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Research 721–750 of 1000+
- BLIMP1 Is Required for Postnatal Epidermal Homeostasis but Does Not Define a Sebaceous Gland Progenitor under Steady-State Conditions
- The hair cycle and Vitamin D receptor
- Defining Skin Fibroblastic Cell Types Beyond CD90
- Epidermal keratinocyte stem cells: their maintenance and regulation
- The Hair Follicle Bulge: A Niche for Adult Stem Cells
- Epidermal stem cells: an update on their potential in regenerative medicine
- Thy1 marks a distinct population of slow-cycling stem cells in the mouse epidermis
- Fibroblast Heterogeneity in Healthy and Wounded Skin
- There and Back Again: Hair Follicle Stem Cell Dynamics
- MmuPV1-Induced Cutaneous Squamous Cell Carcinoma Arises Preferentially from Lgr5+ Epithelial Progenitor Cells
- Reporting Live from the Epidermal Stem Cell Compartment!
- Hair follicle epithelial stem cells contribute to interfollicular epidermis during homeostasis
- Characterisation of CD4+ stem cells of the skin and their role in skin homeostasis and tumourigenesis
- 974 Single-cell analysis identifies heterogeneity of fibroblasts and myeloid-derived adipocytes in regenerating mouse skin wounds
- Understanding Cancer Cells of Origin in Cutaneous Tumors
- 1330 Flexible fate determination ensures robust differentiation in the skin hair follicle
- Rps14 upregulation promotes inner ear progenitor proliferation and hair cell regeneration in the neonatal mouse cochlea
- Basal cells in the epidermis and epidermal differentiation
- Hair follicle stem cell progeny heal blisters while pausing skin development
- Stem Cells Sheltered from Air-Raids Repair Airways
- 1424 Mapping the establishment of fibroblast heterogeneity during skin development and wound repair
- 872 Dermal Wnt/β-catenin signaling controls hair follicle dermal condensate size during development
- Un(MaSC)ing Stem Cell Dynamics in Mammary Branching Morphogenesis
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- EDA2R Is Associated with Androgenetic Alopecia
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- FGFR2 is associated with hair thickness in Asian populations
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family