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Research 631–660 of 1000+
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Secondary Syphilis in Cali, Colombia: New Concepts in Disease Pathogenesis
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Neural Potential of a Stem Cell Population in the Hair Follicle
- Scarless wound healing: Transitioning from fetal research to regenerative healing
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Fabrication of Bilayer Nanofibrous-Hydrogel Scaffold from <i>Bacterial Cellulose</i>, <i>PVA</i>, and <i>Gelatin</i> as Advanced Dressing for Wound Healing and Soft Tissue Engineering
- Vitiligo - Part 2 - classification, histopathology and treatment
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Application of microneedle patches for drug delivery; doorstep to novel therapies
- Hair follicles’ transit-amplifying cells govern concurrent dermal adipocyte production through Sonic Hedgehog
- PRC 2 preserves intestinal progenitors and restricts secretory lineage commitment
- Alkylation of human hair keratin for tunable hydrogel erosion and drug delivery in tissue engineering applications
- Liposomal Packaging Generates Wnt Protein with In Vivo Biological Activity
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- PD-1+CXCR5−CD4+T cells are correlated with the severity of systemic lupus erythematosus
- Production-scale fibronectin nanofibers promote wound closure and tissue repair in a dermal mouse model
- Anabolic androgenic steroids and carcinogenicity focusing on Leydig cell: a literature review
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Narrative Review: Bioactive Potential of Various Mushrooms as the Treasure of Versatile Therapeutic Natural Product
- New insights into the role of Runx1 in epithelial stem cell biology and pathology
- Role of FGFR2-signaling in the pathogenesis of acne
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- Augmenting Endogenous Wnt Signaling Improves Skin Wound Healing
- Comparison of two ASC-derived therapeutics in an in vitro OA model: secretome versus extracellular vesicles
- Receptor activator of NF-κB (RANK) stimulates the proliferation of epithelial cells of the epidermo-pilosebaceous unit
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Sostdc1 defines the size and number of skin appendage placodes