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Research 451–480 of 1000+
- Elevated Dehydroepiandrosterone Sulfate Levels as the Reproductive Phenotype in the Brothers of Women with Polycystic Ovary Syndrome
- The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis
- Central Centrifugal Cicatricial Alopecia: Retrospective Chart Review
- Safe Selection of Genetically Manipulated Human Primary Keratinocytes with Very High Growth Potential Using CD24
- Lifestyle and Physiological Factors Associated with Facial Wrinkling in Men and Women
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer
- Molecular characterization of HOXC8 gene and methylation status analysis of its exon 1 associated with the length of cashmere fiber in Liaoning cashmere goat
- Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Uncovering the complex relationship between balding, testosterone and skin cancers in men
- The disrupted balance between hair follicles and sebaceous glands in<i>Hoxc13</i>‐ablated rabbits
- Efficient expansion of human keratinocyte stem/progenitor cells carrying a transgene with lentiviral vector
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Skin cancer: understanding the journey of transformation from conventional to advanced treatment approaches
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance
- The influence of obesity on Androstenedione to Testosterone ratio in women with polycystic ovary syndrome (PCOS) and hyperandrogenemia
- Alopecia in IL-10-deficient mouse pups is c-kit-dependent and can be triggered by iron deficiency
- The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
- Electrophoretic variability in human head hair: Polyacrylamide gel electrophoresis of hair proteins in the presence of sodium dodecyl sulfate and urea
- Scraggly, a new hair loss mutation on mouse Chromosome 19
- <i>MYC</i> Protooncogenes of Wool and Hair Growth<sup>a</sup>
- Overexpression of alkaline phosphatase improves the hair-inductive capacity of cultured human dermal papilla spheres
- Association of HSPA1B SNP rs6457452 with Alopecia Areata in the Korean Population
- Hairless Up‐Regulates <i>Tgf‐β2</i> Expression via Down‐Regulation of miR‐31 in the Skin of “Hairpoor” (<i>Hr</i><sup><i>Hp</i></sup>) Mice
- A functional polymorphism in interleukin-1α (IL1A) gene is associated with risk of alopecia areata in Chinese populations
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears