Filaggrin deficiency in ichthyosis vulgaris (IV): increase of skin pH and evidence for imbalance of KLK activity in a 3D keratinocytic model for IV

Zaraeva I, Perusquia A, Tarinski T, Seller N, Aufenvenne K, Breitkreuz D, Hausser I, Traupe H, Oji V (2012)

In: Experimental Dermatology, 21(3).

Research article (journal)

Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease.

Oji V, Eckl KM, Aufenvenne K, Nätebus M, Tarinski T, Ackermann K, Seller N, Metze D, Nürnberg G, Fölster-Holst R, Schäfer-Korting M, Hausser I, Traupe H, Hennies HC (2010)

In: American Journal of Human Genetics, 87(2).

Research article (journal)

Peeling skin desease: Elucidation of a rare genetic Disorder of keratinization

Vinzenz O, Eckl KM, Aufenvenne KK, Natebus M, Tarinski T, Seller N, Metze D, Hausser I, Traupe H, Hennies HC (2010)

In: Journal der Deutschen Dermatologischen Gesellschaft, 8(11).

Research article (journal)

Ichthyosis vulgaris: novel FLG mutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup.

Oji V, Seller N, Sandilands A, Gruber R, Gerss J, Hüffmeier U, Hamm H, Emmert S, Aufenvenne K, Metze D, Luger T, Loser K, Hausser I, Traupe H, McLean WH (2009)

In: British Journal of Dermatology, 160(4).

Research article (journal)

Toward enzyme substitution therapy of lamellar ichthyosis: liposomal encapsulation of recombinant transglutaminase 1

Aufenvenne K, Zimmerling K, Walker T, Dathe M, Traupe H (2009)

In: Journal of Investigative Dermatology, 129 Suppl..

Research article (journal)

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Long-term faithful recapitulation of transglutaminase 1-deficient lamellar ichthyosis in a skin-humanized mouse model, and insights from proteomic studies. Aufenvenne K, Rice RH, Hausser I, Oji V, Hennies HC, Rio MD, Traupe H, Larcher F (2012) In: Journal of Investigative Dermatology, 132(7). Research article (journal)
Filaggrin deficiency in ichthyosis vulgaris (IV): increase of skin pH and evidence for imbalance of KLK activity in a 3D keratinocytic model for IV Zaraeva I, Perusquia A, Tarinski T, Seller N, Aufenvenne K, Breitkreuz D, Hausser I, Traupe H, Oji V (2012) In: Experimental Dermatology, 21(3). Research article (journal)
A presentation of ichthyosis with severe atopy due to STS and FLG deficiency Seller N, Bohring A, Hausser I, Steinfeld R, Walker T, Aufenvenne K, Metze D, Luger T, Traupe H, Oji V (2010) In: Journal der Deutschen Dermatologischen Gesellschaft, 8(11). Research article (journal)
Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease. Oji V, Eckl KM, Aufenvenne K, Nätebus M, Tarinski T, Ackermann K, Seller N, Metze D, Nürnberg G, Fölster-Holst R, Schäfer-Korting M, Hausser I, Traupe H, Hennies HC (2010) In: American Journal of Human Genetics, 87(2). Research article (journal)
Expression of LEKTI and normal SPINK5 genotype rule out allelic identity of Peeling skin syndrome type B and Netherton syndrome Oji V, Eckle K, Aufenvenne K, Walker T, Metze D, Seller N, Folster-Holst R, Hausser I, Hennies HC, Traupe H (2010) In: Experimental Dermatology, 19(2). Research article (journal)
Peeling skin desease: Elucidation of a rare genetic Disorder of keratinization Vinzenz O, Eckl KM, Aufenvenne KK, Natebus M, Tarinski T, Seller N, Metze D, Hausser I, Traupe H, Hennies HC (2010) In: Journal der Deutschen Dermatologischen Gesellschaft, 8(11). Research article (journal)
Reconstructed human epidermis demonstrates a severe epidermal barrier defect caused by deficiency of corneodesmosin Eckl K, Oji V, Aufenvenne K, Natebus M, Tarinski T, Ackermann K, Schafer-Korting M, Hausser I, Traupe H, Hennies HC (2010) In: Journal of Investigative Dermatology, 130 Suppl.. Research article (journal)
Ichthyosis vulgaris: novel FLG mutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup. Oji V, Seller N, Sandilands A, Gruber R, Gerss J, Hüffmeier U, Hamm H, Emmert S, Aufenvenne K, Metze D, Luger T, Loser K, Hausser I, Traupe H, McLean WH (2009) In: British Journal of Dermatology, 160(4). Research article (journal)
Novel filaggrin mutations in German ichthyosis vulgaris patients and high presence of CD1a+cells in the epidermis of the atopic subgroup Oji V, Seller N, Sandilands A, Gruber R, Hausser I, Metze D, Walker T, Aufenvenne K, Loser K, McLean I, Traupe H (2009) In: Experimental Dermatology, 18(3). Research article (journal)
Toward enzyme substitution therapy of lamellar ichthyosis: liposomal encapsulation of recombinant transglutaminase 1 Aufenvenne K, Zimmerling K, Walker T, Dathe M, Traupe H (2009) In: Journal of Investigative Dermatology, 129 Suppl.. Research article (journal)