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Research 961–990 of 1000+
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- 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
- 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
- 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
- No Evidence That Human Papillomavirus Is Responsible for the Aggressive Nature of Recessive Dystrophic Epidermolysis Bullosa–Associated Squamous Cell Carcinoma
- Female pattern hair loss—An update
- Integrated Lipidomics in the Secreted Phospholipase A2 Biology
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Genetically determined metabolites in allergic conjunctivitis: A Mendelian randomization study
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- <i>FGF20</i> Secreted From Dermal Papilla Cells Regulate the Proliferation and Differentiation of Hair Follicle Stem Cells in Fine‐Wool Sheep
- Role of sgk1 in cancer: a bibliometric analysis from 2013 to 2023—review article
- The correlation between thyroid hormones, reproductive hormones, body mass index (BMI) and hirsute in Iraqi women with polycystic ovary syndrome (PCOS).
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature