Universität zu Köln

2022

Hake, L., Suessmuth, K., Komlosi, K., Kopp, J., Drerup, C., Metze, D., Traupe, H., Hausser, I, Eckl, K. M., Hennies, H. C., Fischer, J. and Oji, V (2022). Quality of life and clinical characteristics of self-improving congenital ichthyosis within the disease spectrum of autosomal-recessive congenital ichthyosis. J. Eur. Acad. Dermatol. Venereol., 36 (4). S. 582 - 592. HOBOKEN: WILEY. ISSN 1468-3083

2018

Andrews, K., Brennan, L., Blacklock, L., Hennies, H. C., Marriott, A. and Eckl, K. M. (2018). Understanding methylation patterns and histone modification changes in keratinocytes from patients with autosomal recessive congenital ichthyosis. Br. J. Dermatol., 178 (6). S. E425 - 1. HOBOKEN: WILEY. ISSN 1365-2133

Cunha, D. L., Eckl, K. M., Gupta, M., Lingenhel, A., Schmuth, M., Zschocke, J., Saric, T. and Hennies, H. C. (2018). Induced pluripotent stem cell-derived keratinocytes for disease modelling of autosomal recessive congenital ichthyosis and other inherited skin diseases. Br. J. Dermatol., 178 (6). S. E430 - 1. HOBOKEN: WILEY. ISSN 1365-2133

Hennies, H. C., Cunha, D. de Lima, Barragan Vazquez, I., Saric, T. and Eckl, K. M. (2018). TP63 is expressed in adult epidermal and induced pluripotent stem cell-derived melanocytes, furthering the role of Delta Np63 in ectodermal gatekeeping and cell migration to the epidermis. Br. J. Dermatol., 178 (6). S. E415 - 1. HOBOKEN: WILEY. ISSN 1365-2133

Thomforde, S., Plank, R., Yealland, G., Miceli, E., Calderon, M., Hedtrich, S., Eckl, K. M. and Hennies, H. C. (2018). Epidermal proteins as drugs for topical application to the skin. Br. J. Dermatol., 178 (6). S. E430 - 2. HOBOKEN: WILEY. ISSN 1365-2133

Vazquez, I. Barragan, Cunha, D. L., Hockney, S., Kitson, S. T., Eckl, K. M. and Hennies, H. C. (2018). The use of cellular models for the study of epidermal development. Br. J. Dermatol., 178 (6). S. E424 - 2. HOBOKEN: WILEY. ISSN 1365-2133

2017

Gruber, R., Rainer, G., Weiss, A., Udvardi, A., Thiele, H., Eckl, K. M., Schupart, R., Nuernberg, P., Zschocke, J., Schmuth, M., Volc-Platzer, B. and Hennies, H. C. (2017). Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutations. Br. J. Dermatol., 176 (4). S. 1068 - 1074. HOBOKEN: WILEY. ISSN 1365-2133

2016

Plank, R., Eckl, K. M., Yealland, G., Casper, R., Obst, K., Hermann, M., Miceli, E., Calderon, M., Hedtrich, S. and Hennies, H. C. (2016). Nanogel-mediated cutaneous enzyme delivery as protein replacement therapy for autosomal recessive congenital ichthyosis. Br. J. Dermatol., 174 (5). S. E48 - 1. HOBOKEN: WILEY-BLACKWELL. ISSN 1365-2133

2015

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

2014

Cunha, D. L., Eckl, K. M., Rauch, M., Casper, R., Gupta, M., Nurnberg, P., Schmuth, M., Zschocke, J., Saric, T. and Hennies, H. C. (2014). Generation and characterization of induced Pluripotent Stem (iPS) cells from Autosomal Recessive Congenital Ichthyosis patients - a new model system to study rare keratinization disorders. J. Invest. Dermatol., 134. S. S34 - 1. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1523-1747