(PDF) 379 KB105: An HSV-based Gene Therapy Vector

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

Journal of Investigative Dermatology - United Kingdom

doi 10.1016/j.jid.2019.03.455

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May 1, 2019

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Elsevier BV

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

Journal of Investigative Dermatology - United Kingdom

doi 10.1016/j.jid.2019.03.455

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

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

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

380 KB104: An HSV-based Gene Therapy Vector Engineered to Deliver Functional SPINK5 for the Treatment of Netherton Syndrome

Functional Study ofTGM1missense Mutations in Autosomal Recessive Congenital Ichthyosis

NIPAL4 Deletion Identified in an American Bully With Autosomal Recessive Congenital Ichthyosis and Response to Topical Therapy

A Novel Missence Mutation in the Transglutaminase-1 Gene in an Autosomal Recessive Congenital Ichthyosis Patient

Calpain 12 Function Revealed Through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis

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

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