Publications

Footer

Operated by

University of Münster
Division 6.4: Research Information Management
Department 6: Research Affairs
Domplatz 6-7 | 48143 Münster
cris@uni-muenster.de

Top-Links

About the University of Münster
Research profile of the University of Münster
CRIS-Login

living.knowledge

Legal Disclosure | Privacy Statement | Accessibility

Aufenvenne, Karin

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), 1918-1921. Research article (journal) \| Peer reviewed \| Published
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) \| Peer reviewed \| Published
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) \| Published
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), 274-281. Research article (journal) \| Published
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) \| Published
Peeling skin desease: Elucidation of a rare genetic Disorder of keratinization In: .
Reconstructed human epidermis demonstrates a severe epidermal barrier defect caused by deficiency of corneodesmosin In: .
Ichthyosis vulgaris: novel FLG mutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup. In: , -.
Novel filaggrin mutations in German ichthyosis vulgaris patients and high presence of CD1a+cells in the epidermis of the atopic subgroup In: .
Toward enzyme substitution therapy of lamellar ichthyosis: liposomal encapsulation of recombinant transglutaminase 1 In: .

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

(2010)

Journal der Deutschen Dermatologischen Gesellschaft

, 8

(11)

Research article (journal)

| Published

Eckl K, Oji V, Aufenvenne K, Natebus M, Tarinski T, Ackermann K, Schafer-Korting M, Hausser I, Traupe H, Hennies HC

(2010)

Journal of Investigative Dermatology

, 130 Suppl.

Research article (journal)

| Published

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)

British Journal of Dermatology

, 160

(4)

771

781

Research article (journal)

| Published

Oji V, Seller N, Sandilands A, Gruber R, Hausser I, Metze D, Walker T, Aufenvenne K, Loser K, McLean I, Traupe H

(2009)

Experimental Dermatology

, 18

(3)

Research article (journal)

| Published

Aufenvenne K, Zimmerling K, Walker T, Dathe M, Traupe H

(2009)

Journal of Investigative Dermatology

, 129 Suppl.

Research article (journal)

| Published