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Heiko Traupe

Showing results (51-60 of 80) with videos related to

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The Journal of Investigative Dermatology|June 15, 2012
Mutations in the prostaglandin transporter SLCO2A1 cause primary hypertrophic osteoarthropathy with digital clubbingJutta Busch, Valeska Frank, Nadine Bachmann, et al.
The Journal of Investigative Dermatology|June 4, 2004
Meta-analysis of genome-wide studies of psoriasis susceptibility reveals linkage to chromosomes 6p21 and 4q28-q31 in Caucasian and Chinese Hans populationGurdeep S Sagoo, Rachid Tazi-Ahnini, Jonathan W N Barker, et al.
The Journal of Investigative Dermatology|January 19, 2005
Lack of evidence for genetic association to RUNX1 binding site at PSORS2 in different German psoriasis cohortsUlrike Hüffmeier, Heiko Traupe, Harald Burkhardt, et al.
Human Genetics|December 17, 2002
Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab EmiratesKatja Martina Eckl, Howard P Stevens, Gilles G Lestringant, et al.
Acta Dermato-Venereologica|August 16, 2021
Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of ScalingMi-Ran Kim, Vinzenz Oji, Frederic Valentin, et al.
The Journal of Investigative Dermatology|October 22, 2017
Increased Prevalence of Filaggrin Deficiency in 51 Patients with Recessive X-Linked Ichthyosis Presenting for Dermatological ExaminationKira Süßmuth, Robert Gruber, Elke Rodriguez, et al.
American Journal of Human Genetics|August 10, 2010
Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin diseaseVinzenz Oji, Katja-Martina Eckl, Karin Aufenvenne, et al.
The Journal of Investigative Dermatology|January 10, 2009
Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12BKatja-Martina Eckl, Silvia de Juanes, Janine Kurtenbach, et al.
BMC Medical Genetics|August 25, 2017
Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patientsSteffen Uebe, Maria Ehrlicher, Arif Bülent Ekici, et al.
American Journal of Human Genetics|September 28, 2011
Mutations in CSTA, encoding Cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesionDiana C Blaydon, Daniela Nitoiu, Katja-Martina Eckl, et al.
Pageof 8

Showing results (51-60 of 80) with videos related to

Sort By:
Pageof 8
The Journal of Investigative Dermatology|June 15, 2012
Mutations in the prostaglandin transporter SLCO2A1 cause primary hypertrophic osteoarthropathy with digital clubbingJutta Busch, Valeska Frank, Nadine Bachmann, et al.
The Journal of Investigative Dermatology|June 4, 2004
Meta-analysis of genome-wide studies of psoriasis susceptibility reveals linkage to chromosomes 6p21 and 4q28-q31 in Caucasian and Chinese Hans populationGurdeep S Sagoo, Rachid Tazi-Ahnini, Jonathan W N Barker, et al.
The Journal of Investigative Dermatology|January 19, 2005
Lack of evidence for genetic association to RUNX1 binding site at PSORS2 in different German psoriasis cohortsUlrike Hüffmeier, Heiko Traupe, Harald Burkhardt, et al.
Human Genetics|December 17, 2002
Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab EmiratesKatja Martina Eckl, Howard P Stevens, Gilles G Lestringant, et al.
Acta Dermato-Venereologica|August 16, 2021
Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of ScalingMi-Ran Kim, Vinzenz Oji, Frederic Valentin, et al.
The Journal of Investigative Dermatology|October 22, 2017
Increased Prevalence of Filaggrin Deficiency in 51 Patients with Recessive X-Linked Ichthyosis Presenting for Dermatological ExaminationKira Süßmuth, Robert Gruber, Elke Rodriguez, et al.
American Journal of Human Genetics|August 10, 2010
Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin diseaseVinzenz Oji, Katja-Martina Eckl, Karin Aufenvenne, et al.
The Journal of Investigative Dermatology|January 10, 2009
Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12BKatja-Martina Eckl, Silvia de Juanes, Janine Kurtenbach, et al.
BMC Medical Genetics|August 25, 2017
Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patientsSteffen Uebe, Maria Ehrlicher, Arif Bülent Ekici, et al.
American Journal of Human Genetics|September 28, 2011
Mutations in CSTA, encoding Cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesionDiana C Blaydon, Daniela Nitoiu, Katja-Martina Eckl, et al.
Pageof 8