Search
forResearch 10 of 228
- Filaggrin mutations as an archetype for understanding the pathophysiology of atopic dermatitis
- Skin diseases associated with atopic dermatitis
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Overlapping features of atopic dermatitis and alopecia areata: from pathogenesis to treatment
- Editors' Picks
- Plain language summaries
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Cutaneous gain-of-function mutation of LRIG3 leads to alopecia by upregulation of ERBB, PI3K/AKT, NOTCH1 signaling pathways
- Potential genetic associations of acne scar phenotypes: IL1A in fibrotic scarring and CYB5R1 in atrophic scarring
- 9. Immunology and Genetics
Learn
— no results
Try a deeper search in learn →Community
— no results
Try a deeper search in community →