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Journal of Investigative Dermatology

  1. Dermal matrix composition promotes development of aggressive squamous cell carcinoma in recessive dystrophic epidermolysis bullosa

    Ng, Y., Pourreyron, C., Salas-Alanis, J., Cepeda-Valdes, R., Yan, W., Wright, S., Chen, M., Hogg, F., McGrath, J., Murrell, D., Leigh, I., Lane, E. & South, A. May 2012 In : Journal of Investigative Dermatology. 132, p. S20-S20 1 p.

    Research output: Contribution to journalArticle

  2. Expanding the differential diagnosis for pachyonychia congenita

    Wilson, N. J., Hansen, C. D., Azkur, D., Kocabas, C. N., Metin, A., Coskun, Z., Schwartz, M. E., Hull, P. R., McLean, W. H. & Smith, F. J. May 2012 In : Journal of Investigative Dermatology. 132, p. S70-S70 1 p.

    Research output: Contribution to journalArticle

  3. Filaggrin mutations: Prognosis and response to therapy overtime

    Margolis, D. J., Mitra, N., Sandilands, A., McLean, I. & Rebbeck, T. May 2012 In : Journal of Investigative Dermatology. 132, p. S41-S41 1 p.

    Research output: Contribution to journalArticle

  4. Mutations in the SASPase gene (ASPRV1) are not associated with atopic eczema or clinically dry skin

    Sandilands, A., Brown, S. J., Goh, C. S., Pohler, E., Wilson, N. J., Campbell, L. E., Miyamoto, K., Kubo, A., Irvine, A. D., Thawer-Esmail, F., Munro, C. S., McLean, W. H. I., Kudoh, J., Amagai, M. & Matsui, T. May 2012 In : Journal of Investigative Dermatology. 132, 5, p. 1507-1510 4 p.

    Research output: Contribution to journalLetter

  5. Next-generation sequencing identifies Notch receptors as integral tumor suppressors in cutaneous and lung squamous cell carcinomas

    Leigh, I. M. & 24 others Wang, N. J., Sanborn, Z., Arnett, K. L., Bayston, L. J., Liao, W., Proby, C. M., Gordon, P. B., Sharma, M., North, J. P., Vemula, S. S., Mauro, T. M., Neuhaus, I. M., LeBoit, P. E., Kwok, P., Arron, S. T., Bale, A. E., Haussler, D., Cleaver, J. E., Gray, J. W., Spellman, P. T., South, A. P., Aster, J. C., Blacklow, S. C. & Cho, R. J. May 2012 In : Journal of Investigative Dermatology. 132, p. S23-S23 1 p.

    Research output: Contribution to journalArticle

  6. Novel Molecular Therapies for Heritable Skin Disorders

    Uitto, J., Christiano, A. M., McLean, W. H. I. & McGrath, J. A. Mar 2012 In : Journal of Investigative Dermatology. 132, 3, p. 820-828 9 p.

    Research output: Contribution to journalScientific review

  7. One remarkable molecule: filaggrin

    Brown, S. J. & McLean, W. H. I. Mar 2012 In : Journal of Investigative Dermatology. 132, 3, p. 751-762 12 p.

    Research output: Contribution to journalArticle

  8. Intragenic copy number variation within filaggrin contributes to the risk of atopic dermatitis with a dose-dependent effect

    Brown, S. J., Kroboth, K., Sandilands, A., Campbell, L. E., Pohler, E., Kezic, S., Cordell, H. J., McLean, W. H. I. & Irvine, A. D. Jan 2012 In : Journal of Investigative Dermatology. 132, 1, p. 98-104 7 p.

    Research output: Contribution to journalArticle

  9. Development of lentiviral gene therapy for type VII collagen deficient epidermolysis bullosa

    Georgiadis, C., Thrasher, A., South, A. P., McGrath, J., Qasim, W. & Di, W. 2012 In : Journal of Investigative Dermatology. 132, S2, p. S96 1 p., 546

    Research output: Contribution to journalMeeting abstract

  10. Homozygous dominant missense mutation in keratin 17 leads to alopecia in addition to severe pachyonychia congenita

    Wilson, N. J., Pérez, M. L. C., Vahlquist, A., Schwartz, M. E., Hansen, C. D., McLean, W. H. I. & Smith, F. J. D. 2012 In : Journal of Investigative Dermatology.

    Research output: Contribution to journalLetter

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