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Correction

Correction: Dominguez-Meijide et al. Pharmacological Modulators of Tau Aggregation and Spreading. Brain Sci. 2020, 10, 858

by
Antonio Dominguez-Meijide
1,2,
Eftychia Vasili
1 and
Tiago Fleming Outeiro
1,3,4,*
1
Department of Experimental Neurodegeneration, Center for Biostructural Imaging of Neurodegeneration, University Medical Center Goettingen, 37073 Goettingen, Germany
2
Laboratory of Neuroanatomy and Experimental Neurology, Dept. of Morphological Sciences, CIMUS, IDIS, University of Santiago de Compostela, 15782 Santiago de Compostela, Spain
3
Max Planck Institute for Experimental Medicine, 37075 Goettingen, Germany
4
Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Framlington Place, Newcastle Upon Tyne NE2 4HH, UK
*
Author to whom correspondence should be addressed.
Brain Sci. 2024, 14(9), 909; https://doi.org/10.3390/brainsci14090909 (registering DOI)
Submission received: 6 August 2024 / Accepted: 8 August 2024 / Published: 9 September 2024
There was an error in the original publication [1]. References 34, 41, 52, 53, 56, 61, 64, 65, 68, 69, 71, 72, 74, 75, 76, 77, 81, 85, 86, 110, 112, and 114 were not the ones intended, and were unrelated with the main text. A correction has been made to References 34, 41, 52, 53, 56, 61, 64, 65, 68, 69, 71, 72, 74, 75, 76, 77, 81, 85, 86, 110, 112, and 114, and appear as follows:
34.
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69.
Lee, V.M.; Balin, B.J.; Otvos, L., Jr.; Trojanowski, J.Q. A68: A major subunit of paired helical filaments and derivatized forms of normal tau. Science 1991, 251, 675–678.
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Weissmann, C.; Reyher, H.J.; Gauthier, A.; Steinhoff, H.J.; Junge, W.; Brandt, R. Microtubule binding and trapping at the tip of neurites regulate tau motion in living neurons. Traffic 2009, 10, 1655–1668.
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Lathuilière, A.; Valdés, P.; Papin, S.; Cacquevel, M.; Maclachlan, C.; Knott, G.W.; Muhs, A.; Paganetti, P.; Schneider, B.L. Motifs in the tau protein that control binding to microtubules and aggregation determine pathological effects. Sci. Rep. 2017, 7, 13556.
74.
Barthélemy, N.R.; Li, Y.; Joseph-Mathurin, N.; Gordon, B.A.; Hassenstab, J.; Benzinger, T.L.; Buckles, V.; Fagan, A.M.; Perrin, R.J.; Goate, A.M.; et al. A soluble phosphorylated tau signature links tau, amyloid and the evolution of stages of dominantly inherited Alzheimer’s disease. Nat. Med. 2020, 26, 398–407.
75.
Mocanu, M.M.; Nissen, A.; Eckermann, K.; Khlistunova, I.; Biernat, J.; Drexler, D.; Petrova, O.; Schönig, K.; Bujard, H.; Mandelkow, E.; et al. The potential for beta-structure in the repeat domain of tau protein determines aggregation, synaptic decay, neuronal loss, and coassembly with endogenous Tau in inducible mouse models of tauopathy. J. Neurosci. 2008, 28, 737–748.
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Olsen, M.; Aguilar, X.; Sehlin, D.; Fang, X.T.; Antoni, G.; Erlandsson, A.; Syvänen, S. Astroglial Responses to Amyloid-Beta Progression in a Mouse Model of Alzheimer’s Disease. Mol. Imaging Biol. 2018, 20, 605–614.
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Valotassiou, V.; Malamitsi, J.; Papatriantafyllou, J.; Dardiotis, E.; Tsougos, I.; Psimadas, D.; Alexiou, S.; Hadjigeorgiou, G.; Georgoulias, P. SPECT and PET imaging in Alzheimer’s disease. Ann. Nucl. Med. 2018, 32, 583–593.
81.
Ferrer, I.; Andrés-Benito, P.; Zelaya, M.V.; Aguirre, M.E.E.; Carmona, M.; Ausín, K.; Lachén-Montes, M.; Fernández-Irigoyen, J.; Santamaría, E.; Del Rio, J.A. Familial globular glial tauopathy linked to MAPT mutations: Molecular neuropathology and seeding capacity of a prototypical mixed neuronal and glial tauopathy. Acta. Neuropathol. 2020, 139, 735–771.
85.
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Amadoro, G.; Latina, V.; Corsetti, V.; Calissano, P. N-terminal tau truncation in the pathogenesis of Alzheimer’s disease (AD): Developing a novel diagnostic and therapeutic approach. Biochim. Biophys. Acta. Mol. Basis Dis. 2020, 1866, 165584.
110.
Maeda, S.; Sahara, N.; Saito, Y.; Murayama, M.; Yoshiike, Y.; Kim, H.; Miyasaka, T.; Murayama, S.; Ikai, A.; Takashima, A. Granular tau oligomers as intermediates of tau filaments. Biochemistry 2007, 46, 3856–3861.
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Michel, C.H.; Kumar, S.; Pinotsi, D.; Tunnacliffe, A.; St George-Hyslop, P.; Mandelkow, E.; Mandelkow, E.M.; Kaminski, C.F.; Kaminski Schierle, G.S. Extracellular monomeric tau protein is sufficient to initiate the spread of tau protein pathology. J. Biol. Chem. 2014, 289, 956–967.
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The authors state that the scientific conclusions are unaffected. This correction was approved by the Academic Editor. The original publication has also been updated.

Reference

  1. Dominguez-Meijide, A.; Vasili, E.; Outeiro, T.F. Pharmacological Modulators of Tau Aggregation and Spreading. Brain Sci. 2020, 10, 858. [Google Scholar] [CrossRef] [PubMed]
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MDPI and ACS Style

Dominguez-Meijide, A.; Vasili, E.; Outeiro, T.F. Correction: Dominguez-Meijide et al. Pharmacological Modulators of Tau Aggregation and Spreading. Brain Sci. 2020, 10, 858. Brain Sci. 2024, 14, 909. https://doi.org/10.3390/brainsci14090909

AMA Style

Dominguez-Meijide A, Vasili E, Outeiro TF. Correction: Dominguez-Meijide et al. Pharmacological Modulators of Tau Aggregation and Spreading. Brain Sci. 2020, 10, 858. Brain Sciences. 2024; 14(9):909. https://doi.org/10.3390/brainsci14090909

Chicago/Turabian Style

Dominguez-Meijide, Antonio, Eftychia Vasili, and Tiago Fleming Outeiro. 2024. "Correction: Dominguez-Meijide et al. Pharmacological Modulators of Tau Aggregation and Spreading. Brain Sci. 2020, 10, 858" Brain Sciences 14, no. 9: 909. https://doi.org/10.3390/brainsci14090909

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