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Research 601–630 of 1000+
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Androgenetic Alopecia: A Chronic or Pubertal Onset Disease Retarded by Blood Donation
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Genome-Wide Association Studies of Hair Whorl in Pigs
- Chronic Overlapping Pain Conditions and Nociplastic Pain
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Keratin disorders: from gene to therapy
- Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Generalized Vitiligo Associated Autoimmune Diseases in Japanese Patients Their Families
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Metformin therapy for the reproductive and metabolic consequences of polycystic ovary syndrome
- Biochemical Roles of Testosterone and Epitestosterone to 5α-Reductase as Indicators of Male-Pattern Baldness
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- 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
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Polymorphism of genes in patients with new coronavirus infection COVID-19
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Predicting Human Appearance from DNA for Forensic Investigations
- Androgenetic alopecia in women and men is not related to COVID‐19 infection severity: a prospective cohort study of hospitalized COVID‐19 patients
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- Cellular senescence and polycystic ovary syndrome: mechanisms and therapeutic strategies from a new perspective
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep