Tau and tauopathies

Novel Method to Quantify Neuropil Threads in Brains from Elders With or Without Cognitive Impairment

Mitchell, T. W., Nissanov, J., Han, L.-Y., Mufson, E. J., Schneider, J. A., Cochran, E. J., Bennett, D. A., Lee, V. M.-Y., Trojanowski, J. Q., & Arnold, S. E. (2000) · Journal of Histochemistry & Cytochemistry · doi:10.1177/002215540004801206 · Cited by 78

ptl-1, aCaenorhabditis elegansGene Whose Products Are Homologous to the τ Microtubule-Associated Proteins,

McDermott, J. B., Aamodt, S., & Aamodt, E. J. (1996) · Biochemistry · doi:10.1021/bi952646n · Cited by 78

A novel L266V mutation of the tau gene causes frontotemporal dementia with a unique tau pathology

Kobayashi, T., Ota, S., Tanaka, K., Ito, Y., Hasegawa, M., Umeda, Y., Motoi, Y., Takanashi, M., Yasuhara, M., Anno, M., et al. (2002) · Annals of Neurology · doi:10.1002/ana.10447 · Cited by 78

Tau pathology in children and young adults: can you still be unconditionally baptist?

Duyckaerts, C. J. (2011) · Acta Neuropathologica · doi:10.1007/s00401-010-0794-7 · Cited by 77

Neuronal plasticity in hibernation and the proposed role of the microtubule-associated protein tau as a “master switch” regulating synaptic gain in neuronal networks

Arendt, T., & Bullmann, T. (2013) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00117.2013 · Cited by 77

The Neurofibrillary Pathology of Alzheimer's Disease

Goedert, M. (1997) · The Neuroscientist · doi:10.1177/107385849700300212 · Cited by 77

Mixed tau, TDP-43 and p62 pathology in FTLD associated with a C9ORF72 repeat expansion and p.Ala239Thr MAPT (tau) variant

King, A., Al‐Sarraj, S., Troakes, C., Smith, B. N., Maekawa, S., Iovino, M., Spillantini, M. G., & Shaw, C. E. (2012) · Acta Neuropathologica · doi:10.1007/s00401-012-1050-0 · Cited by 76

Amyloid β (Aβ) and phospho-tau (p-tau) as diagnostic biomarkers in Alzheimer's disease

Prvulovic, D., & Hampel, H. J. (2011) · Clinical Chemistry and Laboratory Medicine (CCLM) · doi:10.1515/cclm.2011.087 · Cited by 76

Presenile appearance of abundant Alzheimer's neurofibrillary tangles without senile plaques in the brain in myotonic dystrophy

Kiuchi, A., Otsuka, N., Namba, Y., Nakano, I., & Tomonaga, M. (1991) · Acta Neuropathologica · doi:10.1007/bf00310916 · Cited by 76

Heroin abuse exaggerates age-related deposition of hyperphosphorylated tau and p62-positive inclusions

Kovács, G. G., Horváth, M., Majtényi, K., Lutz, M. I., Hurd, Y. L., & Keller, É. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.07.018 · Cited by 75

Splicing of a Regulated Exon Reveals Additional Complexity in the Axonal Microtubule‐Associated Protein Tau

Wei, M., & Andreadis, A. (1998) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1998.70041346.x · Cited by 75

Tau impacts on growth-factor-stimulated actin remodeling

Sharma, V. M., Litersky, J. M., Bhaskar, K., & Lee, G. S. (2007) · Journal of Cell Science · doi:10.1242/jcs.03378 · Cited by 75

Physiological and Pathophysiological Implications of Synaptic Tau

Regan, P. L., Whitcomb, D. J., & Cho, K. (2016) · The Neuroscientist · doi:10.1177/1073858416633439 · Cited by 75

Seasonal proteomic changes reveal molecular adaptations to preserve and replenish liver proteins during ground squirrel hibernation

Epperson, L. E., Rose, J. C., Carey, H. V., & Martin, S. L. (2009) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00416.2009 · Cited by 74

Neurodegenerative diseases with cytoskeletal pathology: A biochemical classification

Dickson, D. W. (1997) · Annals of Neurology · doi:10.1002/ana.410420403 · Cited by 73

Characterization of Neuronal Tau Protein as a Target of Extracellular Signal-regulated Kinase

Qi, H., Prabakaran, S., Cantrelle, F., Chambraud, B., Gunawardena, J., Lippens, G. M., & Landrieu, I. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.700914 · Cited by 73

Binding of Hsp90 to Tau Promotes a Conformational Change and Aggregation of Tau Protein

Tortosa, E., Santa‐María, I., Moreno, F. J., Lim, F., Pérez, M., & Ávila, J. (2009) · Journal of Alzheimer s Disease · doi:10.3233/jad-2009-1049 · Cited by 72

Dendritic reorganisation in the basal forebrain under degenerative conditions and its defects in Alzheimer's disease. III. The basal forebrain compared with other subcortical areas

Arendt, T., Brückner, M. K., Bigl, V., & Marcova, L. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903510204 · Cited by 72

Activated Mitogenic Signaling Induces a Process of Dedifferentiation in Alzheimer's Disease That Eventually Results in Cell Death

Arendt, T., Holzer, M., Stöbe, A., GÄRTNER, U., Lüth, H., Brückner, M. K., & Ueberham, U. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06931.x · Cited by 72

Principles of rat subcortical forebrain organization: a study using histological techniques and multiple fluorescence labeling

Riedel, A., Härtig, W., Seeger, G., Gärtner, U., Brauer, K., & Arendt, T. (2002) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(01)00142-9 · Cited by 72

Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles

Ghetti, B. F., Tagliavini, F., Giaccone, G., et al. (1994) · Molecular Neurobiology · doi:10.1007/bf02778006 · Cited by 72

Tau associates with actin in differentiating PC12 cells

Yu, J.-Z., & Rasenick, M. M. (2006) · The FASEB Journal · doi:10.1096/fj.05-5206com · Cited by 72

Glial Fibrillary Tangles and JAK/STAT-Mediated Glial and Neuronal Cell Death in a Drosophila Model of Glial Tauopathy

Colodner, K. J., & Feany, M. Β. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2491-10.2010 · Cited by 71

On the identification of low allele frequency mosaic mutations in the brains of Alzheimer’s disease patients

Sala Frigerio, C., Lau, P., Troakes, C., Deramecourt, V., Gele, P., Van Loo, P., Voet, T., & De Strooper, B. (2015) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2015.02.007 · Cited by 71

Dissociation of Alzheimer type pathology in a disconnected piece of cortex

Duyckaerts, C. J., Uchihara, T., Seilhean, D., He, Y., & Hauw, J. (1997) · Acta Neuropathologica · doi:10.1007/s004010050645 · Cited by 71

Pathological τ proteins in postencephalitic parkinsonism: Comparison with Alzheimer's disease and other neurodegenerative disorders

Buée‐Scherrer, V., Buée, L., Leveugle, B., Perl, D. P., Vermersch, P., Hof, P. R., & Delacourte, A. (1997) · Annals of Neurology · doi:10.1002/ana.410420312 · Cited by 71

The Cholinergic System in Aging

Bigl, V., Arendt, T., Fischer, S., Fischer, S., Werner, M., & Arendt, A. (2009) · Gerontology · doi:10.1159/000212872 · Cited by 71

Microtubule Binding and Trapping at the Tip of Neurites Regulate Tau Motion in Living Neurons

Weissmann, C., Reyher, H.-J., Gauthier‐Kemper, A., Steinhoff, H., Junge, W., & Brandt, R. (2009) · Traffic · doi:10.1111/j.1600-0854.2009.00977.x · Cited by 71

Tau imaging in the study of ageing, Alzheimer's disease, and other neurodegenerative conditions

Villemagne, V. L., & Okamura, N. (2015) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2015.09.002 · Cited by 70

Changes in neuronal DNA content variation in the human brain during aging

Fischer, H., Morawski, M., Brückner, M. K., Mittag, A., Tárnok, A., & Arendt, T. (2012) · Aging Cell · doi:10.1111/j.1474-9726.2012.00826.x · Cited by 69

Tau phosphorylation and proteolysis: Insights and perspectives

Johnson, G. V. W. (2006) · Journal of Alzheimer s Disease · doi:10.3233/jad-2006-9s326 · Cited by 69

Prostate-derived Sterile 20-like Kinases (PSKs/TAOKs) Phosphorylate Tau Protein and Are Activated in Tangle-bearing Neurons in Alzheimer Disease

Tavares, I. A., Touma, D., Lynham, S., Troakes, C., Schober, M. S., Čaušević, M., Garg, R., Noble, W. J., Killick, R., Bódi, I., et al. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.448183 · Cited by 69

Examination of the validity of the hierarchical model of neuropathological staging in normal aging and Alzheimer's disease

Gertz, H., Xuereb, J. H., Huppert, F. A., Brayne, C., McGee, M. A., Paykel, E. S., Harrington, C. R., Mukaetova-Ladinska, E., Arendt, T., & Wischik, C. M. (1998) · Acta Neuropathologica · doi:10.1007/s004010050780 · Cited by 69

Relationship of the extended tau haplotype to tau biochemistry and neuropathology in progressive supranuclear palsy

Liu, W.-K., Le, T. V., Adamson, J. L., Baker, M., Cookson, N., Hardy, J., Hutton, M. L., Yen, S.-H. C., & Dickson, D. W. (2001) · Annals of Neurology · doi:10.1002/ana.1159 · Cited by 69

Clinical and pathological features of an Alzheimer's disease patient with the MAPT ΔK280 mutation

Momeni, P., Pittman, A. M., Lashley, T., Vandrovcová, J., Malzer, E., Luk, C. Y., Hulette, C., Lees, A. J., Révész, T., Hardy, J., et al. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.07.013 · Cited by 69

Skeletal muscle proteomics: carbohydrate metabolism oscillates with seasonal and torpor-arousal physiology of hibernation

Hindle, A. G., Karimpour‐Fard, A., Epperson, L. E., Hunter, L., & Martin, S. L. (2011) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00298.2011 · Cited by 69

Neurodegeneration and plasticity

Arendt, T. (2004) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2004.07.007 · Cited by 69

Alzheimer neurofibrillary change in subacute sclerosing panencephalitis

Mandybur, T. I., Nagpaul, A. S., Pappas, Z., & Niklowitz, W. J. (1977) · Annals of Neurology · doi:10.1002/ana.410010112 · Cited by 68

Widespread expression of α-synuclein and τ immunoreactivity in Hallervorden–Spatz syndrome with protracted clinical course

Saito, Y., Kawai, M., Inoue, K., et al. (2000) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(00)00337-3 · Cited by 68

The PSEN1, p.E318G Variant Increases the Risk of Alzheimer's Disease in APOE-ε4 Carriers

Benítez, B. A., Karch, C. M. M., Cai, Y., Jin, S. C., Cooper, B., Carrell, D., Bertelsen, S. E., Chibnik, L. B., Schneider, J. A., Bennett, D., et al. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003685 · Cited by 68

Advances in the development of tau PET radiotracers and their clinical applications

Okamura, N., Harada, R., Furukawa, K., Furumoto, S., Tago, T., Yanai, K., Arai, H., & Kudo, Y. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2015.12.010 · Cited by 68

The Co-Occurrence of Alzheimer's Disease and Huntington's Disease: A Neuropathological Study of 15 Elderly Huntington's Disease Subjects

Davis, M. Y., Keene, C. D., Jayadev, S., et al. (2014) · Journal of Huntington s Disease · doi:10.3233/jhd-140111 · Cited by 67

A polymorphism in the tau gene associated with risk for Alzheimer's disease

Bullido, M. J., Aldudo, J., Frank, A., Coria, F., Ávila, J., & Valdivieso, F. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(99)00893-9 · Cited by 67

Tau gene (MAPT) sequence variation among primates

Holzer, M., Craxton, M., Jakes, R., Arendt, T., & Goedert, M. (2004) · Gene · doi:10.1016/j.gene.2004.07.013 · Cited by 67

Clinical Validity of Aß-Protein Deposition Staging in Brain Aging and Alzheimer Disease

Gold, G., Kövari, E., Corte, G., Herrmann, F. R., Canuto, A., Bussière, T., Hof, P. R., Bouras, C., & Giannakopoulos, P. (2001) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/60.10.946 · Cited by 67

Postmortem changes in the phosphorylation state of tau-protein in the rat brain

Gärtner, U., Janke, C., Holzer, M., Vanmechelen, E., & Arendt, T. (1998) · Neurobiology of Aging · doi:10.1016/s0197-4580(98)00094-3 · Cited by 66

A novel calcium‐binding protein is associated with tau proteins in tauopathy

Vega, I. E., Traverso, E. E., Ferrer‐Acosta, Y., Matos, E., Colon, M., Gonzalez, J., Dickson, D. W., Hutton, M. L., Lewis, J. M., & Yen, S. H. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05339.x · Cited by 66

Analysis of protein-coding genetic variation in 60,706 humans

Atzmon, Palotie, A. V., Ripke, S., Rivas, M. A., Won, H., Freimer, Lyon, Rodríguez-Guillén, Barr, Weisburd, B., et al. (2020) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/akst-av84 · Cited by 66

Disturbance of neuronal plasticity is a critical pathogenetic event in Alzheimer's disease

Arendt, T. (2001) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(01)00007-7 · Cited by 66

Progressive Age-Related Cognitive Decline in Tau Mice

der Jeugd, A. V., Vermaercke, B., Derisbourg, M. J., Lo, A. C., Hamdane, M., Blum, D. L., Buée, L., & D’Hooge, R. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-130110 · Cited by 66

Correlations between cortical and subcortical tau pathology

Attems, J., Thomas, A. J., & Jellinger, K. A. (2011) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2011.01244.x · Cited by 65

Distribution of astrocytic plaques in the corticobasal degeneration brain and comparison with tuft-shaped astrocytes in the progressive supranuclear palsy brain

Hattori, M., Hashizume, Y., Yoshida, M., Iwasaki, Y., Hishikawa, N., Ueda, R., & Ojika, K. (2003) · Acta Neuropathologica · doi:10.1007/s00401-003-0711-4 · Cited by 65

An English kindred with a novel recessive tauopathy and respiratory failure

Nicholl, D. J., Greenstone, M. A., Clarke, C. E., Rizzu, P., Crooks, D. A., Crowe, A., Trojanowski, J. Q., Lee, V. M. ‐., & Heutink, P. (2003) · Annals of Neurology · doi:10.1002/ana.10747 · Cited by 65

Neuronal activation of Ras regulates synaptic connectivity

Arendt, T., Gärtner, U., Seeger, G., Barmashenko, G., Palm, K., Mittmann, T., Li, Y., Huemmeke, M., Behrbohm, J., Brückner, M. K., et al. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2004.03409.x · Cited by 65

Tau hyperphosphorylation and deregulation of calcineurin in mouse models of Huntington’s disease

Gratuze, M., Noël, A., Julien, C., Cisbani, G., Milot-Rousseau, P., Morin, F., Dickler, M., Goupil, C., Bezeau, F., Poitras, I., et al. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddu456 · Cited by 65

Hyperphosphorylation Results in Tau Dysfunction in DNA Folding and Protection

Lü, Y., He, H.-J., Zhou, J., Jun-Ye, M. I. A. O., Lü, J., He, Y.-G., Pan, R., Yan, W., Liu, Y. M., & He, R. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-130602 · Cited by 65

Interaction of Actin Filaments with Microtubules Is Mediated by Microtubule‐Associated Proteins and Regulated by Phosphorylationa

Selden, S. C., & Pollard, T. D. (1986) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1986.tb38464.x · Cited by 65

Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and Lewy body pathology

Wakabayashi, K., Fukushima, T., Koide, R., Horikawa, Y., Hasegawa, M., Watanabe, Y., Noda, T., Eguchi, I., Morita, T., Yoshimoto, M., et al. (2000) · Acta Neuropathologica · doi:10.1007/s004010050049 · Cited by 64

Clinical aspects of argyrophilic grain disease.

Ikeda, K., Akiyama, H., Arai, T., et al. (2001) · PubMed · Cited by 64

Degeneration of rat cholinergic basal forebrain neurons and reactive changes in nerve growth factor expression after chronic neurotoxic injury—II. Reactive expression of the nerve growth factor gene in astrocytes

Arendt, T., Brückner, M. K., Krell, T., Pagliusi, S. R., Kruska, L., & Heumann, R. (1995) · Neuroscience · doi:10.1016/0306-4522(94)00523-8 · Cited by 63

Chronic complement C3 gene expression in the CNS of transgenic mice with astrocyte-targeted interleukin-6 expression

Barnum, S. R., Jones, J. L., Müller-Ladner, U., Samimi, A., & Campbell, I. L. (1996) · Glia · doi:10.1002/(sici)1098-1136(199610)18:2 · Cited by 63

Tau neurotoxicity and rescue in animal models of human Tauopathies

Krüger, L., & Mandelkow, E. (2015) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2015.09.004 · Cited by 63

Non-Alzheimer non-Pick dementia with Fahr's syndrome.

Shibayama, H., Kobayashi, H., Nakagawa, M., et al. (1992) · PubMed · Cited by 62

Frontotemporal lobar degeneration: old knowledge and new insight into the pathogenetic mechanisms of tau mutations

Rossi, G., & Tagliavini, F. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00192 · Cited by 62

A novel tau mutation in exon 9 (1260V) causes a four-repeat tauopathy

Grover, A., England, E., Baker, M., Sahara, N., Adamson, J. L., Granger, B., Houlden, H., Passant, U., Yen, S.-H. C., Deture, M. A., et al. (2003) · Experimental Neurology · doi:10.1016/s0014-4886(03)00393-5 · Cited by 62

Microtubule‐associated protein tau in human prostate cancer cells: Isoforms, phosphorylation, and interactions

Souter, S., & Lee, G. S. (2009) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22287 · Cited by 62

Hereditary prion protein amyloidoses

Ghetti, B. F., Tagliavini, F., Takao, M., Bugiani, O., & Piccardo, P. (2003) · Clinics in Laboratory Medicine · doi:10.1016/s0272-2712(02)00064-1 · Cited by 62

Expression of embryonic tau protein isoforms persist during adult neurogenesis in the hippocampus

Bullmann, T., de Silva, R., Holzer, M., Mori, H., & Arendt, T. (2006) · Hippocampus · doi:10.1002/hipo.20255 · Cited by 62

Mutations in MAPT Gene Cause Chromosome Instability and Introduce Copy Number Variations Widely in the Genome

Rossi, G., Conconi, D., Panzeri, E., Redaelli, S., Piccoli, E., Paoletta, L., Dalprà, L., & Tagliavini, F. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-2012-121633 · Cited by 61

Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family

Lossos, A., Reches, A., Gal, A., Newman, J. P., Soffer, D., Gomori, J. M., Boher, M., Ekstein, D., Biran, I., Meiner, Z., et al. (2003) · Journal of Neurology · doi:10.1007/s00415-003-1074-4 · Cited by 61

Alterserkrankungen des Zentralnervensystems

Braunmühl, A. V. (1957) · Springer eBooks · doi:10.1007/978-3-662-11703-3_5 · Cited by 61

Tau Potentiates Nerve Growth Factor-induced Mitogen-activated Protein Kinase Signaling and Neurite Initiation without a Requirement for Microtubule Binding

Leugers, C. J., & Lee, G. S. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.105387 · Cited by 60

Degeneration of β-amyloid-associated cholinergic structures in transgenic APPSW mice

Lüth, H., Apelt, J., Ihunwo, A., Arendt, T., & Schliebs, R. (2003) · Brain Research · doi:10.1016/s0006-8993(03)02658-1 · Cited by 60

CLINICOPATHOLOGIC STUDY OF ALZHEIMER'S DISEASE

ROTHSCHILD, D. (1936) · Archives of Neurology And Psychiatry · doi:10.1001/archneurpsyc.1936.02260080065004 · Cited by 60

Microtubule‐associated protein tau is required for axonal neurite elaboration by neuroblastoma cells

Shea, T. B., Beermann, M. L., Nixon, R. A., & Fischer, I. (1992) · Journal of Neuroscience Research · doi:10.1002/jnr.490320308 · Cited by 60

TDP-43 pathology in a patient carrying G2019S LRRK2 mutation and a novel p.Q124E MAPT

Ling, H., Kara, E., Bandopadhyay, R., Hardy, J., Holton, J. L., Xiromerisiou, G., Lees, A. J., Houlden, H., & Révész, T. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.04.011 · Cited by 60

