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ClinicalTrials.gov (NCT01492374) Study to Evaluate the Safety, Tolerability and the Effect of BMS-241027 on Cerebrospinal Fluid Biomarkers in Subjects With Mild Alzheimer's Disease. U.S. National Institutes of Health.
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The sterol regulatory element-binding protein 2 is dysregulated by tau alterations in Alzheimer disease.Brain Pathol. 2019 Jul;29(4):530-543. doi: 10.1111/bpa.12691. Epub 2019 Jan 28.
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cPLA2 and desaturases underlie the tau hyperphosphorylation offset induced by BACE knock-down in neuronal primary cultures.Biochim Biophys Acta Mol Basis Dis. 2018 Nov;1864(11):3696-3707. doi: 10.1016/j.bbadis.2018.08.028. Epub 2018 Aug 24.
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P301L tauopathy: confocal immunofluorescence study of perinuclear aggregation of the mutated protein.J Neurol Sci. 2002 Aug 15;200(1-2):85-93. doi: 10.1016/s0022-510x(02)00150-8.
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Inhibition of p25/Cdk5 Attenuates Tauopathy in Mouse and iPSC Models of Frontotemporal Dementia.J Neurosci. 2017 Oct 11;37(41):9917-9924. doi: 10.1523/JNEUROSCI.0621-17.2017. Epub 2017 Sep 14.
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Cholesterol 24-hydroxylase defect is implicated in memory impairments associated with Alzheimer-like Tau pathology.Hum Mol Genet. 2015 Nov 1;24(21):5965-76. doi: 10.1093/hmg/ddv268. Epub 2015 Sep 10.
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Reduction of Nuak1 Decreases Tau and Reverses Phenotypes in a Tauopathy Mouse Model.Neuron. 2016 Oct 19;92(2):407-418. doi: 10.1016/j.neuron.2016.09.022. Epub 2016 Oct 6.
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Phosphorylated TDP-43 Staging of Primary Age-Related Tauopathy.Neurosci Bull. 2019 Apr;35(2):183-192. doi: 10.1007/s12264-018-0300-0. Epub 2018 Oct 31.
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Integrative system biology analyses of CRISPR-edited iPSC-derived neurons and human brains reveal deficiencies of presynaptic signaling in FTLD and PSP.Transl Psychiatry. 2018 Dec 13;8(1):265. doi: 10.1038/s41398-018-0319-z.
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Long-term exposure to ELF-MF ameliorates cognitive deficits and attenuates tau hyperphosphorylation in 3xTg AD mice.Neurotoxicology. 2016 Mar;53:290-300. doi: 10.1016/j.neuro.2016.02.012. Epub 2016 Mar 2.
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Concussion, microvascular injury, and early tauopathy in young athletes after impact head injury and an impact concussion mouse model.Brain. 2018 Feb 1;141(2):422-458. doi: 10.1093/brain/awx350.
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Antileukotriene therapy by reducing tau phosphorylation improves synaptic integrity and cognition of P301S transgenic mice.Aging Cell. 2018 Jun;17(3):e12759. doi: 10.1111/acel.12759. Epub 2018 Apr 1.
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Complement C3aR Inactivation Attenuates Tau Pathology and Reverses an Immune Network Deregulated in Tauopathy Models and Alzheimer's Disease.Neuron. 2018 Dec 19;100(6):1337-1353.e5. doi: 10.1016/j.neuron.2018.10.031. Epub 2018 Nov 8.
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No interaction between tau and TDP-43 pathologies in either frontotemporal lobar degeneration or motor neurone disease.Neuropathol Appl Neurobiol. 2014 Dec;40(7):844-54. doi: 10.1111/nan.12155.
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CX3CR1-deficient microglia shows impaired signalling of the transcription factor NRF2: Implications in tauopathies.Redox Biol. 2019 Apr;22:101118. doi: 10.1016/j.redox.2019.101118. Epub 2019 Feb 6.
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Reduced Adrenomedullin Parallels Microtubule Dismantlement in Frontotemporal Lobar Degeneration.Mol Neurobiol. 2018 Dec;55(12):9328-9333. doi: 10.1007/s12035-018-1079-8. Epub 2018 Apr 18.
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Constitutive Dyrk1A is abnormally expressed in Alzheimer disease, Down syndrome, Pick disease, and related transgenic models. Neurobiol Dis. 2005 Nov;20(2):392-400.
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Constitutive XBP-1s-mediated activation of the endoplasmic reticulum unfolded protein response protects against pathological tau.Nat Commun. 2019 Sep 30;10(1):4443. doi: 10.1038/s41467-019-12070-3.
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Immunophilin FKBP52 induces Tau-P301L filamentous assembly in vitro and modulates its activity in a model of tauopathy.Proc Natl Acad Sci U S A. 2014 Mar 25;111(12):4584-9. doi: 10.1073/pnas.1402645111. Epub 2014 Mar 12.
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Relevance of host tau in tau seeding and spreading in tauopathies.Brain Pathol. 2020 Mar;30(2):298-318. doi: 10.1111/bpa.12778. Epub 2019 Aug 27.
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Imbalance of Hsp70 family variants fosters tau accumulation.FASEB J. 2013 Apr;27(4):1450-9. doi: 10.1096/fj.12-220889. Epub 2012 Dec 27.
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G2019S LRRK2 enhances the neuronal transmission of tau in the mouse brain.Hum Mol Genet. 2018 Jan 1;27(1):120-134. doi: 10.1093/hmg/ddx389.
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Current advances on different kinases involved in tau phosphorylation, and implications in Alzheimer's disease and tauopathies.Curr Alzheimer Res. 2005 Jan;2(1):3-18. doi: 10.2174/1567205052772713.
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Involvement of Oligodendrocytes in Tau Seeding and Spreading in Tauopathies.Front Aging Neurosci. 2019 May 28;11:112. doi: 10.3389/fnagi.2019.00112. eCollection 2019.
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Pin1 has opposite effects on wild-type and P301L tau stability and tauopathy.J Clin Invest. 2008 May;118(5):1877-89. doi: 10.1172/JCI34308.
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Protein Phosphatase 2A and Its Methylation Modulating Enzymes LCMT-1 and PME-1 Are Dysregulated in Tauopathies of Progressive Supranuclear Palsy and Alzheimer Disease.J Neuropathol Exp Neurol. 2018 Feb 1;77(2):139-148. doi: 10.1093/jnen/nlx110.
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Effect of AZD0530 on Cerebral Metabolic Decline in Alzheimer Disease: A Randomized Clinical Trial.JAMA Neurol. 2019 Oct 1;76(10):1219-1229. doi: 10.1001/jamaneurol.2019.2050.
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Delta-secretase (AEP) mediates tau-splicing imbalance and accelerates cognitive decline in tauopathies.J Exp Med. 2018 Dec 3;215(12):3038-3056. doi: 10.1084/jem.20180539. Epub 2018 Oct 29.
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Pathological phosphorylation of tau and TDP-43 by TTBK1 and TTBK2 drives neurodegeneration.Mol Neurodegener. 2018 Feb 6;13(1):7. doi: 10.1186/s13024-018-0237-9.
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Ubiquitin Specific Protease 13 Regulates Tau Accumulation and Clearance in Models of Alzheimer's Disease.J Alzheimers Dis. 2019;72(2):425-441. doi: 10.3233/JAD-190635.
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Gender-Specific Expression of Ubiquitin-Specific Peptidase 9 Modulates Tau Expression and Phosphorylation: Possible Implications for Tauopathies.Mol Neurobiol. 2017 Dec;54(10):7979-7993. doi: 10.1007/s12035-016-0299-z. Epub 2016 Nov 23.
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Correcting miR92a-vGAT-Mediated GABAergic Dysfunctions Rescues Human Tau-Induced Anxiety in Mice.Mol Ther. 2017 Jan 4;25(1):140-152. doi: 10.1016/j.ymthe.2016.10.010. Epub 2017 Jan 4.
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MSUT2 is a determinant of susceptibility to tau neurotoxicity.Hum Mol Genet. 2011 May 15;20(10):1989-99. doi: 10.1093/hmg/ddr079. Epub 2011 Feb 25.
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CREB-activity and nmnat2 transcription are down-regulated prior to neurodegeneration, while NMNAT2 over-expression is neuroprotective, in a mouse model of human tauopathy.Hum Mol Genet. 2012 Jan 15;21(2):251-67. doi: 10.1093/hmg/ddr492. Epub 2011 Oct 25.
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NAD-biosynthetic enzyme NMNAT1 reduces early behavioral impairment in the htau mouse model of tauopathy.Behav Brain Res. 2018 Feb 26;339:140-152. doi: 10.1016/j.bbr.2017.11.030. Epub 2017 Nov 23.
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Role of DJ-1 in Parkinson's disease.J Mol Neurosci. 2006;29(3):215-25. doi: 10.1385/jmn:29:3:215.
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A novel calcium-binding protein is associated with tau proteins in tauopathy.J Neurochem. 2008 Jul;106(1):96-106. doi: 10.1111/j.1471-4159.2008.05339.x. Epub 2008 Jul 1.
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Reinstating plasticity and memory in a tauopathy mouse model with an acetyltransferase activator.EMBO Mol Med. 2018 Nov;10(11):e8587. doi: 10.15252/emmm.201708587.
