Article

Preclinical in vitro and in vivo evidence for targeting CD74 as an effective treatment strategy for cutaneous T-cell lymphomas.
Costanza, M. ORCID: https://orcid.org/0000-0002-8959-1083, Giordano, C., von Brünneck, A.C., Zhao, J., Makky, A., Vinh, K., Montes-Mojarro, I.A., Reisinger, F., Forchhammer, S., Witalisz-Siepracka, A., Edtmayer, S., Stoiber, D., Yin, G., Horst, D., Fischer, A., Siebert, R., Nicolay, J.P., Yin, M., Janz, M. ORCID: https://orcid.org/0000-0002-1127-0044, Fend, F. ORCID: https://orcid.org/0000-0002-5496-293X, Becker, J.C., Schürch, C.M., Kenner, L. ORCID: https://orcid.org/0000-0003-2184-1338, Assaf, C., Merkel, O. and Mathas, S. ORCID: https://orcid.org/0000-0001-9626-1413
British Journal of Dermatology 192 (5): 883-895. May 2025

The tumour suppressor p53 is frequently nonfunctional in Sezary syndrome.
Lamprecht, B., Kreher, S., Moebs, M., Sterry, W., Doerken, B. ORCID: https://orcid.org/0000-0001-7991-3643, Janz, M. ORCID: https://orcid.org/0000-0002-1127-0044, Assaf, C. and Mathas, S. ORCID: https://orcid.org/0000-0001-9626-1413
British Journal of Dermatology 167 (2): 240-246. August 2012

Towards characterization of palmoplantar keratoderma caused by gain-of-function mutation in loricrin: analysis of a family and review of the literature.
Gedicke, M.M., Traupe, H., Fischer, B., Tinschert, S. and Hennies, H.C. ORCID: https://orcid.org/0000-0001-7210-2389
British Journal of Dermatology 154 (1): 167-171. December 2006

Interleukin-10 promoter polymorphism IL10.G and familial early onset psoriasis.
Hensen, P., Asadullah, K., Windemuth, C., Rueschendorf, F., Hueffmeier, U., Staender, M., Schmitt-Egenolf, M., Wienker, T.F., Reis, A. and Traupe, H.
British Journal of Dermatology 149 (2): 381-385. August 2003

HID and KID syndromes are associated with the same connexin 26 mutation.
Van Geel, M., Van Steensel, M.A.M., Kuester, W., Hennies, H.C. ORCID: https://orcid.org/0000-0001-7210-2389, Happle, R., Steijlen, P.M. and Koenig, A.
British Journal of Dermatology 146 (2): 938-942. June 2002

Letter

Coinheritance of biallelic SLURP1 and SLC39A4 mutations cause a severe genodermatosis with skin peeling and hair loss all over the body.
Harms, F.L., Nampoothiri, S., Kortüm, F., Thomas, J., Panicker, V.V., Alawi, M., Altmüller, J. ORCID: https://orcid.org/0000-0003-4372-1521, Yesodharan, D. and Kutsche, K. ORCID: https://orcid.org/0000-0001-8494-8963
British Journal of Dermatology 179 (5): 1192-1194. 1 November 2018

Functional implications of novel ADAM10 mutations in reticulate acropigmentation of Kitamura.
Ralser, D.J., Lestringant, G.G., Du-Thanh, A., Kokordelis, P., Fischer, J., Basmanav, F.B.Ü., Wolf, S., Thiele, H., Altmüller, J. ORCID: https://orcid.org/0000-0003-4372-1521, Nürnberg, P., Oji, V., Fritz, G., Frank, J. and Betz, R.C.
British Journal of Dermatology 177 (6): e340-e343. 8 January 2018

Evidence for a single genetic locus in Clouston's hidrotic ectodermal dysplasia.
Stevens, H.P., Choon, S.E., Hennies, H.C. ORCID: https://orcid.org/0000-0001-7210-2389 and Kelsell, D.P.
British Journal of Dermatology 140 (5): 963-964. 24 May 1999