Transgenic kallikrein 5 mice reproduce major cutaneous and systemic hallmarks of Netherton syndrome
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Title
Transgenic kallikrein 5 mice reproduce major cutaneous and systemic hallmarks of Netherton syndrome
Authors
Keywords
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Journal
JOURNAL OF EXPERIMENTAL MEDICINE
Volume 211, Issue 3, Pages 499-513
Publisher
Rockefeller University Press
Online
2014-02-18
DOI
10.1084/jem.20131797
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Note: Only part of the references are listed.- Mechanism-based selection of a potent kallikrein-related peptidase 7 inhibitor from a versatile library based on the sunflower trypsin inhibitor SFTI-1
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- Non-combinatorial library screening reveals subsite cooperativity and identifies new high-efficiency substrates for kallikrein-related peptidase 14
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- Caspase-14 Is Required for Filaggrin Degradation to Natural Moisturizing Factors in the Skin
- (2011) Esther Hoste et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- Human Keratinocytes' Response to Injury Upregulates CCL20 and Other Genes Linking Innate and Adaptive Immunity
- (2011) Milène Kennedy-Crispin et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- PAR2 absence completely rescues inflammation and ichthyosis caused by altered CAP1/Prss8 expression in mouse skin
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- Elastase 2 is expressed in human and mouse epidermis and impairs skin barrier function in Netherton syndrome through filaggrin and lipid misprocessing
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- New Role for LEKTI in Skin Barrier Formation: Label-Free Quantitative Proteomic Identification of Caspase 14 as a Novel Target for the Protease Inhibitor LEKTI
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- Matriptase initiates activation of epidermal pro-kallikrein and disease onset in a mouse model of Netherton syndrome
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- (2009) Ellen D. Renner et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Kallikrein 5 induces atopic dermatitis–like lesions through PAR2-mediated thymic stromal lymphopoietin expression in Netherton syndrome
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- Th17 cytokines interleukin (IL)-17 and IL-22 modulate distinct inflammatory and keratinocyte-response pathways
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