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Locus Coeruleus Ablation Exacerbates Cognitive Deficits, Neuropathology, and Lethality in P301S Tau Transgenic Mice.J Neurosci. 2018 Jan 3;38(1):74-92. doi: 10.1523/JNEUROSCI.1483-17.2017. Epub 2017 Nov 13.
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PERK activation mitigates tau pathology invitro and invivo.EMBO Mol Med. 2017 Mar;9(3):371-384. doi: 10.15252/emmm.201606664.
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Autoantibodies to Synaptic Receptors and Neuronal Cell Surface Proteins in Autoimmune Diseases of the Central Nervous System.Physiol Rev. 2017 Apr;97(2):839-887. doi: 10.1152/physrev.00010.2016.
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Attenuation of synaptic toxicity and MARK4/PAR1-mediated Tau phosphorylation by methylene blue for Alzheimer's disease treatment.Sci Rep. 2016 Oct 6;6:34784. doi: 10.1038/srep34784.
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Disclosing the Mechanism of Spontaneous Aggregation and Template-Induced Misfolding of the Key Hexapeptide (PHF6) of Tau Protein Based on Molecular Dynamics Simulation.ACS Chem Neurosci. 2019 Dec 18;10(12):4810-4823. doi: 10.1021/acschemneuro.9b00488. Epub 2019 Nov 12.
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Novel Lipidized Analog of Prolactin-Releasing Peptide Improves Memory Impairment and Attenuates Hyperphosphorylation of Tau Protein in a Mouse Model of Tauopathy.J Alzheimers Dis. 2018;62(4):1725-1736. doi: 10.3233/JAD-171041.
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MicroRNA-132 loss is associated with tau exon 10 inclusion in progressive supranuclear palsy.Hum Mol Genet. 2011 Oct 15;20(20):4016-24. doi: 10.1093/hmg/ddr330. Epub 2011 Aug 1.
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RBM4 interacts with an intronic element and stimulates tau exon 10 inclusion.J Biol Chem. 2006 Aug 25;281(34):24479-88. doi: 10.1074/jbc.M603971200. Epub 2006 Jun 15.
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Dysregulation and Dislocation of SFPQ Disturbed DNA Organization in Alzheimer's Disease and Frontotemporal Dementia.J Alzheimers Dis. 2018;61(4):1311-1321. doi: 10.3233/JAD-170659.
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Infantile tauopathies: Hemimegalencephaly; tuberous sclerosis complex; focal cortical dysplasia 2; ganglioglioma.Brain Dev. 2015 Jun;37(6):553-62. doi: 10.1016/j.braindev.2014.08.010. Epub 2014 Oct 19.
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TIA1 regulates the generation and response to toxic tau oligomers.Acta Neuropathol. 2019 Feb;137(2):259-277. doi: 10.1007/s00401-018-1937-5. Epub 2018 Nov 21.
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Mutations in tau gene exon 10 associated with FTDP-17 alter the activity of an exonic splicing enhancer to interact with Tra2 beta.J Biol Chem. 2003 May 23;278(21):18997-9007. doi: 10.1074/jbc.M301800200. Epub 2003 Mar 20.
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DCTN1 F52L mutation case of Perry syndrome with progressive supranuclear palsy-like tauopathy.Parkinsonism Relat Disord. 2018 Jun;51:105-110. doi: 10.1016/j.parkreldis.2018.02.038. Epub 2018 Feb 23.
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Discovery of autism/intellectual disability somatic mutations in Alzheimer's brains: mutated ADNP cytoskeletal impairments and repair as a case study.Mol Psychiatry. 2021 May;26(5):1619-1633. doi: 10.1038/s41380-019-0563-5. Epub 2019 Oct 30.
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Structural Basis of Tau Interaction With BIN1 and Regulation by Tau Phosphorylation.Front Mol Neurosci. 2018 Nov 14;11:421. doi: 10.3389/fnmol.2018.00421. eCollection 2018.
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NAP (davunetide) preferential interaction with dynamic 3-repeat Tau explains differential protection in selected tauopathies.PLoS One. 2019 Mar 13;14(3):e0213666. doi: 10.1371/journal.pone.0213666. eCollection 2019.
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Impact of Swiprosin-1/Efhd2 on Adult Hippocampal Neurogenesis.Stem Cell Reports. 2018 Feb 13;10(2):347-355. doi: 10.1016/j.stemcr.2017.12.010. Epub 2018 Jan 11.
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Loss of Hsp110 leads to age-dependent tau hyperphosphorylation and early accumulation of insoluble amyloid beta.Mol Cell Biol. 2010 Oct;30(19):4626-43. doi: 10.1128/MCB.01493-09. Epub 2010 Aug 2.
