Karin Aufenvenne

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 · 246 citations · Full text

Allergy, Cutaneous Biology, Skin Allergy +7

The α and β Subunits of the Metalloprotease Meprin Are Expressed in Separate Layers of Human Epidermis, Revealing Different Functions in Keratinocyte Proliferation and Differentiation

Christoph Becker‐Pauly, Markus Höwel, Tatjana Walker et al. · Journal of Investigative Dermatology · 2006 · 111 citations

Skin Development, Biochemistry, Medicine +13

SPINK5 and Netherton Syndrome: Novel Mutations, Demonstration of Missing LEKTI, and Differential Expression of Transglutaminases

Michael Raghunath, Lambrini Tontsidou, Vinzenz Oji et al. · Journal of Investigative Dermatology · 2004 · 107 citations · Full text

Missing Lekti, Mendelian Disorder, Genetic Disorder +8

Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype

Vinzenz Oji, J. Mazereeuw‐Hautier, Bijan Ahvazi et al. · Human Molecular Genetics · 2006 · 94 citations

Topical Enzyme-Replacement Therapy Restores Transglutaminase 1 Activity and Corrects Architecture of Transglutaminase-1-Deficient Skin Grafts

Karin Aufenvenne, Fernando Larcher, Blanca Duarte et al. · The American Journal of Human Genetics · 2013 · 67 citations · Full text

Allergy, Scleroderma, Cutaneous Biology +9