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Research 361–390 of 1000+
- Basal Cell Carcinoma, Hedgehog Signaling, and Targeted Therapeutics: The Long and Winding Road
- Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss
- DNA phenotyping: current application in forensic science
- A functional polymorphism in interleukin-1α (IL1A) gene is associated with risk of alopecia areata in Chinese populations
- The relationship among androgens, insulin resistanceand ghrelin polymorphisms in post-adolescent malepatients with severe acne vulgaris
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- CYP21A2 Mutations in Women with Polycystic Ovary Syndrome (PCOS)
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Lentiginosis within plaques of linear atrophoderma of Moulin: a twin-spotting phenomenon?
- Alopecia: Association with Resistance to Thyroid Hormones
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Minoxidil Sulfotransferase Enzyme (SULT1A1) genetic variants predicts response to oral minoxidil treatment for female pattern hair loss
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Adipose and Hair Function: An aPPARent Connection
- Antisense oligonucleotide targeting fibroblast growth factor receptor (FGFR)-1 stimulates cellular activity of hair follicles in an<i>in vitro</i>organ culture system
- Site of beige (<i>bg</i>) and leaden (<i>ln</i>) pigment gene expression determined by recombinant embryonic skin grafts and aggregation mouse chimaeras employing sash (<i>W</i><sup><i>sh</i></sup>) homozygotes
- Increased 25(OH)D3 level in redheaded people: Could redheadedness be an adaptation to temperate climate?
- Narrowband UVB treatment induces expression of WNT7B, WNT10B and TCF7L2 in psoriasis skin
- Association of a polymorphism in the ornithine decarboxylase gene with male androgenetic alopecia
- Frontotemporal dementia with parkinsonism presenting as posterior cortical atrophy
- Diffuse idiopathic skeletal hyperostosis in a 33-year-old woman with PCOS and metabolic syndrome: a rare scenario
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- To study hypoactive sexual desire disorder in a fragile X carrier female successfully treated with local testosterone application
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- Antihelminthic Drugs
- Ischemic Stroke in a Young Adult Male During Finasteride Therapy