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Research 31–60 of 653
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Organ regeneration based on developmental biology: past and future
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- The role of lymphocytes in the development and treatment of alopecia areata
- Selenoproteins Are Essential for Proper Keratinocyte Function and Skin Development
- Sexually dimorphic sail feathers in the Mandarin duck as a model for lifelong developmental modulation
- Protein Kinase C<i>ε</i>, Which Is Linked to Ultraviolet Radiation-Induced Development of Squamous Cell Carcinomas, Stimulates Rapid Turnover of Adult Hair Follicle Stem Cells
- T-Cell Reconstitution after Thymus Xenotransplantation Induces Hair Depigmentation and Loss
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis
- Melatonin membrane receptors in peripheral tissues: Distribution and functions
- Thymosin β4 promotes angiogenesis, wound healing, and hair follicle development
- Wnt signaling in skin organogenesis
- Transient mitochondrial DNA double strand breaks in mice cause accelerated aging phenotypes in a ROS-dependent but p53/p21-independent manner
- Aromatic plants as cosmeceuticals: benefits and applications for skin health
- Developmentally programmed early-age skin localization of iNKT cells supports local tissue development and homeostasis
- Cutaneous gain-of-function mutation of LRIG3 leads to alopecia by upregulation of ERBB, PI3K/AKT, NOTCH1 signaling pathways
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Hox genes in development and beyond
- Development of Heritable Melanoma in Transgenic Mice
- Pax9 is required for filiform papilla development and suppresses skin-specific differentiation of the mammalian tongue epithelium
- Distinct Fibroblast Lineages Give Rise to NG2+ Pericyte Populations in Mouse Skin Development and Repair
- Premature aging and cancer development in transgenic mice lacking functional CYLD
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Effects of the α-ketoglutaric acid on the performance, hair follicle development and antioxidant capacity of Rex rabbits
- WNT10B (wingless-type MMTV integration site family)
- Wnt Signaling Influences the Development of Murine Epidermal Langerhans Cells
- Clinical Application of Development of Nonantibiotic Macrolides That Correct Inflammation-Driven Immune Dysfunction in Inflammatory Skin Diseases