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Research 121–150 of 1000+
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- Two Mechanisms Regulate Keratin K15 Expression In Keratinocytes: Role of PKC/AP-1 and FOXM1 Mediated Signalling
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Ferulic Acid Induces Keratin 6α via Inhibition of Nuclear β-Catenin Accumulation and Activation of Nrf2 in Wound-Induced Inflammation
- Assessing the efficacy of mesotherapy products: Ultra Exo Booster, and Ultra S Line Plus in hair growth: An ex vivo study
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Multi-Modal Imaging to Assess the Follicular Delivery of Zinc Pyrithione
- DNA Damage-Inducible Transcript 4 Is an Innate Surveillant of Hair Follicular Stress in Vitamin D Receptor Knockout Mice and a Regulator of Wound Re-Epithelialization
- Hair follicle immune privilege in autoimmune and immune-mediated alopecias: paths toward reestablishing immune tolerance
- Folliculitis decalvans: a multicentre review of 82 patients
- An Innovative Formula for Keratosis Pilaris Treatment—A Randomized Controlled Study Based on the “Exfoliation‐Dissolution‐Repair” Concept
- Generalized multiple eruptive milia in an infant – An unusual presentation
- Dermatoscopy case of the month: Trichodysplasia spinulosa
- Gate keeping the sebaceous gland
- Extensive Nevus Comedonicus Along the Lines of Blaschko – Through the Eyes of Dermoscope and Histopathology
- Demodicosis of Ophthalmic Concern
- Impaired Notch‐MKP‐1 signalling in hidradenitis suppurativa: an approach to pathogenesis by evidence from translational biology
- Normolipemic xanthoma associated with folliculotropic mycosis fungoides
- What causes acne inversa (or hidradenitis suppurativa)? – the debate continues
- A case of eruptive lichen spinulosus after toxic epidermal necrolysis
- Viewpoint 2
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Traumatic anserine folliculosis
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- The Overexpression of Tβ4 in the Hair Follicle Tissue of Alpas Cashmere Goats Increases Cashmere Yield and Promotes Hair Follicle Development
- What causes acne inversa (or hidradenitis suppurativa)? – The debate continues
- Alopecia Areata in a Dog: Clinical, Dermoscopic and Histological Features
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- The clinicopathological spectrum of preclinical folliculitis keloidalis with correlation to its dermoscopic features: a cross‐sectional analytical study