Dan Vodo
6, Weizmann Street
Tel Aviv, TA 64239, Israel
Tel Aviv, TA 64239, Israel
Last Updated: 09/26/2026
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Found 24 publications
Targeting ST18-mediated pathomechanism in pemphigus vulgaris through voltage-dependent anion channel inhibition.
Journal: Skin health and disease
Published: October 30, 2025
Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4.
Journal: American journal of medical genetics. Part A
Published: June 02, 2023
Syphilis Manifesting with Unilateral Hearing Loss and Tinnitus.
Journal: Indian journal of dermatology
Published: January 24, 2022
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
Epidermolytic epidermal nevus caused by a somatic mutation in KRT2.
Journal: Pediatric dermatology
Published: February 08, 2021
ST18 affects cell-cell adhesion in pemphigus vulgaris in a tumour necrosis factor-α-dependent fashion.
Journal: The British journal of dermatology
Published: November 12, 2020
Atypical presentation of laryngo-onycho-cutaneous syndrome resulting from novel mutations in LAMA3A.
Atypical presentation of laryngo-onycho-cutaneous syndrome resulting from novel mutations in LAMA3A.
Journal: Clinical and experimental dermatology
Published: October 12, 2020
Loss-of-Function Variants in SERPINA12 Underlie Autosomal Recessive Palmoplantar Keratoderma.
Journal: The Journal of investigative dermatology
Published: December 26, 2019
Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 19, 2019
Identification of a recurrent mutation in ATP2C1 demonstrates that papular acantholytic dyskeratosis and Hailey-Hailey disease are allelic disorders.
Journal: The British journal of dermatology
Published: June 27, 2018
Punctate palmoplantar keratoderma: an unusual mutation causing an unusual phenotype.
Journal: The British journal of dermatology
Published: March 02, 2018
Last Updated: 09/26/2026