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Research 61–90 of 757
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- Case of non-Herlitz junctional epidermolysis bullosa with<i>COL17A1</i>mutation
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- 454 Modeling epidermolysis bullosa simplex with cardiomyopathy using KLHL24-mutant pluripotent stem cells.
- Localized variant of junctional epidermolysis bullosa with R795X mutation
- 259 Scalp hair follicle dermal sheath fibroblasts express genes associated with promotion of skin integrity/wound healing and prevention of autoimmune responses in Recessive Dystrophic Epidermolysis Bullosa
- Antiviral drugs prolong survival in murine recessive dystrophic epidermolysis bullosa
- CRISPR/Cas9-mediated Generation of<i>COL7A1</i>-deficient Keratinocyte Model of Recessive Dystrophic Epidermolysis Bullosa
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- 577 Successful allogeneic epidermal grafting of chronic recessive dystrophic epidermolysis bullosa wounds from hematopoietic cell donors in the outpatient setting
- The dental needs of children with Epidermolysis Bullosa and service delivery: a scoping review
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- 301 The Spectrum of PLEC Sequence Variants and Related Plectinopathies Including Novel Association with Epidermolysis Bullosa Pruriginosa
- Three Novel Homozygous Point Mutations and a New Polymorphism in the COL17A1 Gene: Relation to Biological and Clinical Phenotypes of Junctional Epidermolysis Bullosa
- 441 Anti-melanoma gene signature in dermal sheath fibroblasts from scalp hair follicles in Recessive Dystrophic Epidermolysis Bullosa (RDEB)
- Keratins of the Human Hair Follicle
- Keratin gene mutations in disorders of human skin and its appendages
- Keratin disorders: from gene to therapy
- Keratins and disease at a glance
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- Keratins and skin disease
- Mechanical forces in skin disorders
- The keratins and their disorders
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- Thymosin β4 Promotes Dermal Healing
- KERATINS AND SKIN DISORDERS
- The Genetics of Human Skin Disease
- Advances in a rapidly emerging field of hair follicle stem cell research.
- Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids