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Research 691–720 of 1000+
- Replicative stress, stem cells and aging
- Wnt signaling: the good and the bad
- Alopecia areata
- Learning from nudity: lessons from the nude phenotype
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Viewpoint 6
- The nude gene and the skin
- Experimental cutaneous Bacillus anthracis infections in hairless HRS/J mice
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Recent advances on skin‐resident stem/progenitor cell functions in skin regeneration, aging and cancers and novel anti‐aging and cancer therapies
- What causes acne inversa (or hidradenitis suppurativa)? – the debate continues
- What causes acne inversa (or hidradenitis suppurativa)? – The debate continues
- Is knowledge about the genetic and epigenetic alterations in melanoma a basis for targeted therapy?
- 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”
- Morphological Approach to Hair Disorders
- Main Plenary Sessions: Summaries of Papers
- Abstracts
- British Society for Dermatopathology: Summaries of Papers
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Clinical Snippets
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats