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List of works by Katja Martina Eckl

CEDNIK syndrome results from loss-of-function mutations in SNAP29.

scientific article

Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss-of-function mutation in CSTA.

scientific article published on 18 March 2015

Full-thickness human skin models for congenital ichthyosis and related keratinization disorders

scientific article published on 19 May 2011

Genetic and Clinical Heterogeneity in Transgressive Palmoplantar Keratoderma

scientific article published on 01 May 2001

Hallmarks of Atopic Skin Mimicked In Vitro by Means of a Skin Disease Model Based on FLG Knock-down ⬇️

scientific article published on October 1, 2011

Hypoplastic thyroid, growth hormone deficiency, corneal opacities, cataract and hyperkeratotic skin disease: a possible new ichthyosis syndrome associated with endocrinopathies

scientific article published on 05 May 2005

IGFBP7 as a potential therapeutic target in Psoriasis

scientific article published on 12 May 2011

Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates

scientific article

Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.

scientific article published on 8 January 2009

Penetration of normal, damaged and diseased skin--an in vitro study on dendritic core-multishell nanotransporters

scientific article published on 13 April 2014

Update: advanced methods in three-dimensional organotypic tissue engineering for congenital ichthyosis and other rare keratinization disorders

scientific article published on 01 December 2014

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