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High tumour mutational burden and EGFR/MAPK pathway activation are therapeutic targets in metastatic porocarcinoma*.
Published in:
British Journal of Dermatology, 2021, v. 185, n. 6, p. 1186, doi. 10.1111/bjd.20604
By:
- Westphal, D.;
- Garzarolli, M.;
- Sergon, M.;
- Horak, P.;
- Hutter, B.;
- Becker, J.C.;
- Wiegel, M.;
- Maczey, E.;
- Blum, S.;
- Grosche‐Schlee, S.;
- Rütten, A.;
- Ugurel, S.;
- Stenzinger, A.;
- Glimm, H.;
- Aust, D.;
- Baretton, G.;
- Beissert, S.;
- Fröhling, S.;
- Redler, S.;
- Surowy, H.
Publication type:
Article
Exploring the overlap between alopecia areata and major depressive disorder: Epidemiological and genetic perspectives.
Published in:
Journal of the European Academy of Dermatology & Venereology, 2023, v. 37, n. 8, p. 1547, doi. 10.1111/jdv.18921
By:
- Foo, J. C.;
- Redler, S.;
- Forstner, A. J.;
- Basmanav, F. B.;
- Pethukova, L.;
- Guo, J.;
- Streit, F.;
- Witt, S. H.;
- Sirignano, L.;
- Zillich, L.;
- Awasthi, S.;
- Ripke, S.;
- Christiano, A. M.;
- Tesch, F.;
- Schmitt, J.;
- Nöthen, M. M.;
- Betz, R. C.;
- Rietschel, M.;
- Frank, J.
Publication type:
Article
Gene expression profiling in aggressive digital papillary adenocarcinoma sheds light on the architecture of a rare sweat gland carcinoma.
Published in:
British Journal of Dermatology, 2019, v. 180, n. 5, p. 1150, doi. 10.1111/bjd.17446
By:
- Surowy, H.M.;
- Giesen, A.K.;
- Otte, J.;
- Büttner, R.;
- Falkenstein, D.;
- Friedl, H.;
- Meier, F.;
- Petzsch, P.;
- Wachtmeister, T.;
- Westphal, D.;
- Wieczorek, D.;
- Wruck, W.;
- Adjaye, J.;
- Rütten, A.;
- Redler, S.
Publication type:
Article
The oestrogen receptor 2 ( ESR2) gene in female-pattern hair loss: replication of association with rs10137185 in German patients.
Published in:
British Journal of Dermatology, 2014, v. 170, n. 4, p. 982, doi. 10.1111/bjd.12756
By:
- Redler, S.;
- Birch, P.;
- Drichel, D.;
- Hofmann, P.;
- Dobson, K.;
- Böhmer, A.C.;
- Becker, J.;
- Giehl, K.A.;
- Tazi‐Ahnini, R.;
- Kruse, R.;
- Wolff, H.;
- Miesel, A.;
- Fischer, T.;
- Böhm, M.;
- Nuwayhid, R.;
- Garcia Bartels, N.;
- Lutz, G.;
- Becker, T.;
- Blume‐Peytavi, U.;
- Nöthen, M.M.
Publication type:
Article
Investigation of selected cytokine genes suggests that IL2RA and the TNF/ LTA locus are risk factors for severe alopecia areata.
Published in:
British Journal of Dermatology, 2012, v. 167, n. 6, p. 1360, doi. 10.1111/bjd.12004
By:
- Redler, S.;
- Albert, F.;
- Brockschmidt, F.F.;
- Herold, C.;
- Hanneken, S.;
- Eigelshoven, S.;
- Giehl, K.A.;
- Kruse, R.;
- Lutz, G.;
- Wolff, H.;
- Blaumeiser, B.;
- Böhm, M.;
- Becker, T.;
- Nöthen, M.M.;
- Betz, R.C.
Publication type:
Article
Steatocystoma multiplex: keratin 17 - the key player?
Published in:
British Journal of Dermatology, 2012, v. 167, n. 6, p. 1395, doi. 10.1111/j.1365-2133.2012.11073.x
By:
- Antal, A.S.;
- Kulichova, D.;
- Redler, S.;
- Betz, R.C.;
- Ruzicka, T.
Publication type:
Article
Investigation of the male pattern baldness major genetic susceptibility loci AR/ EDA2R and 20p11 in female pattern hair loss.
Published in:
British Journal of Dermatology, 2012, v. 166, n. 6, p. 1314, doi. 10.1111/j.1365-2133.2012.10877.x
By:
- Redler, S.;
- Brockschmidt, F.F.;
- Tazi-Ahnini, R.;
- Drichel, D.;
- Birch, M.P.;
- Dobson, K.;
- Giehl, K.A.;
- Herms, S.;
- Refke, M.;
- Kluck, N.;
- Kruse, R.;
- Lutz, G.;
- Wolff, H.;
- Böhm, M.;
- Becker, T.;
- Nöthen, M.M.;
- Messenger, A.G.;
- Betz, R.C.
Publication type:
Article
Investigation of variants of the aromatase gene ( CYP19A1) in female pattern hair loss.
Published in:
British Journal of Dermatology, 2011, v. 165, n. 3, p. 703, doi. 10.1111/j.1365-2133.2011.10456.x
By:
- Redler, S.;
- Birch, M. P.;
- Drichel, D.;
- Dobson, K.;
- Brockschmidt, F.F.;
- Tazi-Ahnini, R.;
- Giehl, K.A.;
- Kluck, N.;
- Kruse, R.;
- Lutz, G.;
- Wolff, H.;
- Becker, T.;
- Nöthen, M. M.;
- Messenger, A. G.;
- Betz, R. C.
Publication type:
Article
The TRAF1/C5 locus confers risk for familial and severe alopecia areata.
Published in:
British Journal of Dermatology, 2010, v. 162, n. 4, p. 866, doi. 10.1111/j.1365-2133.2009.09598.x
By:
- Redler, S.;
- Brockschmidt, F.F.;
- Forstbauer, L.;
- Giehl, K.A.;
- Herold, C.;
- Eigelshoven, S.;
- Hanneken, S.;
- De Weert, J.;
- Lutz, G.;
- Wolff, H.;
- Kruse, R.;
- Blaumeiser, B.;
- Böhm, M.;
- Becker, T.;
- Nöthen, M.M.;
- Betz, R.C.
Publication type:
Article
The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata.
Published in:
British Journal of Dermatology, 2008, v. 158, n. 2, p. 389, doi. 10.1111/j.1365-2133.2007.08312.x
By:
- Betz, Regina C.;
- König, K.;
- Flaquer, A.;
- Redler, S.;
- Eigelshoven, S.;
- Kortüm, A.-K.;
- Hanneken, S.;
- Hillmer, A.;
- Tüting, T.;
- Lambert, J.;
- De Weert, J.;
- Kruse, R.;
- Lutz, G.;
- Blaumeiser, B.;
- Nöthen, M. M.
Publication type:
Article
A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicism.
Published in:
Clinical & Experimental Dermatology, 2015, v. 40, n. 7, p. 781, doi. 10.1111/ced.12631
By:
- Redler, S.;
- Pasternack, S. M.;
- Wolf, S.;
- Stienen, D.;
- Wenzel, J.;
- Nöthen, M. M.;
- Betz, R. C.
Publication type:
Article
Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis.
Published in:
Clinical & Experimental Dermatology, 2009, v. 34, n. 8, p. e953, doi. 10.1111/j.1365-2230.2009.03644.x
By:
- Düzenli, S.;
- Redler, S.;
- Müller, M.;
- Polat, M.;
- Dogruer, D.;
- Pasternack, S. M.;
- Betz, R. C.
Publication type:
Article

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