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Research 541–570 of 1000+
- Human Hair as a Testing Substrate in the Era of Precision Medicine: Potential Role of ‘Omics-Based Approaches
- Acquired progressive kinking of the hair in a Korean female adolescent
- A unique presentation of trichofolliculoma in amniotic band syndrome
- Expression of the Wnt signaling pathway and hair follicle development in Rex rabbits of different ages
- Functional analysis of the PIP5K1A gene in Liaoning Cashmere goats: an investigation based on bioinformatics, tissue localization, and biological functions
- Effects of FGF5-mediated LncRNA on the skin fibroblast growth of Liaoning Cashmere goats
- Molecular Mechanisms Affecting Development of Animal Fibers and Some Studies on Goats
- Microscopic high-resolution digital volumetric imaging of human hair fibers
- A reciprocal lattice approach to assessing the luster of hair fibers, based on scattering by periodically deformed cylinders
- Book Reviews
- ANNOUNCEMENTS
- Hair shaft disorders
- Efecto Inmunohistoquímico de la Vitamina E y el Ácido Valproico en el Desarrollo de Epidermis y Folículos Pilosos
- Christmas article: Case of uncombable hair syndrome discovered after publication of article in Ugeskrift for Læger
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Two females with hair loss
- Oncogenes and morphogens: intricacies of targeted therapy in cutaneous basal cell carcinoma
- Contents list
- Effect of neurosteroid dehydroepiandrosterone on the higher nervous activity of old non-human primates
- Canine alopecia X
- The human keratins: biology and pathology
- Mechanisms regulating skin immunity and inflammation
- Harmless Herbs? A Review of the Recent Literature
- The Dynamics of the Skin’s Immune System
- Single-cell analysis reveals fibroblast heterogeneity and myeloid-derived adipocyte progenitors in murine skin wounds
- <i>Hoxc13</i> mutant mice lack external hair
- Nutritional factors and hair loss
- Hair follicle differentiation and regulation.
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia