Works matching IS 00016322 AND DT 2020 AND VI 139 AND IP 3

Results: 12

Loss of H3K27 trimethylation by immunohistochemistry is frequent in oligodendroglioma, IDH-mutant and 1p/19q-codeleted, but is neither a sensitive nor a specific marker.
Published in:
Acta Neuropathologica, 2020, v. 139, n. 3, p. 597, doi. 10.1007/s00401-019-02123-8
By:
- Pekmezci, Melike;
- Phillips, Joanna J.;
- Dirilenoglu, Fikret;
- Atasever-Rezanko, Turkan;
- Tihan, Tarik;
- Solomon, David;
- Bollen, Andrew;
- Perry, Arie
Publication type:
Article
cIMPACT-NOW update 5: recommended grading criteria and terminologies for IDH-mutant astrocytomas.
Published in:
Acta Neuropathologica, 2020, v. 139, n. 3, p. 603, doi. 10.1007/s00401-020-02127-9
By:
- Brat, Daniel J.;
- Aldape, Kenneth;
- Colman, Howard;
- Figrarella-Branger, Dominique;
- Fuller, Gregory N.;
- Giannini, Caterina;
- Holland, Eric C.;
- Jenkins, Robert B.;
- Kleinschmidt-DeMasters, Bette;
- Komori, Takashi;
- Kros, Johan M.;
- Louis, David N.;
- McLean, Catriona;
- Perry, Arie;
- Reifenberger, Guido;
- Sarkar, Chitra;
- Stupp, Roger;
- van den Bent, Martin J.;
- von Deimling, Andreas;
- Weller, Michael
Publication type:
Article
Antibody signatures in patients with histopathologically defined multiple sclerosis patterns.
Published in:
Acta Neuropathologica, 2020, v. 139, n. 3, p. 547, doi. 10.1007/s00401-019-02120-x
By:
- Stork, Lidia;
- Ellenberger, David;
- Ruprecht, Klemens;
- Reindl, Markus;
- Beißbarth, Tim;
- Friede, Tim;
- Kümpfel, Tania;
- Gerdes, Lisa A.;
- Gloth, Mareike;
- Liman, Thomas;
- Paul, Friedemann;
- Brück, Wolfgang;
- Metz, Imke
Publication type:
Article
POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, α-dystroglycan hypoglycosylation and a distinctive radiological pattern.
Published in:
Acta Neuropathologica, 2020, v. 139, n. 3, p. 565, doi. 10.1007/s00401-019-02117-6
By:
- Servián-Morilla, E.;
- Cabrera-Serrano, M.;
- Johnson, K.;
- Pandey, A.;
- Ito, A.;
- Rivas, E.;
- Chamova, T.;
- Muelas, N.;
- Mongini, T.;
- Nafissi, S.;
- Claeys, K. G.;
- Grewal, R. P.;
- Takeuchi, M.;
- Hao, H.;
- Bönnemann, C.;
- Lopes Abath Neto, O.;
- Medne, L.;
- Brandsema, J.;
- Töpf, A.;
- Taneva, A.
Publication type:
Article
PrP is a central player in toxicity mediated by soluble aggregates of neurodegeneration-causing proteins.
Published in:
Acta Neuropathologica, 2020, v. 139, n. 3, p. 503, doi. 10.1007/s00401-019-02114-9
By:
- Corbett, Grant T.;
- Wang, Zemin;
- Hong, Wei;
- Colom-Cadena, Marti;
- Rose, Jamie;
- Liao, Meichen;
- Asfaw, Adhana;
- Hall, Tia C.;
- Ding, Lai;
- DeSousa, Alexandra;
- Frosch, Matthew P.;
- Collinge, John;
- Harris, David A.;
- Perkinton, Michael S.;
- Spires-Jones, Tara L.;
- Young-Pearse, Tracy L.;
- Billinton, Andrew;
- Walsh, Dominic M.
Publication type:
Article
Tectal glioma harbors high rates of KRAS G12R and concomitant KRAS and BRAF alterations.
Published in:
Acta Neuropathologica, 2020, v. 139, n. 3, p. 601, doi. 10.1007/s00401-019-02112-x
By:
- Chiang, Jason;
- Li, Xiaoyu;
- Liu, Anthony P. Y.;
- Qaddoumi, Ibrahim;
- Acharya, Sahaja;
- Ellison, David W.
Publication type:
Article
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases.
