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Research 541–570 of 1000+
- Drug Information Analysis Service
- Polycystic Ovary Syndrome
- Polycystic Ovarian Syndrome
- Characterization of metabolic changes in the phenotypes of women with polycystic ovary syndrome in a large Mediterranean population from Sicily
- Appearance and Internal Aging
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Identification of Key Pathways and Genes Related to the Development of Hair Follicle Cycle in Cashmere Goats
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study
- The fiber diameter traits of Tibetan cashmere goats are governed by the inherent differences in stress, hypoxic, and metabolic adaptations: an integrative study of proteome and transcriptome
- Identification and Analysis of MYB Gene Family for Discovering Potential Regulators Responding to Abiotic Stresses in Curcuma wenyujin
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Signature selection analysis reveals candidate genes associated with production traits in Iranian sheep breeds
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Development of a Predictive Model for Iron Levels in Bovine Muscle Tissue Using Hair as a Predictor
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Evaluation of Personalized Skincare Through in-silico Gene Interactive Networks and Cellular Responses to UVR and Oxidative Stress
- Exploring the Complexities of Atopic Dermatitis: Pathophysiological Mechanisms and Therapeutic Approaches
- Uncovering novel biomarkers and drug targets for androgenetic alopecia via metabolite regulation and multi-tissue validation
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene