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Research 211–240 of 1000+
- A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Genomic Analysis of Trichotillomania
- Convergent Decay of Skin-specific Gene Modules in Pangolins
- Exploring climate adaptation in European Merino sheep: a landscape genomics approach
- The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodeling
- Genome-Wide Association Studies of Hair Whorl in Pigs
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- The role of functional variants in the aetiology of polycystic ovary syndrome
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- 481 Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Etiopathogenesis of acne
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Primary Generalized Glucocorticoid Resistance and Hypersensitivity
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Current Perspectives on Less-known Aspects of Headache
- Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
- Organization and Expression of Hair Follicle Genes.
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter