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Research 31–60 of 818
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- CRISPR/Cas9-mediated Generation of<i>COL7A1</i>-deficient Keratinocyte Model of Recessive Dystrophic Epidermolysis Bullosa
- Niche work when you can get it: collagen XVII and the melanocyte stem cell
- New developments in the molecular treatment of ichthyosis: review of the literature
- An <i>mTurq2-Col4a1</i> mouse model allows for live visualization of mammalian basement membrane development
- Hair Follicle Stem Cells Provide a Functional Niche for Melanocyte Stem Cells
- Signature selection analysis reveals candidate genes associated with production traits in Iranian sheep breeds
- Integration Analysis of Transcriptome and Proteome Reveal the Mechanisms of Goat Wool Bending
- Single-Cell Sequencing Reveals Differential Cell Types in Skin Tissues of Liaoning Cashmere Goats and Key Genes Related Potentially to the Fineness of Cashmere Fiber
- Keratinocyte Stem Cells: Role in Aging
- Screening and expression validation of key proteins for secondary hair follicle growth in cashmere goats based on iTRAQ quantitative proteomics technology
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Novel Strategy for Hair Regeneration: Exosomes and Collagenous Sequences of Human a1(XVII) Chain Enhance Hair Follicle Stem Cell Activity by Regulating the hsa-novel-238a-CASP9 Axis
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Whole-genome bisulfite sequencing of goat skins identifies signatures associated with hair cycling
- 129 Genetic transformation of keratoacanthoma-type cutaneous squamous cell carcinoma following intralesional chemotherapy
- 130 Expression of nidogen1 in basal cell carcinoma
- Long-Term Survival of Type XVII Collagen Revertant Cells in an Animal Model of Revertant Cell Therapy
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Ichthyosis with confetti: clinics, molecular genetics and management
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Skin Development and Disease: A Molecular Perspective
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis