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There are 2206 results for: content related to: XBP1 induces WFS1 through an endoplasmic reticulum stress response element-like motif in SH-SY5Y cells

  1. Wolfram syndrome and WFS1 gene

    Clinical Genetics

    Volume 79, Issue 2, February 2011, Pages: 103–117, L Rigoli, F Lombardo and C Di Bella

    Version of Record online : 25 AUG 2010, DOI: 10.1111/j.1399-0004.2010.01522.x

  2. Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disorders

    Clinical Genetics

    Volume 87, Issue 5, May 2015, Pages: 430–439, A. Chaussenot, C. Rouzier, M. Quere, M. Plutino, S. Ait-El-Mkadem, S. Bannwarth, M. Barth, H. Dollfus, P. Charles, M. Nicolino, B. Chabrol, B. Vialettes and V. Paquis-Flucklinger

    Version of Record online : 6 AUG 2014, DOI: 10.1111/cge.12437

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    WFS1 protein modulates the free Ca2+ concentration in the endoplasmic reticulum

    FEBS Letters

    Volume 580, Issue 24, October 16, 2006, Pages: 5635–5640, Daisuke Takei, Hisamitsu Ishihara, Suguru Yamaguchi, Takahiro Yamada, Akira Tamura, Hideki Katagiri, Yoshio Maruyama and Yoshitomo Oka

    Version of Record online : 15 SEP 2006, DOI: 10.1016/j.febslet.2006.09.007

  4. You have full text access to this OnlineOpen article
    The unfolded protein response is required to maintain the integrity of the endoplasmic reticulum, prevent oxidative stress and preserve differentiation in β-cells

    Diabetes, Obesity and Metabolism

    Volume 12, Issue s2, October 2010, Pages: 99–107, R. J. Kaufman, S. H. Back, B. Song, J. Han and J. Hassler

    Version of Record online : 1 OCT 2010, DOI: 10.1111/j.1463-1326.2010.01281.x

  5. Autoimmune disease in a DFNA6/14/38 family carrying a novel missense mutation in WFS1

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 17, 1 September 2008, Pages: 2258–2265, Michael S. Hildebrand, Jessica L. Sorensen, Maren Jensen, William J. Kimberling and Richard J.H. Smith

    Version of Record online : 7 AUG 2008, DOI: 10.1002/ajmg.a.32449

  6. Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease

    Human Mutation

    Volume 22, Issue 4, October 2003, Pages: 275–287, Kim Cryns, Theru A. Sivakumaran, Jody M.W. Van den Ouweland, Ronald J.E. Pennings, Cor W.R.J. Cremers, Kris Flothmann, Terry-Lynn Young, Richard J.H. Smith, Marci M. Lesperance and Guy Van Camp

    Version of Record online : 26 AUG 2003, DOI: 10.1002/humu.10258

  7. Wolfram syndrome 1 (Wfs1) gene expression in the normal mouse visual system

    Journal of Comparative Neurology

    Volume 510, Issue 1, 1 September 2008, Pages: 1–23, June Kawano, Yukio Tanizawa and Koh Shinoda

    Version of Record online : 8 JUL 2008, DOI: 10.1002/cne.21734

  8. You have full text access to this OnlineOpen article
    Analysis of metabolic effects of menthol on WFS1-deficient mice

    Physiological Reports

    Volume 4, Issue 1, January 2016, Marite Ehrlich, Marilin Ivask, Atso Raasmaja and Sulev Kõks

    Version of Record online : 5 JAN 2016, DOI: 10.14814/phy2.12660

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    Wolfram syndrome in French population: Characterization of novel mutations and polymorphisms in the WFS1 gene

    Human Mutation

    Volume 25, Issue 1, January 2005, Pages: 99–100, Fabienne Giuliano, Sylvie Bannwarth, Sophie Monnot, Aline Cano, Brigitte Chabrol, Bernard Vialettes, Bruno Delobel and Veronique Paquis-Flucklinger

    Version of Record online : 16 DEC 2004, DOI: 10.1002/humu.9300

  10. Study of the WFS1 gene and mitochondrial DNA in Spanish Wolfram syndrome families

    Clinical Genetics

    Volume 65, Issue 6, June 2004, Pages: 463–469, E Domènech, M Gómez-Zaera and V Nunes

    Version of Record online : 13 APR 2004, DOI: 10.1111/j.1399-0004.2004.00249.x

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    Distribution of Wfs1 protein in the central nervous system of the mouse and its relation to clinical symptoms of the Wolfram syndrome

    Journal of Comparative Neurology

    Volume 509, Issue 6, 20 August 2008, Pages: 642–660, Hendrik Luuk, Sulev Koks, Mario Plaas, Jens Hannibal, Jens F. Rehfeld and Eero Vasar

    Version of Record online : 12 JUN 2008, DOI: 10.1002/cne.21777

  12. Association of aggression with a novel microRNA binding site polymorphism in the wolframin gene

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 4, June 2013, Pages: 404–412, Reka Kovacs-Nagy, Zsuzsanna Elek, Anna Szekely, Tibor Nanasi, Maria Sasvari-Szekely and Zsolt Ronai

    Version of Record online : 3 MAY 2013, DOI: 10.1002/ajmg.b.32157

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    Wolfram syndrome-associated mutations lead to instability and proteasomal degradation of wolframin

    FEBS Letters

    Volume 580, Issue 16, July 10, 2006, Pages: 4000–4004, Sabine Hofmann and Matthias F. Bauer

    Version of Record online : 22 JUN 2006, DOI: 10.1016/j.febslet.2006.06.036

  14. Wfs1-deficient animals have brain-region-specific changes of Na+, K+-ATPase activity and mRNA expression of α1 and β1 subunits

    Journal of Neuroscience Research

    Volume 93, Issue 3, March 2015, Pages: 530–537, S. Sütt, A. Altpere, R. Reimets, T. Visnapuu, M. Loomets, S. Raud, T. Salum, R. Mahlapuu, C. Kairane, M. Zilmer and E. Vasar

    Version of Record online : 10 NOV 2014, DOI: 10.1002/jnr.23508

  15. You have full text access to this OnlineOpen article
    RNA-sequencing of WFS1-deficient pancreatic islets

    Physiological Reports

    Volume 4, Issue 7, April 2016, Marilin Ivask, Alison Hugill and Sulev Kõks

    Version of Record online : 6 APR 2016, DOI: 10.14814/phy2.12750

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    Genetics of hearing loss: Allelism and modifier genes produce a phenotypic continuum

    The Anatomical Record Part A: Discoveries in Molecular, Cellular, and Evolutionary Biology

    Volume 288A, Issue 4, April 2006, Pages: 370–381, Richard K. Mchugh and Rick A. Friedman

    Version of Record online : 20 MAR 2006, DOI: 10.1002/ar.a.20297

  17. Identification of novel mutations in WFS1 and genotype–phenotype correlation in Wolfram syndrome

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 14, 15 July 2007, Pages: 1605–1612, A. Cano, C. Rouzier, S. Monnot, B. Chabrol, J. Conrath, P. Lecomte, B. Delobel, P. Boileau, R. Valero, V. Procaccio, V. Paquis-Flucklinger and B. Vialettes

    Version of Record online : 13 JUN 2007, DOI: 10.1002/ajmg.a.31809

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    A switch from life to death in endoplasmic reticulum stressed β-cells

    Diabetes, Obesity and Metabolism

    Volume 12, Issue s2, October 2010, Pages: 58–65, C. M. Oslowski and F. Urano

    Version of Record online : 1 OCT 2010, DOI: 10.1111/j.1463-1326.2010.01277.x

  19. You have full text access to this OnlineOpen article
    Wolfram Syndrome protein, Miner1, regulates sulphydryl redox status, the unfolded protein response, and Ca2+ homeostasis

    EMBO Molecular Medicine

    Volume 5, Issue 6, June 2013, Pages: 904–918, Sandra E. Wiley, Alexander Y. Andreyev, Ajit S. Divakaruni, Robert Karisch, Guy Perkins, Estelle A. Wall, Peter van der Geer, Yi-Fan Chen, Ting-Fen Tsai, Melvin I. Simon, Benjamin G. Neel, Jack E. Dixon and Anne N. Murphy

    Version of Record online : 24 MAY 2013, DOI: 10.1002/emmm.201201429

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    Selected terpenoids from medicinal plants modulate endoplasmic reticulum stress in metabolic disorders

    Journal of Pharmacy and Pharmacology

    Volume 66, Issue 11, November 2014, Pages: 1505–1525, Natasha Beukes, Ruby-Ann Levendal and Carminita L. Frost

    Version of Record online : 12 MAY 2014, DOI: 10.1111/jphp.12267