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Research 241–270 of 285
- Genome-Wide Association Study for Body Conformation Traits in Kazakh Fat-Tailed Coarse-Wool Sheep
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Insight into Recent Advances in Degrading Androgen Receptor for Castration-Resistant Prostate Cancer
- Cyberspace Chat
- Incorporation of hair follicles in 3D bioprinted models of human skin
- Comparative Characterization of Human Meibomian Glands, Free Sebaceous Glands, and Hair-Associated Sebaceous Glands Based on Biomarkers, Analysis of Secretion Composition, and Gland Morphology
- Hairless: A nuclear receptor corepressor essential for skin function
- A comprehensive investigation into the molecular mechanism responsible for selective androgen receptor (SARM) tissue-selectivity
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Androgen actions on the human hair follicle: perspectives
- Ligand-Independent Actions of the Vitamin D Receptor Maintain Hair Follicle Homeostasis
- Hairless protein of Jumonji family and hair loss
- [Molecular cloning of full-long cDNA sequences encoding hairless gene in the Kunming mouse].
- Vitamin D receptor: molecular signaling and actions of nutritional ligands in disease prevention
- Androgen Signaling in Sertoli Cells
- Critical Appraisal of Reports on the Treatment of Perioral Dermatitis
- Dermatopathology and molecular genetics
- Molecular Genetics of Alopecias
- Alopecia: Association with Resistance to Thyroid Hormones
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Two females with hair loss
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Madarosis
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
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- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Mediator 1 ablation induces enamel-to-hair lineage conversion in mice through enhancer dynamics