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Research 151–180 of 1000+
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Causes and Management of Hypertrichosis
- Hypotrichosis in a child with olmsted syndrome
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Ichthyosis with confetti: clinics, molecular genetics and management
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Quantification of the Vitamin D Receptor−Coregulator Interaction
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Diseases of Hair
- Diseases of Hair
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Simultaneous Determination of Selected Steroids with Neuroactive Effects in Human Serum by Ultrahigh-Performance Liquid Chromatography–Tandem Mass Spectrometry
- Screening of Protein Related to Wool Development and Fineness in Gansu Alpine Fine-Wool Sheep
- Gray Hair: From Preventive to Treatment
- Endocrinology
- Madarosis: A marker of many Maladies
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Abstracts
- Blank Spots in the Map of Human Skin: The Challenge for Xenotransplantation
- Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency epidemiology, etiopathogenesis, clinical presentation, treatment – a systematic review
- Genetic Defects of Female Sexual Differentiation
- Modelling androgen synthesis and action during human sexual differentiation
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Immunological control of skin development: from homeostasis to developmental pathologies
- Zebrafish Model of Hereditary Pigmentary Disorders