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Heiko Traupe

Showing results (31-40 of 80) with videos related to

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Human Mutation|August 24, 2005
Mutation spectrum and functional analysis of epidermis-type lipoxygenases in patients with autosomal recessive congenital ichthyosisKatja-Martina Eckl, Peter Krieg, Wolfgang Küster, et al.
The Journal of Investigative Dermatology|January 27, 2007
Loss-of-function variants of the filaggrin gene are not major susceptibility factors for psoriasis vulgaris or psoriatic arthritis in German patientsUlrike Hüffmeier, Heiko Traupe, Vinzenz Oji, et al.
The Journal of Investigative Dermatology|March 23, 2012
Long-term faithful recapitulation of transglutaminase 1-deficient lamellar ichthyosis in a skin-humanized mouse model, and insights from proteomic studiesKarin Aufenvenne, Robert H Rice, Ingrid Hausser, et al.
The Journal of Investigative Dermatology|May 8, 2013
Mutations in IL36RN in patients with generalized pustular psoriasisAndreas Körber, Rotraut Mössner, Regina Renner, et al.
Annals of the Rheumatic Diseases|May 15, 2009
Deletion of LCE3C and LCE3B genes at PSORS4 does not contribute to susceptibility to psoriatic arthritis in German patientsUlrike Hüffmeier, Xavier Estivill, Eva Riveira-Munoz, et al.
American Journal of Human Genetics|September 24, 2013
Topical enzyme-replacement therapy restores transglutaminase 1 activity and corrects architecture of transglutaminase-1-deficient skin graftsKarin Aufenvenne, Fernando Larcher, Ingrid Hausser, et al.
Acta Dermato-Venereologica|May 28, 2015
Increased expression of caspase-1 and interleukin-18 in peeling skin disease, and a novel mutation of corneodesmosinFrederic Valentin, Vinzenz Oji, Ingrid Hausser, et al.
Arthritis and Rheumatism|May 29, 2007
TNF polymorphisms in psoriasis: association of psoriatic arthritis with the promoter polymorphism TNF*-857 independent of the PSORS1 risk alleleKristian Reich, Ulrike Hüffmeier, Inke R König, et al.
Arthritis and Rheumatism|November 30, 2006
Lack of genetic association of the interleukin-4 receptor single-nucleotide polymorphisms I50V and Q551R with erosive disease in psoriatic arthritisJesús Lascorz, Ulrike Hüffmeier, Hendrik Schulze-Koops, et al.
The Journal of Investigative Dermatology|August 12, 2004
SPINK5 and Netherton syndrome: novel mutations, demonstration of missing LEKTI, and differential expression of transglutaminasesMichael Raghunath, Lambrini Tontsidou, Vinzenz Oji, et al.
Pageof 8

Showing results (31-40 of 80) with videos related to

Sort By:
Pageof 8
Human Mutation|August 24, 2005
Mutation spectrum and functional analysis of epidermis-type lipoxygenases in patients with autosomal recessive congenital ichthyosisKatja-Martina Eckl, Peter Krieg, Wolfgang Küster, et al.
The Journal of Investigative Dermatology|January 27, 2007
Loss-of-function variants of the filaggrin gene are not major susceptibility factors for psoriasis vulgaris or psoriatic arthritis in German patientsUlrike Hüffmeier, Heiko Traupe, Vinzenz Oji, et al.
The Journal of Investigative Dermatology|March 23, 2012
Long-term faithful recapitulation of transglutaminase 1-deficient lamellar ichthyosis in a skin-humanized mouse model, and insights from proteomic studiesKarin Aufenvenne, Robert H Rice, Ingrid Hausser, et al.
The Journal of Investigative Dermatology|May 8, 2013
Mutations in IL36RN in patients with generalized pustular psoriasisAndreas Körber, Rotraut Mössner, Regina Renner, et al.
Annals of the Rheumatic Diseases|May 15, 2009
Deletion of LCE3C and LCE3B genes at PSORS4 does not contribute to susceptibility to psoriatic arthritis in German patientsUlrike Hüffmeier, Xavier Estivill, Eva Riveira-Munoz, et al.
American Journal of Human Genetics|September 24, 2013
Topical enzyme-replacement therapy restores transglutaminase 1 activity and corrects architecture of transglutaminase-1-deficient skin graftsKarin Aufenvenne, Fernando Larcher, Ingrid Hausser, et al.
Acta Dermato-Venereologica|May 28, 2015
Increased expression of caspase-1 and interleukin-18 in peeling skin disease, and a novel mutation of corneodesmosinFrederic Valentin, Vinzenz Oji, Ingrid Hausser, et al.
Arthritis and Rheumatism|May 29, 2007
TNF polymorphisms in psoriasis: association of psoriatic arthritis with the promoter polymorphism TNF*-857 independent of the PSORS1 risk alleleKristian Reich, Ulrike Hüffmeier, Inke R König, et al.
Arthritis and Rheumatism|November 30, 2006
Lack of genetic association of the interleukin-4 receptor single-nucleotide polymorphisms I50V and Q551R with erosive disease in psoriatic arthritisJesús Lascorz, Ulrike Hüffmeier, Hendrik Schulze-Koops, et al.
The Journal of Investigative Dermatology|August 12, 2004
SPINK5 and Netherton syndrome: novel mutations, demonstration of missing LEKTI, and differential expression of transglutaminasesMichael Raghunath, Lambrini Tontsidou, Vinzenz Oji, et al.
Pageof 8