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Research 61–90 of 178
- DNA Methylation‐Regulated ZDHHC17 Promotes the Risk of Facial Skin Aging
- Dermatologia e Procedimentos Estéticos Ed. XVIII
- Hair-raising Mysteries of the Inner Root Sheath: Unearthing Treasures in Bald Spots
- Wasabi leaf extract changes the expression levels of cytokine related genes in dermal papilla cells, which identified by the whole transcriptome
- Christmas article: Case of uncombable hair syndrome discovered after publication of article in Ugeskrift for Læger
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Inherited Epidermolysis Bullosa: A Clinical Case
- Endocrine Management of Adult Gender-Dysphoric/Gender-Incongruent Persons: A Clinical Practice Guideline from Endocrine Society of India
- Uncombable hair improved by biotin
- Ichthyoses
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Mechanical Stretching Can Modify the Papillary Dermis Pattern and Papillary Fibroblast Characteristics during Skin Regeneration
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- Restoration of Hair Luster via Novel Biomarker COL7A1 by Minoxidil, Caffeine, and Biotin
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Collodion baby to bathing suit ichthyosis: A 6-year follow-up
- 078 The transmembrane protein LRIG1 regulates receptor tyrosine kinases in skin development and homeostasis
- NFATc1 Balances Quiescence and Proliferation of Skin Stem Cells
- The complex relationship between TFEB transcription factor phosphorylation and subcellular localization
- Cell-Type-Specific Chromatin States Differentially Prime Squamous Cell Carcinoma Tumor-Initiating Cells for Epithelial to Mesenchymal Transition