Mozheh Zamiri

Glasgow, SCT G514TF, United Kingdom

Last Updated: 09/26/2026

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Found 15 publications

Dysregulation of Connexin Expression Plays a Pivotal Role in Psoriasis.

Dysregulation of Connexin Expression Plays a Pivotal Role in Psoriasis.

Journal: International journal of molecular sciences

Published: February 22, 2021

A heterozygous mutation in GJB2 (Cx26F142L) associated with deafness and recurrent skin rashes results in connexin assembly deficiencies.

A heterozygous mutation in GJB2 (Cx26F142L) associated with deafness and recurrent skin rashes results in connexin assembly deficiencies.

Journal: Experimental dermatology

Published: May 14, 2020

Generation and Clinical Application of Gene-Modified Autologous Epidermal Sheets in Netherton Syndrome: Lessons Learned from a Phase 1 Trial.

Generation and Clinical Application of Gene-Modified Autologous Epidermal Sheets in Netherton Syndrome: Lessons Learned from a Phase 1 Trial.

Journal: Human gene therapy

Published: July 11, 2019

Novel mutations in desmoglein 1: focal palmoplantar keratoderma in milder phenotypes.

Novel mutations in desmoglein 1: focal palmoplantar keratoderma in milder phenotypes.

Journal: The British journal of dermatology

Published: March 02, 2019

Painful punctate palmoplantar keratoderma due to heterozygous mutations in AAGAB.

Painful punctate palmoplantar keratoderma due to heterozygous mutations in AAGAB.

Journal: The British journal of dermatology

Published: November 20, 2018

Loricrin palmoplantar keratoderma: full-thickness skin grafting for pseudoainhum.

Loricrin palmoplantar keratoderma: full-thickness skin grafting for pseudoainhum.

Journal: Clinical and experimental dermatology

Published: April 28, 2018

Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening.

Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening.

Journal: The British journal of dermatology

Published: August 08, 2016

Novel and recurrent mutations in keratin 1 cause epidermolytic ichthyosis and palmoplantar keratoderma.

Novel and recurrent mutations in keratin 1 cause epidermolytic ichthyosis and palmoplantar keratoderma.

Journal: Clinical and experimental dermatology

Published: July 30, 2016

Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis.

Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis.

Journal: The British journal of dermatology

Published: May 13, 2015

Mutations in GJB6 causing phenotype resembling pachyonychia congenita.

Mutations in GJB6 causing phenotype resembling pachyonychia congenita.

Journal: The British journal of dermatology

Published: November 12, 2014

Avascular necrosis of the hip and diffuse idiopathic skeletal hyperostosis during long-term isotretinoin treatment of epidermolytic ichthyosis due to a novel deletion mutation in KRT10.

Avascular necrosis of the hip and diffuse idiopathic skeletal hyperostosis during long-term isotretinoin treatment of epidermolytic ichthyosis due to a novel deletion mutation in KRT10.

Journal: The British journal of dermatology

Published: April 12, 2014

New and recurrent AAGAB mutations in punctate palmoplantar keratoderma.

New and recurrent AAGAB mutations in punctate palmoplantar keratoderma.

Journal: The British journal of dermatology

Published: March 05, 2014

Showing 1-12 of 15

Last Updated: 09/26/2026