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Research 13
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Iron Metabolism of the Skin: Recycling versus Release
- Characterisation, genomic organisation, expression and function of the mEphA1 receptor Tyrosine Kinase
- An analysis of gene expression data involving examination of signaling pathways activation reveals new insights into the mechanism of action of minoxidil topical foam in men with androgenetic alopecia
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Integrated multiomics analysis reveals the molecular features and crucial regulators of hair follicles in yak (Bos grunniens)
- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- Genome-Wide Association Study for Udder Conformation Traits in Chinese Holstein Cattle
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Presence of Uterine Leiomyomas Has No Significant Impact on Gene Expression Profile in the Scalp of Patients with Central Centrifugal Cicatricial Alopecia
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Iron Deficiency in Immune-Mediated Inflammatory Skin Diseases: A Missing Link Between Systemic Inflammation, Immunometabolism, and Disease Burden
- The molecular anatomy of cashmere goat hair follicle during cytodifferentiation stage