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Research 571–600 of 1000+
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Molecular characterization of HOXC8 gene and methylation status analysis of its exon 1 associated with the length of cashmere fiber in Liaoning cashmere goat
- 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
- 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
- Gene-knockout mice with abnormal epidermal and hair follicular development
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- Combing the genome for the root cause of baldness
- The Association between Exercise and Androgenetic Alopecia: A Survey-Based Study
- A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women
- PLCD1 and Pilar Cysts
- Three-dimensional reconstructions of mechanosensory end organs suggest a unifying mechanism underlying dynamic, light touch
- A Threefold Association Between Vitiligo and Alopecia Areata: Results from a Nationwide Case-control Observational Study
- How Our Microbiome Influences the Pathogenesis of Alopecia Areata
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- Animal fibre: connecting science and production
- Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families
- Sequence Variation in Caprine KRTAP6-2 Affects Cashmere Fiber Diameter
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Spatial variation and associated genes of total hair follicle density in goats
- HLA‐B alleles associated with frontal fibrosing alopecia in Brazil may share similar peptide presentation and T‐cell interaction profiles
- Cyclin‐dependent kinase 4 expression alters the number of keratinocyte stem cells in the mouse hair follicle
- Vitiligo – Study In view of familial occurence
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- CURRENT UNDERSTANDING OF VITILIGO: A COMPREHENSIVE LITERATURE REVIEW
- Unravelling the threads of central centrifugal cicatricial alopecia
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia