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Research 901–930 of 1000+
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- An Extended Epidermal Response Heals Cutaneous Wounds in the Absence of a Hair Follicle Stem Cell Contribution
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Inactivation of the Vitamin D Receptor Enhances Susceptibility of Murine Skin to UV-Induced Tumorigenesis
- WNT Signaling in Disease
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Cell death in the skin
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- The Tissue-dependent Keratin 19 Gene Transcription Is Regulated by GKLF/KLF4 and Sp1
- Small extracellular vesicles from menstrual blood-derived mesenchymal stem cells (MenSCs) as a novel therapeutic impetus in regenerative medicine
- Integument pattern formation involves genetic and epigenetic controls: feather arrays simulated by digital hormone models.
- FGF Family: From Drug Development to Clinical Application
- Cell fate decisions: emerging roles for metabolic signals and cell morphology
- Fluorescence Microscopy—An Outline of Hardware, Biological Handling, and Fluorophore Considerations
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis
- NEDD4 and NEDD4L regulate Wnt signalling and intestinal stem cell priming by degrading LGR5 receptor
- Hox genes in development and beyond
- Recent progress in the manipulation of biochemical and biophysical cues for engineering functional tissues
- KGF and EGF signalling block hair follicle induction and promote interfollicular epidermal fate in developing mouse skin
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Protein kinase Cepsilon is linked to 12-O-tetradecanoylphorbol-13-acetate-induced tumor necrosis factor-alpha ectodomain shedding and the development of metastatic squamous cell carcinoma in protein kinase Cepsilon transgenic mice.
- A Review of the Use of Biotin for Hair Loss
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Hair follicles’ transit-amplifying cells govern concurrent dermal adipocyte production through Sonic Hedgehog
- Roles of the Hedgehog Signaling Pathway in Epidermal and Hair Follicle Development, Homeostasis, and Cancer
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Viral-associated trichodysplasia spinulosa: a case with electron microscopic and molecular detection of the trichodysplasia spinulosa-associated human polyomavirus
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome