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Research 181–210 of 580
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- Current and future pharmacotherapy for alopecia areata
- Biologic Therapies and Small-Molecule Inhibitors for Dissecting Cellulitis of the Scalp: A Systematic Review
- Endocrinologia e Medicina Estética Ed. X
- Would you recognize this lesion as a gumma syphilitica?
- Wnt/β-catenin and ERK pathway activation: The possible mechanism of various light-emitting diode light regulates the proliferation of human outer root sheath cells
- Wound management in hidradenitis suppurativa
- Abstracts from the 17th Congress of the European Society for Dermatology and Psychiatry
- Morphogenesis, Growth Cycle and Molecular Regulation of Hair Follicles
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Matrix Metalloproteinase-9 Is Involved in the Regulation of Hair Canal Formation
- Human Hair Keratin‐Associated Proteins (KAPs)
- Keratins: the hair shaft's backbone revealed
- Dynamic expression of Runx1 in skin affects hair structure
- Keratins of the Human Hair Follicle
- Hair follicle-specific keratins and their diseases
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Morphogenesis and Renewal of Hair Follicles from Adult Multipotent Stem Cells
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Analysis of Apoptotic Cell Death in Human Hair Follicles In Vivo andIn Vitro
- Expression patterns of keratin intermediate filament and keratin associated protein genes in wool follicles
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament