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Research 91–120 of 1000+
- Deciphering gene regulatory programs in mouse embryonic skin through single-cell multiomics analysis
- Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector
- Avaliação do perfil fenotípico, proliferativo e secretório de células-tronco mesenquimais do tecido adiposo captadas por lipoaspiração assistida por laser
- Recent advances in neuropeptide-related omics and gene editing: Spotlight on NPY and somatostatin and their roles in growth and food intake of fish
- 1325 Age-dependent loss of the stemness and antimicrobial defense function of dermal fibroblasts is mediated by TGFbeta
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- 859 Building a functional niche for hair follicle stem cells
- Light-Emitting Hair Follicles: Studying Skin Regeneration With In Vivo Imaging
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- The Genetics of Human Skin Disease
- Biology and Genetics of Hair
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Learning from nudity: lessons from the nude phenotype
- Redefining hormone resistance in prostate cancer
- Platelet-derived growth factor signaling modulates adult hair follicle dermal stem cell maintenance and self-renewal
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Erbium–Yttrium–Aluminum–Garnet Laser Irradiation Ameliorates Skin Permeation and Follicular Delivery of Antialopecia Drugs
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Genetics of Structural Hair Disorders
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Dermatopathology and molecular genetics
- Improving selective androgen receptor modulator discovery and preclinical evaluation
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- STAT3 Partly Inhibits Cell Proliferation via Direct Negative Regulation of FST Gene Expression
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- Dicer- and BSC-dependent miRNAs during murine anagen development
- A computationally inferred regulatory heart aging model including post-transcriptional regulations
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation