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Research 121–150 of 1000+
- In vitro Differentiation of Melanocyte Stem Cells Derived from Vitiligo Patients into Functional Melanocytes
- Molecular heterogeneity of quiescent melanocyte stem cells revealed by single-cell RNA-sequencing
- Human and animal cells under influence of different lighting and stimulus
- Somatic mutations distinguish melanocyte subpopulations in human skin
- Encapsulación en ciclodextrinas de compuestos con actividad frente a la alopecia androgénica masculina.
- High-confidence cancer patient stratification through multiomics investigation of DNA repair disorders
- Understanding, recognizing, and managing toxicities of targeted anticancer therapies
- Genome-Wide Identification and Characterization of the Wnt Gene Family in Donkey (Equus asinus): Phylogenetic Analysis and Expression Profiling
- Recent advances in neuropeptide-related omics and gene editing: Spotlight on NPY and somatostatin and their roles in growth and food intake of fish
- Cornified Epithelial Teeth of Jawless Vertebrates Contain Proteins Similar to Keratin-Associated Proteins of Mammalian Skin Appendages
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- Hox in hair growth and development
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Mandibulofacial dysostosis with alopecia results from ETAR gain-of-function mutations via allosteric effects on ligand binding
- Fibroblast bioelectric signaling drives hair growth
- 5α-Reductase underscores the development of pectoral fin breeding tubercles in zebrafish
- Biomedical applications of organoids in genetic diseases
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- H3K9me3 controls epidermis morphogenesis by regulating RNA Pol II dynamics at developmental promoters and enhancers
- Advancing Aesthetic Medicine Through Exosome-Based Regenerative Therapies with Dr. Face Innovations: Molecular Mechanisms, Nanotechnology Integration, and Data-Driven Insights
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- The Potential of Ginkgo biloba as a Source of Biologically Active Compounds—A Review of the Recent Literature and Patents
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>