(PDF) Patients With Congenital Ichthyosis and TGM1

Patients With Congenital Ichthyosis and TGM1 Mutations Overexpress Other ARCI Genes in the Skin: Part of a Barrier Repair Response?

Experimental Dermatology - United Kingdom

doi 10.1111/exd.13813

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December 21, 2018

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Wiley

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Patients With Congenital Ichthyosis and TGM1 Mutations Overexpress Other ARCI Genes in the Skin: Part of a Barrier Repair Response?

Experimental Dermatology - United Kingdom

doi 10.1111/exd.13813

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

102 Proteins Causing Autosomal Congenital Recessive Ichthyosis (ARCI) Colocalize in Differentiated Primary Keratinocytes and the Interactions Are Altered in Cells From Patients With TGM1 Mutations

379 KB105: An HSV-based Gene Therapy Vector Engineered to Deliver Functional TGM1 to Autosomal Recessive Congenital Ichthyosis (ARCI) Keratinocytes

Autosomal Recessive Congenital Ichthyosis: CERS3 Mutations Identified by a Next Generation Sequencing Panel Targeting Ichthyosis Genes

Comparing Histopathology From Patients With X-Linked Recessive Ichthyosis and Autosomal Recessive Congenital Ichthyosis With Transglutaminase 1 Mutation: A Report From the National Registry for Ichthyosis and Related Skin Disorders

Functional Study ofTGM1missense Mutations in Autosomal Recessive Congenital Ichthyosis

Novel Transglutaminase-1 Mutations and Genotype-Phenotype Investigations of 104 Patients With Autosomal Recessive Congenital Ichthyosis in the USA

Transglutaminase 1 Mutations in Autosomal Recessive Congenital Ichthyosis: Private and Recurrent Mutations in an Isolated Population

383 Preclinical Safety and Pharmacology of KB105, an HSV-based Gene Therapy Vector for the Treatment of Autosomal Recessive Congenital Ichthyosis (ARCI)

Full-Thickness Human Skin Models for Congenital Ichthyosis and Related Keratinization Disorders