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O Sarig

Showing results (11-20 of 35) with videos related to

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The British Journal of Dermatology|December 16, 2014
Extensive lentigo simplex, linear epidermolytic naevus and epidermolytic naevus comedonicus caused by a somatic mutation in KRT10L Samuelov, O Sarig, A Gat, et al.
Clinical and Experimental Dermatology|May 14, 2011
Erythrokeratoderma variabilis caused by a recessive mutation in GJB3D Fuchs-Telem, Y Pessach, B Mevorah, et al.
Clinical and Experimental Dermatology|December 3, 2013
A novel splice-site mutation in the AAGAB gene segregates with hereditary punctate palmoplantar keratoderma and congenital dysplasia of the hip in a large familyO Eytan, O Sarig, S Israeli, et al.
Clinical and Experimental Dermatology|January 19, 2019
PLACK syndrome shows remarkable phenotypic homogeneityJ Mohamad, L Samuelov, D Ben-Amitai, et al.
Clinical and Experimental Dermatology|February 17, 2015
Pyoderma gangrenosum, acne and ulcerative colitis in a patient with a novel mutation in the PSTPIP1 geneT Zeeli, G Padalon-Brauch, E Ellenbogen, et al.
Clinical and Experimental Dermatology|March 19, 2014
New intragenic and promoter region deletion mutations in FERMT1 underscore genetic homogeneity in Kindler syndromeD Fuchs-Telem, J Nousbeck, A Singer, et al.
The British Journal of Dermatology|June 10, 2014
Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genesJ Nousbeck, O Sarig, L Magal, et al.
Clinical and Experimental Dermatology|December 27, 2017
Recessive epidermolytic ichthyosis results from loss of keratin 10 expression, regardless of the mutation locationD Vodo, O Sarig, A Peled, et al.
Clinical and Experimental Dermatology|February 24, 2015
A case for diagnosisL Samuelov, O Sarig, T Goldsmith, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 29, 2018
Immune-regulatory genes as possible modifiers of familial pityriasis rubra pilaris - lessons from a family with PRP and psoriasisI Spoerri, S Herms, O Eytan, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
The British Journal of Dermatology|December 16, 2014
Extensive lentigo simplex, linear epidermolytic naevus and epidermolytic naevus comedonicus caused by a somatic mutation in KRT10L Samuelov, O Sarig, A Gat, et al.
Clinical and Experimental Dermatology|May 14, 2011
Erythrokeratoderma variabilis caused by a recessive mutation in GJB3D Fuchs-Telem, Y Pessach, B Mevorah, et al.
Clinical and Experimental Dermatology|December 3, 2013
A novel splice-site mutation in the AAGAB gene segregates with hereditary punctate palmoplantar keratoderma and congenital dysplasia of the hip in a large familyO Eytan, O Sarig, S Israeli, et al.
Clinical and Experimental Dermatology|January 19, 2019
PLACK syndrome shows remarkable phenotypic homogeneityJ Mohamad, L Samuelov, D Ben-Amitai, et al.
Clinical and Experimental Dermatology|February 17, 2015
Pyoderma gangrenosum, acne and ulcerative colitis in a patient with a novel mutation in the PSTPIP1 geneT Zeeli, G Padalon-Brauch, E Ellenbogen, et al.
Clinical and Experimental Dermatology|March 19, 2014
New intragenic and promoter region deletion mutations in FERMT1 underscore genetic homogeneity in Kindler syndromeD Fuchs-Telem, J Nousbeck, A Singer, et al.
The British Journal of Dermatology|June 10, 2014
Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genesJ Nousbeck, O Sarig, L Magal, et al.
Clinical and Experimental Dermatology|December 27, 2017
Recessive epidermolytic ichthyosis results from loss of keratin 10 expression, regardless of the mutation locationD Vodo, O Sarig, A Peled, et al.
Clinical and Experimental Dermatology|February 24, 2015
A case for diagnosisL Samuelov, O Sarig, T Goldsmith, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 29, 2018
Immune-regulatory genes as possible modifiers of familial pityriasis rubra pilaris - lessons from a family with PRP and psoriasisI Spoerri, S Herms, O Eytan, et al.
Pageof 4