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Research 481–510 of 1000+
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Facial pore refining by targeting dermal and epidermal functions: Assessment across age and gender
- Pigment epithelium‑derived factor short peptides facilitate full‑thickness cutaneous wound healing by promoting epithelial basal cell and hair follicle stem cell proliferation
- Metabolic Regulation of Stem Cells in Aging
- A Hair Growth-Enhancing Component of Hydrolysate of Human Placenta: In vitro and In vivo Assessments
- Novel anti-Mullerian hormone receptor 2 binding peptide prevents chemotherapy-related ovarian follicle loss in a mouse model
- Analysis of Keratin-Associated Protein-7 (KRTAP7) protein structure and function in Indian dromedary camel (Camelus dromedarius)
- Enzymes
- ダブルストロボレンジファインダの開発(特別講演)(画像センシングおよび一般)
- Nutritional factors and hair loss
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Mechanical and biological properties of keratose biomaterials
- Thymosin β4 promotes angiogenesis, wound healing, and hair follicle development
- Expression of vascular endothelial growth factor (VEGF) in various compartments of the human hair follicle
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Structure of human type II 5 alpha-reductase gene
- Real-time iTRAQ-based proteome profiling revealed the central metabolism involved in nitrogen starvation induced lipid accumulation in microalgae
- Characterizing Wool Keratin
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- The Enzymic Derivation of Citrulline Residues from Arginine Residues In Situ during the Biosynthesis of Hair Proteins that are Cross-Linked by Isopeptide Bonds
- Novel de novo pathogenic variant in the <i>ODC1</i> gene in a girl with developmental delay, alopecia, and dysmorphic features
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Serine-rich ultra high sulfur protein gene expression in murine hair and skin during the hair cycle.
- Isolation and Characterization of a Novel Hair Follicle–Specific Gene, Hacl-1
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Protein deficiency in a colony of western lowland gorillas (Gorilla g. gorilla)