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Research 601–630 of 1000+
- Apoptotic cells represent a dynamic stem cell niche governing proliferation and tissue regeneration
- Suppression of Wnt/β-catenin signaling by EGF receptor is required for hair follicle development
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- From basic biology to engineered therapies: the keratinocyte stem cell playbook
- Natural products and their derivatives as candidate treatments for hair greying: from drug discovery to molecular mechanisms
- Ca <sup>2+</sup> -mediated protein citrullination regulates proliferation in the regenerating and malignant CNS
- IL-17a induces age-related olfactory dysfunction by impairing regeneration and promoting respiratory metaplasia in mice
- Immunological control of skin development: from homeostasis to developmental pathologies
- Human and animal cells under influence of different lighting and stimulus
- Epithelial Skin Biology
- Quality of life in patients with alopecia areata: a hospital‐based cross‐sectional study
- Mesenchymal Stem Cell Secretome: Toward Cell-Free Therapeutic Strategies in Regenerative Medicine
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- scINSIGHT for interpreting single-cell gene expression from biologically heterogeneous data
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Serum Level of Macrophage Migration Inhibitory Factor (MIF) in Egyptians With Alopecia Areata and Its Relation to the Clinical Severity of the Disease
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Chronic overlapping pain conditions and nociplastic pain
- Mendelian randomization study highlights hypothyroidism as a causal determinant of alopecia areata
- Genetically predicted levels of circulating cytokines and the risk of six immune skin diseases: a two-sample Mendelian randomization study
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Minoxidil may suppress androgen receptor-related functions
- The genetic link between thyroid dysfunction and alopecia areata: a bidirectional two-sample Mendelian randomization study
- Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
- Fibrotic enzymes modulate wound‐induced skin tumorigenesis