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Research 811–840 of 1000+
- Drug Repurposing for Rare Diseases
- Challenges, Progress, and Prospects of Developing Therapies to Treat Autoimmune Diseases
- Mitochondrial Complex I Activity Suppresses Inflammation and Enhances Bone Resorption by Shifting Macrophage-Osteoclast Polarization
- The Biological Actions of Dehydroepiandrosterone Involves Multiple Receptors
- Patched1 Functions as a Gatekeeper by Promoting Cell Cycle Progression
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Skin Pigmentation Types, Causes and Treatment—A Review
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Recurrent implantation failure: A comprehensive summary from etiology to treatment
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Frizzled Receptors in Development and Disease
- The structure of people’s hair
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Trichoscopy in alopecias: Diagnosis simplified
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Secondary Syphilis in Cali, Colombia: New Concepts in Disease Pathogenesis
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Aging of the hair follicle pigmentation system
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Physiopathology of polycystic ovary syndrome in endocrinology, metabolism and inflammation
- Hair Tissue Mineral Analysis and Metabolic Syndrome
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Scoping Review on the Use of Drugs Targeting JAK/STAT Pathway in Atopic Dermatitis, Vitiligo, and Alopecia Areata