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Research 271–300 of 727
- Role of the Notch Ligand Delta1 in Embryonic and Adult Mouse Epidermis
- The keratin 19 promoter is potent for cell-specific targeting of genes in transgenic mice
- Clock genes, hair growth and aging
- Structure and Mechanical Properties of Human Trichocyte Keratin Intermediate Filament Protein
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Overexpression of Bcl-2 Protects from Ultraviolet B-Induced Apoptosis but Promotes Hair Follicle Regression and Chemotherapy-Induced Alopecia
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- Activin B Promotes Epithelial Wound Healing In Vivo through RhoA-JNK Signaling Pathway
- Hypoxia in Cell Reprogramming and the Epigenetic Regulations
- Interleukin-25-Mediated-IL-17RB Upregulation Promotes Cutaneous Wound Healing in Diabetic Mice by Improving Endothelial Cell Functions
- The influence of interferon on healthy and diseased skin
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Keratinocyte-derived follistatin regulates epidermal homeostasis and wound repair
- Recombinant human hair keratin proteins for halting bleeding
- PPAR‐γ signalling as a key mediator of human hair follicle physiology and pathology
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- IL-12/IL-23 neutralization is ineffective for alopecia areata in mice and humans
- Human hair follicle stem cell differentiation into contractile smooth muscle cells is induced by transforming growth factor-β1 and platelet-derived growth factor BB
- Cutaneous gene therapy
- Investigation of a non-invasive method of assessing the equine circadian clock using hair follicle cells
- Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids
- A human vitamin D receptor mutation causes rickets and impaired Th1/Th17 responses
- Ligand‐Independent Actions of the Vitamin D Receptor: More Questions Than Answers
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Epidermal PPARγ Is a Key Homeostatic Regulator of Cutaneous Inflammation and Barrier Function in Mouse Skin
- Epiregulin promotes hair growth via EGFR‐medicated epidermal and ErbB4‐mediated dermal stimulation
- Phosphatase Regulator NIPP1 Restrains Chemokine-Driven Skin Inflammation
- Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study