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Research 511–540 of 1000+
- Orai1 expression pattern in tooth and craniofacial ectodermal tissues and potential functions during ameloblast differentiation
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- Atrichia with papular lesions
- Alteration in Hair Texture Following Regrowth in Alopecia Areata
- Psychological Aspects of Hair Disorders: Consideration for Dermatologists, Cosmetologists, Aesthetic, and Plastic Surgeons
- Common causes of paediatric alopecia
- Trichoscopy pattern in alopecia areata: A systematic review and meta‐analysis
- Not just thinning: A case of alopecia universalis after mild COVID-19
- Physiology of Skin, Hair, and Nails as Differentiated by Sex and Age
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Viva questions from the IJDVL
- Mesoterapia. Una revisión crítica
- Hair follicle immune privilege and its collapse in alopecia areata
- Molecular Mechanisms Regulating Hair Follicle Development
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Mineral Malnutrition Following Bariatric Surgery
- Human hair keratin and its-based biomaterials for biomedical applications
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Progressive Alopecia Reveals Decreasing Stem Cell Activation Probability during Aging of Mice with Epidermal Deletion of DNA Methyltransferase 1
- Chemical Composition of Different Hair Types
- Hair regrowth in alopecia areata patients following Stem Cell Educator therapy
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Alopecia areata: What’s new in the epidemiology, comorbidities, and pathogenesis?
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- CD34 <sup>+</sup> cell–derived fibroblast-macrophage cross-talk drives limb ischemia recovery through the OSM-ANGPTL signaling axis
- Ichthyosis with confetti: clinics, molecular genetics and management
- Runx3 is involved in hair shape determination
- Clinical and histological challenge in the differential diagnosis of diffuse alopecia: female androgenetic alopecia, telogen effluvium and alopecia areata – part II
- Genetic Hair Disorders: A Review