Bibliography about the Tau family (71 articles)
Add article(s) associated with Tau family
- Sequestosome 1/p62 shuttles polyubiquitinated tau for proteasomal degradation.
- Babu J.R., Geetha T., Wooten M.W. et al
2005, J. Neurochem. (94) 192-203 - Proteomic analysis of in vivo phosphorylated synaptic proteins.
- Collins M.O., Yu L., Coba M.P. et al
2005, J. Biol. Chem. (280) 5972-5982 - Large-scale characterization of HeLa cell nuclear phosphoproteins.
- Beausoleil S.A., Jedrychowski M., Schwartz D. et al
2004, Proc. Natl. Acad. Sci. U.S.A. (101) 12130-12135 - Tau gene (MAPT) sequence variation among primates.
- Holzer M., Craxton M., Jakes R. et al
2004, Gene (341) 313-322 - Tau gene delN296 mutation, Parkinson's disease, and atypical supranuclear palsy.
- Oliva R., Pastor P.
2004, Ann. Neurol. (55) 448-449 - Progressive supranuclear palsy and Parkinson's disease in a family with a new mutation in the tau gene.
- Rossi G., Gasparoli E., Pasquali C. et al
2004, Ann. Neurol. (55) 448-448 - Reversible paired helical filament-like phosphorylation of tau is an adaptive process associated with neuronal plasticity in hibernating animals.
- Arendt T., Stieler J., Strijkstra A.M. et al
2003, J. Neurosci. (23) 6972-6981 - Elevated gene expression levels distinguish human from non-human primate brains.
- Caceres M., Lachuer J., Zapala M.A. et al
2003, Proc. Natl. Acad. Sci. U.S.A. (100) 13030-13035 - A novel L266V mutation of the tau gene causes frontotemporal dementia with a unique tau pathology.
- Kobayashi T., Ota S., Tanaka K. et al
2003, Ann. Neurol. (53) 133-137 - An English kindred with a novel recessive tauopathy and respiratory failure.
- Nicholl D.J., Greenstone M.A., Clarke C.E. et al
2003, Ann. Neurol. (54) 682-686 - Tau (MAPT) mutation arg406trp presenting clinically with Alzheimer disease does not share a common founder in western Europe.
- Rademakers R., Dermaut B., Peeters K. et al
2003, Hum. Mutat. (22) 409-411 - Late-onset frontotemporal dementia with a novel exon 1 (Arg5His) tau gene mutation.
- Hayashi S., Toyoshima Y., Hasegawa M. et al
2002, Ann. Neurol. (51) 525-530 - An R5L tau mutation in a subject with a progressive supranuclear palsy phenotype.
- Poorkaj P., Muma N.A., Zhukareva V. et al
2002, Ann. Neurol. (52) 511-516 - A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease.
- Rosso S.M., Van, Herpen E. et al
2002, Ann. Neurol. (51) 373-376 - Early-onset, rapidly progressive familial tauopathy with R406W mutation.
- Saito Y., Geyer A., Sasaki R. et al
2002, Neurology (58) 811-813 - Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
- Strausberg R.L., Feingold E.A., Grouse L.H. et al
2002, Proc. Natl. Acad. Sci. U.S.A. (99) 16899-16903 - Clinical and genetic studies of families with the tau N279K mutation (FTDP-17).
- Tsuboi Y., Baker M., Hutton M.L. et al
2002, Neurology (59) 1791-1793 - Functional effects of tau gene mutations deltaN296 and N296H.
- Yoshida H., Crowther R.A., Goedert M. et al
2002, J. Neurochem. (80) 548-551 - Effects of FTDP-17 mutations on the in vitro phosphorylation of tau by glycogen synthase kinase 3beta identified by mass spectrometry demonstrate certain mutations exert long-range conformational changes.
- Connell J.W., Gibb G.M., Betts J.C. et al
2001, FEBS Lett. (493) 40-44 - Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells.
- Iseki E., Matsumura T., Marui W. et al
2001, Acta Neuropathol. (102) 285-292 - Pick's disease associated with the novel Tau gene mutation K369I.
- Neumann M., Schulz-Schaeffer W., Crowther R.A. et al
2001, Ann. Neurol. (50) 503-513 - Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene.
- Pastor P., Pastor E., Carnero C. et al
2001, Ann. Neurol. (49) 263-267 - 1H NMR study on the binding of Pin1 Trp-Trp domain with phosphothreonine peptides.
- Wintjens R., Wieruszeski J.M., Drobecq H. et al
2001, J. Biol. Chem. (276) 25150-25156 - Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene.
- Arima K., Kowalska A., Hasegawa M. et al
2000, Neurology (54) 1787-1795 - Tau mutations in frontotemporal dementia FTDP-17 and their relevance for Alzheimer's disease.
- Goedert M., Spillantini M.G.
2000, Biochim. Biophys. Acta (1502) 110-121 - Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation.
- Lippa C.F., Zhukareva V., Kawarai T. et al
2000, Ann. Neurol. (48) 850-858 - Interaction of tau with the neural membrane cortex is regulated by phosphorylation at sites that are modified in paired helical filaments.
- Maas T., Eidenmueller J., Brandt R. et al
2000, J. Biol. Chem. (275) 15733-15740 - Pick's disease is associated with mutations in the tau gene.
- Pickering-Brown S., Baker M., Yen S.-H. et al
2000, Ann. Neurol. (48) 859-867 - Tau gene mutation K257T causes a tauopathy similar to Pick's disease.
- Rizzini C., Goedert M., Hodges J.R. et al
2000, J. Neuropathol. Exp. Neurol. (59) 990-1001 - A Japanese patient with frontotemporal dementia and parkinsonism by a tau P301S mutation.
- Yasuda M., Yokoyama K., Nakayasu T. et al
2000, Neurology (55) 1224-1227 - Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.
- Bugiani O., Murrell J.R., Giaccone G. et al
1999, J. Neuropathol. Exp. Neurol. (58) 667-677 - A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy.
- Delisle M.-B., Murrell J.R., Richardson R. et al
1999, Acta Neuropathol. (98) 62-77 - Mutational analysis of the tau gene in progressive supranuclear palsy.
- Higgins J.J., Adler R.L., Loveless J.M. et al
1999, Neurology (53) 1421-1424 - A distinct familial presenile dementia with a novel missense mutation in the tau gene.
- Iijima M., Tabira T., Poorkaj P. et al
1999, NeuroReport (10) 497-501 - Tau gene mutation G389R causes a tauopathy with abundant pick body- like inclusions and axonal deposits.
- Murrell J.R., Spillantini M.G., Zolo P. et al
1999, J. Neuropathol. Exp. Neurol. (58) 1207-1226 - Accelerated filament formation from tau protein with specific FTDP-17 missense mutations.
- Nacharaju P., Lewis J., Easson C. et al
1999, FEBS Lett. (447) 195-199 - High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands.
- Rizzu P., Van, Swieten J.C. et al
1999, Am. J. Hum. Genet. (64) 414-421 - A mutation in the microtubule-associated protein tau in pallido- nigro-luysian degeneration.
- Yasuda M., Kawamata T., Komure O. et al
1999, Neurology (53) 864-868 - Pathogenic implications of mutations in the tau gene in pallido- ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17.
- Clark L.N., Poorkaj P., Wszolek Z. et al
1998, Proc. Natl. Acad. Sci. U.S.A. (95) 13103-13107 - Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.
- Dumanchin C., Camuzat A., Campion D. et al
1998, Hum. Mol. Genet. (7) 1825-1829 - Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17.
- Hutton M., Lendon C.L., Rizzu P. et al
1998, Nature (393) 702-705 - The endogenous and cell cycle-dependent phosphorylation of tau protein in living cells: implications for Alzheimer's disease.
- Illenberger S., Zheng-Fischhofer Q., Preuss U. et al
1998, Mol. Biol. Cell (9) 1495-1512 - Tau is a candidate gene for chromosome 17 frontotemporal dementia.
- Poorkaj P., Bird T.D., Wijsman E. et al
1998, Ann. Neurol. (43) 815-825 - Phosphorylation of tau at both Thr 231 and Ser 262 is required for maximal inhibition of its binding to microtubules.
- Sengupta A., Kabat J., Novak M. et al
1998, Arch. Biochem. Biophys. (357) 299-309 - Characterization of in vitro glycation sites of tau.
- Nacharaju P., Ko L., Yen S.H. et al
1997, J. Neurochem. (69) 1709-1719 - The microtubule-associated protein tau is extensively modified with O-linked N-acetylglucosamine.
- Arnold C.S., Johnson G.V.W., Cole R.N. et al
1996, J. Biol. Chem. (271) 28741-28744 - Molecular evolution of tau protein: implications for Alzheimer's disease.
- Nelson P.T., Stefansson K., Gulcher J. et al
1996, J. Neurochem. (67) 1622-1632 - Microtubule-associated protein/microtubule affinity-regulating kinase (p110mark). A novel protein kinase that regulates tau-microtubule interactions and dynamic instability by phosphorylation at the Alzheimer-specific site serine 262.
- Drewes G., Trinczek B., Illenberger S. et al
1995, J. Biol. Chem. (270) 7679-7688 - Expression of three- and four-repeat tau isoforms in mouse liver.
- Kenner L., el-Shabrawi Y., Hutter H. et al
1994, Hepatology (20) 1086-1089 - Diversity of high-molecular-weight tau proteins in different regions of the nervous system.
- Mavilia C., Couchie D., Nunez J. et al
1994, J. Neurochem. (63) 2300-2306 - Complete sequence of 3'-untranslated region of tau from rat central nervous system. Implications for mRNA heterogeneity.
- Sadot E., Marx R., Barg J. et al
1994, J. Mol. Biol. (241) 325-331 - Molecular diversity at the carboxyl terminus of human and rat tau.
- Sawa A., Oyama F., Matsushita M. et al
1994, Brain Res. Mol. Brain Res. (27) 111-117 - High molecular weight tau proteins and acquisition of neuronal polarity in peripheral nervous system.
- Couchie D., Gache Y., Mavilia C. et al
1993, C. R. Acad. Sci. III, Sci. Vie (316) 404-409 - Expression of high molecular weight tau in the central and peripheral nervous systems.
- Georgieff I.S., Liem R.K.H., Couchie D. et al
1993, J. Cell Sci. (105) 729-737 - In vivo phosphorylation sites in fetal and adult rat tau.
- Watanabe A., Hasegawa M., Suzuki M. et al
1993, J. Biol. Chem. (268) 25712-25717 - Structure and novel exons of the human tau gene.
- Andreadis A., Brown W.M., Kosik K.S. et al
1992, Biochemistry (31) 10626-10633 - Primary structure of high molecular weight tau present in the peripheral nervous system.
- Couchie D., Mavilia C., Georgieff I.S. et al
1992, Proc. Natl. Acad. Sci. U.S.A. (89) 4378-4381 - Cloning of a big tau microtubule-associated protein characteristic of the peripheral nervous system.
- Goedert M., Spillantini M.G., Crowther R.A. et al
1992, Proc. Natl. Acad. Sci. U.S.A. (89) 1983-1987 - Protein sequence and mass spectrometric analyses of tau in the Alzheimer's disease brain.
- Hasegawa M., Morishima-Kawashima M., Takio K. et al
1992, J. Biol. Chem. (267) 17047-17054 - Molecular characterization of microtubule-associated proteins tau and MAP2.
- Goedert M., Crowther R.A., Garner C.C. et al
1991, Trends Neurosci. (14) 193-199 - Identification of 3- and 4-repeat tau isoforms within the PHF in Alzheimer's disease.
- Jakes R., Novak M., Davison M. et al
1991, EMBO J. (10) 2725-2729 - 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. et al
1989, Neuron (3) 519-526 - Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats: differential expression of tau protein mRNAs in human brain.
- Goedert M., Spillantini M.G., Potier M.C. et al
1989, EMBO J. (8) 393-399 - Structure of the bovine tau gene: alternatively spliced transcripts generate a protein family.
- Himmler A.
1989, Mol. Cell. Biol. (9) 1389-1396 - Tau consists of a set of proteins with repeated C-terminal microtubule-binding domains and variable N-terminal domains.
- Himmler A., Drechsel D., Kirschner M.W. et al
1989, Mol. Cell. Biol. (9) 1381-1388 - Expression of multiple tau isoforms and microtubule bundle formation in fibroblasts transfected with a single tau cDNA.
- Kanai Y., Takemura R., Oshima T. et al
1989, J. Cell Biol. (109) 1173-1184 - Developmentally regulated expression of specific tau sequences.
- Kosik K.S., Orecchio L.D., Bakalis S. et al
1989, Neuron (2) 1389-1397 - The microtubule binding domain of tau protein.
- Lee G., Neve R.L., Kosik K.S. et al
1989, Neuron (2) 1615-1624 - A distinct form of tau is selectively incorporated into Alzheimer's paired helical filaments.
- Mori H., Hamada Y., Kawaguchi M. et al
1989, Biochem. Biophys. Res. Commun. (159) 1221-1226 - Cloning and sequencing of the cDNA encoding a core protein of the paired helical filament of Alzheimer disease: identification as the microtubule-associated protein tau.
- Goedert M., Wischik C., Crowther R. et al
1988, Proc. Natl. Acad. Sci. U.S.A. (85) 4051-4055 - The primary structure and heterogeneity of tau protein from mouse brain.
- Lee G., Cowan N.J., Kirschner M. et al
1988, Science (239) 285-288