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Research 211–240 of 1000+
- Correlation analysis of four KRTAP gene polymorphisms and cashmere fiber diameters in two cashmere goat breeds
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- Human Peptidylarginine Deiminase Type III: Molecular Cloning and Nucleotide Sequence of the cDNA, Properties of the Recombinant Enzyme, and Immunohistochemical Localization in Human Skin
- MultiKano: an automatic cell type annotation tool for single-cell multi-omics data based on Kolmogorov–Arnold network and data augmentation
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- The Genetic Landscape of Androgenetic Alopecia: Current Knowledge and Future Perspectives
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics
- Genetic variants in AR and SHBG and resistance to hormonal castration in prostate cancer
- Keratinocyte Cytokine Networks Associated with Human Melanocytic Nevus Development
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Vitamin D Receptor, UVR, and Skin Cancer: A Potential Protective Mechanism
- Keratinic amyloid deposition in canine hair follicle tumors
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- BJD Editor's Choice
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Dietary and Genetic Aspects of Polycystic Ovary Syndrome (PCOS) in Polish Women-Part II: Association of
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Algorithms For Preventive Measures For Disease Prevention And Antioxidant Protection
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Hepatitis C virus: host, environmental and viral factors promoting spontaneous clearance