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Research 271–300 of 1000+
- 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 EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- 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
- 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
- Molecular basis of congenital atrichia in humans and mice.
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Severe diffuse non-scarring hair loss in systemic lupus erythematosus - clinical and histopathological analysis of four cases
- 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
- Pathophysiology of the Burn Scar
- Atrichia with papular lesions
- Alopecia: Association with Resistance to Thyroid Hormones
- Lectinhistochemistry of Dorsal Skin of Wistar-derived Hypotrichotic WBN/Ila-Ht Rats.
- Alopecia in children
- In vitro skin permeation of hinokitiol loaded in vesicles composed of behenyltrimethylammonium chloride and stearic acid
- Congenital atrichia with papular lesions
- Another Way to Look at Donor Harvesting Effects with FUE
- Werewolf, there wolf: variants in <i>Hairless</i> associated with hypotrichia and roaning in the lykoi cat breed
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Terapia por el arte
- Automated quantitative analysis of coat and skin coloration in laboratory animals
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