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Research 151–180 of 1000+
- FoxN1 in K14 promoter-driven epithelium is required for generation and maintenance of 3D-thymus medulla and preventing nude phenotype in the skin (36.33)
- Distinct fibroblast lineages determine dermal architecture in skin development and repair
- The Rotterdam Study: 2016 objectives and design update
- The Rotterdam Study: 2014 objectives and design update
- Laser hair removal
- Hedgehog signalling in skin development and cancer
- Bioprinting of skin constructs for wound healing
- Microencapsulating Alginate-Based Polymers for Probiotics Delivery Systems and Their Application
- Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat (Capra hircus)
- Human Epidermal Neural Crest Stem Cells (hEPI-NCSC)—Characterization and Directed Differentiation into Osteocytes and Melanocytes
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Simple and rapid method to isolate and culture follicular papillae from human scalp hair follicles
- Non-Edg family LPA receptors: the cutting edge of LPA research
- Integrated analysis of long non-coding RNA and mRNA expression in different colored skin of koi carp
- Reorganization of hair follicles in human skin organ culture induced by cultured human follicle-derived cells
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Sprouty/FGF signaling regulates the proximal–distal feather morphology and the size of dermal papillae
- The role of activins and follistatins in skin and hair follicle development and function
- Macrophages are necessary for skin regeneration during tissue expansion
- D’orenone blocks polarized tip growth of root hairs by interfering with the PIN2‐mediated auxin transport network in the root apex
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Whole-Cell Bioprocessing of Human Fetal Cells for Tissue Engineering of Skin
- A Review of Barbed Sutures—Evolution, Applications and Clinical Significance
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Contact Dermatitis Associated With Nail Care Products: Retrospective Analysis of North American Contact Dermatitis Group Data, 2001–2016
- Yellow facial papules associated with frontal fibrosing alopecia: A distinct histologic pattern and response to isotretinoin
- The scope of the dermoscope
- Basonuclin as a cell marker in the formation and cycling of the murine hair follicle
- Induction of ornithine decarboxylase in specific subpopulations of murine epidermal cells following multiple exposures to 12-<i>O</i>-tetradecanoylphorbol-13-acetate, mezerein and ethyl phenylpropriolate