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Research 151–180 of 1000+
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Comprehensive analysis of circRNAs from cashmere goat skin by next generation RNA sequencing (RNA-seq)
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Nanocarrier Systems for Transdermal Drug Delivery
- Early-onset baldness and the risk of aggressive prostate cancer: findings from a case–control study
- Encapsulación en ciclodextrinas de compuestos con actividad frente a la alopecia androgénica masculina.
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Ichthyosis
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Female Androgenetic (?) Alopecia
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- Assessing Causality Between Androgenetic Alopecia with Depression: A Bidirectional Mendelian Randomization Study
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- FGF5 is a crucial regulator of hair length in humans
- Update on hidradenitis suppurativa: connecting the tracts
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Insertional mutation of the hairless locus on mouse Chromosome 14
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- GLOMERULAR MEMBRANOUS NEPHROPATHY AND WERNER SYNDROME: A CASE REPORT
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- 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