Ausgabe 5/2023
Inhalt (12 Artikel)
Biomarkers for parkinsonian disorders in CNS-originating EVs: promise and challenges
Suman Dutta, Simon Hornung, Hash Brown Taha, Gal Bitan
Urinary tract infections trigger synucleinopathy via the innate immune response
Wouter Peelaerts, Gabriela Mercado, Sonia George, Marie Villumsen, Alysa Kasen, Miguel Aguileta, Christian Linstow, Alexandra B. Sutter, Emily Kuhn, Lucas Stetzik, Rachel Sheridan, Liza Bergkvist, Lindsay Meyerdirk, Allison Lindqvist, Martha L. Escobar Gavis, Chris Van den Haute, Scott J. Hultgren, Veerle Baekelandt, J. Andrew Pospisilik, Tomasz Brudek, Susana Aznar, Jennifer A. Steiner, Michael X. Henderson, Lena Brundin, Magdalena I. Ivanova, Tom J. Hannan, Patrik Brundin
New SNCA mutation and structures of α-synuclein filaments from juvenile-onset synucleinopathy
Yang Yang, Holly J. Garringer, Yang Shi, Sofia Lövestam, Sew Peak-Chew, Xianjun Zhang, Abhay Kotecha, Mehtap Bacioglu, Atsuo Koto, Masaki Takao, Maria Grazia Spillantini, Bernardino Ghetti, Ruben Vidal, Alexey G. Murzin, Sjors H. W. Scheres, Michel Goedert
Phosphatidylinositol-3,4,5-trisphosphate interacts with alpha-synuclein and initiates its aggregation and formation of Parkinson’s disease-related fibril polymorphism
Chi-Jing Choong, César Aguirre, Keita Kakuda, Goichi Beck, Hiroki Nakanishi, Yasuyoshi Kimura, Shuichi Shimma, Kei Nabekura, Makoto Hideshima, Junko Doi, Keiichi Yamaguchi, Kichitaro Nakajima, Tomoya Wadayama, Hideki Hayakawa, Kousuke Baba, Kotaro Ogawa, Toshihide Takeuchi, Shaymaa Mohamed Mohamed Badawy, Shigeo Murayama, Seiichi Nagano, Yuji Goto, Yohei Miyanoiri, Yoshitaka Nagai, Hideki Mochizuki, Kensuke Ikenaka
Dysregulation of astrocytic Ca2+ signaling and gliotransmitter release in mouse models of α-synucleinopathies
Carmen Nanclares, Jonah Poynter, Hector A. Martell-Martinez, Scott Vermilyea, Alfonso Araque, Paulo Kofuji, Michael K. Lee, Ana Covelo
Spinal astrocyte dysfunction drives motor neuron loss in late-onset spinal muscular atrophy
Linda-Isabell Schmitt, Christina David, Rebecca Steffen, Stefanie Hezel, Andreas Roos, Ulrike Schara-Schmidt, Christoph Kleinschnitz, Markus Leo, Tim Hagenacker
A point mutation in GPI-attachment signal peptide accelerates the development of prion disease
Atsushi Kobayashi, Tetsuya Hirata, Taishi Shimazaki, Yoshiko Munesue, Keisuke Aoshima, Takashi Kimura, Junko Nio-Kobayashi, Rie Hasebe, Atsuko Takeuchi, Yuichi Matsuura, Satoshi Kusumi, Daisuke Koga, Yasushi Iwasaki, Taroh Kinoshita, Shirou Mohri, Tetsuyuki Kitamoto
Molecular characterisation defines clinically-actionable heterogeneity within Group 4 medulloblastoma and improves disease risk-stratification
Jack Goddard, Jemma Castle, Emily Southworth, Anya Fletcher, Stephen Crosier, Idoia Martin-Guerrero, Miguel García-Ariza, Aurora Navajas, Julien Masliah-Planchon, Franck Bourdeaut, Christelle Dufour, Olivier Ayrault, Tobias Goschzik, Torsten Pietsch, Martin Sill, Stefan M. Pfister, Stefan Rutkowski, Stacey Richardson, Rebecca M. Hill, Daniel Williamson, Simon Bailey, Edward C. Schwalbe, Steven C. Clifford, Debbie Hicks
Glioneuronal tumor with ATRX alteration, kinase fusion and anaplastic features (GTAKA): a molecularly distinct brain tumor type with recurrent NTRK gene fusions
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
Mutations in ARHGEF15 cause autosomal dominant hereditary cerebral small vessel disease and osteoporotic fracture
Xuebing Ding, Yongkang Chen, Cancan Guo, Yu Fu, Chi Qin, Qingyong Zhu, Jiuqi Wang, Rui Zhang, Haiyan Tian, Renyi Feng, Han Liu, Dongxiao Liang, Guanghui Wang, Junfang Teng, Jinchen Li, Beisha Tang, Xuejing Wang
Cross-β helical filaments of Tau and TMEM106B in gray and white matter of multiple system tauopathy with presenile dementia
Md. Rejaul Hoq, Sakshibeedu R. Bharath, Grace I. Hallinan, Anllely Fernandez, Frank S. Vago, Kadir A. Ozcan, Daoyi Li, Holly J. Garringer, Ruben Vidal, Bernardino Ghetti, Wen Jiang
Correction to: Isoform-specific patterns of tau burden and neuronal degeneration in MAPT-associated frontotemporal lobar degeneration
Lucia A. A. Giannini, Daniel T. Ohm, Annemieke J. M. Rozemuller, Laynie Dratch, EunRan Suh, Vivianna M. van Deerlin, John Q. Trojanowski, Edward B. Lee, John C. van Swieten, Murray Grossman, Harro Seelaar, David J. Irwin