Tau Structures

Amyloid oligomers exacerbate tau pathology in a mouse model of tauopathy

Selenica, M.-L. B., Brownlow, M., Jimenez, J. P., Lee, D. C., Pena, G., Dickey, C. A., Gordon, M. N., & Morgan, D. (2013) · Neurodegenerative Diseases · doi:10.1159/000337230 · Cited by 10,359

Abnormal phosphorylation of the microtubule-associated protein tau (tau) in Alzheimer cytoskeletal pathology.

Grundke-Iqbal, I., Iqbal, K., Tung, Y. C., Quinlan, M., Wisniewski, H. M., & Binder, L. I. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.13.4913 · Cited by 3,676

A protein factor essential for microtubule assembly

Weingarten, M. D., Lockwood, A. H., Hwo, S. Y., & Kirschner, M. W. (1975) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.72.5.1858 · Cited by 3,089

A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation

Patel, A., Lee, H. O., Jawerth, L. M., Maharana, S., Jahnel, M., Hein, M. Y., Stoynov, S., Mahamid, J., Saha, S., Franzmann, T. M., et al. (2015) · Cell · doi:10.1016/j.cell.2015.07.047 · Cited by 2,927

Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease

Goedert, M., Spillantini, M. G., Jakes, R., Rutherford, D., & Crowther, R. A. (1989) · Neuron · doi:10.1016/0896-6273(89)90210-9 · Cited by 2,492

Tau in physiology and pathology

Wang, Y., & Mandelkow, E. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2015.1 · Cited by 2,251

Paclitaxel (Taxol)

Rowinsky, E. K., & Donehower, R. C. (1995) · New England Journal of Medicine · doi:10.1056/nejm199504133321507 · Cited by 1,924

Dendritic Function of Tau Mediates Amyloid-β Toxicity in Alzheimer's Disease Mouse Models

Ittner, L. M., Ke, Y. D., Delerue, F., Bi, M., Gladbach, A., van Eersel, J., Wölfing, H., Chieng, B. C., Christie, M. J., Napier, I. A., et al. (2010) · Cell · doi:10.1016/j.cell.2010.06.036 · Cited by 1,821

Transmission and spreading of tauopathy in transgenic mouse brain

Clavaguera, F., Bolmont, T., Crowther, R. A., Abramowski, D., Frank, S., Probst, A., Fraser, G., Stalder, A. K., Beibel, M., Staufenbiel, M., et al. (2009) · Nature Cell Biology · doi:10.1038/ncb1901 · Cited by 1,803

Microtubule-associated protein tau. A component of Alzheimer paired helical filaments.

Grundke, I., Iqbal, K., Quinlan, M., Tung, Y. C., Zaidi, M. S., & Wisniewski, H. M. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)38495-8 · Cited by 1,780

Epigallocatechin -3- gallate mitigates diazinon neurotoxicity via suppression of pro-inflammatory genes and upregulation of antioxidant pathways

Onukak, C. E., Femi-Akinlosotu, O. M., Obasa, A. A., Folarin, O. R., Ajibade, T. O., Igado, O. O., Esan, O. O., Oyagbemi, T. O., Adeogun, A. V., Oyagbemi, A. A., et al. (2025) · BMC Neuroscience · doi:10.1186/s12868-025-00943-x · Cited by 4

Polyphenols as Potential Therapeutic Drugs in Neurodegeneration

de Laureto, P. P., Palazzi, L., & Acquasaliente, L. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.89575 · Cited by 3

Spectroscopic investigation of tau protein conformational changes by static magnetic field exposure

Darwish, S. M., & Darwish, I. M. (2022) · Journal of Physics Communications · doi:10.1088/2399-6528/ac7d3a · Cited by 3

Probing the Interactions of LRP1 Ectodomain-Derived Peptides with Fibrillar Tau Protein and Its Impact on Cellular Internalization

Boder, E. J., Goncalves, B. G., Lebedenko, C. G., & Banerjee, I. A. (2023) · Applied Sciences · doi:10.3390/app13020853 · Cited by 4

Association between glioma and neurodegenerative diseases risk: a two-sample bi-directional Mendelian randomization analysis

Liu, Y., Chen, Y., Gao, M., Luo, J., Wang, Y., Wang, Y., Gao, Y., Yang, L., Wang, J., & Wang, N. (2024) · Frontiers in Neurology · doi:10.3389/fneur.2024.1413015 · Cited by 5

The increase in TDP-43 and neurogranin blood levels at different stages of cognitive impairment in the elderly people: A cross-sectional study

Ochneva, A., Zakurazhnaya, V., Zorkina, Y., Abramova, O. V., Ushakova, V. M., Tsurina, A. M., Golubeva, E., Gurina, O. I., Berdalin, A., Syunyakov, T., et al. (2025) · Journal of Alzheimer s Disease · doi:10.1177/13872877251350385 · Cited by 2

The Interplay of Tau and Amyloid Beta Pathologies in Alzheimer's Disease

Harith, M. (2023) · Journal of Student Research · doi:10.47611/jsrhs.v12i4.5732 · Cited by 2

Protein aggregation in health and disease: A looking glass of two faces

de Andrade, G. C., Mota, M. F., Moreira-Ferreira, D. N., Silva, J. L., de Oliveira, G. A. P., & Marques, M. A. (2024) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2024.09.010 · Cited by 2

Molecular etiopathogenesis of neurodegenerative diseases

Divya, D., Thekkekkara, D., Sai, T. E., Ramakrishna, D., Manjula, S. N., & Goswami, S. K. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-28822-7.00002-7 · Cited by 2

The Prion-like Properties of Amyloid-beta Peptide and Tau: Is there Any Risk of Transmitting Alzheimer's Disease During Neurosurgical Interventions?

Padilla-Zambrano, H., García-Ballestas, E., Quiñones-Ossa, G. A., Sibaja-Perez, A. E., Agrawal, A., Moscote‐Salazar, L. R., & Menéndez‐González, M. (2020) · Current Alzheimer Research · doi:10.2174/1567205017666201204164220 · Cited by 2

Histological and Memory Alterations in an Innovative Alzheimer’s Disease Animal Model by Vanadium Pentoxide Inhalation

Dorado-Martínez, C., Montiel-Flores, E., Ordóñez-Librado, J. L., Gutiérrez-Valdez, A. L., Caballero, C. A. G., Sánchez-Betancourt, J., Erazo, L. R., Tron-Alvarez, R., Rodríguez-Lara, V., & Ávila-Costa, M. R. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-230818 · Cited by 3

Progressive supranuclear palsy: an updated approach on diagnosis, treatment, risk factors and outlook in Mexico

Gomez‐Virgilio, L., Gutierrez‐Malacara, A., Rivera‐Osorio, J., Silva‐Lucero, M., Padilla-Mendoza, J. R., Gómez-Ramírez, D. E., & Cárdenas-Aguayo, M. D. C. (2024) · Gaceta Médica de México · doi:10.24875/gmm.m24000930 · Cited by 1

Tau conformation, distribution and PET imaging correlations in progressive supranuclear palsy

Dong, C., Ma, J., Qiao, H., Tamagnan, G. D., Chan, P., & Liu, S. (2026) · Translational Neurodegeneration · doi:10.1186/s40035-026-00545-5 · Cited by 2

HIV-1 Tat and gp120 as key drivers of neurodegeneration in the central nervous system

Cecchetto, R., Diani, E., Lotti, V., Palmisano, A., Lagni, A., Mantoan, M., Turrina, S., Raniero, D., Paolone, G., Mazzariol, A., et al. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1895162 · Cited by 2

Current Advancements in the Treatment of Alzheimer’s Disease

Ajith, V., & Kalam, A. (2022) · Journal of Student Research · doi:10.47611/jsrhs.v11i4.3691 · Cited by 1

Protein–Protein Interactions in Neurodegenerative Diseases

Poluri, K. M., Gulati, K., Tripathi, D. K., & Nagar, N. (2023) · Springer eBooks · doi:10.1007/978-981-99-2423-3_3 · Cited by 2

Homology Modeling of Tubulin Isotypes to Investigate MT-Tau Interactions

Bhandare, V. V. (2021) · IntechOpen eBooks · doi:10.5772/intechopen.95792 · Cited by 1

Molekularne podłoże proteinopatii: przyczyna zespołów otępiennych i zaburzeń motorycznych

Zgórzyńska, E., Krawczyk, K., Bełdzińska, P., & Walczewska, A. (2021) · Postępy Higieny i Medycyny Doświadczalnej · doi:10.5604/01.3001.0014.9513

Siebte Schweizer Familienrecht§Tage

Schwenzer, I., Büchler, A., & Fankhauser, R. (2014) · Stämpfli eBooks

Analysis of Adult Hippocampal Neurogenesis in Neurodegenerative disease

HAN, G. (2022) · Cronfa (Swansea University) · doi:10.23889/suthesis.62147

Editorial Special Issue Neuroscience “Tauopathies”

Ávila, J., Santa‐María, I., & Sotiropulos, I. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.03.021

Dinámica molecular de grano grueso de la proteína tau

Robert-Jimenez, L., Figueroa-Gerstenmaier, S., Basurto‐Islas, G., & Herrera-Velarde, S. (2023) · Revista Mexicana de Física · doi:10.31349/revmexfis.69.031701 · Cited by 1

Linking the Meso and Macroscale Determinants of Cerebral AgeingPreprint

Paolo, R. D., Deery, H. A., & Jamadar, S. D. (2023) · PsyArXiv (OSF Preprints) · doi:10.31234/osf.io/8n4ud

Association of tau protein and Alzheimer’s disease

Lin, K. (2023) · Theoretical and Natural Science · doi:10.54254/2753-8818/6/20230194

Structural polymorphism in amyloids—states within proteins’ solid-state

Dhakal, S., & Rangachari, V. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-21809-5.00024-7

Histopathological and Behavioral Irreversible Damage Derived from Chronic Exposure to Vanadium Pentoxide Is Similar to that Found in Alzheimer’s Disease

Ávila-Costa, M. R., Dorado-Martínez, C., Montiel-Flores, E., Ordóñez-Librado, J. L., Gutiérrez-Valdez, A. L., Caballero, C. A. G., Sánchez-Betancourt, J., Erazo, L. R., Tron-Alvarez, R., Rodríguez-Lara, V., et al. (2024) · IntechOpen eBooks · doi:10.5772/intechopen.1007924

Imaging Markers of Amyloid and Tau in Alzheimer Disease

Tarawneh, R. M. (2025) · Springer eBooks · doi:10.1007/978-3-031-80849-4_20

Tau-Cytoskeleton and their interaction with other neurodegenerative proteins

Sahu, S., Rangappa, N., Chinnathambi, S., & Mishra, M. (2025) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2025.10.032

Heparin and fluoride drive distinct tau (4R/1 N) aggregation pathways to fibrils and granular oligomers, as revealed by Raman spectroscopy

Rouhbakhsh, H., Farkhari, N., Khatami, S. H., Ehtiati, S., Hosseini, M. M., Soleimani, Y., Rashidi, M., Tajalli, H., Ahmadi-Kandjani, S., Boostanipour, A., et al. (2025) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2025.2598636

Histidine behaviors effect on β-sheet-rich dimer formation of Tau R3 fragment: New insights on primary nucleation processes

Shi, H., Li, J., Sun, Y., Wang, L., Yan, L., & Pu, X. (2026) · Biophysical Chemistry · doi:10.1016/j.bpc.2026.107602

Dérégulation de l’homéostasie calcique du réticulum endoplasmique dans la maladie d’Alzheimer : rôle du récepteur de la ryanodine et de l’isoforme SERCA1 tronquée

Bussiere, R. (2018) · theses.fr (ABES) · doi:10.70675/2334ca11z42bfz4e8bza53bz02e8bbacc38e

Caractérisation d'anticorps à domaine unique dirigés contre la protéine Tau

Danis, C. (2018) · theses.fr (ABES) · doi:10.70675/c783a062zb57bz4024z85d0z509baaed8a1b

Interaction entre la protéine Tau et la protéine p54nrb : effet sur la maturation des miARN au sein des paraspeckles

Denéchaud, M. (2022) · theses.fr (ABES) · doi:10.70675/623e7224z0cb0z47b1z8a22z549acf553ac0

Therapeutic strategies for Tau and Alzheimer’s disease

Karthikeyan, K., & Chinnathambi, S. (2026) · Advances in pharmacology · doi:10.1016/bs.apha.2026.06.001

Targeting mtDNA to Modulate Mitochondrial Dysfunction in Neurodegenerative Diseases

Pramanik, S., Debnath, B., Chakraborty, A. J., Islam, A., Mullick, S., Chaudhary, P., Nath, R., Chellappan, D. K., Mondal, M., & Ashique, S. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-06008-2

Phase separation and protein aggregation in neurodegenerative diseases

Seiglière, H. D. L., Letourneur, Æ., Ichas, F., & Giorgi, F. D. (2026) · Biophysical Chemistry · doi:10.1016/j.bpc.2026.107678 · Cited by 1

Modulatory Effects of Camellia sinensis (Green Tea) on Glyphosate-Induced Neurobehavioural Deficits and Tau Gene Dysregulation in Wistar RatsPreprint

Bukoye, M. A., Oyewole, O. I., & Adetunji, J. B. (2026) · SSRN Electronic Journal · doi:10.2139/ssrn.7119392

Investigating the role of EFhd2 protein in modulating tau pathology in a tauopathy mouse model

Soliman, A. S., Umstead, A., & Vega, I. E. (2026) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2026.1833887

Pathological depositions in human disease: converging mechanisms in atherosclerosis, Alzheimer's disease, and related disorders

Ragolia, L. (2026) · Molecular Biomedicine · doi:10.1186/s43556-026-00552-y

Neurochemical and neurobehavioural alterations in glyphosate-intoxicated Wistar rats treated with green tea (Camellia sinensis)

Bukoye, M. A., Oyewole, O. I., & Adetunji, J. B. (2026) · Pharmacological Research - Reports · doi:10.1016/j.prerep.2026.100105

Tau in physiology and pathology

Wang, Y., & Mandelkow, E. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2015.1 · Cited by 2,251

It’s all about tau

Tapia‐Rojas, C., Cabezas-Opazo, F., Deaton, C. A., Vergara, E. H., Johnson, G. V. W., & Quintanilla, R. A. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.12.005 · Cited by 207

Probing forces generated and architectures mediated by Tau on microtubules

Chung, P. J. (2016) · eScholarship (California Digital Library)

Tau Protein Function in Axonal Formation

Paglini, M. G., Peris, L., Mascotti, F., Quiroga, S., & Cáceres, A. (2000) · Neurochemical Research · doi:10.1023/a:1007531230651 · Cited by 50

Tau: It’s Not What You Think

Baas, P. W., & Qiang, L. (2019) · Trends in Cell Biology · doi:10.1016/j.tcb.2019.02.007 · Cited by 123