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Research 211–240 of 1000+
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Converging physiological roles of the anthrax toxin receptors
- Bikunin, a Serine Protease Inhibitor, is Present on the Cell Boundary of Epidermis
- Female pattern hair loss—An update
- Pharmacotherapy of plexiform neurofibromas in patients with neurofibromatosis type 1. Possible adverse events and their management
- Expression of Hypothalamic–Pituitary–Thyroid Axis RelatedGenes in the Human Skin
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- YAP1 promotes adipogenesis by regulating the negative feedback mechanism of the Hippo signaling pathway via LATS2
- Polymorphisms in androgen and estrogen receptor genes: effects on male aging
- The Genetics of Human Skin Disease
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Targeted expression of SV40 T antigen in the hair follicle of transgenic mice produces an aberrant hair phenotype
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- The cutaneous serotoninergic/melatoninergic system: securing a place under the sun
- In vivo transcriptional governance of hair follicle stem cells by canonical Wnt regulators
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Vitamin D Receptor Gene Polymorphism In Chronic Telogen Effluvium; A Case-Control Study
- The urine as a diagnostic key for a homozygous EGFR mutation
- Methylated CpG dinucleotides in 5-α reductase 2 gene might explain the finasteride-resistance in BPE patients
- Safety Profile of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors: A Disproportionality Analysis of FDA Adverse Event Reporting System
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Dietary isoflavone increases insulin-like growth factor-I production, thereby promoting hair growth in mice
- Comparative study on seasonal hair follicle cycling by analysis of the transcriptomes from cashmere and milk goats
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Role of vitamin D and calcium signaling in epidermal wound healing
- Androgen Receptor in Human Health: A Potential Therapeutic Target
- Single-cell chromatin landscapes of mouse skin development
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters