T. Tarinski

Loss of Corneodesmosin Leads to Severe Skin Barrier Defect, Pruritus, and Atopy: Unraveling the Peeling Skin Disease

Vinzenz Oji, Katja‐Martina Eckl, Karin Aufenvenne et al. · The American Journal of Human Genetics · 2010 · 247 citations · Full text

Medicine, Dermatology, Pathology +16

Complete filaggrin deficiency in ichthyosis vulgaris is associated with only moderate changes in epidermal permeability barrier function profile

Ana María Perusquía‐Ortiz, Vinzenz Oji, Maria Cristina Sauerland et al. · Journal of the European Academy of Dermatology and Venereology · 2013 · 38 citations

Medicine, Dermatology, Genetics +14

Increased Prevalence of Filaggrin Deficiency in 51 Patients with Recessive X-Linked Ichthyosis Presenting for Dermatological Examination

Kira Süßmuth, Robert Gruber, Elke Rodríguez et al. · Journal of Investigative Dermatology · 2017 · 19 citations · Full text

Medicine, Dermatology, Pathology +9

Development of a pathogenesis‐based therapy for peeling skin syndrome type 1*

Frederic Valentin, Henning Wiegmann, T. Tarinski et al. · British Journal of Dermatology · 2020 · 17 citations · Full text

Medicine, Dermatology, Molecular Biology +15

LEKTI domains D6, D7 and D8+9 serve as substrates for transglutaminase 1: implications for targeted therapy of Netherton syndrome

Henning Wiegmann, Frederic Valentin, T. Tarinski et al. · British Journal of Dermatology · 2019 · 11 citations

Life Sciences, Biochemistry, Molecular Biology +13