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Papers matching “polyglutamine diseases” 19

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

Aaron Voigt, Sabine Hamm, Dierk Niessing

0

citations
Development of mAb-based polyglutamine-dependent and polyglutamine length-independent huntingtin quantification assays with cross-site validation
2022 PLoS ONE article Neuroscience Genetic Neurodegenerative Diseases Open access

David F. Fischer, Sipke Dijkstra, Kimberly Lo, Johnny Suijker, Ana C. P. Correia, Patricia Naud, +6 more

8

citations
ConvNets for automatic detection of polyglutamine SCAs from brain MRIs: state of the art applications
2022 Medical & Biological Engineering & Computing article Neuroscience Genetic Neurodegenerative Diseases Open access

Robin Cabeza-Ruiz, Luis Velázquez‐Pérez, Roberto Pérez‐Rodríguez, Kathrin Reetz

0

citations
Polyglutamine-expanded ataxin-3: a target engagement marker for Spinocerebellar ataxia type 3 in peripheral blood
2021 Research Square preprint Neuroscience Genetic Neurodegenerative Diseases Open access

Jeannette Hübener‐Schmid, Kirsten Kuhlbrodt, Julien Peladan, Jennifer Faber, Magda M. Santana, Holger Hengel, +17 more

0

citations
Polyglutamine‐Expanded Ataxin‐3: A Target Engagement Marker for Spinocerebellar Ataxia Type 3 in Peripheral Blood
2021 Movement Disorders article Neuroscience Genetic Neurodegenerative Diseases Open access

Jeannette Hübener‐Schmid, Kirsten Kuhlbrodt, Julien Peladan, Jennifer Faber, Magda M. Santana, Holger Hengel, +17 more

36

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
Polyglutamine expansion induced dynamic misfolding of androgen receptor
2025 Protein Science article Neuroscience Genetic Neurodegenerative Diseases Open access

Laurens W.H.J. Heling, Vahid Sheikhhassani, Alba Jiménez‐Panizo, Andrea Alegre‐Martí, Jaie C. Woodard, Willeke van Roon‐Mom, +3 more

1

citations
Polyglutamine expansion induced dynamic misfolding of Androgen Receptor
2024 bioRxiv (Cold Spring Harbor Laboratory) preprint Neuroscience Genetic Neurodegenerative Diseases Open access

Laurens W.H.J. Heling, Vahid Sheikhhassani, Alba Jiménez‐Panizo, Andrea Alegre‐Martí, Jaie C. Woodard, Willeke van Roon‐Mom, +3 more

0

citations
B002 The Dutch CureQ consortium: using IPSC modelling and clinical and biomarker data from patients to predict, delay and cure polyglutamine caused neurodegeneration
2024 conference-abstract Neuroscience Genetic Neurodegenerative Diseases Open access

Willeke van Roon‐Mom, Ineke L L E Bolt, Jurre Hageman, Bart Baselmans, Harm H. Kampinga, Monique T. Mulder, +5 more

0

citations
Accurate Quantification of Mutant and Wild-Type polyQ Proteins Using Simple Western Capillary Immunoassays
2025 Molecular Neurobiology article Neuroscience Genetic Neurodegenerative Diseases Open access

Bas Röttgering, Janwillem Testerink, Rudie Weij, Chantal Beekman, Nicole A. Datson

0

citations
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
Sex- and Depression-specific Effects of Non-pathogenic CAG Repeats in HTT, ATXN3 and CACNA1A on Sleep
2025 SSRN Electronic Journal preprint Neuroscience Genetic Neurodegenerative Diseases Open access

Linjun Ao, Raymond Noordam, N. Ahmad Aziz, Tariq O. Faquih, See PDF

0

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
Loss of astrocytic markers and impaired metabolic function in spinocerebellar ataxia type 7 patient-derived neural cultures
2026 Neurobiology of Disease article Neuroscience Genetic Neurodegenerative Diseases Open access

Linde F. Bouwman, Ronald A.M. Buijsen, Linda M. van der Graaf, Barry A. Pepers, Bas J. B. Voesenek, Hailiang Mei, +2 more

0

citations
FibrilPaints for visualisation and ubiquitination of Huntingtin amyloid fibrils
2025 bioRxiv (Cold Spring Harbor Laboratory) preprint Neuroscience Genetic Neurodegenerative Diseases Open access

Françoise A. Dekker, Emile van Weert, Tommaso Garfagnini, Júlia Aragonès Pedrola, Alfred C.O. Vertegaal, Assaf Friedler, +1 more

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
The MID1 Protein: A Promising Therapeutic Target in Huntington’s Disease
2021 Frontiers in Genetics article Neuroscience Genetic Neurodegenerative Diseases Open access

Annika Heinz, Judith Schilling, Willeke van Roon‐Mom, Sybille Krauß

18

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

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