An IL-17–dominant immune profile is shared across the major orphan forms of ichthyosis - Journal of Allergy and Clinical Immunology
ABHD5 knock out mouse | Mouse Models - Ximbio
13 Harlequin Ichthyosis | Plastic Surgery Key
Self-Improvement of Keratinocyte Differentiation Defects During Skin Maturation in ABCA12-Deficient Harlequin Ichthyosis Model Mice - The American Journal of Pathology
Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009 - Journal of the American Academy of Dermatology
Harlequin ichthyosis model mouse reveals alveolar collapse and severe fetal skin barrier defects
![PDF] Defects in Stratum Corneum Desquamation Are the Predominant Effect of Impaired ABCA12 Function in a Novel Mouse Model of Harlequin Ichthyosis | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/a849e063c74e39d86e52c0a6c753fa0586b01a8d/6-Figure1-1.png "PDF] Defects in Stratum Corneum Desquamation Are the Predominant Effect of Impaired ABCA12 Function in a Novel Mouse Model of Harlequin Ichthyosis | Semantic Scholar")
PDF] Defects in Stratum Corneum Desquamation Are the Predominant Effect of Impaired ABCA12 Function in a Novel Mouse Model of Harlequin Ichthyosis | Semantic Scholar
Defects in Stratum Corneum Desquamation Are the Predominant Effect of Impaired ABCA12 Function in a Novel Mouse Model of Harlequin Ichthyosis | PLOS ONE
![PDF] A Mouse Model of Harlequin Ichthyosis Delineates a Key Role for Abca12 in Lipid Homeostasis | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/e8fbbef28129e15499469ef5ca366ec16b5be081/3-Figure1-1.png "PDF] A Mouse Model of Harlequin Ichthyosis Delineates a Key Role for Abca12 in Lipid Homeostasis | Semantic Scholar")
PDF] A Mouse Model of Harlequin Ichthyosis Delineates a Key Role for Abca12 in Lipid Homeostasis | Semantic Scholar
Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis - Journal of Allergy and Clinical Immunology
Identification of a novel lethal form of autosomal recessive ichthyosis caused by UDP‐glucose ceramide glucosyltransferase deficiency - Monies - 2018 - Clinical Genetics - Wiley Online Library
A Mouse Model of Harlequin Ichthyosis Delineates a Key Role for Abca12 in Lipid Homeostasis | PLOS Genetics
PAR2 absence completely rescues inflammation and ichthyosis caused by altered CAP1/Prss8 expression in mouse skin | Nature Communications
A Mouse Model of Harlequin Ichthyosis Delineates a Key Role for Abca12 in Lipid Homeostasis | PLOS Genetics
Topical Aminosalicylic Acid Improves Keratinocyte Differentiation in an Inducible Mouse Model of Harlequin Ichthyosis
PNPLA1 Deficiency in Mice and Humans Leads to a Defect in the Synthesis of Omega-O-Acylceramides - ScienceDirect
Cx26-G45E transgenic mice develop skin abnormalities. Animals were... | Download High-Resolution Scientific Diagram
A,B. Mutant newborn mice exhibited a protruding tongue (black arrow in... | Download Scientific Diagram
Ichthyosis Awareness Ribbon Mouse Pad : Office Products - Amazon.com
Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger–Hue¨t anom
Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis. - Abstract - Europe PMC
13 Harlequin Ichthyosis | Plastic Surgery Key
Lamellar Ichthyosis: Practice Essentials, Pathophysiology, Epidemiology
Ichthyosis - Wikipedia
Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice | Cell Death & Disease
Figure 2 from Harlequin ichthyosis model mouse reveals alveolar collapse and severe fetal skin barrier defects. | Semantic Scholar
Dermatology - Musculoskeletal and Cutaneous Surgery - Laboratories | Nagoya University GraduateSchool of Medicine
