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Reuven Bergman

Showing results (141-150 of 163) with videos related to

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Archives of Dermatology|April 23, 2003
Epidermolysis bullosa simplex in Israel: clinical and genetic featuresDan Ciubotaru, Reuven Bergman, David Baty, et al.
The Journal of Allergy and Clinical Immunology|May 3, 2007
Major differences in inflammatory dendritic cells and their products distinguish atopic dermatitis from psoriasisEmma Guttman-Yassky, Michelle A Lowes, Judilyn Fuentes-Duculan, et al.
Journal of the American Academy of Dermatology|March 22, 2002
Junctional epidermolysis bullosa in the Middle East: clinical and genetic studies in a series of consanguineous familiesAoi Nakano, Gilles G Lestringant, Tamar Paperna, et al.
The Journal of Allergy and Clinical Immunology|December 17, 2009
Broad defects in epidermal cornification in atopic dermatitis identified through genomic analysisEmma Guttman-Yassky, Mayte Suárez-Fariñas, Andrea Chiricozzi, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 5, 2008
Low expression of the IL-23/Th17 pathway in atopic dermatitis compared to psoriasisEmma Guttman-Yassky, Michelle A Lowes, Judilyn Fuentes-Duculan, et al.
The Journal of Biological Chemistry|November 5, 2005
Targeting perlecan in human keratinocytes reveals novel roles for perlecan in epidermal formationIfat Sher, Simona Zisman-Rozen, Liat Eliahu, et al.
The Journal of Allergy and Clinical Immunology|March 16, 2010
Atopic dermatitis keratinocytes exhibit normal T(H)17 cytokine responsesKristine E Nograles, Mayte Suárez-Fariñas, Avner Shemer, et al.
American Journal of Human Genetics|September 9, 2006
Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14Jennie Lugassy, Peter Itin, Akemi Ishida-Yamamoto, et al.
Nature Genetics|May 11, 2004
Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosisOrit Topaz, Daniel L Shurman, Reuven Bergman, et al.
The Journal of Investigative Dermatology|January 8, 2004
Phenotypic diversity and mutation spectrum in hypotrichosis with juvenile macular dystrophyMargarita Indelman, Christian P Hamel, Reuven Bergman, et al.
Pageof 17

Showing results (141-150 of 163) with videos related to

Sort By:
Pageof 17
Archives of Dermatology|April 23, 2003
Epidermolysis bullosa simplex in Israel: clinical and genetic featuresDan Ciubotaru, Reuven Bergman, David Baty, et al.
The Journal of Allergy and Clinical Immunology|May 3, 2007
Major differences in inflammatory dendritic cells and their products distinguish atopic dermatitis from psoriasisEmma Guttman-Yassky, Michelle A Lowes, Judilyn Fuentes-Duculan, et al.
Journal of the American Academy of Dermatology|March 22, 2002
Junctional epidermolysis bullosa in the Middle East: clinical and genetic studies in a series of consanguineous familiesAoi Nakano, Gilles G Lestringant, Tamar Paperna, et al.
The Journal of Allergy and Clinical Immunology|December 17, 2009
Broad defects in epidermal cornification in atopic dermatitis identified through genomic analysisEmma Guttman-Yassky, Mayte Suárez-Fariñas, Andrea Chiricozzi, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 5, 2008
Low expression of the IL-23/Th17 pathway in atopic dermatitis compared to psoriasisEmma Guttman-Yassky, Michelle A Lowes, Judilyn Fuentes-Duculan, et al.
The Journal of Biological Chemistry|November 5, 2005
Targeting perlecan in human keratinocytes reveals novel roles for perlecan in epidermal formationIfat Sher, Simona Zisman-Rozen, Liat Eliahu, et al.
The Journal of Allergy and Clinical Immunology|March 16, 2010
Atopic dermatitis keratinocytes exhibit normal T(H)17 cytokine responsesKristine E Nograles, Mayte Suárez-Fariñas, Avner Shemer, et al.
American Journal of Human Genetics|September 9, 2006
Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14Jennie Lugassy, Peter Itin, Akemi Ishida-Yamamoto, et al.
Nature Genetics|May 11, 2004
Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosisOrit Topaz, Daniel L Shurman, Reuven Bergman, et al.
The Journal of Investigative Dermatology|January 8, 2004
Phenotypic diversity and mutation spectrum in hypotrichosis with juvenile macular dystrophyMargarita Indelman, Christian P Hamel, Reuven Bergman, et al.
Pageof 17