Works matching IS 00016322 AND DT 2013 AND VI 125 AND IP 3

Results: 14

Secretory meningiomas are defined by combined KLF4 K409Q and TRAF7 mutations.

Published in:

Acta Neuropathologica, 2013, v. 125, n. 3, p. 351, doi. 10.1007/s00401-013-1093-x

By:

Reuss, David;
Piro, Rosario;
Jones, David;
Simon, Matthias;
Ketter, Ralf;
Kool, Marcel;
Becker, Albert;
Sahm, Felix;
Pusch, Stefan;
Meyer, Jochen;
Hagenlocher, Christian;
Schweizer, Leonille;
Capper, David;
Kickingereder, Phillipp;
Mucha, Jana;
Koelsche, Christian;
Jäger, Natalie;
Santarius, Thomas;
Tarpey, Patrick;
Stephens, Philip

Publication type:

Article

DNA methylation profiling of medulloblastoma allows robust subclassification and improved outcome prediction using formalin-fixed biopsies.

Published in:

Acta Neuropathologica, 2013, v. 125, n. 3, p. 359, doi. 10.1007/s00401-012-1077-2

By:

Schwalbe, Edward;
Williamson, Daniel;
Lindsey, Janet;
Hamilton, Dolores;
Ryan, Sarra;
Megahed, Hisham;
Garami, Miklós;
Hauser, Peter;
Dembowska-Baginska, Bożena;
Perek, Danuta;
Northcott, Paul;
Taylor, Michael;
Taylor, Roger;
Ellison, David;
Bailey, Simon;
Clifford, Steven

Publication type:

Article

OTX2 sustains a bivalent-like state of OTX2-bound promoters in medulloblastoma by maintaining their H3K27me3 levels.

Published in:

Acta Neuropathologica, 2013, v. 125, n. 3, p. 385, doi. 10.1007/s00401-012-1069-2

By:

Bunt, Jens;
Hasselt, Nancy;
Zwijnenburg, Danny;
Koster, Jan;
Versteeg, Rogier;
Kool, Marcel

Publication type:

Article

Aberrant patterns of H3K4 and H3K27 histone lysine methylation occur across subgroups in medulloblastoma.

Published in:

Acta Neuropathologica, 2013, v. 125, n. 3, p. 373, doi. 10.1007/s00401-012-1070-9

By:

Dubuc, Adrian;
Remke, Marc;
Korshunov, Andrey;
Northcott, Paul;
Zhan, Shing;
Mendez-Lago, Maria;
Kool, Marcel;
Jones, David;
Unterberger, Alexander;
Morrissy, A.;
Shih, David;
Peacock, John;
Ramaswamy, Vijay;
Rolider, Adi;
Wang, Xin;
Witt, Hendrik;
Hielscher, Thomas;
Hawkins, Cynthia;
Vibhakar, Rajeev;
Croul, Sidney

Publication type:

Article

Polymorphonuclear neutrophil infiltration into ischemic infarctions: myth or truth?

Published in:

2013

By:

Kalimo, Hannu;
del Zoppo, Gregory;
Paetau, Anders;
Lindsberg, Perttu

Publication type:

Editorial

Erratum to: APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38.

Published in:

2013

By:

Moro, Maria;
Giaccone, Giorgio;
Lombardi, Raffaella;
Indaco, Antonio;
Uggetti, Andrea;
Morbin, Michela;
Saccucci, Stefania;
Fede, Giuseppe;
Catania, Marcella;
Walsh, Dominic;
Demarchi, Andrea;
Rozemuller, Annemieke;
Bogdanovic, Nenad;
Bugiani, Orso;
Ghetti, Bernardino;
Tagliavini, Fabrizio

Publication type:

Correction Notice

Nervous system involvement in von Hippel-Lindau disease: pathology and mechanisms.

Published in:

Acta Neuropathologica, 2013, v. 125, n. 3, p. 333, doi. 10.1007/s00401-013-1091-z

By:

Vortmeyer, Alexander;
Falke, Eric;
Gläsker, Sven;
Li, Jie;
Oldfield, Edward

Publication type:

Article

hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations.

Published in:

Acta Neuropathologica, 2013, v. 125, n. 3, p. 413, doi. 10.1007/s00401-013-1088-7

By:

Mori, Kohji;
Lammich, Sven;
Mackenzie, Ian;
Forné, Ignasi;
Zilow, Sonja;
Kretzschmar, Hans;
Edbauer, Dieter;
Janssens, Jonathan;
Kleinberger, Gernot;
Cruts, Marc;
Herms, Jochen;
Neumann, Manuela;
Broeckhoven, Christine;
Arzberger, Thomas;
Haass, Christian

Publication type:

Article

Lysosomal storage and advanced senescence in the brain of LAMP-2-deficient Danon disease.

Published in:

2013

By:

Furuta, Akiko;
Wakabayashi, Koichi;
Haratake, Joji;
Kikuchi, Hisae;
Kabuta, Tomohiro;
Mori, Fumiaki;
Tokonami, Fusao;
Katsumi, Yukinori;
Tanioka, Fumihiko;
Uchiyama, Yasuo;
Nishino, Ichizo;
Wada, Keiji

Publication type:

Letter

Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid.

Published in:

2013

By:

Bigio, Eileen;
Wu, Jane;
Deng, Han-Xiang;
Bit-Ivan, Esther;
Mao, Qinwen;
Ganti, Rakhee;
Peterson, Melanie;
Siddique, Nailah;
Geula, Changiz;
Siddique, Teepu;
Mesulam, Marsel

Publication type:

Letter

Evolving neurobiology of tuberous sclerosis complex.

Published in:

Acta Neuropathologica, 2013, v. 125, n. 3, p. 317, doi. 10.1007/s00401-013-1085-x

By:

Crino, Peter

Publication type:

Article

Sequence variants in eukaryotic translation initiation factor 4-gamma (eIF4G1) are associated with Lewy body dementia.

Published in:

Acta Neuropathologica, 2013, v. 125, n. 3, p. 425, doi. 10.1007/s00401-012-1059-4

By:

Fujioka, Shinsuke;
Sundal, Christina;
Strongosky, Audrey;
Castanedes, Monica;
Rademakers, Rosa;
Ross, Owen;
Vilariño-Güell, Carles;
Farrer, Matthew;
Wszolek, Zbigniew;
Dickson, Dennis

Publication type:

Article

VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy.

Published in:

Acta Neuropathologica, 2013, v. 125, n. 3, p. 439, doi. 10.1007/s00401-012-1073-6

By:

Ramachandran, Nivetha;
Munteanu, Iulia;
Wang, Peixiang;
Ruggieri, Alessandra;
Rilstone, Jennifer;
Israelian, Nyrie;
Naranian, Taline;
Paroutis, Paul;
Guo, Ray;
Ren, Zhi-Ping;
Nishino, Ichizo;
Chabrol, Brigitte;
Pellissier, Jean-Francois;
Minetti, Carlo;
Udd, Bjarne;
Fardeau, Michel;
Tailor, Chetankumar;
Mahuran, Don;
Kissel, John;
Kalimo, Hannu

Publication type:

Article

The neurovascular unit as a selective barrier to polymorphonuclear granulocyte (PMN) infiltration into the brain after ischemic injury.

Published in:

Acta Neuropathologica, 2013, v. 125, n. 3, p. 395, doi. 10.1007/s00401-012-1076-3

By:

Enzmann, Gaby;
Mysiorek, Caroline;
Gorina, Roser;
Cheng, Yu-Jung;
Ghavampour, Sharang;
Hannocks, Melanie-Jane;
Prinz, Vincent;
Dirnagl, Ulrich;
Endres, Matthias;
Prinz, Marco;
Beschorner, Rudi;
Harter, Patrick;
Mittelbronn, Michel;
Engelhardt, Britta;
Sorokin, Lydia

Publication type:

Article