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Research 481–510 of 1000+
- Syndromes of Severe Insulin Resistance (SSIRs)
- Testing the impact of trait prevalence priors in Bayesian-based genetic prediction modeling of human appearance traits
- Lack of classic histology should not prevent diagnosis of necrolytic acral erythema
- A New CARASIL Family: Recurrent Lobar Hemorrhage as a Novel Characteristic of the Disease
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Utilising SNP Association Analysis as a Prospective Approach for Personalising Androgenetic Alopecia Treatment
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Serum interleukin-37 and its gene polymorphism (rs3811047) in Egyptian patients with alopecia areata
- Behavioural characterization of Vitamin D receptor knockout mice
- Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat
- Acne Syndromes and Mosaicism
- Two parietal cephaloceles in a female neonate
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- The Tumor Suppressor Actions of the Vitamin D Receptor in Skin
- Investigating the Genetic Association of Selected Candidate Loci with Alopecia Areata Susceptibility in Jordanian Patients
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Amplicon-based sequencing and co-occurence network analysis reveals notable differences of microbial community structure in healthy and dandruff scalps
- Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep
- MITF E318K naevus phenotype: the modifying role of MC1R Red Hair Variants
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- The Rho GTPase exchange factor Vav2 promotes extensive age-dependent rewiring of the hair follicle stem cell transcriptome
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing