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Research 31–60 of 1000+
- Skin-type-dependent development of murine mechanosensory neurons
- Humanized CXCL12 antibody delays onset and modulates immune response in alopecia areata mice: insights from single-cell RNA sequencing
- Type 2 Cytokine–Dependent Skin Barrier Regulation in Personalized 2-Dimensional and 3-Dimensional Skin Models of Atopic Dermatitis: A Pilot Study
- Promoter Methylation Changes in KRT17: A Novel Epigenetic Marker for Wool Production in Angora Rabbit
- Repairing the lungs one breath at a time: How dedicated or facultative are you?
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- Anagen hair follicles transplanted into mature human scars remodel fibrotic tissue
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- KRT6A derived from mesenchymal stem cells as a potential biomarker and therapeutic target for alopecia areata: insights from multi-omics analysis and experimental evidence
- Unlocking the genetic secrets of Dorper sheep: insights into wool shedding and hair follicle development
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Epithelial stem cells and implications for wound repair
- Hedgehog signaling maintains hair follicle stem cell phenotype in young and aged human skin
- Dermatopathology and molecular genetics
- Establishment of a culture model for the prolonged maintenance of chicken feather follicles structure in vitro
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- A novel point mutation of keratin 17 (<i>KRT17</i>) in a Japanese family with pachyonychia congenita type 2: an RNA-based genetic analysis using a single hair bulb
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep
- The Vitamin D Receptor Is a Wnt Effector that Controls Hair Follicle Differentiation and Specifies Tumor Type in Adult Epidermis
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Ovine Hair Follicle Stem Cells Derived from Single Vibrissae Reconstitute Haired Skin
- The Transcriptional Regulator Prdm1 Is Essential for the Early Development of the Sensory Whisker Follicle and Is Linked to the Beta-Catenin First Dermal Signal
- Screening of Protein Related to Wool Development and Fineness in Gansu Alpine Fine-Wool Sheep
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Keratins and disease at a glance