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

Ofer Sarig

Showing results (51-60 of 71) with videos related to

Pageof 8
Sort By:
American Journal of Human Genetics|July 31, 2012
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutationOfer Sarig, Sagi Nahum, Debora Rapaport, et al.
Experimental Dermatology|May 6, 2015
RBM28, a protein deficient in ANE syndrome, regulates hair follicle growth via miR-203 and p63Emily Warshauer, Liat Samuelov, Ofer Sarig, et al.
Pediatric Dermatology|October 12, 2023
Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosaShir Bergson, Daniel Daniely, David Bomze, et al.
The Journal of Investigative Dermatology|May 15, 2018
Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type AJanan Mohamad, Ofer Sarig, Lisa M Godsel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 28, 2020
Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosisLiron Malki, Ofer Sarig, Nicole Cesarato, et al.
The American Journal of Dermatopathology|January 26, 2017
Epidermolytic Ichthyosis Sine EpidermolysisMarina Eskin-Schwartz, Marianna Drozhdina, Ofer Sarig, et al.
The British Journal of Dermatology|September 8, 2023
MicroRNA-200b-mediated reversion of a spectrum of epithelial-to-mesenchymal transition states in recessive dystrophic epidermolysis bullosa squamous cell carcinomasJulia Illmer, Roland Zauner, Josefina Piñón Hofbauer, et al.
The Journal of Investigative Dermatology|August 30, 2019
The Role of Desmoglein 1 in Gap Junction Turnover Revealed through the Study of SAM SyndromeEran Cohen-Barak, Lisa M Godsel, Jennifer L Koetsier, et al.
The New England Journal of Medicine|February 15, 2019
Variant <i>PADI3</i> in Central Centrifugal Cicatricial AlopeciaLiron Malki, Ofer Sarig, Maria-Teresa Romano, et al.
The Journal of Allergy and Clinical Immunology|September 25, 2018
Loss-of-function mutations in caspase recruitment domain-containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitisAlon Peled, Ofer Sarig, Guangping Sun, et al.
Pageof 8

Showing results (51-60 of 71) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|July 31, 2012
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutationOfer Sarig, Sagi Nahum, Debora Rapaport, et al.
Experimental Dermatology|May 6, 2015
RBM28, a protein deficient in ANE syndrome, regulates hair follicle growth via miR-203 and p63Emily Warshauer, Liat Samuelov, Ofer Sarig, et al.
Pediatric Dermatology|October 12, 2023
Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosaShir Bergson, Daniel Daniely, David Bomze, et al.
The Journal of Investigative Dermatology|May 15, 2018
Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type AJanan Mohamad, Ofer Sarig, Lisa M Godsel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 28, 2020
Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosisLiron Malki, Ofer Sarig, Nicole Cesarato, et al.
The American Journal of Dermatopathology|January 26, 2017
Epidermolytic Ichthyosis Sine EpidermolysisMarina Eskin-Schwartz, Marianna Drozhdina, Ofer Sarig, et al.
The British Journal of Dermatology|September 8, 2023
MicroRNA-200b-mediated reversion of a spectrum of epithelial-to-mesenchymal transition states in recessive dystrophic epidermolysis bullosa squamous cell carcinomasJulia Illmer, Roland Zauner, Josefina Piñón Hofbauer, et al.
The Journal of Investigative Dermatology|August 30, 2019
The Role of Desmoglein 1 in Gap Junction Turnover Revealed through the Study of SAM SyndromeEran Cohen-Barak, Lisa M Godsel, Jennifer L Koetsier, et al.
The New England Journal of Medicine|February 15, 2019
Variant <i>PADI3</i> in Central Centrifugal Cicatricial AlopeciaLiron Malki, Ofer Sarig, Maria-Teresa Romano, et al.
The Journal of Allergy and Clinical Immunology|September 25, 2018
Loss-of-function mutations in caspase recruitment domain-containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitisAlon Peled, Ofer Sarig, Guangping Sun, et al.
Pageof 8