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JDDG - Journal of the German Society of Dermatology, ISSN 1610-0379, 11/2015, Volume 13, Issue 11, pp. 1125 - 1134
Journal Article
J D D G, ISSN 1610-0379, 11/2015, Volume 13, Issue 11, pp. 1125 - 1134
The term epidermolysis bullosa (EB) includes a group of rare genodermatoses characterized by mutational impairment of the structural and functional integrity... 
Journal Article
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, ISSN 1610-0379, 04/2019, Volume 17, Issue 4, pp. 448 - 450
Journal Article
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, ISSN 1610-0379, 11/2015, Volume 13, Issue 11, pp. 1125 - 1134
Epidermolysis bullosa (EB) umfasst eine Gruppe seltener erblicher Hauterkrankungen, die durch mutationsbedingte Störung der strukturellen und funktionellen... 
Epidermolysis bullosa | Gentherapie | Genodermatosen
Journal Article
Journal Article
Der Hautarzt, ISSN 0017-8470, 03/2015, Volume 66, Issue 3, p. 203
Primare und/oder sekundare Extrakutanmanifestationen mit diversen Organkomplikationen, fruher Krankheitsbeginn und progressiver, durch relevante Morbiditat und... 
Orphans | Analysis | Mortality
Journal Article
Annals of Dermatology, ISSN 1013-9087, 2017, Volume 29, Issue 6, p. 667
Stem cells are undifferentiated cells capable of generating, sustaining, and replacing terminally differentiated cells and tissues. They can be isolated from... 
Epidermal stem cells | Wound healing | Epidermolysis bullosa | Induced pluripotent stem cells | Mesenchymal multipotent stromal cells | Stem cell therapy
Journal Article
Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 04/2019, Volume 17, Issue 4, pp. 448 - 450
Journal Article
HAUTARZT, ISSN 0017-8470, 03/2015, Volume 66, Issue 3, pp. 203 - 211
Journal Article
Nature, ISSN 0028-0836, 11/2017, Volume 551, Issue 7680, pp. 327 - 332
Journal Article
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, ISSN 1610-0379, 12/2015, Volume 13, Issue 12, pp. 1257 - 1266
Journal Article
JDDG - Journal of the German Society of Dermatology, ISSN 1610-0379, 03/2015, Volume 13, Issue 3, pp. 261 - 264
Journal Article
The Keio Journal of Medicine, ISSN 0022-9717, 2015
In the past few years, substantial preclinical and experimental advances have been made in the treatment of the severe monogenic skin blistering disease... 
epidermolysis bullosa | gene/cell therapy
Journal Article
Journal der Deutschen Dermatologischen Gesellschaft, ISSN 1610-0379, 03/2015, Volume 13, Issue 3, p. 261
Journal Article
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, ISSN 1610-0379, 03/2015, Volume 13, Issue 3, pp. 261 - 264
Journal Article
Archives of Dermatological Research, ISSN 0340-3696, 07/2011, Volume 303, Issue 5, pp. 371 - 374
Darier's disease (DD, OMIM 124200) is an autosomal dominant inherited genodermatosis characterized by warty papules and plaques in seborrheic areas, and loss... 
ATP2A2 | Darier-White | Mutation | Morbus Darier | PHENOTYPE | FEATURES | DERMATOLOGY | Humans | Middle Aged | Male | Darier Disease - pathology | Austria | Adolescent | Darier Disease - genetics | Polymerase Chain Reaction | Adult | Female | Aged | Sarcoplasmic Reticulum Calcium-Transporting ATPases - genetics | Protein Isoforms - genetics | Genetic aspects | Adenosine triphosphatase | Index Medicus
Journal Article
Journal Article
Molecular Therapy, ISSN 1525-0016, 11/2017, Volume 25, Issue 11, pp. 2573 - 2584
Designer nucleases allow specific and precise genomic modifications and represent versatile molecular tools for the correction of disease-associated mutations.... 
CRISPR/Cas9 | homology-directed repair | epidermolysis bullosa | COL7A1 | MEDICINE, RESEARCH & EXPERIMENTAL | CRISPR-CAS9 | MINICIRCLE DNA | MECHANISMS | TRANSPLANTATION | PLURIPOTENT STEM-CELLS | REPAIR | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | IN-VIVO | MOUSE MODEL | DISEASE | GENETICS & HEREDITY | GENE-THERAPY | Exons | Humans | Transplantation, Heterologous | Molecular Targeted Therapy | Epidermolysis Bullosa Dystrophica - pathology | Base Sequence | Keratinocytes - transplantation | Collagen Type VII - metabolism | Epidermolysis Bullosa Dystrophica - metabolism | Epidermolysis Bullosa Dystrophica - therapy | Gene Expression | Collagen Type VII - genetics | Treatment Outcome | Plasmids - metabolism | Keratinocytes - pathology | Animals | Keratinocytes - metabolism | Mice, Nude | CRISPR-Cas Systems | Plasmids - chemistry | Gene Editing - methods | High-Throughput Nucleotide Sequencing | Mice | Epidermolysis Bullosa Dystrophica - genetics | Mutation | Primary Cell Culture | Disease | Homology | Transplantation | Genomes | Proteins | Design | Reversion | Next-generation sequencing | Efficiency | Phenotypic reversion | Skin diseases | Nuclease | Localization | Deoxyribonucleic acid--DNA | CRISPR | Epidermolysis bullosa | Cloning | Immunodeficiency | Keratinocytes | Vectors (Biology) | Microscopy | Collagen | Skin | Gene therapy | Binding sites | Dystrophic epidermolysis bullosa | Index Medicus | Cas9 | Original
Journal Article
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