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Research 331–360 of 1000+
- Tracing the cellular origin of cancer
- Evidence that Myc activation depletes the epidermal stem cell compartment by modulating adhesive interactions with the local microenvironment
- Dynamic interplay between IL-1 and WNT pathways in regulating dermal adipocyte lineage cells during skin development and wound regeneration
- Glutamate transporter Slc1a3 mediates inter‐niche stem cell activation during skin growth
- Premature aging and cancer development in transgenic mice lacking functional CYLD
- Inhibition of the CoREST Repressor Complex Promotes Wound Re-Epithelialization through the Regulation of Keratinocyte Migration
- Exploiting the origins of Ras mediated squamous cell carcinoma to develop novel therapeutic interventions
- 877 Loss of UBE2N in keratinocytes leads to skin inflammation and immune infiltration through IRAK1/4-mediated processes
- Characterization of the Role of Transferrin receptor 1 (Tfr1) in the Intestinal Epithelium, Pancreas, and Skin
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- Patched1 Functions as a Gatekeeper by Promoting Cell Cycle Progression
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary cilia
- Aberrant Wnt Signaling Induces Comedo-Like Changes in the Murine Upper Hair Follicle
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Author response: Hair follicle epidermal stem cells define a niche for tactile sensation
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Characterisation, genomic organisation, expression and function of the mEphA1 receptor Tyrosine Kinase
- Brain and muscle Arnt-like protein-1 (BMAL1) controls circadian cell proliferation and susceptibility to UVB-induced DNA damage in the epidermis
- Conditional Gene Expression in the Epidermis of Transgenic Mice Using the Tetracycline-Regulated Transactivators tTA and rTA Linked to the Keratin 5 Promoter
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- Long-term expansion and differentiation of adult murine epidermal stem cells in 3D organoid cultures
- The effect of dietary modulation of sulfur amino acids on cystathionine β synthase–deficient mice
- Suppression of eukaryotic initiation factor 4E prevents chemotherapy-induced alopecia
- <i>PIK3CA</i> gain-of-function mutation in Schwann cells leads to severe neuropathy and aerobic glycolysis through a non-cell autonomous effect
- Blank Spots in the Map of Human Skin: The Challenge for Xenotransplantation
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- CRF Receptor Antagonist Astressin-B Reverses and Prevents Alopecia in CRF Over-Expressing Mice