Published in:
Acta Neuropathologica, 2020, v. 139, n. 3, p. 415, doi. 10.1007/s00401-019-02109-6
By:
- Perenthaler, Elena;
- Nikoncuk, Anita;
- Yousefi, Soheil;
- Berdowski, Woutje M.;
- Alsagob, Maysoon;
- Capo, Ivan;
- van der Linde, Herma C.;
- van den Berg, Paul;
- Jacobs, Edwin H.;
- Putar, Darija;
- Ghazvini, Mehrnaz;
- Aronica, Eleonora;
- van IJcken, Wilfred F. J.;
- de Valk, Walter G.;
- Medici-van den Herik, Evita;
- van Slegtenhorst, Marjon;
- Brick, Lauren;
- Kozenko, Mariya;
- Kohler, Jennefer N.;
- Bernstein, Jonathan A.
Publication type:
Article
Human subiculo-fornico-mamillary system in Alzheimer's disease: Tau seeding by the pillar of the fornix.
Published in:
Acta Neuropathologica, 2020, v. 139, n. 3, p. 443, doi. 10.1007/s00401-019-02108-7
By:
- Thierry, Manon;
- Boluda, Susana;
- Delatour, Benoît;
- Marty, Serge;
- Seilhean, Danielle;
- Brainbank Neuro-CEB Neuropathology Network;
- Letournel, Franck;
- Martin-Négrier, Marie-Laure;
- Chapon, Françoise;
- Godfraind, Catherine;
- Maurage, Claude-Alain;
- Deramecourt, Vincent;
- Meyronnet, David;
- Streichenberger, Nathalie;
- de Paula, André Maues;
- Rigau, Valérie;
- Vandenbos-Burel, Fanny;
- Duyckaerts, Charles;
- Plu, Isabelle;
- Milin, Serge
Publication type:
Article
Necrosome complex detected in granulovacuolar degeneration is associated with neuronal loss in Alzheimer's disease.
Published in:
Acta Neuropathologica, 2020, v. 139, n. 3, p. 463, doi. 10.1007/s00401-019-02103-y
By:
- Koper, Marta J.;
- Van Schoor, Evelien;
- Ospitalieri, Simona;
- Vandenberghe, Rik;
- Vandenbulcke, Mathieu;
- von Arnim, Christine A. F.;
- Tousseyn, Thomas;
- Balusu, Sriram;
- De Strooper, Bart;
- Thal, Dietmar Rudolf
Publication type:
Article
ACE2 activation protects against cognitive decline and reduces amyloid pathology in the Tg2576 mouse model of Alzheimer's disease.
Published in:
Acta Neuropathologica, 2020, v. 139, n. 3, p. 485, doi. 10.1007/s00401-019-02098-6
By:
- Evans, Charles E.;
- Miners, James S.;
- Piva, Giulia;
- Willis, Christine L.;
- Heard, David M.;
- Kidd, Emma J.;
- Good, Mark A.;
- Kehoe, Patrick G.
Publication type:
Article
Shortening heparan sulfate chains prolongs survival and reduces parenchymal plaques in prion disease caused by mobile, ADAM10-cleaved prions.
Published in:
Acta Neuropathologica, 2020, v. 139, n. 3, p. 527, doi. 10.1007/s00401-019-02085-x
By:
- Aguilar-Calvo, Patricia;
- Sevillano, Alejandro M.;
- Bapat, Jaidev;
- Soldau, Katrin;
- Sandoval, Daniel R.;
- Altmeppen, Hermann C.;
- Linsenmeier, Luise;
- Pizzo, Donald P.;
- Geschwind, Michael D.;
- Sanchez, Henry;
- Appleby, Brian S.;
- Cohen, Mark L.;
- Safar, Jiri G.;
- Edland, Steven D.;
- Glatzel, Markus;
- Nilsson, K. Peter R.;
- Esko, Jeffrey D.;
- Sigurdson, Christina J.
Publication type:
Article
Transcriptional profiling of medulloblastoma with extensive nodularity (MBEN) reveals two clinically relevant tumor subsets with VSNL1 as potent prognostic marker.
Published in:
Acta Neuropathologica, 2020, v. 139, n. 3, p. 583, doi. 10.1007/s00401-019-02102-z
By:
- Korshunov, Andrey;
- Okonechnikov, Konstantin;
- Sahm, Felix;
- Ryzhova, Marina;
- Stichel, Damian;
- Schrimpf, Daniel;
- Ghasemi, David R.;
- Pajtler, Kristian W.;
- Antonelli, Manila;
- Donofrio, Vittoria;
- Mastronuzzi, Angela;
- Rossi, Sabrina;
- Camassei, Francesca Diomedi;
- Buccoliero, Anna Maria;
- Haberler, Christine;
- Slavc, Irene;
- Dahiya, Sonika;
- Casalini, Belen;
- Sievers, Philipp;
- Meyer, Jochen
Publication type:
Article