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Research 361–390 of 1000+
- In vivo monitoring of hair cycle stages via bioluminescence imaging of hair follicle NG2 cells
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Virilizing insulinoma
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Hair follicle development and related gene and protein expression of skins in Rex rabbits during the first 8 weeks of life
- The relationship among androgens, insulin resistanceand ghrelin polymorphisms in post-adolescent malepatients with severe acne vulgaris
- The role of versican in the skin ECM and its interaction with hyaluronic acid
- Effect of inhibiting prolactin secretion on secondary hair follicle development in cashmere goats
- Pilomatrixoma of the Forearm in an Elderly Male
- Genetic Fate Mapping Using Site-Specific Recombinases
- Supplementary Methods, Tables 1-2 and Figures from Tumor Stroma–Derived Wnt5a Induces Differentiation of Basal Cell Carcinoma of <i>Ptch</i>-Mutant Mice via CaMKII
- Characterization of Human KAP24.1, A Cuticular Hair Keratin-Associated Protein with Unusual Amino-Acid Composition and Repeat Structure
- Recombinant Goat VEGF164 Increases Hair Growth by Painting Process on the Skin of Shaved Mouse
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Recently Identified Forms of Epidermolysis Bullosa
- Persistent hair growth during treatment with the EGFR inhibitor erlotinib
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Impaired wound healing in transgenic mice overexpressing the activin antagonist follistatin in the epidermis
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Intratumoral <i>De Novo</i> Steroid Synthesis Activates Androgen Receptor in Castration-Resistant Prostate Cancer and Is Upregulated by Treatment with CYP17A1 Inhibitors
- Human Hair Keratin‐Associated Proteins (KAPs)
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Novel Type I Hair Keratins K39 and K40 Are the Last to be Expressed in Differentiation of the Hair: Completion of the Human Hair Keratin Catalog