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Serine protease activity and residual LEKTI expression determine phenotype in Netherton syndrome
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2006 (English)In: Journal of Investigative Dermatology, ISSN 0022-202X, E-ISSN 1523-1747, Vol. 126, no 7, 1609-21 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2006. Vol. 126, no 7, 1609-21 p.
Keyword [en]
Abnormalities; Multiple/*genetics, Adolescent, Adult, Animals, Carrier Proteins/*genetics/physiology, Cell Membrane Permeability/physiology, Child, Dermatitis; Atopic/*genetics/*pathology, Desmocollins, Desmoglein 1/physiology, Desmosomes/physiology/ultrastructure, Enzyme Activation, Epidermis/chemistry/pathology, Gene Expression Regulation, Hair Follicle/*abnormalities/physiopathology, Humans, Ichthyosis; Lamellar/*genetics/*pathology, Kallikreins/analysis, Membrane Glycoproteins/physiology, Mice, Mice; Transgenic, Mutation, Phenotype, Proteinase Inhibitory Proteins; Secretory, Serine Endopeptidases/*metabolism, Severity of Illness Index, Syndrome
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URN: urn:nbn:se:umu:diva-6741DOI: 10.1038/sj.jid.5700288PubMedID: 16601670OAI: oai:DiVA.org:umu-6741DiVA: diva2:146411
Available from: 2007-12-17 Created: 2007-12-17 Last updated: 2017-12-14Bibliographically approved

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Publisher's full textPubMedhttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=16601670&dopt=Citation

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Brattsand, MariaEgelrud, Torbjorn
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Dermatology and Venerology
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