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Svenja Alter

Showing results (1-10 of 22) with videos related to

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The British Journal of Dermatology|January 23, 2023
Adding up the desmosomal genes causing syndromes with hair and skin involvement: identification of TUFT1 by state-of-the-art whole-genome sequencingJudith Fischer, Svenja Alter
Frontiers in Plant Science|October 14, 2014
The beginning of a seed: regulatory mechanisms of double fertilizationAndrea Bleckmann, Svenja Alter, Thomas Dresselhaus
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|February 29, 2024
Julie Claude Schroeder, Svenja Alter, Judith Fischer, et al.
Genes|March 25, 2022
First Description of Inheritance of a Postzygotic <i>OPA1</i> Mosaic VariantSvenja Alter, Navid Farassat, Sebastian Küchlin, et al.
Pediatric Dermatology|January 20, 2023
Lipoid proteinosis: Novel ECM1 pathogenic variants and intrafamilial variability in four unrelated Arab familiesMingfeng Li, Judith Fischer, Sylvia Safwat, et al.
Database : the Journal of Biological Databases and Curation|May 17, 2015
DroughtDB: an expert-curated compilation of plant drought stress genes and their homologs in nine speciesSvenja Alter, Kai C Bader, Manuel Spannagl, et al.
Frontiers in Immunology|April 25, 2022
Case Report: Diagnostic and Therapeutic Challenges in Severe Mechanobullous Epidermolysis Bullosa AcquisitaFranziska Schauer, Alexander Nyström, Manfred Kunz, et al.
JIMD Reports|September 9, 2020
Neonatal presentation of COG6-CDG with prominent skin phenotypeKatalin Komlosi, Selina Gläser, Julia Kopp, et al.
Journal of Medical Genetics|August 21, 2020
Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in <i>protein kinase D1</i>Svenja Alter, Andreas David Zimmer, Misun Park, et al.
The British Journal of Dermatology|January 23, 2023
Pathogenic variants in the SPTLC1 gene cause hyperkeratosis lenticularis perstansSabine Jägle, Hao-Hsiang Hsu, Hazem A Juratli, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
The British Journal of Dermatology|January 23, 2023
Adding up the desmosomal genes causing syndromes with hair and skin involvement: identification of TUFT1 by state-of-the-art whole-genome sequencingJudith Fischer, Svenja Alter
Frontiers in Plant Science|October 14, 2014
The beginning of a seed: regulatory mechanisms of double fertilizationAndrea Bleckmann, Svenja Alter, Thomas Dresselhaus
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|February 29, 2024
Julie Claude Schroeder, Svenja Alter, Judith Fischer, et al.
Genes|March 25, 2022
First Description of Inheritance of a Postzygotic <i>OPA1</i> Mosaic VariantSvenja Alter, Navid Farassat, Sebastian Küchlin, et al.
Pediatric Dermatology|January 20, 2023
Lipoid proteinosis: Novel ECM1 pathogenic variants and intrafamilial variability in four unrelated Arab familiesMingfeng Li, Judith Fischer, Sylvia Safwat, et al.
Database : the Journal of Biological Databases and Curation|May 17, 2015
DroughtDB: an expert-curated compilation of plant drought stress genes and their homologs in nine speciesSvenja Alter, Kai C Bader, Manuel Spannagl, et al.
Frontiers in Immunology|April 25, 2022
Case Report: Diagnostic and Therapeutic Challenges in Severe Mechanobullous Epidermolysis Bullosa AcquisitaFranziska Schauer, Alexander Nyström, Manfred Kunz, et al.
JIMD Reports|September 9, 2020
Neonatal presentation of COG6-CDG with prominent skin phenotypeKatalin Komlosi, Selina Gläser, Julia Kopp, et al.
Journal of Medical Genetics|August 21, 2020
Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in <i>protein kinase D1</i>Svenja Alter, Andreas David Zimmer, Misun Park, et al.
The British Journal of Dermatology|January 23, 2023
Pathogenic variants in the SPTLC1 gene cause hyperkeratosis lenticularis perstansSabine Jägle, Hao-Hsiang Hsu, Hazem A Juratli, et al.
Pageof 3