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Ofer Sarig

Showing results (61-70 of 71) with videos related to

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The Journal of Investigative Dermatology|September 8, 2019
Coagulation Factor XIII-A Subunit Missense Mutation in the Pathobiology of Autosomal Dominant Multiple DermatofibromasChavalit Supsrisunjai, Chao-Kai Hsu, Magdalene Michael, et al.
American Journal of Human Genetics|July 28, 2009
RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndromeLina Basel-Vanagaite, Ofer Sarig, Dov Hershkovitz, et al.
The Journal of Allergy and Clinical Immunology|June 16, 2015
Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakinMaeve A McAleer, Elizabeth Pohler, Frances J D Smith, et al.
Plos Genetics|October 14, 2016
Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle MorphogenesisAlon Peled, Ofer Sarig, Liat Samuelov, 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.
Experimental Dermatology|March 31, 2021
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern populationJanan Mohamad, Liat Samuelov, Natalia Malchin, et al.
The Journal of Investigative Dermatology|March 23, 2012
Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgarisOfer Sarig, Sivan Bercovici, Lilach Zoller, et al.
The Journal of Experimental Medicine|February 20, 2025
HMCN1 variants aggravate epidermolysis bullosa simplex phenotypeShir Bergson, Ofer Sarig, Moshe Giladi, et al.
Nature Genetics|August 27, 2013
Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wastingLiat Samuelov, Ofer Sarig, Robert M Harmon, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
The Journal of Investigative Dermatology|September 8, 2019
Coagulation Factor XIII-A Subunit Missense Mutation in the Pathobiology of Autosomal Dominant Multiple DermatofibromasChavalit Supsrisunjai, Chao-Kai Hsu, Magdalene Michael, et al.
American Journal of Human Genetics|July 28, 2009
RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndromeLina Basel-Vanagaite, Ofer Sarig, Dov Hershkovitz, et al.
The Journal of Allergy and Clinical Immunology|June 16, 2015
Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakinMaeve A McAleer, Elizabeth Pohler, Frances J D Smith, et al.
Plos Genetics|October 14, 2016
Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle MorphogenesisAlon Peled, Ofer Sarig, Liat Samuelov, 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.
Experimental Dermatology|March 31, 2021
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern populationJanan Mohamad, Liat Samuelov, Natalia Malchin, et al.
The Journal of Investigative Dermatology|March 23, 2012
Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgarisOfer Sarig, Sivan Bercovici, Lilach Zoller, et al.
The Journal of Experimental Medicine|February 20, 2025
HMCN1 variants aggravate epidermolysis bullosa simplex phenotypeShir Bergson, Ofer Sarig, Moshe Giladi, et al.
Nature Genetics|August 27, 2013
Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wastingLiat Samuelov, Ofer Sarig, Robert M Harmon, et al.
Pageof 8