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Heliyon|January 6, 2025
Lipid imbalance and inflammatory oxylipin cascade at the maternal-fetal interface in recurrent spontaneous abortionHao Liu, Huijia Chen, Ting Han, et al.
The Journal of Allergy and Clinical Immunology|July 13, 2010
Raman profiles of the stratum corneum define 3 filaggrin genotype-determined atopic dermatitis endophenotypesGráinne M O'Regan, Patrick M J H Kemperman, Aileen Sandilands, et al.
Human Molecular Genetics|May 3, 2015
Second-generation compound for the modulation of utrophin in the therapy of DMDSimon Guiraud, Sarah E Squire, Benjamin Edwards, et al.
The Journal of Allergy and Clinical Immunology|February 11, 2012
Filaggrin loss-of-function mutations are associated with enhanced expression of IL-1 cytokines in the stratum corneum of patients with atopic dermatitis and in a murine model of filaggrin deficiencySanja Kezic, Gráinne M O'Regan, René Lutter, et al.
Human Mutation|November 23, 2007
The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseasesIldiko Szeverenyi, Andrew J Cassidy, Cheuk Wang Chung, et al.
The Journal of Allergy and Clinical Immunology|September 9, 2008
Analysis of the individual and aggregate genetic contributions of previously identified serine peptidase inhibitor Kazal type 5 (SPINK5), kallikrein-related peptidase 7 (KLK7), and filaggrin (FLG) polymorphisms to eczema riskStephan Weidinger, Hansjörg Baurecht, Stefan Wagenpfeil, et al.
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