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Research 691–720 of 1000+
- Invasion and increased expression of S100A4 and CYR61 in mesenchymal transformed breast cancer cells is downregulated by GnRH
- Scalp microbiome of healthy women wearing hijab compared to those not wearing hijab: a cross-sectional study
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Primary High‐Grade Ovarian Sertoli–Leydig Cell Tumor With Bilateral Adnexal Involvement in a Patient Diagnosed With Peutz–Jeghers Syndrome
- Repurposing of approved cardiovascular drugs
- Specific Citrullination Causes Assembly of a Globular S100A3 Homotetramer
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Exosome-based cell therapy for diabetic foot ulcers: Present and prospect
- Hutchinson-Gilford progeria syndrome - A brief introduction
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Functional Skin Grafts: Where Biomaterials Meet Stem Cells
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Eyelash Trichomegaly: A Rare Presenting Feature of Systemic Lupus Erythematosus.
- Evidence for 1,25-Dihydroxyvitamin D3-independent Transactivation by the Vitamin D Receptor
- The role of the microbiome in scalp hair follicle biology and disease
- Whole Neonatal Cochlear Explants as an <em>In vitro</em> Model
- Role of Sulfur Metabolism Gene and High-Sulfur Gene Expression in Wool Growth Regulation in the Cashmere Goat
- hUC-MSC-exosomes deliver Let-7b/7f-5p to dermal papilla cells for a multi-target synergistic treatment of androgenetic alopecia
- The Wound Healing: A Mystery Still to Be Solved—What Is the Future?
- Smart bacteriophage release from bovine β-lactoglobulin fibrils based hydrogel with anti-MRSA, biofilm degradation and hair follicle regeneration functions for infected burn wound