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Research 751–780 of 1000+
- A new path in defining light parameters for hair growth: Discovery and modulation of photoreceptors in human hair follicle
- Transcutaneous implantation of valproic acid-encapsulated dissolving microneedles induces hair regrowth
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Adipose mesenchymal stem cells combined with platelet-rich plasma accelerate diabetic wound healing by modulating the Notch pathway
- Congenital atrichia and hypotrichosis
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response
- Glucocorticoid and Sex Hormone Receptors: Clinical Implications and Therapeutic Relevance
- γδ17 T cell-stromal networks modulate matrix composition and vascularity in foreign body response
- Follicular Neutrophilic Inflammation (Hidradenitis Suppurativa)
- Cutaneous signals of immune system disease
- Carboxytherapy in Aesthetic Medicine
- A Novel Secretory Vesicle from Deer Antlerogenic Mesenchymal Stem Cell-Conditioned Media (DaMSC-CM) Promotes Tissue Regeneration
- Botanicals With Dermatologic Properties Derived From First Nations Healing: Part 1—Trees
- Progeroide Syndrome
- Induction of Skin-Derived Precursor Cells from Human Induced Pluripotent Stem Cells
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Advances In Mesenchymal Cell Therapy In Dermatology And Aesthetic Medicine
- Ovine KRT81 Variants and Their Influence on Selected Wool Traits of Commercial Value
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- Autophagy Controls the Protein Composition of Hair Shafts
- Detection of a Second KAP22 Family Member in Sheep and Analysis of Its Genetic Variation and Associations with Selected Wool Fibre Traits
- Defective trophoblast function in mice with a targeted mutation of Ets2
- More than one way to skin . . .
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Transcriptomic regulation of seasonal coat color change in hares
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes