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Papers matching “cell aggregation” 20

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Small-molecule modulators of TRMT2A decrease PolyQ aggregation and PolyQ-induced cell death
2021 Computational and Structural Biotechnology Journal article Neuroscience Genetic Neurodegenerative Diseases Open access

Michael A. Margreiter, Monika Witzenberger, Yasmine Wasser, Elena Davydova, Robert Janowski, Jonas Metz, +12 more

19

citations
Small-molecule modulators of TRMT2A decrease PolyQ aggregation and PolyQ-induced cell death
2021 bioRxiv (Cold Spring Harbor Laboratory) preprint Neuroscience Genetic Neurodegenerative Diseases Open access

Michael A. Margreiter, Monika Witzenberger, Yasmine Wasser, Elena Davydova, Robert Janowski, Carina Sobisch, +11 more

0

citations
Glutamine missense suppressor transfer RNAs inhibit polyglutamine aggregation
2024 Molecular Therapy — Nucleic Acids article Neuroscience Genetic Neurodegenerative Diseases Open access

Rasangi Tennakoon, Teija M.I. Bily, Farah Hasan, Sunidhi Syal, Aaron Voigt, Tuğçe B. Balcı, +2 more

4

citations
Surface‐modified protein crowders influence mutant huntingtin exon 1 aggregation via crowding effects, crowder association, and crowder solution stability
2025 Protein Science article Neuroscience Genetic Neurodegenerative Diseases Open access

Jakub Haduła, Sabrina T. Krepel, Dhanya Babu, Meng‐Ruo Huang, Arnold J. Boersma

3

citations
Structural Features of Pathogenic Aggregates Correlate with Cell Pathology in Differentiated Cells
2025 Research Square preprint Neuroscience Genetic Neurodegenerative Diseases Open access

Vered Raz, Sander D. Mallon, Erik Bos, Vahid Sheikhhassani, Milad Shademan, Lenard M. Voortman, +2 more

0

citations
New Insights into the Neuromyogenic Spectrum of a Gain of Function Mutation in SPTLC1
2022 Genes article Neuroscience Hereditary Neurological Disorders Open access

Heike Kölbel, Florian Kraft, Andreas Hentschel, Artur Czech, Andrea Gangfuß, Payam Mohassel, +5 more

7

citations
Polyalanine Expansion in PABPN1 Alters the Structure and Dynamics of Its Nuclear Aggregates in Differentiated Muscle Cells
2025 The FASEB Journal article Neuroscience Genetic Neurodegenerative Diseases Open access

Sander D. Mallon, Erik Bos, Vahid Sheikhhassani, Milad Shademan, Lenard M. Voortman, Alireza Mashaghi, +2 more

6

citations
Spinocerebellar Ataxia Type 1 Characteristics in Patient‐Derived Fibroblast and iPSC ‐Derived Neuronal Cultures
2023 Movement Disorders article Neuroscience Genetic Neurodegenerative Diseases Open access

Ronald A.M. Buijsen, Michel H. Y. Hu, Maria Sáez González, Sofia Notopoulou, Eleni Mina, Winette Koning, +10 more

16

citations
DNA Methyltransferase 1 (DNMT1) Acts on Neurodegeneration by Modulating Proteostasis-Relevant Intracellular Processes
2020 International Journal of Molecular Sciences article Neuroscience Genetic Neurodegenerative Diseases Open access

Cathrin Bayer, Georg Pitschelatow, Nina Hannemann, Jenice Linde, Julia Reichard, Daniel Pensold, +1 more

21

citations
I13 Polyqure- inhibiton of TRMT2A to cure polyQ diseases
2022 conference-abstract Neuroscience Genetic Neurodegenerative Diseases

Aaron Voigt, Sabine Hamm, Dierk Niessing

0

citations
Glucocorticoid receptor antagonist CORT113176 attenuates motor and neuropathological symptoms of Huntington's disease in R6/2 mice
2024 Experimental Neurology article Neuroscience Genetic Neurodegenerative Diseases Open access

Max Gentenaar, Fleur L. Meulmeester, Ximaine R. van der Burg, Anna T. Hoekstra, Hazel Hunt, Jan Kroon, +2 more

7

citations
Autoimmune signatures in neurodegenerative dementias: from peripheral immune activation to CNS pathology
2026 Frontiers in Immunology review Neuroscience Neuroinflammation and Neurodegeneration Mechanisms Open access

Xin Zhao, Guifeng Zhang, Zheng Wang, D J Zhang, Zhangyong Xia, Chengju Huo

0

citations
Developing HDAC4-Selective Protein Degraders To Investigate the Role of HDAC4 in Huntington’s Disease Pathology
2022 Journal of Medicinal Chemistry article Neuroscience Genetic Neurodegenerative Diseases Open access

Natsuko Macabuag, William Esmieu, Perla Breccia, Rebecca E. Jarvis, Wesley Blackaby, Ovadia Lazari, +19 more

34

citations
A pathogenic proteolysis–resistant huntingtin isoform induced by an antisense oligonucleotide maintains huntingtin function
2022 JCI Insight article Neuroscience Genetic Neurodegenerative Diseases Open access

Hyeongju Kim, Sophie Lenoir, Angela Helfricht, Tae‐Yang Jung, Zhana K. Karneva, Wouter Beumer, +11 more

14

citations
Pathogenic LRSAM1 RING Domain Variants Disrupt Intracellular Protein Localization in Charcot–Marie–Tooth Disease Type 2P
2026 Human Mutation article Neuroscience Hereditary Neurological Disorders Open access

Johanna E. Hakonen, Tom P. Hellings, Esther Dingemanse, Bo Laman, Olaf J. Froncek, NynkeWienholts, +5 more

0

citations
Neurofilaments in spinocerebellar ataxia type 3: blood biomarkers at the preataxic and ataxic stage in humans and mice
2020 EMBO Molecular Medicine article Neuroscience Genetic Neurodegenerative Diseases Open access

Carlo Wilke, Eva Haas, Kathrin Reetz, Jennifer Faber, Héctor García‐Moreno, Magda M. Santana, +30 more

108

citations
Influence of ATXN2 intermediate CAG repeats, 9bp duplication and alternative splicing on SCA3 pathogenesis
2025 Acta Neuropathologica Communications article Neuroscience Genetic Neurodegenerative Diseases Open access

Marilena Lauerer, Jennifer Faber, Nicolas Casadei, Magda M. Santana, Georg W. J. Auburger, Michaela Pogoda, +22 more

3

citations
The DNA methyltransferase 1 (DNMT1) acts on neurodegeneration by modulating proteostasis-relevant intracellular processes
2020 bioRxiv (Cold Spring Harbor Laboratory) preprint Neuroscience Genetic Neurodegenerative Diseases Open access

Cathrin Bayer, Georg Pitschelatow, Nina Hannemann, Jenice Linde, Julia Reichard, Daniel Pensold, +1 more

9

citations
Exon 1-targeting miRNA reduces the pathogenic exon 1 HTT protein in Huntington's disease models
2024 Brain article Neuroscience Genetic Neurodegenerative Diseases Open access

Marina Sogorb-González, Christian Landles, Nicholas S. Caron, Anouk Stam, Georgina F Osborne, Michael R. Hayden, +5 more

26

citations
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss
2021 Human Molecular Genetics article Neuroscience Hearing, Cochlea, Tinnitus, Genetics Open access

Sissy Bassani, Edward S. A. van Beelen, Mireille Rossel, Norine Voisin, Anna Morgan, Yoan Arribat, +20 more

13

citations

20 results