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Archives of Dermatology
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April 23, 2003
Epidermolysis bullosa simplex in Israel: clinical and genetic features
Dan 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 psoriasis
Emma 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 families
Aoi 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 analysis
Emma 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 psoriasis
Emma 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 formation
Ifat 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 responses
Kristine 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 KRT14
Jennie 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 calcinosis
Orit 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 dystrophy
Margarita Indelman, Christian P Hamel, Reuven Bergman, et al.
Page
of 17
Search research articles
Search
Showing results (141-150 of 163) with videos related to
Sort By:
Page
of 17
Archives of Dermatology
|
April 23, 2003
Epidermolysis bullosa simplex in Israel: clinical and genetic features
Dan 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 psoriasis
Emma 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 families
Aoi 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 analysis
Emma 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 psoriasis
Emma 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 formation
Ifat 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 responses
Kristine 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 KRT14
Jennie 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 calcinosis
Orit 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 dystrophy
Margarita Indelman, Christian P Hamel, Reuven Bergman, et al.
Page
of 17