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Research 841–870 of 1000+
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- p63: a crucial player in epithelial stemness regulation
- Mesenchymal Stem Cell-Derived Extracellular Vesicles for Therapeutic Use and in Bioengineering Applications
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Effects of microenvironment and biological behavior on the paracrine function of stem cells
- Expression of truncated latent TGF-β-binding protein modulates TGF-β signaling
- Graphene oxide and indole-3-acetic acid cotreatment regulates the root growth of Brassica napus L. via multiple phytohormone pathways
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Disentangling the Coronavirus Disease 2019 Health Disparities in African Americans: Biological, Environmental, and Social Factors
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11
- Regulatory T cells in dominant immunologic tolerance
- Genetic and molecular aspects of androgenetic alopecia
- The Genetic Architecture of Alopecia Areata
- μ-Crystallin, Thyroid Hormone-binding Protein, is Expressed Abundantly in the Murine Inner Root Sheath Cells
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- IL-1 Receptor–Knockout Mice Develop Epidermal Cysts and Show an Altered Innate Immune Response after Exposure to UVB Radiation
- Persistently curly hair phenotype with the use of nivolumab for squamous cell lung cancer
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Exploring the relationship between anastasis and mitochondrial ROS-mediated ferroptosis in metastatic chemoresistant cancers: a call for investigation
- COVID-19-Related Neuropathic Pain: A Systematic Review and Meta-Analysis
- miR-761-hepcidin/Gpx4 pathway contribute to unexplained liver dysfunction in polycystic ovary syndrome by regulating liver iron overload and ferroptosis
- Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- Stratum-Specific Expression of Human Transferrin Receptor Increases Iron in Mouse Epidermis
- Exosomes Derived From Human Adipose-Derived Stem Cells Inhibit Lipogenesis Involving Hedgehog Signaling Pathway