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Research 571–600 of 1000+
- LOS ANGELES DERMATOLOGICAL SOCIETY
- Sequence and expression of human hair keratin genes
- Structural Hierarchy of Trichocyte Keratin Intermediate Filaments
- Identification of differentially expressed Gnαs and Gnα11 in sheep ( Ovis aries ) skins associated with white and black coat colors
- Retinoic Acid-Induced Epidermal Transdifferentiation in Skin
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Effect of Sonic Hedgehog on the Regeneration of Epidermal Texture Patterns
- Congenital milia En plaque on scalp
- Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis
- Immunolocalization of Scaffoldin, a Trichohyalin‐Like Protein, in the Epidermis of the Chicken Embryo
- Dermoscopy of skin infestations and infections (entomodermoscopy) – Part I: dermatozoonoses and bacterial infections
- Differential gene expression profiles in foetal skin of Rex rabbits with different wool density
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Changes in distribution pattern of CD8 lymphocytes in the scalp in alopecia areata during treatment with diphencyprone
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Skin development in the gray short‐tailed opossum (<i>Monodelphis domestica</i>)—From skin respiration to thermoregulation
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Enigma of Folliculitis Decalvans in Two Pediatric Sisters, Treated with Low-Dose Isotretinoin and Erythromycin
- Male Pattern Baldness – Symptoms, Causes, and Treatments
- Genetic analysis of a novel antioxidant multi-target iron chelator, M30 protecting against chemotherapy-induced alopecia in mice
- Hair growth control by follistatin
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia
- Pattern hair loss distribution: a novel presentation for alopecia areata
- Ultrastructure of the contrasting types of keratinization seen in the tail epidermis of the laboratory mouseMus musculus
- Transient agonism of the sonic hedgehog pathway triggers a permanent transition of skin appendage fate in the chicken embryo
- CPC12 Coinheritance of <i>BRCA2</i> and <i>CYLD</i> germline pathogenic variants associated with targetable metastatic malignant cylindroma