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Research 601–630 of 1000+
- Molecular characterization of HOXC8 gene and methylation status analysis of its exon 1 associated with the length of cashmere fiber in Liaoning cashmere goat
- Phenotype of Normal Hairline Maturation
- Prevalence and Etiology of Central Centrifugal Cicatricial Alopecia
- Adrenal Gland Disease in Ferrets
- Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic?
- 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 twisting tale of woolly hair: a trait with many causes
- Efficient expansion of human keratinocyte stem/progenitor cells carrying a transgene with lentiviral vector
- Making Waves with Hairs
- Merkel cell carcinoma: updates in tumor biology, emerging therapies, and preclinical models
- The aetiology and pathogenesis of alopecia areata
- Alopecia Areata
- Bad medicine: misconceptions and misuses revealed, from distance healing to vitamin O
- Female Pattern Hair Loss
- Scraggly, a new hair loss mutation on mouse Chromosome 19
- Female pattern hair loss—An update
- Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
- Syndrome of Birt–Hogg–Dubé, a Histopathological Pitfall With Similarities to Tuberous Sclerosis
- DNA phenotyping: current application in forensic science
- Inherited Disorders of Corneocyte Proteins
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Biology of the hair follicle and mechanisms of nonscarring and scarring alopecia
- Longitudinal Assessment of the Prevalence of Actinic Keratosis and Extensive Risk Factor Evaluation: An Update from the Rotterdam Study
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Genome‐wide association study identifies variants associated with hair length in Brangus cattle
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle