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Research 331–360 of 1000+
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Differential Auxin-Transporting Activities of PIN-FORMED Proteins in Arabidopsis Root Hair Cells
- Tissue Engineering and Regenerative Medicine: Achievements, Future, and Sustainability in Asia
- 9 Role of 5α-reductase in health and disease
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Melanocytes: The new Black
- 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
- The Cytology and Cytochemistry of the Wool Follicle
- Biocomposite nanofiber matrices to support ECM remodeling by human dermal progenitors and enhanced wound closure
- Olfactory receptor OR2AT4 regulates human hair growth
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Mitoxantrone
- Identification of microRNAs in Wool Follicles during Anagen, Catagen, and Telogen Phases in Tibetan Sheep
- Hairless is a nuclear receptor corepressor essential for skin function
- Histologic comparison of microscopic treatment zones induced by fractional lasers and radiofrequency
- Suppression of Wnt/β-catenin signaling by EGF receptor is required for hair follicle development
- Regulation of melanocyte stem cell behavior by the niche microenvironment
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Establishment of keratinocyte cell lines from human hair follicles
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Twist1 Contributes to the Maintenance of Some Biological Properties of Dermal Papilla Cells in vitro by Forming a Complex With Tcf4 and β-Catenin
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- Hair regenerative effect of silk fibroin hydrogel with incorporation of FGF-2-liposome and its potential mechanism in mice with testosterone-induced alopecia areata
- The Endoscopic Brow Lift
- Hair coat characteristics in Friesian heifers in the Netherlands and Kenya : experimental data and a review of literature