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Research 151–180 of 1000+
- The role of macrophages in skin homeostasis
- Calcineurin/Nfatc1 signaling links skin stem cell quiescence to hormonal signaling during pregnancy and lactation
- Are fingernails a key to unlocking the puzzle of mammalian limb regeneration?
- Chapter 23. Therapeutic Control of Androgen Action
- γδ17 T cell-stromal networks modulate matrix composition and vascularity in foreign body response
- Characterization of Primary Cilia and Intraflagellar Transport 20 in the Epidermis
- Understanding Polycystic Ovary Syndrome
- Subject Index
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Fibroblast heterogeneity and functions: insights from single-cell sequencing in wound healing, breast cancer, ovarian cancer and melanoma
- Sox2 in the dermal papilla regulates hair follicle pigmentation
- Autophagy critically controls skin inflammation and apoptosis-induced stem cell activation
- A Subset of TREM2+ Dermal Macrophages Secretes Oncostatin M to Maintain Hair Follicle Stem Cell Quiescence and Inhibit Hair Growth
- Hair & Cutaneous Development
- Epidermal Notch signalling: differentiation, cancer and adhesion
- Lymphatic vessels interact dynamically with the hair follicle stem cell niche during skin regeneration <i>in vivo</i>
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Regional Variation in Androgen Receptor Expression and Biomechanical Properties May Contribute to Cryptorchidism Susceptibility in the LE/orl Rat
- 176 Myeloid cell-specific deletion of mTOR suppresses psoriasis-like skin inflammation in C57BL/6 mice
- Spatiotemporal dynamics of sensory neuron and Merkel-cell remodeling are decoupled during epidermal homeostasis
- Wounding induces dedifferentiation of epidermal Gata6+ cells and acquisition of stem cell properties
- Hair Follicles as Micro-Organs: MicroRNA-Mediated Control of Growth, Cycling, and Fiber Traits
- Skin abnormalities generated by temporally controlled RXRα mutations in mouse epidermis
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Pathophysiological mechanisms implicated in postpartum depression
- Recent advances in treatment for Benign Prostatic Hyperplasia
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- Regulatory T cell dysfunction and immunotherapeutic breakthroughs in type 1 diabetes