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Research 421–450 of 1000+
- Dynamic expression of Runx1 in skin affects hair structure
- Alleviation of Severe Skin Insults Following High-Dose Irradiation with Isolated Human Fetal Placental Stromal Cells
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Signaling Involved in Hair Follicle Morphogenesis and Development
- ATRICHIA WITH PAPULAR LESIONS – A CASE REPORT
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- DNA Methylation as an Epigenetic Memory Keeper during Skin Development and Regeneration
- A decade of neglecting sublingual mass: A case report of epidermoid cyst
- A Scarless Healing Tale: Comparing Homeostasis and Wound Healing of Oral Mucosa With Skin and Oesophagus
- Aging in the sebaceous gland
- Molecular Mechanisms Regulating Hair Follicle Development
- Identification of Stem Cell Populations in Sweat Glands and Ducts Reveals Roles in Homeostasis and Wound Repair
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Tissue engineering of skin and regenerative medicine for wound care
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- WNT Signaling in Disease
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- The Role of Vitamins and Minerals in Hair Loss: A Review
- Cell death in the skin
- Integument pattern formation involves genetic and epigenetic controls: feather arrays simulated by digital hormone models.
- Development and homeostasis of the sebaceous gland
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Keratins and disease at a glance
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions