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Research 781–810 of 1000+
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Monilethrix
- Monilethrix in three generations
- Genetic Susceptibility to Alopecia
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Beyond Wavy Hairs
- An Update of Congenital Adrenal Hyperplasia
- Delayed Wound Healing in Keratin 6a Knockout Mice
- WNT Signaling in Disease
- Regulatory T Cells: the Many Faces of Foxp3
- Frizzled Receptors in Development and Disease
- Concise Review: Wnt Signaling Pathways in Skin Development and Epidermal Stem Cells
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Melanocytes: The new Black
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Generalized atrophic benign epidermolysis bullosa.
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- Lymphoid Enhancer-binding Factor-1 (LEF1) Interacts with the DNA-binding Domain of the Vitamin D Receptor
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- The Dynamic Duo: Niche/Stem Cell Interdependency
- Hairless is a nuclear receptor corepressor essential for skin function
- The vitamin D receptor, the skin and stem cells
- The ITGB6 gene: its role in experimental and clinical biology