Search Results

There are 131571 results for: content related to: FUS gene mutations cause essential tremor: A surprise but also confirms genetic heterogeneity of essential tremor

  1. TARDBP and FUS Mutations Associated with Amyotrophic Lateral Sclerosis: Summary and Update

    Human Mutation

    Volume 34, Issue 6, June 2013, Pages: 812–826, Serena Lattante, Guy A. Rouleau and Edor Kabashi

    Version of Record online : 29 APR 2013, DOI: 10.1002/humu.22319

  2. You have free access to this content
    Physiological functions and pathobiology of TDP-43 and FUS/TLS proteins

    Journal of Neurochemistry

    Volume 138, Issue S1, August 2016, Pages: 95–111, Antonia Ratti and Emanuele Buratti

    Version of Record online : 15 JUN 2016, DOI: 10.1111/jnc.13625

  3. RNA quality control and protein aggregates in amyotrophic lateral sclerosis: A review

    Muscle & Nerve

    Volume 47, Issue 3, March 2013, Pages: 330–338, Ashok Verma and Rup Tandan

    Version of Record online : 4 FEB 2013, DOI: 10.1002/mus.23673

  4. Genetic analysis of the FUS/TLS gene in essential tremor

    European Journal of Neurology

    Volume 20, Issue 3, March 2013, Pages: 534–539, N. Parmalee, K. Mirzozoda, S. Kisselev, N. Merner, P. Dion, G. Rouleau, L. Clark and E. D. Louis

    Version of Record online : 31 OCT 2012, DOI: 10.1111/ene.12023

  5. The impact of rare variants in FUS in essential tremor

    Movement Disorders

    Volume 30, Issue 5, 15 April 2015, Pages: 721–724, Franziska Hopfner, Giovanni Stevanin, Stefanie H. Müller, Emeline Mundwiller, May Bungeroth, Alexandra Durr, Manuela Pendziwiat, Mathieu Anheim, Susanne A. Schneider, Lukas Tittmann, Stephan Klebe, Delia Lorenz, Günther Deuschl, Alexis Brice and Gregor Kuhlenbäumer

    Version of Record online : 28 JAN 2015, DOI: 10.1002/mds.26145

  6. Novel FUS mutations identified through molecular screening in a large cohort of familial and sporadic amyotrophic lateral sclerosis

    European Journal of Neurology

    Volume 22, Issue 11, November 2015, Pages: 1474–1481, C. Tarlarini, C. Lunetta, L. Mosca, F. Avemaria, N. Riva, V. Mantero, E. Maestri, A. Quattrini, M. Corbo, M. G. Melazzini and S. Penco

    Version of Record online : 15 JUL 2015, DOI: 10.1111/ene.12772

  7. You have full text access to this OnlineOpen article
    Spliceosome integrity is defective in the motor neuron diseases ALS and SMA

    EMBO Molecular Medicine

    Volume 5, Issue 2, February 2013, Pages: 221–234, Hitomi Tsuiji, Yohei Iguchi, Asako Furuya, Ayane Kataoka, Hiroyuki Hatsuta, Naoki Atsuta, Fumiaki Tanaka, Yoshio Hashizume, Hiroyasu Akatsu, Shigeo Murayama, Gen Sobue and Koji Yamanaka

    Version of Record online : 25 JAN 2013, DOI: 10.1002/emmm.201202303

  8. RNA-binding proteins involved in RNA localization and their implications in neuronal diseases

    European Journal of Neuroscience

    Volume 35, Issue 12, June 2012, Pages: 1818–1836, Marco Tolino, Martin Köhrmann and Michael A. Kiebler

    Version of Record online : 19 JUN 2012, DOI: 10.1111/j.1460-9568.2012.08160.x

  9. RNA-binding proteins in neurodegenerative disease: TDP-43 and beyond

    Wiley Interdisciplinary Reviews: RNA

    Volume 3, Issue 2, March/April 2012, Pages: 265–285, Keith A. Hanson, Sang Hwa Kim and Randal S. Tibbetts

    Version of Record online : 25 OCT 2011, DOI: 10.1002/wrna.111

  10. You have free access to this content
    TDP-43 and FUS/TLS: sending a complex message about messenger RNA in amyotrophic lateral sclerosis?

    The FEBS Journal

    Volume 278, Issue 19, October 2011, Pages: 3569–3577, Michael J. Strong and Kathryn Volkening

    Version of Record online : 6 SEP 2011, DOI: 10.1111/j.1742-4658.2011.08277.x

  11. You have free access to this content
    TDP-43 and FUS/TLS: cellular functions and implications for neurodegeneration

    The FEBS Journal

    Volume 278, Issue 19, October 2011, Pages: 3550–3568, Fabienne C. Fiesel and Philipp J. Kahle

    Version of Record online : 24 AUG 2011, DOI: 10.1111/j.1742-4658.2011.08258.x

  12. Genotype–phenotype relationships in familial amyotrophic lateral sclerosis with FUS/TLS mutations in Japan

    Muscle & Nerve

    Volume 54, Issue 3, September 2016, Pages: 398–404, Tetsuya Akiyama, Hitoshi Warita, Masaaki Kato, Ayumi Nishiyama, Rumiko Izumi, Chikako Ikeda, Masaki Kamada, Naoki Suzuki and Masashi Aoki

    Version of Record online : 23 FEB 2016, DOI: 10.1002/mus.25061

  13. You have free access to this content
    Poster Presentations

    Movement Disorders

    Volume 30, Issue S1, June 2015, Pages: S1–S567,

    Version of Record online : 12 JUN 2015, DOI: 10.1002/mds.26295

  14. You have free access to this content
    FUS stimulates microRNA biogenesis by facilitating co-transcriptional Drosha recruitment

    The EMBO Journal

    Volume 31, Issue 24, December 12, 2012, Pages: 4502–4510, Mariangela Morlando, Stefano Dini Modigliani, Giulia Torrelli, Alessandro Rosa, Valerio Di Carlo, Elisa Caffarelli and Irene Bozzoni

    Version of Record online : 12 DEC 2012, DOI: 10.1038/emboj.2012.319

  15. Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis

    Muscle & Nerve

    Volume 42, Issue 2, August 2010, Pages: 170–176, Rosa Rademakers, Heather Stewart, Mariely Dejesus-Hernandez, Charles Krieger, Neill Graff-Radford, Marife Fabros, Hannah Briemberg, Neil Cashman, Andrew Eisen and Ian R.A. Mackenzie

    Version of Record online : 16 APR 2010, DOI: 10.1002/mus.21665

  16. You have free access to this content
    Stress granules in neurodegeneration – lessons learnt from TAR DNA binding protein of 43 kDa and fused in sarcoma

    The FEBS Journal

    Volume 280, Issue 18, September 2013, Pages: 4348–4370, Eva Bentmann, Christian Haass and Dorothee Dormann

    Version of Record online : 9 MAY 2013, DOI: 10.1111/febs.12287

  17. A Japanese patient with familial ALS and a p.K510M mutation in the gene for FUS (FUS) resulting in the totally locked-in state

    Neuropathology

    Volume 34, Issue 5, October 2014, Pages: 504–509, Yoko Mochizuki, Akihiro Kawata, Hirofumi Maruyama, Taku Homma, Kazuhiko Watabe, Hideshi Kawakami, Takashi Komori, Toshio Mizutani and Shiro Matsubara

    Version of Record online : 19 MAY 2014, DOI: 10.1111/neup.12130

  18. Screening of the FUS gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin

    European Journal of Neurology

    Volume 19, Issue 7, July 2012, Pages: 977–983, Z.-Y. Zou, Y. Peng, X.-H. Feng, X.-N. Wang, Q. Sun, M.-S. Liu, X.-G. Li and L.-Y. Cui

    Version of Record online : 16 FEB 2012, DOI: 10.1111/j.1468-1331.2012.03662.x

  19. FUS/TLS assembles into stress granules and is a prosurvival factor during hyperosmolar stress

    Journal of Cellular Physiology

    Volume 228, Issue 11, November 2013, Pages: 2222–2231, Reddy Ranjith K. Sama, Catherine L. Ward, Laura J. Kaushansky, Nathan Lemay, Shinsuke Ishigaki, Fumihiko Urano and Daryl A. Bosco

    Version of Record online : 25 JUL 2013, DOI: 10.1002/jcp.24395

  20. You have free access to this content
    The FUS about arginine methylation in ALS and FTLD

    The EMBO Journal

    Volume 31, Issue 22, November 14, 2012, Pages: 4249–4251, Hannah M Kaneb, Patrick A Dion and Guy A Rouleau

    Version of Record online : 19 OCT 2012, DOI: 10.1038/emboj.2012.291