Syndrome de Netherton : un modèle d’étude de la régulation de la desquamation
Author:
Publisher
EDP Sciences
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Link
http://www.medecinesciences.org/10.1051/medsci/2005215457/pdf
Reference11 articles.
1. Références
2. ComelM. Ichtyosis linearis circumflexa.Dermatologica1949; 98 : 133–6.
3. Netherton EW. A unique case ofTrichorrexis Invaginata.Arch Dermatol1958; 78 : 483–7.
4. Fartasch M, Williams ML, Elias PM. Altered lamellar body secretion and stratum corneum membrane structure in Netherton syndrome.Arch Dermatol1999; 135 : 823–32.
5. Chavanas S, Bodemer C, Rochat A,et al.Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome.Nat Genet2000; 25 : 141–2.
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1. Attenuated kallikrein‐related peptidase activity disrupts desquamation and leads to stratum corneum thickening in human skin equivalent models;British Journal of Dermatology;2016-12-22
2. Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine;Archives de Pédiatrie;2011-03
3. L’élastase 2, une nouvelle protéase épidermique impliquée dans l’établissement de la barrière cutanée;médecine/sciences;2010-08
4. Proteolytic processing of human growth hormone by multiple tissue kallikreins and regulation by the serine protease inhibitor Kazal-Type5 (SPINK5) protein;Clinica Chimica Acta;2007-02
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