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Research 631–660 of 1000+
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Roles of the Hedgehog Signaling Pathway in Epidermal and Hair Follicle Development, Homeostasis, and Cancer
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Cylindroma as Tumor of Hair Follicle Origin
- Multiple cyclic nucleotide‐gated channels coordinate calcium oscillations and polar growth of root hairs
- Embryonic hair follicle fate change by augmented β-catenin through Shh and Bmp signaling
- Identification of Ectodysplasin Target Genes Reveals the Involvement of Chemokines in Hair Development
- Regulation of a hair follicle keratin intermediate filament gene promoter
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- Morphological Approach to Hair Disorders
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle
- Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity
- State-dependent signaling by Ca<sub>v</sub>1.2 regulates hair follicle stem cell function
- Cholesterol homeostasis: Links to hair follicle biology and hair disorders
- hKAP1.6 and hKAP1.7, Two Novel Human High Sulfur Keratin-Associated Proteins are Expressed in the Hair Follicle Cortex
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Molecular Conversations and the Development of the Hair Follicle and Basal Cell Carcinoma
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- UDP-GlcNAc-1-Phosphotransferase Is a Clinically Important Regulator of Human and Mouse Hair Pigmentation
- Structural optimization of pep7, a small peptide extracted from epimorphin, for effective induction of hair follicle anagen
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Congenital atrichia with papular lesions
- The Dark Side of Gefitinib: Reflectance Confocal Microscopy Applied to Hair Hyperpigmentation
- Porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus: Is nomenclature “porokeratotic adnexal ostial nevus” more appropriate?
- Monilethrix, a rare inherited hair shaft disorder in siblings