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Research 481–510 of 1000+
- The role of macrophages in skin homeostasis
- Regulatory T cells in inflammatory skin disease: from mice to humans
- Skin diseases in consequence of endocrine alterations
- Spironolactone May Reduce the Risk of Incident Rosacea
- 272 Structural changes in human skin after topical application of glucocorticoids assessed by in vivo imaging technologies
- GSDMA deficiency impairs cutaneous squamous cell carcinoma growth
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- 269 Down-regulatory role of cholecystokinin on psoriatic epidermal inflammation
- General Dermatology
- Emerging Therapies for Acne Vulgaris
- Alopecia Areata and Vitamin D3 Deficiency: The Potential of Calcipotriol as a Treatment
- Severe cutaneous adverse reactions to drugs
- Oral Manifestations of Hematologic and Nutritional Diseases
- Dermal Papilla Cells Serially Cultured with Wnt-10b Sustain their Hair Follicle Induction Activity after Transplantation into Nude Mice
- Various Applications of Tofacitinib and Ruxolitinib (Janus Kinase Inhibitors) in Dermatology and Rheumatology: A Review of Current Evidence and Future Perspective
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Stem cell dynamics, migration and plasticity during wound healing
- Vitamin D increases expression of cathelicidin in cultured sebocytes
- Mechanisms regulating skin immunity and inflammation
- Acne, the Skin Microbiome, and Antibiotic Treatment
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Next generation human skin constructs as advanced tools for drug development
- Mechanisms of Disease: selective inhibition of 11β-hydroxysteroid dehydrogenase type 1 as a novel treatment for the metabolic syndrome
- Skin disorders in Parkinson’s disease: potential biomarkers and risk factors
- What does acne genetics teach us about disease pathogenesis?
- Alopecia Areata
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Polymorphisms in androgen and estrogen receptor genes: effects on male aging
- Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia