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Research 571–600 of 1000+
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Aqueous Dispersion of Unmodified Fullerene C60: Stimulation of Hair Growth and Study of a New Molecular Target for Interaction
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- Correlation analysis of four KRTAP gene polymorphisms and cashmere fiber diameters in two cashmere goat breeds
- Cutaneous wound healing: recruiting developmental pathways for regeneration
- New aspects of vitamin D metabolism and action — addressing the skin as source and target
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- Biotin and biotinidase deficiency
- Impaired wound healing in transgenic mice overexpressing the activin antagonist follistatin in the epidermis
- Fibroblast growth factors: key players in regeneration and tissue repair
- Estrogen and androgen signaling in the pathogenesis of BPH
- Agouti and Agouti-related Protein: Analogies and Contrasts
- Intracrine androgen biosynthesis, metabolism and action revisited
- What’s Sex Got to Do With COVID-19? Gender-Based Differences in the Host Immune Response to Coronaviruses
- TRP Channels in Skin Biology and Pathophysiology
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Targeting of Smoothened for therapeutic gain
- Disturbance of the Circadian System in Shift Work and Its Health Impact
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Notch Signaling Regulates Late-Stage Epidermal Differentiation and Maintains Postnatal Hair Cycle Homeostasis
- Unmet Medical Needs in Chronic, Non-communicable Inflammatory Skin Diseases
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation