Aileen Sandilands
James Arrott Drive
Dundee, SCT DD19SY, United Kingdom
Dundee, SCT DD19SY, United Kingdom
Last Updated: 09/26/2026
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Found 19 publications
The CNC-bZIP transcription factor Nrf2 controls expression of matrix metalloproteases in murine macrophages.
Journal: Journal of leukocyte biology
Published: October 14, 2025
CD5L is a target of transcription factor Nrf2.
Journal: Biochemical and biophysical research communications
Published: May 22, 2025
Therapeutic Prospects of Exon Skipping for Epidermolysis Bullosa.
Journal: International journal of molecular sciences
Published: October 14, 2021
A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis.
Journal: The Journal of investigative dermatology
Published: May 05, 2017
Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants.
Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants.
Journal: The Journal of allergy and clinical immunology
Published: February 17, 2017
Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening.
Journal: The British journal of dermatology
Published: August 08, 2016
Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis.
Journal: The Journal of investigative dermatology
Published: March 28, 2016
Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis.
Journal: The British journal of dermatology
Published: May 13, 2015
A new filaggrin gene mutation in a Korean patient with ichthyosis vulgaris.
Journal: European journal of dermatology : EJD
Published: August 14, 2014
Filaggrin-stratified transcriptomic analysis of pediatric skin identifies mechanistic pathways in patients with atopic dermatitis.
Journal: The Journal of allergy and clinical immunology
Published: March 05, 2014
Loss-of-function mutations in the gene encoding filaggrin underlie a Japanese family with food-dependent exercise-induced anaphylaxis.
Journal: Journal of the European Academy of Dermatology and Venereology : JEADV
Published: October 11, 2013
South African amaXhosa patients with atopic dermatitis have decreased levels of filaggrin breakdown products but no loss-of-function mutations in filaggrin.
Journal: The Journal of allergy and clinical immunology
Published: August 06, 2013
Last Updated: 09/26/2026