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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 complex
Marcel 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 simplex
Lionel Fontao, Kaisa Tasanen, Marcel Huber, et al.
Frontiers in Immunology
|
August 30, 2013
Activin a inhibits antigen-induced allergy in murine epicutaneous sensitization
Magdalini 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 Syndrome
Andrey 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 Meleda
Fabrice Chimienti, Ronald C Hogg, Laure Plantard, et al.
EMBO Molecular Medicine
|
October 9, 2023
NRF3 suppresses squamous carcinogenesis, involving the unfolded protein response regulator HSPA5
Selina 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 carcinogenesis
Maria 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 Meleda
Bertrand 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 simplex
Marcel Huber, Michaela Floeth, Luca Borradori, et al.
Human Molecular Genetics
|
March 1, 2006
A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis
Felix B Müller, Marcel Huber, Tamar Kinaciyan, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 39) with videos related to
Sort By:
Page
of 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 complex
Marcel 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 simplex
Lionel Fontao, Kaisa Tasanen, Marcel Huber, et al.
Frontiers in Immunology
|
August 30, 2013
Activin a inhibits antigen-induced allergy in murine epicutaneous sensitization
Magdalini 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 Syndrome
Andrey 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 Meleda
Fabrice Chimienti, Ronald C Hogg, Laure Plantard, et al.
EMBO Molecular Medicine
|
October 9, 2023
NRF3 suppresses squamous carcinogenesis, involving the unfolded protein response regulator HSPA5
Selina 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 carcinogenesis
Maria 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 Meleda
Bertrand 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 simplex
Marcel Huber, Michaela Floeth, Luca Borradori, et al.
Human Molecular Genetics
|
March 1, 2006
A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis
Felix B Müller, Marcel Huber, Tamar Kinaciyan, et al.
Page
of 4