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Research 391–420 of 1000+
- DNA phenotyping: current application in forensic science
- Exploring imputation performance of phenotype-associated SNPs for forensic prediction models
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Minoxidil may suppress androgen receptor-related functions
- Long noncoding RNA and gene expression analysis of melatonin-exposed Liaoning cashmere goat fibroblasts indicating cashmere growth
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- Banding Pattern on Polarized Hair Microscopic Examination and Unilateral Polymicrogyria in a Patient With Steroid Sulfatase Deficiency
- Characterization and expression analysis of KAP7.1, KAP8.2 gene in Liaoning new-breeding cashmere goat hair follicle
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss
- Variation in the ovine keratin-associated protein 15-1 gene affects wool yield
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Association of Gly972Arg variant of insulin receptor subtrate-1 and Gly1057Asp variant of insulin receptor subtrate-2 with polycystic ovary syndrome in the Chinese population
- Abstracts
- Genome wide association analysis of root hair traits in rice reveals novel genomic regions controlling epidermal cell differentiation
- Hormonal and Genetic Etiology of Male Androgenetic Alopecia
- 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
- Biology of hair pigmentation and its role in premature canities
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Potassium Channel Openers Increase Aortic Elastic Fiber Formation and Reverse the Genetically Determined Elastin Deficit in the BN Rat
- Peroxisome proliferator-activated receptors (PPARs) and PPAR agonists: the ‘future’ in dermatology therapeutics?
- Male Androgenetic Alopecia
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Understanding sex and gender disparities in COVID-19 mortality: a narrative review beyond biology
- Synopsis: 2005 Annual Meeting of the American Society of Andrology
- Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic?
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia