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Research 631–660 of 1000+
- Is knowledge about the genetic and epigenetic alterations in melanoma a basis for targeted therapy?
- ENZYMES
- Follicular and Scarring Disorders in Skin of Color: Presentation and Management
- Regulation of cashmere fineness traits by noncoding RNA in Jiangnan cashmere goats
- Comparative aspects of the inner root sheath in adult and developing hairs of mammals in relation to the evolution of hairs
- Melanocytes in regenerative medicine applications and disease modeling
- The Functional Relevance of the Type 1 Cytokines IFN-γ and IL-2 in Alopecia Areata of C3H/HeJ Mice
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Symposium Proceedings of the 4th Intercontinental Meeting of Hair Research Societies: “The World of Hair 2004”
- The Distribution of Estrogen Receptor β Is Distinct to That of Estrogen Receptor α and the Androgen Receptor in Human Skin and the Pilosebaceous Unit
- Cultured Peribulbar Dermal Sheath Cells Can Induce Hair Follicle Development and Contribute to the Dermal Sheath and Dermal Papilla
- The role of androgen and androgen receptor in skin-related disorders
- Gender aspects in skin diseases
- Androgen receptor gene polymorphisms and risk for androgenetic alopecia: a meta-analysis
- Gene expression of type 2 17β hydroxysteroid dehydrogenase in scalp hairs of hirsute women
- The great atopic diseases epidemic: does chemical exposure play a role?
- Significance of iron status in hair loss in women
- Main Plenary Sessions: Summaries of Papers
- Cutaneous Androgen Metabolism: Basic Research and Clinical Perspectives
- Obesity and the skin
- Oxidative Activity of the Type 2 Isozyme of 17β-Hydroxysteroid Dehydrogenase (17β-HSD) Predominates in Human Sebaceous Glands
- Morphological Approach to Hair Disorders
- Macrophage-Stimulating Protein Promotes Hair Growth Ex Vivo and Induces Anagen from Telogen Stage Hair Follicles In Vivo
- Clinical relevance of hair microscopy in alopecia
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- Main Plenary Sessions: Summaries of Papers
- Abstracts
- British Society for Dermatopathology: Summaries of Papers
- Lentiginosis within plaques of linear atrophoderma of Moulin: a twin-spotting phenomenon?