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Movement disorders with neuronal antibodies: syndromic approach, genetic parallels and pathophysiology.Brain. 2018 Jan 1;141(1):13-36. doi: 10.1093/brain/awx189.
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A Novel Microtubule-Tau Association Enhancer and Neuroprotective Drug Candidate: Ac-SKIP.Front Cell Neurosci. 2019 Oct 1;13:435. doi: 10.3389/fncel.2019.00435. eCollection 2019.
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Resveratrol induces dephosphorylation of Tau by interfering with the MID1-PP2A complex.Sci Rep. 2017 Oct 23;7(1):13753. doi: 10.1038/s41598-017-12974-4.
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Alpha-Synuclein contributes to GSK-3beta-catalyzed Tau phosphorylation in Parkinson's disease models.FASEB J. 2009 Sep;23(9):2820-30. doi: 10.1096/fj.08-120410. Epub 2009 Apr 15.
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Early structural and functional defects in synapses and myelinated axons in stratum lacunosum moleculare in two preclinical models for tauopathy.PLoS One. 2014 Feb 3;9(2):e87605. doi: 10.1371/journal.pone.0087605. eCollection 2014.
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Tau deletion exacerbates the phenotype of Niemann-Pick type C mice and implicates autophagy in pathogenesis.Hum Mol Genet. 2009 Mar 1;18(5):956-65. doi: 10.1093/hmg/ddn423. Epub 2008 Dec 12.
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Sugar Kick Prevents Memory Impairment.J Med Chem. 2019 Nov 27;62(22):10059-10061. doi: 10.1021/acs.jmedchem.9b01668. Epub 2019 Oct 31.
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Inhibition of O-GlcNAcase leads to elevation of O-GlcNAc tau and reduction of tauopathy and cerebrospinal fluid tau in rTg4510 mice.Mol Neurodegener. 2017 May 18;12(1):39. doi: 10.1186/s13024-017-0181-0.
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Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration.Acta Neuropathol. 2014 Feb;127(2):271-82. doi: 10.1007/s00401-013-1193-7.
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Tau interactome mappingbased identification of Otub1 as Tau deubiquitinase involved in accumulation of pathological Tau forms in vitro and in vivo.Acta Neuropathol. 2017 May;133(5):731-749. doi: 10.1007/s00401-016-1663-9. Epub 2017 Jan 12.
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Cerebrovascular inflammation is associated with tau pathology in Guam parkinsonism dementia.J Neural Transm (Vienna). 2018 Jul;125(7):1013-1025. doi: 10.1007/s00702-018-1883-3. Epub 2018 Apr 26.
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Memantine mediates astrocytic activity in response to excitotoxicity induced by PP2A inhibition.Neurosci Lett. 2019 Mar 23;696:179-183. doi: 10.1016/j.neulet.2018.12.034. Epub 2018 Dec 23.
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Enhanced tau pathology via RanBP9 and Hsp90/Hsc70 chaperone complexes.Hum Mol Genet. 2017 Oct 15;26(20):3973-3988. doi: 10.1093/hmg/ddx284.
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Why Microtubules Should Be Considered as One of the Supplementary Targets for Designing Neurotherapeutics.ACS Chem Neurosci. 2019 Mar 20;10(3):1118-1120. doi: 10.1021/acschemneuro.9b00002. Epub 2019 Jan 18.
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S-nitrosylation of E3 ubiquitin-protein ligase RNF213 alters non-canonical Wnt/Ca+2 signaling in the P301S mouse model of tauopathy.Transl Psychiatry. 2019 Jan 29;9(1):44. doi: 10.1038/s41398-019-0388-7.
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Secernin-1 is a novel phosphorylated tau binding protein that accumulates in Alzheimer's disease and not in other tauopathies.Acta Neuropathol Commun. 2019 Dec 3;7(1):195. doi: 10.1186/s40478-019-0848-6.
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Loss of Tau results in defects in photoreceptor development and progressive neuronal degeneration in Drosophila.Dev Neurobiol. 2014 Dec;74(12):1210-25. doi: 10.1002/dneu.22199. Epub 2014 Jun 18.
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SIRT1 Deacetylates SC35 and Suppresses Its Function in Tau Exon 10 Inclusion.J Alzheimers Dis. 2018;61(2):561-570. doi: 10.3233/JAD-170418.
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The Q7R Saitohin gene polymorphism is not associated with Alzheimer disease.Neurosci Lett. 2003 Aug 28;347(3):143-6. doi: 10.1016/s0304-3940(03)00670-0.
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SYNJ1 gene associated with neonatal onset of neurodegenerative disorder and intractable seizure.Mol Genet Genomic Med. 2018 Jan;6(1):109-113. doi: 10.1002/mgg3.341. Epub 2017 Nov 27.
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