Browse by Journal Title

2023

Extracellular matrix remodeling in atopic dermatitis harnesses the onset of an asthmatic phenotype and is a potential contributor to the atopic march.
Graff, P. and Woerz, D. and Wilzopolski, J. and Voss, A. and Sarrazin, J. and Blimkie, T.M. and Weiner, J. and Kershaw, O. and Panwar, P. and Hackett, T. and Lau, S. and Brömme, D. and Beule, D. and Lee, Y.A. and Hancock, R.E.W. and Gruber, A.D. and Bäumer, W. and Hedtrich, S.
Journal of Investigative Dermatology 13 October 2023 (In Press)

2022

Sox9 is required for nail bed differentiation and digit tip regeneration.
Lao, M. and Hurtado, A. and de Castro, A.C. and Burgos, M. and Jiménez, R. and Barrionuevo, F.J.
Journal of Investigative Dermatology 142 (10): 2613-2622. October 2022

Skin sodium accumulates in psoriasis and reflects disease severity.
Maifeld, A. and Wild, J. and Karlsen, T.V. and Rakova, N. and Wistorf, E. and Linz, P. and Jung, R. and Birukov, A. and Gimenez-Rivera, V.A. and Wilck, N. and Bartolomaeus, T. and Dechend, R. and Kleinewietfeld, M. and Forslund, S.K. and Krause, A. and Kokolakis, G. and Philipp, S. and Clausen, B.E. and Brand, A. and Waisman, A. and Kurschus, F.C. and Wegner, J. and Schultheis, M. and Luft, F.C. and Boschmann, M. and Kelm, M. and Wiig, H. and Kuehne, T. and Müller, D.N. and Karbach, S. and Markó, L.
Journal of Investigative Dermatology 142 (1): 166-178. January 2022

2019

Transglutaminase 1 replacement therapy successfully mitigates the autosomal recessive congenital ichthyosis phenotype in full-thickness skin disease equivalents.
Plank, R. and Yealland, G. and Miceli, E. and Lima Cunha, D. and Graff, P. and Thomforde, S. and Gruber, R. and Moosbrugger-Martinz, V. and Eckl, K. and Calderón, M. and Hennies, H.C. and Hedtrich, S.
Journal of Investigative Dermatology 139 (5): 1191-1195. May 2019

2018

SMARCAD1 haploinsufficiency underlies Huriez syndrome and associated skin cancer susceptibility.
Günther, C. and Lee-Kirsch, M.A. and Eckhard, J. and Matanovic, A. and Kerscher, T. and Rüschendorf, F. and Klein, B. and Berndt, N. and Zimmermann, N. and Flachmeier, C. and Thuß, T. and Lucas, N. and Marenholz, I. and Esparza-Gordillo, J. and Hübner, N. and Traupe, H. and Delaporte, E. and Lee, Y.A.
Journal of Investigative Dermatology 138 (6): 1428-1431. June 2018

NF-κB participates in mouse hair cycle control and plays distinct roles in the various pelage hair follicle types.
Krieger, K. and Millar, S.E. and Mikuda, N. and Krahn, I. and Kloepper, J.E. and Bertolini, M. and Scheidereit, C. and Paus, R. and Schmidt-Ullrich, R.
Journal of Investigative Dermatology 138 (2): 256-264. February 2018

2017

Patched receptors sense, interpret and establish an epidermal Hedgehog signalling gradient.
Adolphe, C. and Junker, J.P. and Lyubimova, A. and van Oudenaarden, A. and Wainwright, B.
Journal of Investigative Dermatology 137 (1): 179-186. January 2017

2016

Influence of Th2 cytokines on the cornified envelope, tight junction proteins, and ß-defensins in filaggrin-deficient skin equivalents.
Hönzke, S. and Wallmeyer, L. and Ostrowski, A. and Radbruch, M. and Mundhenk, L. and Schäfer-Korting, M. and Hedtrich, S.
Journal of Investigative Dermatology 136 (3): 631-639. March 2016

2015

GORAB missense mutations disrupt RAB6 and ARF5 binding and golgi targeting.
Egerer, J. and Emmerich, D. and Fischer-Zirnsak, B. and Chan, W.L. and Meierhofer, D. and Tuysuz, B. and Marschner, K. and Sauer, S. and Barr, F.A. and Mundlos, S. and Kornak, U.
Journal of Investigative Dermatology 135 (10): 2368-2376. October 2015

Pathogenicity of POFUT1 in Dowling-Degos disease: additional mutations and clinical overlap with reticulate acropigmentation of kitamura.
Basmanav, F.B. and Fritz, G. and Lestringant, G.G. and Pachat, D. and Hoffjan, S. and Fischer, J. and Wehner, M. and Wolf, S. and Thiele, H. and Altmüller, J. and Pulimood, S.A. and Rütten, A. and Kruse, R. and Hanneken, S. and Frank, J. and Danda, S. and Bygum, A. and Betz, R.C.
Journal of Investigative Dermatology 135 (2): 615-618. February 2015

2014

NF-κB activity is required for anagen maintenance in human hair follicles in vitro.
Kloepper, J.E. and Ernst, N. and Krieger, K. and Bodo, E. and Biro, T. and Haslam, I.S. and Schmidt-Ullrich, R. and Paus, R.
Journal of Investigative Dermatology 134 (7): 2036-2038. 11 February 2014

2011

Association screening in the epidermal differentiation complex (EDC) identifies an SPRR3 repeat number variant as a risk factor for eczema.
Marenholz, I. and Rivera, V.A. and Esparza-Gordillo, J. and Bauerfeind, A. and Lee-Kirsch, M.A. and Ciechanowicz, A. and Kurek, M. and Piskackova, T. and Macek, M. and Lee, Y.A.
Journal of Investigative Dermatology 131 (8): 1644-1649. August 2011

2006

Loss of proapoptotic Bcl-2-related multidomain proteins in primary melanomas is associated with poor prognosis.
Fecker, L.F. and Geilen, C.C. and Tchernev, G. and Trefzer, U. and Assaf, C. and Kurbanov, B.M. and Schwarz, C. and Daniel, P.T. and Eberle, J.
Journal of Investigative Dermatology 126 : 1366-1371. June 2006

2003

Self-healing collodion baby: a dynamic phenotype explained by a particular transglutaminase-1 mutation.
Raghunath, M. and Hennies, H.C. and Ahvazi, B. and Vogel, M. and Reis, A. and Steinert, P.M. and Traupe, H.
Journal of Investigative Dermatology 120 (2): 224-228. February 2003

2001

The Bax/Bcl-2 ratio determines the susceptibility of human melanoma cells to CD95/Fas-mediated apoptosis.
Raisova, M. and Hossini, A.M. and Eberle, J. and Riebeling, C. and Wieder, T. and Sturm, I. and Daniel, P.T. and Orfanos, C.E. and Geilen, C.C.
Journal of Investigative Dermatology 117 (2): 333-340. 1 August 2001

Genetic and clinical heterogeneity in transgressive palmoplantar keratoderma.
Lestringant, G.G. and Frossard, P.M. and Eckl, K.M. and Reis, A. and Hennies, H.C.
Journal of Investigative Dermatology 116 (5): 825-827. 1 January 2001

2000

Assignment of the gene for a new hereditary nail disorder, isolated congenital nail dysplasia, to chromosome 17p13.
Krebsova, A. and Hamm, H. and Karl, S. and Reis, A. and Hennies, H.C.
Journal of Investigative Dermatology 115 (4): 664-667. 1 October 2000

1999

Promoter polymorphism at -238 of the tumor necrosis factor alpha gene is not associated with early onset psoriasis when tested by the transmission disequilibrium test.
Jacob, N. and Rueschendorf, F. and Schmitt-Egenolf, M. and Hennies, H.C. and Friedl, G. and Stander, M. and Wienker, T.F. and Reis, A. and Traupe, H.
Journal of Investigative Dermatology 112 : 514-515. 1 April 1999

1998

Neurotrophin-3 involvement in the regulation of hair follicle morphogenesis.
Botchkarev, V.A. and Botchkareva, N.V. and Albers, K.M. and van der Veen, C. and Lewin, G.R. and Paus, R.
Journal of Investigative Dermatology 111 : 279-285. 1 January 1998

1996

Impaired immunosuppressive response to ultraviolet radiation in interleukin-10-deficient mice.
Beissert, S. and Hosoi, J. and Kühn, R. and Rajewsky, K. and Müller, W. and Granstein, R.D.
Journal of Investigative Dermatology 107 (4): 553-557. October 1996