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Research 361–390 of 737
- Molecular basis of androgen insensitivity
- The Photoprotective Effect of S-Methylmethionine Sulfonium in Skin
- Proteolysis‐Targeting Chimera (PROTAC): Current Applications and Future Directions
- Identification of functional circRNAs regulating ovarian follicle development in goats
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Isoginkgetin, a natural biflavonoid from Ginkgo biloba, inhibits inflammatory response in endothelial cells via suppressing NF-κB activation
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Regulatory mechanisms of LGR4 on cancer and cancer stem cell properties
- Myotonic Dystrophy—A Progeroid Disease?
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- <i>miR‐124</i> promotes neural differentiation in mouse bulge stem cells by repressing <i>Ptbp1</i> and <i>Sox9</i>
- Phosphatase Regulator NIPP1 Restrains Chemokine-Driven Skin Inflammation
- Epigenetics of Colorectal Cancer
- Impaired wound healing in transgenic mice overexpressing the activin antagonist follistatin in the epidermis
- WNT Signaling in Disease
- Corticotropin releasing hormone and the skin
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Hair Defects and Pup Loss in Mice with Targeted Deletion of the First Cut Repeat Domain of theCux/CDPHomeoprotein Gene
- Epithelial–mesenchymal transition in keloid tissues and TGF‐β1–induced hair follicle outer root sheath keratinocytes
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- The Molecular Biology of the Vitamin D Receptor
- Finasteride Enhances the Generation of Human Myeloid-Derived Suppressor Cells by Up-Regulating the COX2/PGE2 Pathway
- The Peach RGF/GLV Signaling Peptide pCTG134 Is Involved in a Regulatory Circuit That Sustains Auxin and Ethylene Actions
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- ALKBH5-mediated m6A demethylation fuels cutaneous wound re-epithelialization by enhancing PELI2 mRNA stability
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Ectopic expression of FGF5s induces wool growth in Chinese merino sheep
- Regulation of cashmere fineness traits by noncoding RNA in Jiangnan cashmere goats
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Repigmentation by combined narrow‑band ultraviolet B/adipose‑derived stem cell transplantation in the mouse model: Role of Nrf2/HO‑1‑mediated Ca<sup>2+</sup> homeostasis