Works matching IS 00016322 AND DT 2023 AND VI 146 AND IP 2

Results: 11

Mutation ∆K281 in MAPT causes Pick's disease.
Published in:
Acta Neuropathologica, 2023, v. 146, n. 2, p. 211, doi. 10.1007/s00401-023-02598-6
By:
- Schweighauser, Manuel;
- Garringer, Holly J.;
- Klingstedt, Therése;
- Nilsson, K. Peter R.;
- Masuda-Suzukake, Masami;
- Murrell, Jill R.;
- Risacher, Shannon L.;
- Vidal, Ruben;
- Scheres, Sjors H. W.;
- Goedert, Michel;
- Ghetti, Bernardino;
- Newell, Kathy L.
Publication type:
Article
A T-cell antigen atlas for meningioma: novel options for immunotherapy.
Published in:
Acta Neuropathologica, 2023, v. 146, n. 2, p. 173, doi. 10.1007/s00401-023-02605-w
By:
- Medici, Gioele;
- Freudenmann, Lena K.;
- Velz, Julia;
- Wang, Sophie Shih-Yüng;
- Kapolou, Konstantina;
- Paramasivam, Nagarajan;
- Mühlenbruch, Lena;
- Kowalewski, Daniel J.;
- Vasella, Flavio;
- Bilich, Tatjana;
- Frey, Beat M.;
- Dubbelaar, Marissa L.;
- Patterson, Angelica Brooke;
- Zeitlberger, Anna Maria;
- Silginer, Manuela;
- Roth, Patrick;
- Weiss, Tobias;
- Wirsching, Hans-Georg;
- Krayenbühl, Niklaus;
- Bozinov, Oliver
Publication type:
Article
Individual myasthenia gravis autoantibody clones can efficiently mediate multiple mechanisms of pathology.
Published in:
Acta Neuropathologica, 2023, v. 146, n. 2, p. 319, doi. 10.1007/s00401-023-02603-y
By:
- Pham, Minh C.;
- Masi, Gianvito;
- Patzina, Rosa;
- Obaid, Abeer H.;
- Oxendine, Seneca R.;
- Oh, Sangwook;
- Payne, Aimee S.;
- Nowak, Richard J.;
- O'Connor, Kevin C.
Publication type:
Article
Defective cerebellar ryanodine receptor type 1 and endoplasmic reticulum calcium 'leak' in tremor pathophysiology.
Published in:
Acta Neuropathologica, 2023, v. 146, n. 2, p. 301, doi. 10.1007/s00401-023-02602-z
By:
- Martuscello, Regina T.;
- Chen, Meng-Ling;
- Reiken, Steven;
- Sittenfeld, Leah R.;
- Ruff, David S.;
- Ni, Chun-Lun;
- Lin, Chih-Chun;
- Pan, Ming-Kai;
- Louis, Elan D.;
- Marks, Andrew R.;
- Kuo, Sheng-Han;
- Faust, Phyllis L.
Publication type:
Article
Tau seeding and spreading in vivo is supported by both AD-derived fibrillar and oligomeric tau.
Published in:
Acta Neuropathologica, 2023, v. 146, n. 2, p. 191, doi. 10.1007/s00401-023-02600-1
By:
- Mate De Gerando, Anastasie;
- Welikovitch, Lindsay A.;
- Khasnavis, Anita;
- Commins, Caitlin;
- Glynn, Calina;
- Chun, Joshua E.;
- Perbet, Romain;
- Hyman, Bradley T.
Publication type:
Article
Transcriptomic profiling of Parkinson's disease brains reveals disease stage specific gene expression changes.
Published in:
Acta Neuropathologica, 2023, v. 146, n. 2, p. 227, doi. 10.1007/s00401-023-02597-7
By:
- Cappelletti, Chiara;
- Henriksen, Sandra Pilar;
- Geut, Hanneke;
- Rozemuller, Annemieke J. M.;
- van de Berg, Wilma D. J.;
- Pihlstrøm, Lasse;
- Toft, Mathias
Publication type:
Article
From methylation to myelination: epigenomic and transcriptomic profiling of chronic inactive demyelinated multiple sclerosis lesions.
Published in:
Acta Neuropathologica, 2023, v. 146, n. 2, p. 283, doi. 10.1007/s00401-023-02596-8
By:
- Tiane, Assia;
- Schepers, Melissa;
- Reijnders, Rick A.;
- van Veggel, Lieve;
- Chenine, Sarah;
- Rombaut, Ben;
- Dempster, Emma;
- Verfaillie, Catherine;
- Wasner, Kobi;
- Grünewald, Anne;
- Prickaerts, Jos;
- Pishva, Ehsan;
- Hellings, Niels;
- van den Hove, Daniel;
- Vanmierlo, Tim
Publication type:
Article
Mutant LRRK2 exacerbates immune response and neurodegeneration in a chronic model of experimental colitis.
Published in:
Acta Neuropathologica, 2023, v. 146, n. 2, p. 245, doi. 10.1007/s00401-023-02595-9
By:
- Cabezudo, Diego;
- Tsafaras, George;
- Van Acker, Eva;
- Van den Haute, Chris;
- Baekelandt, Veerle
Publication type:
Article
Central and peripheral myeloid-derived suppressor cell-like cells are closely related to the clinical severity of multiple sclerosis.
Published in:
Acta Neuropathologica, 2023, v. 146, n. 2, p. 263, doi. 10.1007/s00401-023-02593-x
By:
- Ortega, María Cristina;
- Lebrón-Galán, Rafael;
- Machín-Díaz, Isabel;
- Naughton, Michelle;
- Pérez-Molina, Inmaculada;
- García-Arocha, Jennifer;
- Garcia-Dominguez, Jose Manuel;
- Goicoechea-Briceño, Haydee;
- Vila-del Sol, Virginia;
- Quintanero-Casero, Víctor;
- García-Montero, Rosa;
- Galán, Victoria;
- Calahorra, Leticia;
- Camacho-Toledano, Celia;
- Martínez-Ginés, María Luisa;
- Fitzgerald, Denise C.;
- Clemente, Diego
Publication type:
Article
SCA34 caused by ELOVL4 L168F mutation is a lysosomal lipid storage disease sharing pathology features with neuronal ceroid lipofuscinosis and peroxisomal disorders.
Published in:
Acta Neuropathologica, 2023, v. 146, n. 2, p. 337, doi. 10.1007/s00401-023-02582-0
By:
- Ellezam, Benjamin;
- Kaseka, Matsanga L.;
- Nguyen, Dang Khoa;
- Michaud, Jean
Publication type:
Article
AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model.
Published in:
Acta Neuropathologica, 2023, v. 146, n. 2, p. 353, doi. 10.1007/s00401-023-02579-9
By:
- Deng, Ruizhi;
- Medico-Salsench, Eva;
- Nikoncuk, Anita;
- Ramakrishnan, Reshmi;
- Lanko, Kristina;
- Kühn, Nikolas A.;
- van der Linde, Herma C.;
- Lor-Zade, Sarah;
- Albuainain, Fatimah;
- Shi, Yuwei;
- Yousefi, Soheil;
- Capo, Ivan;
- van den Herik, Evita Medici;
- van Slegtenhorst, Marjon;
- van Minkelen, Rick;
- Geeven, Geert;
- Mulder, Monique T.;
- Ruijter, George J. G.;
- Lütjohann, Dieter;
- Jacobs, Edwin H.
Publication type:
Article