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Research 91–120 of 202
- PBX homeobox 1 enhances hair follicle mesenchymal stem cell proliferation and reprogramming through activation of the AKT/glycogen synthase kinase signaling pathway and suppression of apoptosis
- The epidermis: rising to the surface
- Identification of novel glucocorticoid receptor-regulated genes involved in epidermal homeostasis and hair follicle differentiation
- Molecular Evolution and Protein Structure Variation of Dkk Family
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Dermal fibroblast in cutaneous development and healing
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Distinct Regulatory Programs Control the Latent Regenerative Potential of Dermal Fibroblasts during Wound Healing
- Skin tissue engineering
- Whole-genome resequencing to investigate the genetic diversity and the molecular basis underlying key economic traits in indigenous sheep breeds adapted to hypoxic environments
- Temporal Layering of Signaling Effectors Drives Chromatin Remodeling during Hair Follicle Stem Cell Lineage Progression
- Human iPS Cell-Derived Cell Aggregates Exhibited Dermal Papilla Cell Properties in in vitro Three-Dimensional Assemblage Mimicking Hair Follicle Structures
- Role of regeneration in tissue repairing and therapies
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- Developmental Mechanisms Controlling Cell Fate, Evolution of
- Feather arrays are patterned by interacting signalling and cell density waves
- Brg1 Governs a Positive Feedback Circuit in the Hair Follicle for Tissue Regeneration and Repair
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Retinoic Acid and Mouse Skin Morphogenesis. II. Role of Epidermal Competence in Hair Glandular Metaplasia
- Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Fibroblasts – the cellular choreographers of wound healing
- The role of WNT10B in physiology and disease: A 10-year update