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Research 331–360 of 1000+
- Hair loss evolving into a lifestyle and metabolic phenotype: A hypothesis exploring oxidative stress and acquired androgen sensitivity through reactive oxygen species
- Restoring neuropetide Y levels in the hypothalamus ameliorates premature aging phenotype in mice
- A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- Phenotypic Characterization of Patients with Polycystic Ovary Syndrome in a Population from the Ecuadorian Andes: A Cross-Sectional Study
- The Cross-section Trichometer: A New Device for Measuring Hair Quantity, Hair Loss, and Hair Growth
- New clinico‐genetic classification of trichothiodystrophy
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- A missense mutation in Lama3 causes androgen alopecia
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- The Glucocorticoid Resistance Syndrome. Two Cases of a Novel Pathogenic Variant in the Glucocorticoid Receptor Gene
- The physical and physiological effects of vacuum massage on the different skin layers: a current status of the literature
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- A mutation in MAP2 is associated with prenatal hair follicle density
- Health-related quality of life in adult Mediterranean women with polycystic ovary syndrome attending to a tertiary hospital: a case-control study.
- Familial aggregation of phenotypic expression of premature hair hypopigmentation in the craniofacial region
- The Cross-section Trichometer
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- FoxN1 in K14 promoter-driven epithelium is required for generation and maintenance of 3D-thymus medulla and preventing nude phenotype in the skin (36.33)
- Permanent hair dyes and bladder cancer risk
- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- 0439 Temporal–phenotype signatures of alopecia associated with GLP-1–based therapies: A PRISMA-ScR scoping review
- Engineered Bilayer Hydrogel with Spatiotemporal Drug and Oxygen Delivery for Diabetic Wound Microenvironment Reprogramming
- Rancangan televisyen: Menyangga atau menyanggah bahasa dan budaya?
- SCA-1+ Cells with an Adipocyte Phenotype in Neonatal Mouse Skin
- Experimental Modulation of the Differentiated Phenotype of Keratinocytes from Epidermis and Hair Follicle Outer Root Sheath and Matrix Cells
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- 652 Short cell cycle duration is a phenotype of human epidermal stem cells
- Weathering of the hairless scalp: a study using skin capacitance imaging and ultraviolet light-enhanced visualization