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Research 211–240 of 1000+
- Molecular Regulation and Cellular Heterogeneity in Skin Repair and Hair Follicle Regeneration
- Microporous Dermal-Like Electrospun Scaffolds Promote Accelerated Skin Regeneration
- Faculty Opinions recommendation of Bald scalp in men with androgenetic alopecia retains hair follicle stem cells but lacks CD200-rich and CD34-positive hair follicle progenitor cells.
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- α3β1-integrin regulates hair follicle but not interfollicular morphogenesis in adult epidermis
- Elucidating the roles of three β-glucuronosyltransferases (GLCATs) acting on arabinogalactan-proteins using a CRISPR-Cas9 multiplexing approach in Arabidopsis
- Hair Disorders
- Biocompatibility of hair follicle stem cells and heterogeneous bladder acellular matrixat
- [Netherton's syndrome in two sisters].
- Defective trophoblast function in mice with a targeted mutation of Ets2
- [Mechanism of rat sciatic nerve regeneration induced by human hair keratin].
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- P-18 THREE BODY PROBLEM PATIENT: EHLER DANLOS SYNDROME COMBINED WITH HYPOPHOSPHATASIA AND FATTY ACID OXIDATION DEFECT
- The Evaluation and Treatment of Hirsute Women
- Extracellular vesicles released from irradiated neonatal mouse cheek tissue increased cell survival after radiation
- Vitamin Deficiency, Dependency, and Toxicity
- Skin Graft
- Free skin grafts in dogs-A review
- Glycogen content of tissues during healing of skin wounds in albino mice
- Calcitriol-resistant rickets with alopecia
- Alopecia totalis in an infant
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Extra-Intestinal Manifestation of Celiac Disease in Children
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Scalp Alopecia Reconstruction
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- A Rare Case of Acrodermatitis Enteropathica in a One Year Old Child