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Research 841–870 of 1000+
- A complete guide to human microbiomes: Body niches, transmission, development, dysbiosis, and restoration
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- The palette of techniques for cell cycle analysis
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- <i>NUDT15</i>,<i>FTO</i>, and<i>RUNX1</i>genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases
- Dietary supplementation with Essential-oils-cobalt for improving growth performance, meat quality and skin cell capacity of goats
- Optimal processing for proteomic genotyping of single human hairs
- Autofluorescence as a Signal to Sort Developing Glandular Trichomes by Flow Cytometry
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Formation of regulator/target gene relationships during evolution
- The Genetics of Human Skin Disease
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Pmg-1 and Pmg-2 constitute a novel family of KAP genes differentially expressed during skin and mammary gland development
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Spatial Distribution and Functional Impact of Human Scalp Hair Follicle Microbiota
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Alterations of gut microbiota composition in post-finasteride patients: a pilot study
- Cellular heterogeneity and microenvironmental control of skin cancer
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Developmentally programmed early-age skin localization of iNKT cells supports local tissue development and homeostasis
- Ranitidine and finasteride inhibit the synthesis and release of trimethylamine N-oxide and mitigates its cardiovascular and renal damage through modulating gut microbiota