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Robert Gruber

Showing results (51-60 of 56) with videos related to

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The Journal of Allergy and Clinical Immunology|June 16, 2015
Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakinMaeve A McAleer, Elizabeth Pohler, Frances J D Smith, et al.
Dermatology and Therapy|July 15, 2026
Consensus Recommendations for Management of Darier Disease: A Practical ApproachCristina Has, Valentina Ruffo di Calabria, Marzia Caproni, et al.
Nature Genetics|April 10, 2007
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczemaAileen Sandilands, Ana Terron-Kwiatkowski, Peter R Hull, et al.
Genes|January 13, 2021
Meta-Analysis of Mutations in <i>ALOX12B</i> or <i>ALOXE3</i> Identified in a Large Cohort of 224 PatientsAlrun Hotz, Julia Kopp, Emmanuelle Bourrat, et al.
The British Journal of Dermatology|October 29, 2024
Biologics in congenital ichthyosis: are they effective?Juliette Mazereeuw-Hautier, Céline Granier Tournier, Angela Hernandez-Martin, et al.
American Journal of Human Genetics|October 18, 2016
Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of ComplementInes Kapferer-Seebacher, Melanie Pepin, Roland Werner, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
The Journal of Allergy and Clinical Immunology|June 16, 2015
Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakinMaeve A McAleer, Elizabeth Pohler, Frances J D Smith, et al.
Dermatology and Therapy|July 15, 2026
Consensus Recommendations for Management of Darier Disease: A Practical ApproachCristina Has, Valentina Ruffo di Calabria, Marzia Caproni, et al.
Nature Genetics|April 10, 2007
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczemaAileen Sandilands, Ana Terron-Kwiatkowski, Peter R Hull, et al.
Genes|January 13, 2021
Meta-Analysis of Mutations in <i>ALOX12B</i> or <i>ALOXE3</i> Identified in a Large Cohort of 224 PatientsAlrun Hotz, Julia Kopp, Emmanuelle Bourrat, et al.
The British Journal of Dermatology|October 29, 2024
Biologics in congenital ichthyosis: are they effective?Juliette Mazereeuw-Hautier, Céline Granier Tournier, Angela Hernandez-Martin, et al.
American Journal of Human Genetics|October 18, 2016
Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of ComplementInes Kapferer-Seebacher, Melanie Pepin, Roland Werner, et al.
Pageof 6