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Research 931–960 of 1000+
- Comparative Analysis of Chloroplast Genomes in Sansevieria Reveals Phylogenetic Relationships and High Variability Molecular Markers
- Screened of long non-coding RNA related to wool development and fineness in Gansu alpine fine-wool sheep
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Effects of KRTAP20-1 Gene Variation on Wool Traits in Chinese Tan Sheep
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Hair & Cutaneous Development
- The Role of the Mammalian Target of Rapamycin (mTOR) in Pulmonary Fibrosis
- Obesity and Polycystic Ovary Syndrome: Implications for Pathogenesis and Novel Management Strategies
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Ginseng for Health Care: A Systematic Review of Randomized Controlled Trials in Korean Literature
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Physiopathology of polycystic ovary syndrome in endocrinology, metabolism and inflammation
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Genetic predictors of testosterone and their associations with cardiovascular disease and risk factors: A Mendelian randomization investigation
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Progenitor Cell Dysfunctions Underlie Some Diabetic Complications
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Regeneration Genetics
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Ichthyosis with confetti: clinics, molecular genetics and management
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess
- Infrared and Raman Diagnostic Modeling of Phosphate Adsorption on Ceria Nanoparticles
- Molecular characterization of HOXC8 gene and methylation status analysis of its exon 1 associated with the length of cashmere fiber in Liaoning cashmere goat
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations