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Research 631–660 of 1000+
- Molecular characterisation of keratin-associated protein-7 (KRTAP7) gene for hair quality in Indian Dromedary Camel
- Genetic Association Between Polycystic Ovary Syndrome and the <i>APOA5</i> rs662799 and <i>PLIN1</i> rs894160 Metabolic Variants in the Western Saudi Population: A Case-Control Study
- Ovine KRTAP36-2: A New Keratin-Associated Protein Gene Related to Variation in Wool Yield
- Genetics and Epigenetics of Polycystic Ovary Syndrome
- Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Female Pattern Hair Loss: An Overview with Focus on the Genetics
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Dermatological diseases from a genetic perspective
- Case of autosomal recessive woolly hair/hypotrichosis with compound heterozygous mutations in the <i>LIPH</i> gene at c.742C > A and c.614A > G: The first Japanese case
- Genetic Single Nucleotide Polymorphisms of IL-16 and its Concentration of Patients Infected with Alopecia Areata in Diyala Province, Iraq
- Policistisko olnīcu sindroms pusaudzēm – starppaaudžu, ģenētiskie, dzīves kvalitātes un negausīgas ēšanas aspekti. Promocijas darbs
- Genes of Congenital Dermatologic Disorders in Dogs—A Review
- Polymorphisms in Genes Involved in Steroidogenesis in the Development of Severe Acne
- Generation of Genetically Modified Rats Using CRISPR/Cas9 Genome-Editing System to Reveal Novel Vitamin D Actions
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- Mutation analysis of the typeIIhair keratin gene in a family of Han nationality with monilethrix
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Genetics of Progeria and Aging
- Generating hair follicle inductive dermal papillae cells from adipose derived mesenchymal stem cells
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- 516 Functional annotation of genes underlying hair disorders
- Generation of iPS-derived model cells for the analysis of hair development
- Estudo da diversidade dos genes MC1R e SLC24A5 em populações globais: avaliação de aspectos evolutivos e ambientais
- Genetic Defects of Female Sexual Differentiation
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Generating LacZ-reporter transgenic mice to identify α1 (XIX) Collagen (Col19a1) expression in Dermal Papilla Cells
- Application of genetically modified umbilical cord blood cells and direct gene therapy for treatment of skin wounds in rats
- Genetics
- Genetic characterization of congenital defects in dogs : caudal dysplasia, ectodermal dysplasia and mucopolysaccharidosis VII