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Research 61–90 of 1000+
- Management of tinea capitis in childhood
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Case Series: Gene Expression Analysis in Canine Vogt-Koyanagi-Harada/Uveodermatologic Syndrome and Vitiligo Reveals Conserved Immunopathogenesis Pathways Between Dog and Human Autoimmune Pigmentary Disorders
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS
- Analysis of Genetic Diversity and Construction of a Core Collection of Ginkgo biloba Germplasm Using EST-SSR Markers
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Neurosarcoidosis Occurring 6 Years after Onset of Vogt-Koyanagi-Harada Disease
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- The Impact of Vitamin D Receptor Gene Polymorphisms (FokI, ApaI, TaqI) in Correlation with Oxidative Stress and Hormonal and Dermatologic Manifestations in Polycystic Ovary Syndrome
- The Relationship between Seborrheic Dermatitis and Androgenetic Alopecia in Patients Referred to a Skin Clinic in Tehran, Iran: A Retrospective Study
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Relationship between the bacterial community structures on human hair and scalp
- A novel chitosan-peptide system for cartilage tissue engineering with adipose-derived stromal cells
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications