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Research 421–450 of 1000+
- Handbook of Mouse Mutations with Skin and Hair Abnormalities: Animal Models and Biomedical Tools
- The role of vitamin D receptor mutations in the development of alopecia
- Biology and Genetics of Hair
- Learning from nudity: lessons from the nude phenotype
- Development and progression of alopecia in the vitamin D receptor null mouse
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- 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.
- Beauty is skin deep: the fascinating biology of the epidermis and its appendages.
- Quantification of the Vitamin D Receptor−Coregulator Interaction
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Increased rate of hair keratin gene loss in the cetacean lineage
- The nude gene and the skin
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- The development of several organs and appendages is impaired in mice lacking Sp6
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Sheep vibrissa dermal papillae induce hair follicle formation in heterotypic skin equivalents
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Molecular basis of congenital atrichia in humans and mice.
- Dermatopathology and molecular genetics
- Hair Restoration Surgery in Patients with Hypotrichosis of the Pubis
- A mutation in MAP2 is associated with prenatal hair follicle density
- A RARE FORM OF SUPPURATING AND CICATRIZING DISEASE OF THE SCALP
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Pleiotropic effects of the nude mutation.