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Ofer Sarig

Showing results (11-20 of 71) with videos related to

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Harefuah|January 14, 2020
[LINEAR MYCOSIS FUNGOIDES IN A BLASCHKOID DISTRIBUTION]Yehonatan Kaplan, Ofer Sarig, Tom Rabinowitz, et al.
The Journal of Investigative Dermatology|December 17, 2010
Functional characterization of SAMD9, a protein deficient in normophosphatemic familial tumoral calcinosisDov Hershkovitz, Yonit Gross, Sagi Nahum, et al.
American Journal of Human Genetics|March 29, 2011
A mutation in LIPN, encoding epidermal lipase N, causes a late-onset form of autosomal-recessive congenital ichthyosisShirli Israeli, Ziyad Khamaysi, Dana Fuchs-Telem, et al.
The British Journal of Dermatology|January 7, 2022
Neonatal inflammatory skin and bowel disease type 1 caused by a complex genetic defect and responsive to combined anti-tumour necrosis factor-α and interleukin-12/23 blockadeLiat Samuelov, Ofer Sarig, Kiril Malovitski, et al.
Dermatology (Basel, Switzerland)|March 1, 2014
Molecular analysis of a series of Israeli families with Comèl-Netherton syndromeShirli Israeli, Ofer Sarig, Ben Zion Garty, et al.
The Journal of Investigative Dermatology|August 28, 2009
Insulin-like growth factor-binding protein 7 regulates keratinocyte proliferation, differentiation and apoptosisJanna Nousbeck, Ofer Sarig, Nili Avidan, et al.
Pediatric Dermatology|May 19, 2025
Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads (PLACK) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two PatientsFiona Haxho, Richard M Haber, Janan Mohamad, et al.
American Journal of Human Genetics|August 9, 2011
A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphiaJanna Nousbeck, Bettina Burger, Dana Fuchs-Telem, 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.
The British Journal of Dermatology|May 20, 2023
Defective cathepsin Z affects EGFR expression and causes autosomal dominant palmoplantar keratodermaKiril Malovitski, Ofer Sarig, Yarden Feller, et al.
Pageof 8

Showing results (11-20 of 71) with videos related to

Sort By:
Pageof 8
Harefuah|January 14, 2020
[LINEAR MYCOSIS FUNGOIDES IN A BLASCHKOID DISTRIBUTION]Yehonatan Kaplan, Ofer Sarig, Tom Rabinowitz, et al.
The Journal of Investigative Dermatology|December 17, 2010
Functional characterization of SAMD9, a protein deficient in normophosphatemic familial tumoral calcinosisDov Hershkovitz, Yonit Gross, Sagi Nahum, et al.
American Journal of Human Genetics|March 29, 2011
A mutation in LIPN, encoding epidermal lipase N, causes a late-onset form of autosomal-recessive congenital ichthyosisShirli Israeli, Ziyad Khamaysi, Dana Fuchs-Telem, et al.
The British Journal of Dermatology|January 7, 2022
Neonatal inflammatory skin and bowel disease type 1 caused by a complex genetic defect and responsive to combined anti-tumour necrosis factor-α and interleukin-12/23 blockadeLiat Samuelov, Ofer Sarig, Kiril Malovitski, et al.
Dermatology (Basel, Switzerland)|March 1, 2014
Molecular analysis of a series of Israeli families with Comèl-Netherton syndromeShirli Israeli, Ofer Sarig, Ben Zion Garty, et al.
The Journal of Investigative Dermatology|August 28, 2009
Insulin-like growth factor-binding protein 7 regulates keratinocyte proliferation, differentiation and apoptosisJanna Nousbeck, Ofer Sarig, Nili Avidan, et al.
Pediatric Dermatology|May 19, 2025
Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads (PLACK) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two PatientsFiona Haxho, Richard M Haber, Janan Mohamad, et al.
American Journal of Human Genetics|August 9, 2011
A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphiaJanna Nousbeck, Bettina Burger, Dana Fuchs-Telem, 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.
The British Journal of Dermatology|May 20, 2023
Defective cathepsin Z affects EGFR expression and causes autosomal dominant palmoplantar keratodermaKiril Malovitski, Ofer Sarig, Yarden Feller, et al.
Pageof 8