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Research 601–630 of 1000+
- The influence of interferon on healthy and diseased skin
- Using WGCNA (weighted gene co-expression network analysis) to identify the hub genes of skin hair follicle development in fetus stage of Inner Mongolia cashmere goat
- Iron Metabolism of the Skin: Recycling versus Release
- Establishment of Tsc2-deficient rat embryonic stem cells
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- Paxillin regulates androgen receptor expression associated with granulosa cell focal adhesions
- The Rho guanosine nucleotide exchange factors Vav2 and Vav3 modulate epidermal stem cell function
- TRPV3 Ion Channel: From Gene to Pharmacology
- The Immunological Intersection of Psoriasis and Autoimmune Diseases: Shared Pathways and Clinical Implications
- Integrative skin phenotypic and transcriptomic analyses reveal candidate genes for coat color and fiber length in four Chinese goat breeds (<i>Capra hircus</i>)
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Research advances of tissue-derived extracellular vesicles in cancers
- Blank Spots in the Map of Human Skin: The Challenge for Xenotransplantation
- Improving human forensics through advances in genetics, genomics and molecular biology
- Miz1 is required for hair follicle structure and hair morphogenesis
- Past, Present and Future Perspectives of Forensic Genetics
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- C‐reactive protein as a novel biomarker for vitamin D deficiency in alopecia areata
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- What’s Sex Got to Do With COVID-19? Gender-Based Differences in the Host Immune Response to Coronaviruses
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- A Ca <sup>2+</sup> /calmodulin-dependent protein kinase required for symbiotic nodule development: Gene identification by transcript-based cloning
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- TRPA1 Modulates Mechanotransduction in Cutaneous Sensory Neurons
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Dermal β-catenin activity in response to epidermal Wnt ligands is required for fibroblast proliferation and hair follicle initiation