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Gilly Padalon-Brauch

Showing results (1-10 of 6) with videos related to

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Nucleic Acids Research|February 13, 2008
Small RNAs encoded within genetic islands of Salmonella typhimurium show host-induced expression and role in virulenceGilly Padalon-Brauch, Ruth Hershberg, Maya Elgrably-Weiss, et al.
The Journal of Investigative Dermatology|April 23, 2013
Semidominant inheritance in epidermolytic ichthyosisJanna Nousbeck, Gilly Padalon-Brauch, Dana Fuchs-Telem, 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.
Experimental Dermatology|March 27, 2013
The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12Tomer Goldsmith, Dana Fuchs-Telem, Shirli Israeli, et al.
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.
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.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Nucleic Acids Research|February 13, 2008
Small RNAs encoded within genetic islands of Salmonella typhimurium show host-induced expression and role in virulenceGilly Padalon-Brauch, Ruth Hershberg, Maya Elgrably-Weiss, et al.
The Journal of Investigative Dermatology|April 23, 2013
Semidominant inheritance in epidermolytic ichthyosisJanna Nousbeck, Gilly Padalon-Brauch, Dana Fuchs-Telem, 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.
Experimental Dermatology|March 27, 2013
The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12Tomer Goldsmith, Dana Fuchs-Telem, Shirli Israeli, et al.
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.
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.
Pageof 1