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Research 30 of 121
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Transcriptome Profile at Different Physiological Stages Reveals Potential Mode for Curly Fleece in Chinese Tan Sheep
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Comparative proteomic analyses using iTRAQ-labeling provides insights into fiber diversity in sheep and goats
- m6A Methylation Analysis Reveals Networks and Key Genes Underlying the Coarse and Fine Wool Traits in a Full-sib Merino Family
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- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia.
- 481 Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Study on the expression patterns of inner root sheath-specific genes in Tan sheep hair follicle during different developmental stages
- 120 Identification of post-translationally modified trichohyalin epitopes responsible for triggering autoimmunity in alopecia areata
- Entdeckung von Autoantigenen bei der Haarverluststörung Alopecia areata: Implikation von posttranslationalen Modifikationen
- Uncombable hair syndrome and beyond
- Unravelling the threads of central centrifugal cicatricial alopecia
- Melatonin regulates the periodic growth of secondary hair follicles through the nuclear receptor RORα
- Identification of Trichohyalin-Like 1, an S100 Fused-Type Protein Selectively Expressed in Hair Follicles
- Variation in the ovine trichohyalin gene and its association with wool curvature
- The biology and genetics of curly hair
- Autoantigen Discovery in the Hair Loss Disorder, Alopecia Areata: Implication of Post-Translational Modifications
- 138 Characterization of xenobiotic metabolizing enzymes of a reconstructed human epidermal model from adult hair follicles
- The pathogenesis of alopecia areata
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Whole-genome bisulfite sequencing of goat skins identifies signatures associated with hair cycling