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Marcel Huber

Showing results (21-30 of 39) with videos related to

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The Journal of Investigative Dermatology|April 28, 2005
Isolation and characterization of human repetin, a member of the fused gene family of the epidermal differentiation complexMarcel Huber, Georges Siegenthaler, Nicolae Mirancea, et al.
The Journal of Investigative Dermatology|February 14, 2004
Molecular consequences of deletion of the cytoplasmic domain of bullous pemphigoid 180 in a patient with predominant features of epidermolysis bullosa simplexLionel Fontao, Kaisa Tasanen, Marcel Huber, et al.
Frontiers in Immunology|August 30, 2013
Activin a inhibits antigen-induced allergy in murine epicutaneous sensitizationMagdalini Kypriotou, Dianelys Rivero, Sergio Haller, et al.
The Journal of Investigative Dermatology|May 24, 2025
Integrative Molecular Analysis of Skin Tumors from Patients with CYLD Cutaneous SyndromeAndrey A Yurchenko, Hiba Sharkhith, Fatemeh Rajabi, et al.
Human Molecular Genetics|September 25, 2003
Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of Mal de MeledaFabrice Chimienti, Ronald C Hogg, Laure Plantard, et al.
EMBO Molecular Medicine|October 9, 2023
NRF3 suppresses squamous carcinogenesis, involving the unfolded protein response regulator HSPA5Selina Gurri, Beat Siegenthaler, Michael Cangkrama, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 15, 2013
Mast cells are dispensable for normal and activin-promoted wound healing and skin carcinogenesisMaria Antsiferova, Caroline Martin, Marcel Huber, et al.
The Journal of Investigative Dermatology|September 30, 2006
SLURP1 is a late marker of epidermal differentiation and is absent in Mal de MeledaBertrand Favre, Laure Plantard, Lorène Aeschbach, et al.
The Journal of Investigative Dermatology|February 20, 2002
Deletion of the cytoplasmatic domain of BP180/collagen XVII causes a phenotype with predominant features of epidermolysis bullosa simplexMarcel Huber, Michaela Floeth, Luca Borradori, et al.
Human Molecular Genetics|March 1, 2006
A human keratin 10 knockout causes recessive epidermolytic hyperkeratosisFelix B Müller, Marcel Huber, Tamar Kinaciyan, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
The Journal of Investigative Dermatology|April 28, 2005
Isolation and characterization of human repetin, a member of the fused gene family of the epidermal differentiation complexMarcel Huber, Georges Siegenthaler, Nicolae Mirancea, et al.
The Journal of Investigative Dermatology|February 14, 2004
Molecular consequences of deletion of the cytoplasmic domain of bullous pemphigoid 180 in a patient with predominant features of epidermolysis bullosa simplexLionel Fontao, Kaisa Tasanen, Marcel Huber, et al.
Frontiers in Immunology|August 30, 2013
Activin a inhibits antigen-induced allergy in murine epicutaneous sensitizationMagdalini Kypriotou, Dianelys Rivero, Sergio Haller, et al.
The Journal of Investigative Dermatology|May 24, 2025
Integrative Molecular Analysis of Skin Tumors from Patients with CYLD Cutaneous SyndromeAndrey A Yurchenko, Hiba Sharkhith, Fatemeh Rajabi, et al.
Human Molecular Genetics|September 25, 2003
Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of Mal de MeledaFabrice Chimienti, Ronald C Hogg, Laure Plantard, et al.
EMBO Molecular Medicine|October 9, 2023
NRF3 suppresses squamous carcinogenesis, involving the unfolded protein response regulator HSPA5Selina Gurri, Beat Siegenthaler, Michael Cangkrama, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 15, 2013
Mast cells are dispensable for normal and activin-promoted wound healing and skin carcinogenesisMaria Antsiferova, Caroline Martin, Marcel Huber, et al.
The Journal of Investigative Dermatology|September 30, 2006
SLURP1 is a late marker of epidermal differentiation and is absent in Mal de MeledaBertrand Favre, Laure Plantard, Lorène Aeschbach, et al.
The Journal of Investigative Dermatology|February 20, 2002
Deletion of the cytoplasmatic domain of BP180/collagen XVII causes a phenotype with predominant features of epidermolysis bullosa simplexMarcel Huber, Michaela Floeth, Luca Borradori, et al.
Human Molecular Genetics|March 1, 2006
A human keratin 10 knockout causes recessive epidermolytic hyperkeratosisFelix B Müller, Marcel Huber, Tamar Kinaciyan, et al.
Pageof 4