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There are 8585195 results for: content related to: The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome

  1. FTDP-17 with Pick body-like inclusions associated with a novel tau mutation, p.E372G

    Brain Pathology

    Volume 27, Issue 5, September 2017, Pages: 612–626, Pawel Tacik, Michael A. DeTure, Yari Carlomagno, Wen-Lang Lin, Melissa E. Murray, Matthew C. Baker, Keith A. Josephs, Bradley F. Boeve, Zbigniew K. Wszolek, Neill R. Graff-Radford, Joseph E. Parisi, Leonard Petrucelli, Rosa Rademakers, Richard S. Isaacson, Kenneth M. Heilman, Ronald C. Petersen, Dennis W. Dickson and Naomi Kouri

    Version of Record online : 5 OCT 2016, DOI: 10.1111/bpa.12428

  2. You have full text access to this OnlineOpen article
    Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging

    Neuropathology and Applied Neurobiology

    Volume 41, Issue 1, February 2015, Pages: 24–46, Bernardino Ghetti, Adrian L. Oblak, Bradley F. Boeve, Keith A. Johnson, Bradford C. Dickerson and Michel Goedert

    Version of Record online : 29 JAN 2015, DOI: 10.1111/nan.12213

    Corrected by:

    Corrigendum: Corrigendum

    Vol. 41, Issue 4, 571, Version of Record online: 13 MAY 2015

  3. You have free access to this content
    Removing endogenous tau does not prevent tau propagation yet reduces its neurotoxicity

    The EMBO Journal

    Volume 34, Issue 24, 14 December 2015, Pages: 3028–3041, Susanne Wegmann, Eduardo A Maury, Molly J Kirk, Lubna Saqran, Allyson Roe, Sarah L DeVos, Samantha Nicholls, Zhanyun Fan, Shuko Takeda, Ozge Cagsal-Getkin, Christopher M William, Tara L Spires-Jones, Rose Pitstick, George A Carlson, Amy M Pooler and Bradley T Hyman

    Version of Record online : 4 NOV 2015, DOI: 10.15252/embj.201592748

  4. Tau isoform regulation is region- and cell-specific in mouse brain

    Journal of Comparative Neurology

    Volume 511, Issue 6, 20 December 2008, Pages: 788–803, Pamela McMillan, Elena Korvatska, Parvoneh Poorkaj, Zana Evstafjeva, Linda Robinson, Lynne Greenup, James Leverenz, Gerard D. Schellenberg and Ian D'Souza

    Version of Record online : 16 OCT 2008, DOI: 10.1002/cne.21867

  5. Tau and α-synuclein in susceptibility to, and dementia in, Parkinson's disease

    Annals of Neurology

    Volume 62, Issue 2, August 2007, Pages: 145–153, An Goris, Caroline H. Williams-Gray, Graeme R. Clark, Thomas Foltynie, Simon J. G. Lewis, Joanne Brown, Maria Ban, Maria G. Spillantini, Alastair Compston, David J. Burn, Patrick F. Chinnery, Roger A. Barker and Stephen J. Sawcer

    Version of Record online : 7 AUG 2007, DOI: 10.1002/ana.21192

  6. SNCA, MAPT, and GSK3B in Parkinson disease: a gene–gene interaction study

    European Journal of Neurology

    Volume 18, Issue 6, June 2011, Pages: 876–881, C. Wider, C. Vilariño-Güell, M. G. Heckman, B. Jasinska-Myga, A. I. Ortolaza-Soto, N. N. Diehl, J. E. Crook, S. A. Cobb, J. A. Bacon, J. O. Aasly, J. M. Gibson, T. Lynch, R. J. Uitti, Z. K. Wszolek, M. J. Farrer and O. A. Ross

    Version of Record online : 15 DEC 2010, DOI: 10.1111/j.1468-1331.2010.03297.x

  7. Correlation of MAPT scores with clinical and radiographic assessment of patients awaiting THR/TKR

    ANZ Journal of Surgery

    Volume 81, Issue 7-8, July/August 2011, Pages: 543–546, Vikram Mohan David, George Bousounis, Theo Kapakoulakis, Robert Champion, Kevin Masman and Keith McCullough

    Version of Record online : 17 NOV 2010, DOI: 10.1111/j.1445-2197.2010.05572.x

  8. You have free access to this content
    Poster Presentations

    Movement Disorders

    Volume 27, Issue S1, June 2012, Pages: S1–S523,

    Version of Record online : 19 JUN 2012, DOI: 10.1002/mds.25051

  9. Glycogen synthase kinase-3β and tau genes interact in Alzheimer's disease

    Annals of Neurology

    Volume 64, Issue 4, October 2008, Pages: 446–454, John B. J. Kwok, Clement T. Loy, Gillian Hamilton, Edmond Lau, Marianne Hallupp, Julie Williams, Michael J. Owen, G. Anthony Broe, Nelson Tang, Linda Lam, John F. Powell, Simon Lovestone and Peter R. Schofield

    Version of Record online : 7 NOV 2008, DOI: 10.1002/ana.21476

  10. The MAPT gene is differentially methylated in the progressive supranuclear palsy brain

    Movement Disorders

    Volume 31, Issue 12, December 2016, Pages: 1883–1890, Vincent Huin, Vincent Deramecourt, Dominique Caparros-Lefebvre, Claude-Alain Maurage, Charles Duyckaerts, Eniko Kovari, Florence Pasquier, Valérie Buée-Scherrer, Julien Labreuche, Hélène Behal, Luc Buée, Claire-Marie Dhaenens and Bernard Sablonnière

    Version of Record online : 6 OCT 2016, DOI: 10.1002/mds.26820

  11. Independent and joint effects of the MAPT and SNCA genes in Parkinson disease

    Annals of Neurology

    Volume 69, Issue 5, May 2011, Pages: 778–792, Alexis Elbaz, Owen A. Ross, John P. A. Ioannidis, Alexandra I. Soto-Ortolaza, Frédéric Moisan, Jan Aasly, Grazia Annesi, Maria Bozi, Laura Brighina, Marie-Christine Chartier-Harlin, Alain Destée, Carlo Ferrarese, Alessandro Ferraris, J. Mark Gibson, Suzana Gispert, Georgios M. Hadjigeorgiou, Barbara Jasinska-Myga, Christine Klein, Rejko Krüger, Jean-Charles Lambert, Katja Lohmann, Simone van de Loo, Marie-Anne Loriot, Timothy Lynch, George D. Mellick, Eugénie Mutez, Christer Nilsson, Grzegorz Opala, Andreas Puschmann, Aldo Quattrone, Manu Sharma, Peter A. Silburn, Leonidas Stefanis, Ryan J. Uitti, Enza Maria Valente, Carles Vilariño-Güell, Karin Wirdefeldt, Zbigniew K. Wszolek, Georgia Xiromerisiou, Demetrius M. Maraganore, Matthew J. Farrer and on behalf of the Genetic Epidemiology of Parkinson's Disease (GEO-PD) consortium

    Version of Record online : 9 MAR 2011, DOI: 10.1002/ana.22321

  12. Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance images

    European Journal of Neurology

    Volume 22, Issue 5, May 2015, Pages: 745–752, J. L. Whitwell, B. F. Boeve, S. D. Weigand, M. L. Senjem, J. L. Gunter, M. C. Baker, M. DeJesus-Hernandez, D. S. Knopman, Z. K. Wszolek, R. C. Petersen, R. Rademakers, C. R. Jack Jr and K. A. Josephs

    Version of Record online : 12 FEB 2015, DOI: 10.1111/ene.12675

  13. DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E In Vitro

    Movement Disorders

    Volume 29, Issue 13, November 2014, Pages: 1606–1614, Kirsten G. Coupland, George D. Mellick, Peter A. Silburn, Karen Mather, Nicola J. Armstrong, Perminder S. Sachdev, Henry Brodaty, Yue Huang, Glenda M. Halliday, Marianne Hallupp, Woojin S. Kim, Carol Dobson-Stone and John B.J. Kwok

    Version of Record online : 27 DEC 2013, DOI: 10.1002/mds.25784

    Corrected by:

    Corrigendum: Corrigendum

    Vol. 31, Issue 5, 768, Version of Record online: 31 MAR 2016

  14. Bottom-up Design of Small Molecules that Stimulate Exon 10 Skipping in Mutant MAPT Pre-mRNA


    Volume 15, Issue 14, September 22, 2014, Pages: 2041–2044, Dr. Yiling Luo and Prof. Dr. Matthew D. Disney

    Version of Record online : 12 AUG 2014, DOI: 10.1002/cbic.201402069

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    Genetics of FTLD: overview and what else we can expect from genetic studies

    Journal of Neurochemistry

    Volume 138, Issue S1, August 2016, Pages: 32–53, Cyril Pottier, Thomas A. Ravenscroft, Monica Sanchez-Contreras and Rosa Rademakers

    Version of Record online : 9 AUG 2016, DOI: 10.1111/jnc.13622

  16. Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer’s disease

    Neuropathology and Applied Neurobiology

    Volume 32, Issue 4, August 2006, Pages: 374–387, A.-M. Shiarli, R. Jennings, J. Shi, K. Bailey, Y. Davidson, J. Tian, E. H. Bigio, B. Ghetti, J. R. Murrell, M. B. Delisle, S. Mirra, B. Crain, P. Zolo, K. Arima, E. Iseki, S. Murayama, H. Kretzschmar, M. Neumann, C. Lippa, G. Halliday, J. MacKenzie, N. Khan, R. Ravid, D. Dickson, Z. Wszolek, T. Iwatsubo, S. M. Pickering-Brown and D. M. A. Mann

    Version of Record online : 7 JUL 2006, DOI: 10.1111/j.1365-2990.2006.00736.x

  17. Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) due to microtubule-associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathy

    Neuropathology and Applied Neurobiology

    Volume 43, Issue 3, April 2017, Pages: 200–214, P. Tacik, M. Sanchez-Contreras, M. DeTure, M. E. Murray, R. Rademakers, O. A. Ross, Z. K. Wszolek, J. E. Parisi, D. S. Knopman, R. C. Petersen and D. W. Dickson

    Version of Record online : 8 MAR 2017, DOI: 10.1111/nan.12367

  18. You have full text access to this OnlineOpen article
    Functional role of the Tau protein in epithelial ovarian cancer cells

    Reproductive Medicine and Biology

    Volume 16, Issue 2, April 2017, Pages: 143–151, Aisa Yamauchi, Asami Kobayashi, Hiroe Oikiri and Yoshihito Yokoyama

    Version of Record online : 20 MAR 2017, DOI: 10.1002/rmb2.12019

  19. Interaction of α-synuclein and tau genotypes in Parkinson's disease

    Annals of Neurology

    Volume 57, Issue 3, March 2005, Pages: 439–443, Catherine E. Mamah, Timothy G. Lesnick, Sarah J. Lincoln, Kari J. Strain, Mariza de Andrade, James H. Bower, J. Eric Ahlskog, Walter A. Rocca, Matthew J. Farrer and Demetrius M. Maraganore

    Version of Record online : 24 FEB 2005, DOI: 10.1002/ana.20387

  20. The role of tau (MAPT) in frontotemporal dementia and related tauopathies

    Human Mutation

    Volume 24, Issue 4, October 2004, Pages: 277–295, R. Rademakers, M. Cruts and C. van Broeckhoven

    Version of Record online : 30 AUG 2004, DOI: 10.1002/humu.20086