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Research 181–210 of 764
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- Lab Quality Management and Methodology
- Association Between Retinoid X Receptor Gene Variants and Dyslipidemia Risk in an Iranian Population
- A genome‐wide association study identified a genetic variant associated with hair thinning in Japanese women
- Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia
- Compilation of a comprehensive gene panel for systematic assessment of genes that govern an individual’s drug responses
- AKT2 Gene Polymorphisms, sRANKL/OPG and Hormone Measurements in Polycystic Ovarian Syndrome (PCOS) Women
- Lipin 1 Gene Polymorphisms in Polycystic Ovary Syndrome
- Cells to Surgery Quiz: April 2020
- Pilot study: genetic distribution of AR, FGF5, SULT1A1 and CYP3A5 polymorphisms in male Mexican population with androgenetic alopecia.
- Sex dependent influence of a functional polymorphism in steroid 5‐α‐reductase type 2 (<i>SRD5A2</i>) on post‐traumatic stress symptoms
- Genetic association of complement component 2 polymorphism with systemic lupus erythematosus
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- Variation in the ovine trichohyalin gene and its association with wool curvature
- Genome-based analysis of the genetic pattern of black sheep in Qira sheep
- Single nucleotide polymorphisms associated with elevated alanine aminotransferase in patients receiving asunaprevir plus daclatasvir combination therapy for chronic hepatitis C
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- Genomic Portraiture: The Science and Ethics of DNA Phenotyping in Identity Prediction
- 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Genome-Wide Association Studies of Hair Whorl in Pigs
- Natural Killer Group 2 Type D (NKG2D) Gene Polymorphism in Systemic Lupus Erythematosus-Suez Canal Region - Egypt
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Evaluation of Personalized Skincare Through in-silico Gene Interactive Networks and Cellular Responses to UVR and Oxidative Stress
- Polymorphisms and association of FAT1 gene with wool quality traits in Chinese Merino sheep