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Research 121–150 of 625
- Physiologic functions of PP2A: Lessons from genetically modified mice
- Epidermal Notch1 recruits RORγ+ group 3 innate lymphoid cells to orchestrate normal skin repair
- Replicative stress, stem cells and aging
- The role of nuclear hormone receptors in cutaneous wound repair
- Identification and characterization of an antisense RNA transcript (gfg) from the human basic fibroblast growth factor gene.
- Abstracts of Communications
- Keratin cytoskeletons in epithelial cells of internal organs
- Identification of a link between Wnt/β-catenin signalling and the cell fusion pathway
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- FOXP3 <sup>+</sup> regulatory T cells and age‐related diseases
- Delayed hair cycle in mnd2 mutant mice lacking HtrA2 serine protease activity
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- RANKL Induces Organized Lymph Node Growth by Stromal Cell Proliferation
- Mouse Intestinal Krt15+ Crypt Cells Are Radio-Resistant and Tumor Initiating
- CD80 on skin stem cells promotes local expansion of regulatory T cells upon injury to orchestrate repair within an inflammatory environment
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Pathogenesis of graft-versus-host-disease
- Author response: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Over-, ectopic-expression of FoxN1 at early life adversely influences lymphopoiesis (HEM3P.280)
- MCMV Infection Lowers the Threshold for the Development of Clinical GvHD after Allogeneic Bone Marrow Transplantation.
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Commensal Microbes and Hair Follicle Morphogenesis Coordinately Drive Treg Migration into Neonatal Skin
- Hox genes in development and beyond
- Conserved γδ T cell selection by BTNL proteins limits progression of human inflammatory bowel disease
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Cell death in skin function, inflammation, and disease
- Biomaterials Mimicking Mechanobiology: A Specific Design for a Specific Biological Application
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- TGFβ‐mediated inhibition of hypodermal adipocyte progenitor differentiation promotes wound‐induced skin fibrosis