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Research 331–360 of 1000+
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
- EdnrB Governs Regenerative Response of Melanocyte Stem Cells by Crosstalk with Wnt Signaling
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- Prediction of male-pattern baldness from genotypes
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- <i>WNT10A</i> , dermatology and dentistry
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Uncovering the complex relationship between balding, testosterone and skin cancers in men
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
- Genetic links between atopy, allergy, and alopecia areata: insights from a Mendelian randomization study
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Polymorphism of genes in patients with new coronavirus infection COVID-19
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- Association between genetically predicted rheumatoid arthritis and alopecia areata: a two-sample Mendelian randomization study
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria