Image

    A Spontaneous Fatp4/Slc27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis

    November 2012 in “ PLoS ONE
    Jianning Tao, Maranke I. Koster, Wilbur R. Harrison … Paul A. Overbeek
    Studysummary This study identified a novel recessive mutation in mice causing lethal congenital lamellar ichthyosis, with skin and hair follicle alterations similar to human congenital ichthyoses, linked to a specific genetic defect affecting Fatp4.
    Automatically generated from the study's abstract, not written by a person, and not a review of the full paper. Not medical advice or a treatment recommendation. Read the original study, and consult a qualified healthcare professional before changing treatment. Full disclaimer
    Read the full study on journals.plos.org →
    Discuss this study in the Community →

    Research cited in this study 5

    1. Very-Long-Chain Acyl-CoA Synthetases Journal of Biological Chemistry · 2007
    2. Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency ˜The œjournal of investigative dermatology/Journal of investigative dermatology · 2005
    3. Cloning of Wrinkle-Free, a Previously Uncharacterized Mouse Mutation, Reveals Crucial Roles for Fatty Acid Transport Protein 4 in Skin and Hair Development Proceedings of the National Academy of Sciences of the United States of America · 2003
    4. Inhibition of BMP Signaling Affects Growth and Differentiation in the Anagen Hair Follicle The EMBO Journal · 2000
    5. The Biology of Hair Follicles The New England Journal of Medicine · 1999

    Related research 1

    1. Immunohistochemical Expression of Keratins in Normal Ovine Skin and in Chronic Dermatitis Due to Sarcoptes Scabiei Journal of comparative pathology · 2021