Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis. - Abstract - Europe PMC
Autosomal Recessive Congenital Ichthyosis | Actas Dermo-Sifiliográficas
Harlequin ichthyosis and other autosomal recessive congenital ichthyoses: The underlying genetic defects and pathomechanisms - Journal of Dermatological Science
Dermatology - Musculoskeletal and Cutaneous Surgery - Laboratories | Nagoya University GraduateSchool of Medicine
Defects in Stratum Corneum Desquamation Are the Predominant Effect of Impaired ABCA12 Function in a Novel Mouse Model of Harlequin Ichthyosis | PLOS ONE
ABHD5 knock out mouse | Mouse Models - Ximbio
Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger–Hue¨t anom
Figure 2 from Harlequin ichthyosis model mouse reveals alveolar collapse and severe fetal skin barrier defects. | Semantic Scholar
13 Harlequin Ichthyosis | Plastic Surgery Key
Genetics of Inherited Ichthyoses and Related Diseases | HTML | Acta Dermato-Venereologica
Topical Aminosalicylic Acid Improves Keratinocyte Differentiation in an Inducible Mouse Model of Harlequin Ichthyosis
Requirement of Fatty Acid Transport Protein 4 for Development, Maturation, and Function of Sebaceous Glands in a Mouse Model of Ichthyosis Prematurity Syndrome* - Journal of Biological Chemistry
Filaggrin Genotype in Ichthyosis Vulgaris Predicts Abnormalities in Epidermal Structure and Function - The American Journal of Pathology
The Cx26-G45E mutation displays increased hemichannel activity in a mouse model of the lethal form of keratitis-ichthyosis-deafness syndrome | Molecular Biology of the Cell
An IL-17–dominant immune profile is shared across the major orphan forms of ichthyosis - Journal of Allergy and Clinical Immunology
![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
Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice | Cell Death & Disease
Ichthyosis Awareness Ribbon Mouse Pad : Office Products - Amazon.com
Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis - Journal of Allergy and Clinical Immunology
PAR2 absence completely rescues inflammation and ichthyosis caused by altered CAP1/Prss8 expression in mouse skin | Nature Communications
Ichthyosis: A Road Model for Skin Research | HTML | Acta Dermato-Venereologica
Cx26-G45E transgenic mice develop skin abnormalities. Animals were... | Download High-Resolution Scientific Diagram
PNPLA1 Deficiency in Mice and Humans Leads to a Defect in the Synthesis of Omega-O-Acylceramides - ScienceDirect
A Mouse Model of Harlequin Ichthyosis Delineates a Key Role for Abca12 in Lipid Homeostasis | PLOS Genetics
Characterization of dermatitis arising spontaneously in DS-Nh mice maintained under conventional conditions: another possible model for atopic dermatitis - Journal of Dermatological Science
Lamellar Ichthyosis: Practice Essentials, Pathophysiology, Epidemiology
