Shir Bergson
Tel Aviv, TA, Israel
Last Updated: 09/26/2026
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Found 11 publications
Targeting ST18-mediated pathomechanism in pemphigus vulgaris through voltage-dependent anion channel inhibition.
Journal: Skin health and disease
Published: October 30, 2025
HMCN1 variants aggravate epidermolysis bullosa simplex phenotype.
Journal: The Journal of experimental medicine
Published: May 11, 2024
Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa.
Journal: Pediatric dermatology
Published: June 30, 2023
MicroRNA-200b-mediated reversion of a spectrum of epithelial-to-mesenchymal transition states in recessive dystrophic epidermolysis bullosa squamous cell carcinomas.
Journal: The British journal of dermatology
Published: March 21, 2023
Defective cathepsin Z affects EGFR expression and causes autosomal dominant palmoplantar keratoderma.
Journal: The British journal of dermatology
Published: March 04, 2023
Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expression.
Journal: Scientific reports
Published: November 24, 2021
Loss-of-function variants in KLF4 underlie autosomal dominant palmoplantar keratoderma.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 29, 2021
Neonatal inflammatory skin and bowel disease type 1 caused by a complex genetic defect and responsive to combined anti-tumour necrosis factor-α and interleukin-12/23 blockade.
Journal: The British journal of dermatology
Published: September 20, 2021
Viral Bcl-2 Encoded by the Kaposi's Sarcoma-Associated Herpesvirus Is Vital for Virus Reactivation.
Journal: Journal of virology
Published: January 13, 2015
Showing 1-11 of 11
Last Updated: 09/26/2026