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There are 8209 results for: content related to: Collapse of the keratin filament network through the expression of mutant keratin 6c observed in a case of focal plantar keratoderma

  1. You have full text access to this OnlineOpen article
    The molecular genetic analysis of the expanding pachyonychia congenita case collection

    British Journal of Dermatology

    Volume 171, Issue 2, August 2014, Pages: 343–355, N.J. Wilson, E.A. O'Toole, L.M. Milstone, C.D. Hansen, A.A. Shepherd, E. Al-Asadi, M.E. Schwartz, W.H.I. McLean, E. Sprecher and F.J.D. Smith

    Version of Record online : 6 AUG 2014, DOI: 10.1111/bjd.12958

  2. You have free access to this content
    Hereditary palmoplantar keratoderma “clinical and genetic differential diagnosis”

    The Journal of Dermatology

    Volume 43, Issue 3, March 2016, Pages: 264–274, Tomo Sakiyama and Akiharu Kubo

    Version of Record online : 5 MAR 2016, DOI: 10.1111/1346-8138.13219

  3. You have free access to this content
    Keratosis palmoplantaris: klinische und genetische Aspekte

    JDDG: Journal der Deutschen Dermatologischen Gesellschaft

    Volume 14, Issue 2, February 2016, Pages: 123–142, Cristina Has and Kristin Technau-Hafsi

    Version of Record online : 27 JAN 2016, DOI: 10.1111/ddg.150_12930

  4. Diffuse and focal palmoplantar keratoderma can be caused by a keratin 6c mutation

    British Journal of Dermatology

    Volume 165, Issue 6, December 2011, Pages: 1290–1292, E. Akasaka, H. Nakano, A. Nakano, Y. Toyomaki, N. Takiyoshi, D. Rokunohe, Y. Nishikawa, A. Korekawa, Y. Matsuzaki, Y. Mitsuhashi and D. Sawamura

    Version of Record online : 24 NOV 2011, DOI: 10.1111/j.1365-2133.2011.10552.x

  5. Focal PPK secondary to a novel KRT6C mutation (Pachyonychia congenita-K6c)

    Journal of the European Academy of Dermatology and Venereology

    J.S. Wee, F.J.D. Smith, N.J. Wilson and E.A. O'Toole

    Version of Record online : 24 AUG 2015, DOI: 10.1111/jdv.13259

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    Palmoplantar keratodermas: clinical and genetic aspects

    JDDG: Journal der Deutschen Dermatologischen Gesellschaft

    Volume 14, Issue 2, February 2016, Pages: 123–140, Cristina Has and Kristin Technau-Hafsi

    Version of Record online : 27 JAN 2016, DOI: 10.1111/ddg.12930

  7. The effect of polyphosphate kinase gene deletion on polyhydroxyalkanoate accumulation and carbon metabolism in Pseudomonas putida KT2440

    Environmental Microbiology Reports

    Volume 5, Issue 5, October 2013, Pages: 740–746, William T. Casey, Jasmina Nikodinovic-Runic, Pilar Fonseca Garcia, Maciej W. Guzik, John W. McGrath, John P. Quinn, Gerard Cagney, Maria Auxiliadora Prieto and Kevin E. O'Connor

    Version of Record online : 18 AUG 2013, DOI: 10.1111/1758-2229.12076

  8. Novel and recurrent keratin 6A (KRT6A) mutations in Chinese patients with pachyonychia congenita type 1

    British Journal of Dermatology

    Volume 160, Issue 6, June 2009, Pages: 1327–1329, Y.M. Lv, S. Yang, Z. Zhang, Y. Cui, C. Quan, F.S. Zhou, Q.Y. Fang, W.H. Du, F.R. Zhang, J.M. Chang, X.P. Tao, A.L. Zhang, R.H. Kang, W.D. Du and X.J. Zhang

    Version of Record online : 11 MAR 2009, DOI: 10.1111/j.1365-2133.2009.09062.x

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    Palmoplantar keratoderma (PPK): acquired and genetic causes of a not so rare disease

    JDDG: Journal der Deutschen Dermatologischen Gesellschaft

    Volume 12, Issue 9, September 2014, Pages: 781–788, Stina Schiller, Christina Seebode, Hans Christian Hennies, Kathrin Giehl and Steffen Emmert

    Version of Record online : 29 AUG 2014, DOI: 10.1111/ddg.12418

  10. Mutations of KRT6A are more frequent than those of KRT16 in pachyonychia congenita type 1: report of a novel and a recently reported mutation in two unrelated Chinese families

    British Journal of Dermatology

    Volume 159, Issue 1, July 2008, Pages: 238–240, Z-L. Bai, Y-G. Feng, S-S. Tan, X-Y. Wang, S-X. Xiao, H. Wang, H-Q. Jia, J-W. Wu, D-L. He and R-H. Kang

    Version of Record online : 16 MAY 2008, DOI: 10.1111/j.1365-2133.2008.08603.x

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    Inherited ichthyosis: Non-syndromic forms

    The Journal of Dermatology

    Volume 43, Issue 3, March 2016, Pages: 242–251, Takuya Takeichi and Masashi Akiyama

    Version of Record online : 5 MAR 2016, DOI: 10.1111/1346-8138.13243

  12. Mutations in KRT5 and KRT14 cause epidermolysis bullosa simplex in 75% of the patients

    British Journal of Dermatology

    Volume 164, Issue 3, March 2011, Pages: 637–644, M.C. Bolling, H.H. Lemmink, G.H.L. Jansen and M.F. Jonkman

    Version of Record online : 17 FEB 2011, DOI: 10.1111/j.1365-2133.2010.10146.x

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    Deciphering TGF-β3 function in medial edge epithelium specification and fusion during mouse secondary palate development

    Developmental Dynamics

    Volume 243, Issue 12, December 2014, Pages: 1536–1543, Jiu-Zhen Jin, Dennis R. Warner, Qingxian Lu, M. Michele Pisano, Robert M. Greene and Jixiang Ding

    Version of Record online : 30 AUG 2014, DOI: 10.1002/dvdy.24177

  14. Pachyonychia congenita patients with mutations in KRT6A have more extensive disease compared with patients who have mutations in KRT16

    British Journal of Dermatology

    Volume 166, Issue 4, April 2012, Pages: 875–878, K.M. Spaunhurst, A.M. Hogendorf, F.J.D. Smith, B. Lingala, M.E. Schwartz, A. Cywinska-Bernas, K.J. Zeman and J.Y. Tang

    Version of Record online : 27 MAR 2012, DOI: 10.1111/j.1365-2133.2011.10745.x

  15. Molecular Genetics of Inherited Disorders of Epidermal Keratins

    Standard Article

    eLS

    Eli Sprecher

    Published Online : 15 MAR 2009, DOI: 10.1002/9780470015902.a0021472

  16. Expanding the keratin mutation database: novel and recurrent mutations and genotype–phenotype correlations in 28 patients with epidermolytic ichthyosis

    British Journal of Dermatology

    Volume 164, Issue 2, February 2011, Pages: 442–447, M.J. Arin, V. Oji, S. Emmert, I. Hausser, H. Traupe, T. Krieg and G. Grimberg

    Version of Record online : 28 JAN 2011, DOI: 10.1111/j.1365-2133.2010.10096.x

  17. Mapping of a novel locus for an autosomal recessive form of palmoplantar keratoderma on chromosome 3q27.2-q29

    British Journal of Dermatology

    Volume 163, Issue 4, October 2010, Pages: 711–718, S. Khan, S. Muzaffar, M. Tariq, A. Khan, S. Basit and W. Ahmad

    Version of Record online : 1 JUN 2010, DOI: 10.1111/j.1365-2133.2010.09881.x

  18. Pachyonychia Congenita: A Spectrum of KRT6a Mutations in Australian Patients

    Pediatric Dermatology

    Volume 33, Issue 3, May/June 2016, Pages: 337–342, Charlotte E. Forrest, Genevieve Casey, Dylan A. Mordaunt, Elizabeth M. Thompson and Lynne Gordon

    Version of Record online : 4 APR 2016, DOI: 10.1111/pde.12841

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    Crystal structure of a polyphosphate kinase and its implications for polyphosphate synthesis

    EMBO reports

    Volume 6, Issue 7, July 2005, Pages: 681–687, Ye Zhu, Weijun Huang, Sam S K Lee and Wenqing Xu

    Version of Record online : 1 JUL 2005, DOI: 10.1038/sj.embor.7400448

  20. Keratins and Keratin Diseases

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    eLS

    MA Rogers

    Published Online : 27 JAN 2006, DOI: 10.1038/npg.els.0005905