Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Dan Vodo

Showing results (1-10 of 18) with videos related to

Pageof 2
Sort By:
Frontiers in Medicine|August 30, 2018
The Genetics of Pemphigus VulgarisDan Vodo, Ofer Sarig, Eli Sprecher
Indian Journal of Dermatology|January 24, 2022
Syphilis Manifesting with Unilateral Hearing Loss and TinnitusDan Vodo, Liron Spitzer, Tomer Goldsmith, et al.
Experimental Dermatology|June 30, 2015
Autosomal-dominant cutis laxa resulting from an intronic mutation in ELNDan Vodo, Ofer Sarig, Alon Peled, et al.
Pediatric Dermatology|February 8, 2021
Epidermolytic epidermal nevus caused by a somatic mutation in KRT2Janan Mohamad, Liat Samuelov, Sari Assaf, et al.
The Journal of Investigative Dermatology|July 27, 2012
Digenic inheritance in epidermolysis bullosa simplexGilly Padalon-Brauch, Dani Ben Amitai, Dan Vodo, et al.
Scientific Reports|April 9, 2022
Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expressionSari Assaf, Dan Vodo, Kiril Malovitski, et al.
Pediatric Dermatology|April 19, 2016
Somatic Mosaicism for a "Lethal" GJB2 Mutation Results in a Patterned Form of Spiny Hyperkeratosis without Eccrine InvolvementMarina Eskin-Schwartz, Yoav Metzger, Alon Peled, et al.
American Journal of Medical Genetics. Part A|September 19, 2023
Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4Alon Peled, Ofer Sarig, Janan Mohamad, et al.
Skin Health and Disease|April 2, 2026
Targeting ST18-mediated pathomechanism in pemphigus vulgaris through voltage-dependent anion channel inhibitionSari Assaf, Ofer Sarig, Rawaa Ishtewy, et al.
The Journal of Investigative Dermatology|April 6, 2020
Loss-of-Function Variants in SERPINA12 Underlie Autosomal Recessive Palmoplantar KeratodermaJanan Mohamad, Ofer Sarig, Liron Malki, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Frontiers in Medicine|August 30, 2018
The Genetics of Pemphigus VulgarisDan Vodo, Ofer Sarig, Eli Sprecher
Indian Journal of Dermatology|January 24, 2022
Syphilis Manifesting with Unilateral Hearing Loss and TinnitusDan Vodo, Liron Spitzer, Tomer Goldsmith, et al.
Experimental Dermatology|June 30, 2015
Autosomal-dominant cutis laxa resulting from an intronic mutation in ELNDan Vodo, Ofer Sarig, Alon Peled, et al.
Pediatric Dermatology|February 8, 2021
Epidermolytic epidermal nevus caused by a somatic mutation in KRT2Janan Mohamad, Liat Samuelov, Sari Assaf, et al.
The Journal of Investigative Dermatology|July 27, 2012
Digenic inheritance in epidermolysis bullosa simplexGilly Padalon-Brauch, Dani Ben Amitai, Dan Vodo, et al.
Scientific Reports|April 9, 2022
Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expressionSari Assaf, Dan Vodo, Kiril Malovitski, et al.
Pediatric Dermatology|April 19, 2016
Somatic Mosaicism for a "Lethal" GJB2 Mutation Results in a Patterned Form of Spiny Hyperkeratosis without Eccrine InvolvementMarina Eskin-Schwartz, Yoav Metzger, Alon Peled, et al.
American Journal of Medical Genetics. Part A|September 19, 2023
Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4Alon Peled, Ofer Sarig, Janan Mohamad, et al.
Skin Health and Disease|April 2, 2026
Targeting ST18-mediated pathomechanism in pemphigus vulgaris through voltage-dependent anion channel inhibitionSari Assaf, Ofer Sarig, Rawaa Ishtewy, et al.
The Journal of Investigative Dermatology|April 6, 2020
Loss-of-Function Variants in SERPINA12 Underlie Autosomal Recessive Palmoplantar KeratodermaJanan Mohamad, Ofer Sarig, Liron Malki, et al.
Pageof 2