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- Function and interactions of the Ysc84/SH3yl1 family of actin- and lipid-binding proteins
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Conditional knock out of N-WASP in keratinocytes causes skin barrier defects and atopic dermatitis-like inflammation
- Careless talk costs lives: fibroblast growth factor receptor signalling and the consequences of pathway malfunction
- PAK4 signaling in health and disease: defining the PAK4–CREB axis
- What does acne genetics teach us about disease pathogenesis?
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