Ultrastructural characterization of the tau-immunoreactive tubules in the oligodendroglial perikarya and their inner loop processes in progressive supranuclear palsy

Arima, K., Nakamura, M., Sunohara, N., Ogawa, M., Anno, M., Izumiyama, Y., Hirai, S., & Ikeda, K. (1997) · Acta Neuropathologica · doi:10.1007/s004010050652 · Cited by 59

Molecular flexibility in microtubule proteins: proton nuclear magnetic resonance characterization

Woody, R. W., Clark, D. C., Roberts, G. C. K., Martin, S. R., & Bayley, P. M. (1983) · Biochemistry · doi:10.1021/bi00278a020 · Cited by 59

MAPT S305I mutation: implications for argyrophilic grain disease

Kovács, G., Pittman, A., Révész, T., Luk, C., Lees, A., Kiss, É., Tariska, P., Laszlo, L., Molnár, K., Molnár, M., et al. (2008) · Acta Neuropathologica · doi:10.1007/s00401-007-0322-6 · Cited by 59

Neuroglial alterations in rats submitted to the okadaic acid-induced model of dementia

Costa, A. P., Tramontina, A. C., Biasibetti, R., Batassini, C., Lopes, M. W., Wartchow, K. M., Bernardi, C. L., Tortorelli, L. S., Leal, R. B., & Gonçalves, C. A. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.09.035 · Cited by 59

Familial dementia with swollen achromatic neurons and corticobasal inclusion bodies: a clinical and pathological study

Brown, J., Lantos, P. L., Roques, P. K., et al. (1996) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(95)00236-u · Cited by 59

Brain evolution and Alzheimer's disease.

Рапопорт, С. И. (1988) · PubMed · Cited by 59

A neuroprotective role for the DNA damage checkpoint in tauopathy

Khurana, V., Merlo, P., DuBoff, B., Fulga, T. A., Sharp, K. A., Campbell, S. D., Götz, J., & Feany, M. Β. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2011.00778.x · Cited by 58

Increased tau accumulation in senile plaques as a hallmark in Alzheimer's disease.

Shin, R., Ogomori, K., Kitamoto, T., & Tateishi, J. (1989) · Europe PMC (PubMed Central) · doi:10.11501/3054141 · Cited by 58

Degeneration of rat cholinergic basal forebrain neurons and reactive changes in nerve growth factor expression after chronic neurotoxic injury—I. Degeneration and plastic response of basal forebrain neurons

Arendt, T., Brückner, M. K., Pagliusi, S. R., & Krell, T. (1995) · Neuroscience · doi:10.1016/0306-4522(94)00526-b · Cited by 58

Axotrophin/MARCH7 acts as an E3 ubiquitin ligase and ubiquitinates tau protein in vitro impairing microtubule binding

Flach, K., Ramminger, E., Hilbrich, I., Arsalan-Werner, A., Albrecht, F., Herrmann, L., Goedert, M., Arendt, T., & Holzer, M. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.05.029 · Cited by 58

ApoE3 binding to tau tandem repeat I is abolished by tau serine262 phosphorylation

Huang, D. Y., Weisgraber, K. H., Goedert, M., Saunders, A. M., Roses, A. D., & Strittmatter, W. J. (1995) · Neuroscience Letters · doi:10.1016/0304-3940(95)11649-h · Cited by 57

The proline-rich domain and the microtubule binding domain of protein tau acting as RNA binding domains.

Wang, X.-S., Wang, D., Zhao, J., Qu, M.-H., Zhou, X.-H., He, H., & He, R.-Q. (2006) · Protein Peptide Letters · doi:10.2174/092986606777790566 · Cited by 57

Function of tau protein in adult newborn neurons

Fuster-Matanzo, A., de Barreda, E. G., Dawson, H. N., Vitek, M. P., Avila, J., & Hernández, F. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.08.017 · Cited by 57

Preferential binding of hog brain microtubule-associated proteins to mouse satellite versus bulk DNA preparations

Wiche, G., Corces, V. G., & Ávila, J. (1978) · Nature · doi:10.1038/273403a0 · Cited by 57

Pantothenate kinase‐associated neurodegeneration is not a synucleinopathy

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A τ Fragment Containing a Repetitive Sequence Induces Bundling of Actin Filaments

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