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Full-Thickness Human Skin Models for Congenital Ichthyosis and Related Keratinization DisordersECKL, Katja-Martina; ALEF, Thomas; TORRES, Serena et al.Journal of investigative dermatology. 2011, Vol 131, Num 9, pp 1938-1942, issn 0022-202X, 5 p.Article

Hallmarks of Atopic Skin Mimicked In Vitro by Means of a Skin Disease Model Based on FLG Knock-downKÜCHLER, Sarah; HENKES, Dominika; ECKL, Katja-Martina et al.ATLA. Alternatives to laboratory animals. 2011, Vol 39, Num 5, pp 471-480, issn 0261-1929, 10 p.Article

Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab EmiratesECKL, Katja Martina; STEVENS, Howard P; REIS, André et al.Human genetics. 2003, Vol 112, Num 1, pp 50-56, issn 0340-6717, 7 p.Article

Molecular Analysis of 250 Patients with Autosomal Recessive Congenital Ichthyosis: Evidence for Mutation Hotspots in ALOXE3 and Allelic Heterogeneity in ALOX12BECKL, Katja-Martina; DE JUANES, Silvia; HAREL, Avikam et al.Journal of investigative dermatology. 2009, Vol 129, Num 6, pp 1421-1428, issn 0022-202X, 8 p.Article

Mutations in CSTA, Encoding Cystatin A, Underlie Exfoliative Ichthyosis and Reveal a Role for This Protease Inhibitor in Cell-Cell AdhesionBLAYDON, Diana C; NITOIU, Daniela; ZVULUNOV, Alex et al.American journal of human genetics. 2011, Vol 89, Num 4, pp 564-571, issn 0002-9297, 8 p.Article

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