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- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Application of genetically modified umbilical cord blood cells and direct gene therapy for treatment of skin wounds in rats
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Fetal wound healing using a genetically modified murine model: the contribution of P-selectin
- Generation of Genetically Modified Rats Using CRISPR/Cas9 Genome-Editing System to Reveal Novel Vitamin D Actions
- Triton modified polyethyleneimine conjugates assembled with growth arrest-specific protein 6 for androgenetic alopecia transdermal gene therapy
- Physiologic functions of PP2A: Lessons from genetically modified mice
- The Effect of Conditioned Medium from Angiopoietin-1 Gene-Modified Mesenchymal Stem Cells on Wound Healing in a Diabetic Mouse Model
- Feasibility of repairing skin defects by VEGF<sub>165</sub> gene‐modified iPS‐HFSCs seeded on a 3D printed scaffold containing astragalus polysaccharide
- Vascularization of skin substitute constructed by vascular endothelial growth factor 165 gene-modified hair follicle stem cells compounded with three-dimensional gelatin-chondroitin sulfate-hyaluronic acid
- [Experimental study on vascular endothelial growth factor 165 gene-modified rat hair follicle stem cells mediated by lentiviral vector].
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Rapid Genetic Analysis of Epithelial-Mesenchymal Signaling During Hair Regeneration
- Generating iPSCs with a High-Efficient, Non-Invasive Method—An Improved Way to Cultivate Keratinocytes from Plucked Hair for Reprogramming
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
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- ESGCT and FSGT Collaborative Congress Helsinki, Finland September 17–20, 2015 Abstracts
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Epidermal Differentiation Complex: A Review on Its Epigenetic Regulation and Potential Drug Targets.
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Electrical stimulation to human dermal papilla cells for hair regenerative medicine
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- Skin wound healing in humans and mice: Challenges in translational research
- Exosomes and Their Bioengineering Strategies in the Cutaneous Wound Healing and Related Complications: Current Knowledge and Future Perspectives
- Advances in skin grafting and treatment of cutaneous wounds
- GROWTH FACTORS IN HAIR ORGAN DEVELOPMENT AND THE HAIR GROWTH CYCLE