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Research 931–960 of 1000+
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Hepatic Adenoma in an Adolescent With Elevated Androgen Levels
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Esrp1-Regulated Splicing of Arhgef11 Isoforms Is Required for Epithelial Tight Junction Integrity
- Hair and nail diseases in the mature patient
- Isolation and Characterization of a Novel Hair Follicle–Specific Gene, Hacl-1
- Preparation and hemostatic mechanism of bioactive glass-based membrane-like structure camouflage composite particles
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- Prevention of Follicular Penetration: Barrier-Enhancing Formulations against the Penetration of Pollen Allergens into Hair Follicles
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- [Retracted] Fibroblasts in Scar Formation: Biology and Clinical Translation
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Current and future outlook of loaded components in hydrogel composites for the treatment of chronic diabetic ulcers
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- Gynecologic and andrologic dermatology and the metabolic syndrome
- Multiple potential roles of thymosin β4 in the growth and development of hair follicles
- A second <i>KRT</i>71 allele in curly coated dogs
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Structure and expression of the ovine Hoxc-13 gene
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Engineering strategies to enhance the research progress of mesenchymal stem cells in wound healing
- ACKR2 limits skin fibrosis and hair loss through IFN‐β
- Different synaptic stimulation patterns influence the local androgenic and estrogenic neurosteroid availability triggering hippocampal synaptic plasticity in the male rat
- Use of a Sustained Release Preparation of Clotrimazole to Treat Dermatophytosis in a Siamang (Hylobates syndactylus)
- Topical spermine and putrescine stimulated DNA synthesis in the hairless mouse epidermis
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- Chitosan Hydrogel as Tissue Engineering Scaffolds for Vascular Regeneration Applications