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Research 31–60 of 1000+
- Genetic architecture of mouse skin inflammation and tumour susceptibility
- Epidermal Wnt/β-catenin signaling regulates adipocyte differentiation via secretion of adipogenic factors
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- A role of melatonin in neuroectodermal‐mesodermal interactions: the hair follicle synthesizes melatonin and expresses functional melatonin receptors
- The Keratins of the Human Beard Hair Medulla: The Riddle in the Middle
- Anti-ageing effect of a lactococcal strain: analysis using senescence-accelerated mice
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- NUDT15 R139C-related thiopurine leukocytopenia is mediated by 6-thioguanine nucleotide-independent mechanism in Japanese patients with inflammatory bowel disease
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Bioengineering a 3D integumentary organ system from iPS cells using an in vivo transplantation model
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- A new catalyst for organic synthesis: mercuric triflate
- Beta-caryophyllene enhances wound healing through multiple routes
- Measurement of Skin Permeation/Penetration of Nanoparticles for Their Safety Evaluation
- Hair organ regeneration via the bioengineered hair follicular unit transplantation
- Ethanol Patch Test—A Simple and Sensitive Method for Identifying ALDH Phenotype
- Life before and beyond blistering: The role of collagen XVII in epidermal physiology
- Sex Steroid Hormone Receptors in Human Skin Appendage and its Neoplasms
- Vitamin D‐dependent rickets type I and type II
- Hair Regeneration Therapy: Application of Adipose-Derived Stem Cells
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- Embryonic hair follicle fate change by augmented β-catenin through Shh and Bmp signaling
- Phospholipase C‐δ1 is an essential molecule downstream of <i>Foxnl,</i> the gene responsible for the nude mutation, in normal hair development
- An immunohistochemical study of the apocrine type of cutaneous mixed tumors with special reference to their follicular and sebaceous differentiation
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Effects of aromatase inhibitors on human osteoblast and osteoblast-like cells: A possible androgenic bone protective effects induced by exemestane
- Pharmacological Mobilization of Endogenous Stem Cells Significantly Promotes Skin Regeneration after Full-Thickness Excision: The Synergistic Activity of AMD3100 and Tacrolimus
- Epithelial skirt and bulge of human facial vellus hair follicles and and associated Merkel cell-nerve complex