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Research 61–90 of 93
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Association of follicle-stimulating hormone receptor gene ser680 asn (rs6166) polymorphism with polycystic ovarian syndrome
- Association of insulin-like growth factor 2 Apa1 A820G gene (rs680) polymorphism with polycystic ovarian syndrome
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- Molecular Diagnostics and Control of Zoonotic Dermatophytosis: First Detection of Trichophyton indotineae in a Dog in Africa
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Neurosarcoidosis Occurring 6 Years after Onset of Vogt-Koyanagi-Harada Disease
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- 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
- Association of JAK 1 and JAK 2 gene polymorphism with alopecia areata risk: a case–control genetic study
- Stratum corneum dysfunction in dandruff
- 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
- The itchy scalp - scratching for an explanation
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Management of tinea capitis in childhood
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- 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
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Application of PCR Technique to Detect Polymorphism of the KRTAP1.1 Gene in Three Sheep Breeds - A Review
- 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
- Oral Presentation Abstracts
- Glutathione S-transferase gene polymorphism, total antioxidant status, and blood pressure changes in androgenic alopecia