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There are 4393 results for: content related to: TMEM 106B p.T185S regulates TMEM 106B protein levels: implications for frontotemporal dementia

  1. You have free access to this content
    The FTLD risk factor TMEM106B and MAP6 control dendritic trafficking of lysosomes

    The EMBO Journal

    Volume 33, Issue 5, 3 March 2014, Pages: 450–467, Benjamin M Schwenk, Christina M Lang, Sebastian Hogl, Sabina Tahirovic, Denise Orozco, Kristin Rentzsch, Stefan F Lichtenthaler, Casper C Hoogenraad, Anja Capell, Christian Haass and Dieter Edbauer

    Version of Record online : 20 DEC 2013, DOI: 10.1002/embj.201385857

  2. You have full text access to this OnlineOpen article
    Transmembrane protein 106A is silenced by promoter region hypermethylation and suppresses gastric cancer growth by inducing apoptosis

    Journal of Cellular and Molecular Medicine

    Volume 18, Issue 8, August 2014, Pages: 1655–1666, Dong Xu, Liujing Qu, Jia Hu, Ge Li, Ping Lv, Dalong Ma, Mingzhou Guo and Yingyu Chen

    Version of Record online : 28 JUN 2014, DOI: 10.1111/jcmm.12352

  3. A novel TMEM16A splice variant lacking the dimerization domain contributes to calcium-activated chloride secretion in human sweat gland epithelial cells

    Experimental Dermatology

    Volume 23, Issue 11, November 2014, Pages: 825–831, Torsten Ertongur-Fauth, Andreas Hochheimer, Joerg Martin Buescher, Stefan Rapprich and Michael Krohn

    Version of Record online : 1 OCT 2014, DOI: 10.1111/exd.12543

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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

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    TMEM106B and frontotemporal lobar degeneration: can over-expression tell us how reductions are beneficial?

    Journal of Neurochemistry

    Volume 126, Issue 6, September 2013, Pages: 696–698, Steven W. Barger

    Version of Record online : 22 JUL 2013, DOI: 10.1111/jnc.12357

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    Impairment of endothelial-mesenchymal transformation during atrioventricular cushion formation in Tmem100 null embryos

    Developmental Dynamics

    Volume 244, Issue 1, January 2015, Pages: 31–42, Ken Mizuta, Masahide Sakabe, Aya Hashimoto, Tomoko Ioka, Chihiro Sakai, Kazuki Okumura, Miwa Hattammaru, Masahide Fujita, Mutsumi Araki, Satoshi Somekawa, Yoshihiko Saito and Osamu Nakagawa

    Version of Record online : 7 NOV 2014, DOI: 10.1002/dvdy.24216

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    Plasticity of PI4KIIIα interactions at the plasma membrane

    EMBO reports

    Volume 16, Issue 3, March 2015, Pages: 312–320, Jeeyun Chung, Fubito Nakatsu, Jeremy M Baskin and Pietro De Camilli

    Version of Record online : 21 JAN 2015, DOI: 10.15252/embr.201439151

  8. TMEM16E (GDD1) Exhibits Protein Instability and Distinct Characteristics in Chloride Channel/Pore Forming Ability

    Journal of Cellular Physiology

    Volume 229, Issue 2, February 2014, Pages: 181–190, Ta To Tran, Kei Tobiume, Chikara Hirono, Shinichi Fujimoto, Kuniko Mizuta, Kazumi Kubozono, Hiroshi Inoue, Mitsuo Itakura, Makoto Sugita and Nobuyuki Kamata

    Version of Record online : 25 OCT 2013, DOI: 10.1002/jcp.24431

  9. Chloride ion transport and overexpression of TMEM16A in a guinea-pig asthma model

    Clinical & Experimental Allergy

    Volume 47, Issue 6, June 2017, Pages: 795–804, M. Kondo, M. Tsuji, K. Hara, K. Arimura, O. Yagi, E. Tagaya, K. Takeyama and J. Tamaoki

    Version of Record online : 20 FEB 2017, DOI: 10.1111/cea.12887

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    9-Phenanthrol inhibits recombinant and arterial myocyte TMEM16A channels

    British Journal of Pharmacology

    Volume 172, Issue 10, May 2015, Pages: 2459–2468, Sarah K Burris, Qian Wang, Simon Bulley, Zachary P Neeb and Jonathan H Jaggar

    Version of Record online : 24 MAR 2015, DOI: 10.1111/bph.13077

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    Expression of TMEM16 paralogs during murine embryogenesis

    Developmental Dynamics

    Volume 237, Issue 9, September 2008, Pages: 2566–2574, Jason R. Rock and Brian D. Harfe

    Version of Record online : 26 AUG 2008, DOI: 10.1002/dvdy.21676

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    Formation of the transition zone by Mks5/Rpgrip1L establishes a ciliary zone of exclusion (CIZE) that compartmentalises ciliary signalling proteins and controls PIP2 ciliary abundance

    The EMBO Journal

    Volume 34, Issue 20, 14 October 2015, Pages: 2537–2556, Victor L Jensen, Chunmei Li, Rachel V Bowie, Lara Clarke, Swetha Mohan, Oliver E Blacque and Michel R Leroux

    Version of Record online : 21 SEP 2015, DOI: 10.15252/embj.201488044

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    A TMEM16F point mutation causes an absence of canine platelet TMEM16F and ineffective activation and death-induced phospholipid scrambling

    Journal of Thrombosis and Haemostasis

    Volume 13, Issue 12, December 2015, Pages: 2240–2252, M. B. Brooks, J. L. Catalfamo, R. MacNguyen, D. Tim, S. Fancher and J. A. McCardle

    Version of Record online : 20 NOV 2015, DOI: 10.1111/jth.13157

  14. Molecular Genetics of Frontotemporal Dementia

    Standard Article


    Raffaele Ferrari, Avinash Thumma and Parastoo Momeni

    Published Online : 15 MAY 2013, DOI: 10.1002/9780470015902.a0024457

  15. Identification of Tmem10/Opalin as an oligodendrocyte enriched gene using expression profiling combined with genetic cell ablation


    Volume 56, Issue 11, 15 August 2008, Pages: 1176–1186, Neev Golan, Konstantin Adamsky, Elena Kartvelishvily, Damian Brockschnieder, Wiebke Möbius, Ivo Spiegel, Alejandro D. Roth, Christine E. Thomson, Gideon Rechavi and Elior Peles

    Version of Record online : 20 JUN 2008, DOI: 10.1002/glia.20688

  16. TMEM16A is a Ca2+-activated Cl channel expressed in the renal collecting duct

    Acta Physiologica

    Volume 212, Issue 2, October 2014, Pages: 166–174, P. Svenningsen, M. R. Nielsen, N. Marcussen, S. Walter and B. L. Jensen

    Version of Record online : 26 JUN 2014, DOI: 10.1111/apha.12323

  17. TMEM107 Is a Critical Regulator of Ciliary Protein Composition and Is Mutated in Orofaciodigital Syndrome

    Human Mutation

    Volume 37, Issue 2, February 2016, Pages: 155–159, Natalia A. Shylo, Kasey J. Christopher, Alejandro Iglesias, Aaron Daluiski and Scott D. Weatherbee

    Version of Record online : 23 NOV 2015, DOI: 10.1002/humu.22925

  18. Whole-Exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99

    Human Mutation

    Volume 36, Issue 1, January 2015, Pages: 98–105, Jiangxia Li, Xiaohan Zhao, Qian Xin, Shan Shan, Baichun Jiang, Yecheng Jin, Huijun Yuan, Pu Dai, Ruo Xiao, Qingyan Zhang, Jingjing Xiao, Changshun Shao, Yaoqin Gong and Qiji Liu

    Version of Record online : 28 NOV 2014, DOI: 10.1002/humu.22712

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    TiME for TMEM106B

    The EMBO Journal

    Volume 33, Issue 5, 3 March 2014, Pages: 405–406, Solène Debaisieux and Giampietro Schiavo

    Version of Record online : 4 FEB 2014, DOI: 10.1002/embj.201387697

  20. Generation of mice with a conditional and reporter allele for Tmem100


    Volume 48, Issue 11, November 2010, Pages: 673–678, Eun-Hye Moon, Mi-Jung Kim, Keum Soun Ko, Yoo Sung Kim, Jiyoung Seo, S. Paul Oh and Young Jae Lee

    Version of Record online : 30 OCT 2010, DOI: 10.1002/dvg.20674