satgunaseelan, Ina Kurth, Annekatrin Seidlitz, Christine L. White, Ho-Keung Ng, Zhi-Feng Shi, Christine Haberler, Martina Deckert, Marco Timmer, Roland Goldbrunner, Arnault Tauziède-Espariat, Pascale Varlet, Sebastian Brandner, Sanda Alexandrescu, Matija Snuderl, Kenneth Aldape, Andrey Korshunov, Olaf Witt, Christel Herold-Mende, Andreas Unterberg, Wolfgang Wick, Stefan M. Pfister, Andreas von Deimling, David T. W. Jones, Felix Sahm, Philipp Sievers

Publikováno v: Bogumil, H, Sill, M, Schrimpf, D, Ismer, B, Blume, C, Rahmanzade, R, Hinz, F, Cherkezov, A, Banan, R, Friedel, D, Reuss, D E, Selt, F, Ecker, J, Milde, T, Pajtler, K W, Schittenhelm, J, Hench, J, Frank, S, Boldt, H B, Kristensen, B W, Scheie, D, Melchior, L C, Olesen, V, Sehested, A, Boué, D R, Abdullaev, Z, Satgunaseelan, L, Kurth, I, Seidlitz, A, White, C L, Ng, H K, Shi, Z F, Haberler, C, Deckert, M, Timmer, M, Goldbrunner, R, Tauziède-Espariat, A, Varlet, P, Brandner, S, Alexandrescu, S, Snuderl, M, Aldape, K, Korshunov, A, Witt, O, Herold-Mende, C, Unterberg, A, Wick, W, Pfister, S M, von Deimling, A, Jones, D T W, Sahm, F & Sievers, P 2023, ' Glioneuronal tumor with ATRX alteration, kinase fusion and anaplastic features (GTAKA) : a molecularly distinct brain tumor type with recurrent NTRK gene fusions ', Acta Neuropathologica, vol. 145, pp. 667–680 . https://doi.org/10.1007/s00401-023-02558-0

Glioneuronal tumors are a heterogenous group of CNS neoplasms that can be challenging to accurately diagnose. Molecular methods are highly useful in classifying these tumors—distinguishing precise classes from their histological mimics and identify

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Clear cell meningiomas are defined by a highly distinct DNA methylation profile and mutations in SMARCE1

Publikováno v: Acta Neuropathologica, 141, 281-290
Acta Neuropathologica, 141, 2, pp. 281-290
Sievers, P, Sill, M, Blume, C, Tauziede-Espariat, A, Schrimpf, D, Stichel, D, Reuss, D E, Dogan, H, Hartmann, C, Mawrin, C, Hasselblatt, M, Stummer, W, Schick, U, Hench, J, Frank, S, Ketter, R, Schweizer, L, Schittenhelm, J, Puget, S, Brandner, S, Jaunmuktane, Z, Küsters, B, Abdullaev, Z, Pekmezci, M, Snuderl, M, Ratliff, M, Herold-Mende, C, Unterberg, A, Aldape, K, Ellison, D W, Wesseling, P, Reifenberger, G, Wick, W, Perry, A, Varlet, P, Pfister, S M, Jones, D T W, von Deimling, A, Sahm, F & The German Consortium “Aggressive Meningiomas” 2021, ' Clear cell meningiomas are defined by a highly distinct DNA methylation profile and mutations in SMARCE1 ', Acta Neuropathologica, vol. 141, no. 2, pp. 281-290 . https://doi.org/10.1007/s00401-020-02247-2
Acta Neuropathologica, 141(2), 281-290. Springer Verlag
Acta Neuropathologica

Clear cell meningioma represents an uncommon variant of meningioma that typically affects children and young adults. Although an enrichment of loss-of-function mutations in the SMARCE1 gene has been reported for this subtype, comprehensive molecular

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