Basis for abnormal desquamation and permeability barrier dysfunction in RXLI
about
Modeling of diffusion with partitioning in stratum corneum using a finite element modelIFAP syndrome is caused by deficiency in MBTPS2, an intramembrane zinc metalloprotease essential for cholesterol homeostasis and ER stress responsePathogenesis of permeability barrier abnormalities in the ichthyoses: inherited disorders of lipid metabolismAn update of the defensive barrier function of skinDistinguishing ichthyoses by protein profilingInvolvement of corneodesmosome degradation and lamellar granule transportation in the desquamation processAbca12-mediated lipid transport and Snap29-dependent trafficking of lamellar granules are crucial for epidermal morphogenesis in a zebrafish model of ichthyosisRegulation of ABCG1 expression in human keratinocytes and murine epidermis.High-temperature gas chromatography-mass spectrometry for skin surface lipids profilingThematic review series: skin lipids. The role of epidermal lipids in cutaneous permeability barrier homeostasis.A mutation in LIPN, encoding epidermal lipase N, causes a late-onset form of autosomal-recessive congenital ichthyosis.Disturbed skin barrier in children with chronic kidney diseaseReduction of amyloid angiopathy and Abeta plaque burden after enriched housing in TgCRND8 mice: involvement of multiple pathways.Stratum corneum defensive functions: an integrated view.Cellular changes that accompany shedding of human corneocytes.Acute modulations in permeability barrier function regulate epidermal cornification: role of caspase-14 and the protease-activated receptor type 2Inherited ichthyoses/generalized Mendelian disorders of cornification.Mice deficient in involucrin, envoplakin, and periplakin have a defective epidermal barrierAbnormal barrier function in the pathogenesis of ichthyosis: therapeutic implications for lipid metabolic disorders.The stratum corneum: a double paradox.Role of cholesterol sulfate in epidermal structure and function: lessons from X-linked ichthyosis.Order and disorder in corneocyte adhesion.Updated molecular genetics and pathogenesis of ichthiyoses.Bicelles: lipid nanostructured platforms with potential dermal applications.Pathogenesis-based therapies in ichthyoses.Multifaceted pathways protect human skin from UV radiation.Epidermal barrier disorders and corneodesmosome defects.The biology and regulation of corneodesmosomes.Encapsulation of cosmetic active ingredients for topical application--a review.Cholesterol sulfate and Ca(2+) modulate the mixing properties of lipids in stratum corneum model mixturesHigh levels of oxysterol sulfates in serum of patients with steroid sulfatase deficiency.Skin Barrier Function Is Not Impaired and Kallikrein 7 Gene Polymorphism Is Frequently Observed in Korean X-linked Ichthyosis Patients Diagnosed by Fluorescence in Situ Hybridization and Array Comparative Genomic Hybridization.Epidermal Differentiation in Barrier Maintenance and Wound Healing.C/EBPalpha and beta couple interfollicular keratinocyte proliferation arrest to commitment and terminal differentiation.Pathogenesis of the cutaneous phenotype in inherited disorders of cholesterol metabolism: Therapeutic implications for topical treatment of these disorders.Skin penetration by metal compounds with special reference to copper.Regulation of ABCA1 expression in human keratinocytes and murine epidermis.Sampling of disease biomarkers from skin for theranostic applications.Deletion of the Sox21 gene drastically affects hair lipids.X-linked recessive ichthyosis: an impaired barrier function evokes limited gene responses before and after moisturizing treatments.
P2860
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P2860
Basis for abnormal desquamation and permeability barrier dysfunction in RXLI
description
2004 nî lūn-bûn
@nan
2004 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Basis for abnormal desquamation and permeability barrier dysfunction in RXLI
@ast
Basis for abnormal desquamation and permeability barrier dysfunction in RXLI
@en
Basis for abnormal desquamation and permeability barrier dysfunction in RXLI
@nl
type
label
Basis for abnormal desquamation and permeability barrier dysfunction in RXLI
@ast
Basis for abnormal desquamation and permeability barrier dysfunction in RXLI
@en
Basis for abnormal desquamation and permeability barrier dysfunction in RXLI
@nl
prefLabel
Basis for abnormal desquamation and permeability barrier dysfunction in RXLI
@ast
Basis for abnormal desquamation and permeability barrier dysfunction in RXLI
@en
Basis for abnormal desquamation and permeability barrier dysfunction in RXLI
@nl
P2093
P3181
P1476
Basis for abnormal desquamation and permeability barrier dysfunction in RXLI
@en
P2093
Debra Crumrine
Gopinathan K Menon
Jean-Pierre Hachem
Kenneth R Feingold
Laura Leypoldt
Mary L Williams
Monica Hoi Wun Choy
Peter M Elias
Ulrich Rassner
Wenyan Man
P3181
P356
10.1046/J.1523-1747.2003.22258.X
P407
P577
2004-02-01T00:00:00Z
P5875
P6179
1049438364