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
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
Ichthyosis: A Road Model for Skin Research | HTML | Acta Dermato-Venereologica
Identification of a novel lethal form of autosomal recessive ichthyosis caused by UDP‐glucose ceramide glucosyltransferase deficiency - Monies - 2018 - Clinical Genetics - Wiley Online Library
Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice | Cell Death & Disease
Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis - Journal of Allergy and Clinical Immunology
Ichthyosis - Wikipedia
THE ICHTHYOSIS MOUSE: HISTOLOGIC, HISTOCHEMICAL, ULTRASTRUCTURAL, AND AUTORADIOGRAPHIC STUDIES OF INTERFOLLICULAR EPIDERMIS
Defects in Stratum Corneum Desquamation Are the Predominant Effect of Impaired ABCA12 Function in a Novel Mouse Model of Harlequin Ichthyosis | PLOS ONE
Harlequin ichthyosis and other autosomal recessive congenital ichthyoses: The underlying genetic defects and pathomechanisms - Journal of Dermatological Science
Characterization of dermatitis arising spontaneously in DS-Nh mice maintained under conventional conditions: another possible model for atopic dermatitis - Journal of Dermatological Science
![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
Autosomal Recessive Congenital Ichthyosis | Actas Dermo-Sifiliográficas
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
Ichthyosis Awareness Month: Shannon and Lauren's story ~ “Our community has no single country, no identified boundaries. Information is shared with a click of the mouse…Hugs have gone virtual.” “
![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
Lamellar Ichthyosis: Practice Essentials, Pathophysiology, Epidemiology
A,B. Mutant newborn mice exhibited a protruding tongue (black arrow in... | Download Scientific Diagram
Self-Improvement of Keratinocyte Differentiation Defects During Skin Maturation in ABCA12-Deficient Harlequin Ichthyosis Model Mice - The American Journal of Pathology
