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Journal Article
Ammann, S., Schulz, A., Kraegeloh-Mann, I., Schoening, M., von Bernuth, H., zur Stadt, U., Lehmberg, K., Ehl, S. and Hennies, H. (2014). AP3D Deficiency Defines a New Type of Hermansky-Pudlak Syndrome. J. Clin. Immunol., 34. S. S148 - 1. NEW YORK: SPRINGER/PLENUM PUBLISHERS. ISSN 1573-2592
Eckl, K., Cunha, D., Saric, T., Plank, R. and Hennies, H. (2016). Patient-specific induced pluripotent stem cell-derived melanocytes for three-dimensional monogenic disease modelling. Br. J. Dermatol., 174 (5). S. E62 - 1. HOBOKEN: WILEY-BLACKWELL. ISSN 1365-2133
Plank, R., Casper, R., Obst, K., Hermann, M., Caldern, M., Hedtrich, S., Eckl, K. M. and Hennies, H. (2015). Nanogel coupled cutaneous enzyme delivery as protein replacement therapy for autosomal recessive congenital ichthyosis (ARCI). J. Invest. Dermatol., 135. S. S55 - 1. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1523-1747
Plank, R., Rauch, M., Casper, R., Obst, K., Kuechler, S., Eckl, K. and Hennies, H. (2014). 3D-skin models for protein substitution in autosomal recessive congenital ichthyosis. J. Invest. Dermatol., 134. S. S54 - 1. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1523-1747