Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A-Reference-Cited by-同舟云学术

Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A

Published:2018-08 Issue:8 Volume:138 Page:1736-1743
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Mohamad Janan,Sarig Ofer,Godsel Lisa M.,Peled Alon,Malchin Natalia,Bochner Ron,Vodo Dan,Rabinowitz Tom,Pavlovsky Mor,Taiber Shahar,Fried Maya,Eskin-Schwartz Marina,Assi Siwar,Shomron Noam,Uitto Jouni,Koetsier Jennifer L.,Bergman Reuven,Green Kathleen J.,Sprecher Eli

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference33 articles.

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3. Generalized ichthyotic peeling skin syndrome due to FLG2 mutations;Bolling;J Invest Dermatol,2018

4. Repeated short climatic change affects the epidermal differentiation program and leads to matrix remodeling in a human organotypic skin model;Boutrand;Clin Cosmet Investig Dermatol,2017

5. Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndrome;Cabral;Genomics,2012

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