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Research 61–90 of 594
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- WNT10B (wingless-type MMTV integration site family)
- Developmental signals in skin morphogenesis
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- LncRNA-599547 contributes the inductive property of dermal papilla cells in cashmere goat through miR-15b-5p/Wnt10b axis
- Wnt Signaling Influences the Development of Murine Epidermal Langerhans Cells
- Premature aging and cancer development in transgenic mice lacking functional CYLD
- AIRE Deficiency Leads to the Development of Alopecia Areata‒Like Lesions in Mice
- Molecular and Functional Characterization of Clonogenic Human Thymic Epithelial Cells
- MCMV Infection Lowers the Threshold for the Development of Clinical GvHD after Allogeneic Bone Marrow Transplantation.
- Cyclin D3 deficiency inhibits skin tumor development, but does not affect normal keratinocyte proliferation
- The role of PEDF in ageing and development: reduction of oxidative damage and support for stem cells
- CD34 Expression by Hair Follicle Stem Cells Is Required for Skin Tumor Development in Mice
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Inhibition of T-cell activity in alopecia areata: recent developments and new directions
- The Skin Microenvironment: A Dynamic Regulator of Hair Follicle Development, Cycling and Disease
- 078 The transmembrane protein LRIG1 regulates receptor tyrosine kinases in skin development and homeostasis
- Expression of caspase-14 and keratin-19 in the human epidermis and appendages during fetal skin development
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Adipose tissue remodeling via TSLP-mediated IL-4/IL-13 signaling: Implications for atopic dermatitis and skin barrier
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis.
- FoxN1 in K14 promoter-driven epithelium is required for generation and maintenance of 3D-thymus medulla and preventing nude phenotype in the skin (36.33)
- Patterns of desmocollin synthesis in human epithelia: immunolocalization of desmocollins 1 and 3 in special epithelia and in cultured cells.
- Homeostatic Control of Sebaceous Glands by Innate Lymphoid Cells Regulates Commensal Bacteria Equilibrium
- Squamous epithelial proliferation induced by walleye dermal sarcoma retrovirus cyclin in transgenic mice
- Role of bulge epidermal stem cells and TSLP signaling in psoriasis
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- Developing Human Skin Contains Lymphocytes Demonstrating a Memory Signature