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Dan Vodo

Showing results (11-20 of 18) with videos related to

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Plos Genetics|May 6, 2016
Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 GeneDan Vodo, Ofer Sarig, Shamir Geller, 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.
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.
Nature Genetics|November 8, 2016
Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragilityZhimiao Lin, Shuo Li, Cheng Feng, et al.
Experimental Dermatology|November 29, 2016
SVEP1 plays a crucial role in epidermal differentiationLiat Samuelov, Qiaoli Li, Ron Bochner, et al.
The Journal of Investigative Dermatology|October 23, 2016
Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital IchthyosisRon Bochner, Liat Samuelov, Ofer Sarig, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Plos Genetics|May 6, 2016
Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 GeneDan Vodo, Ofer Sarig, Shamir Geller, 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.
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.
Nature Genetics|November 8, 2016
Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragilityZhimiao Lin, Shuo Li, Cheng Feng, et al.
Experimental Dermatology|November 29, 2016
SVEP1 plays a crucial role in epidermal differentiationLiat Samuelov, Qiaoli Li, Ron Bochner, et al.
The Journal of Investigative Dermatology|October 23, 2016
Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital IchthyosisRon Bochner, Liat Samuelov, Ofer Sarig, et al.
Pageof 2