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Research 631–660 of 1000+
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Structural features and sites of expression of a new murine 65 kD and 48 kD hair-related keratin pair, associated with a special type of parakeratotic epithelial differentiation
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Formation of regulator/target gene relationships during evolution
- GATA3 inhibits proliferation and induces expression of both early and late differentiation markers in keratinocytes of the human epidermis
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- The Molecular Biology of the Vitamin D Receptor
- Selective Expression of Calcium-Binding Proteins S100A8 and S100A9 at Distinct Sites of Hair Follicles
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- Tβ4-overexpression based on the piggyBac transposon system in cashmere goats alters hair fiber characteristics
- Analysis of familial factors using the basic and specific (BASP) classification in Korean patients with androgenetic alopecia
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Structure and site of expression of a murine type II hair keratin
- 4 Vitamin D resistance
- Androgen regulation of a specific gene in hamster flank organs
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- CtBP1 Overexpression in Keratinocytes Perturbs Skin Homeostasis
- The Mask Mutation Identifies TMPRSS6 as an Essential Suppressor of Hepcidin Gene Expression, Required for Normal Uptake of Dietary Iron.
- Hair follicle morphogenesis and epidermal homeostasis in we/we wal/wal mice with postnatal alopecia
- URB expression in human dermal papilla cells
- Reconstructive Hair Transplantation of the Face and Scalp
- Oral Finasteride Presents With Sexual-Unrelated Withdrawal in Long-Term Treated Androgenic Alopecia in Men.
- Enhancement of hair growth through stimulation of hair follicle stem cells by prostaglandin E2 collagen matrix
- Lipid signaling in keratinocytes: Lipin-1 plays a PArt
- Decoding the ZmNF-YC1–ZmAPRG pathway for phosphorus efficiency
- Role of DNA Methylation in the Pathogenesis of Skin Disorders: Mechanisms, Inhibitors of Methylation‐Related Enzyme, and Molecular Docking Studies
- Extensive Challenges and Pending Advances in the Study of 5-Alpha-Reductase Isoenzymes. A Literature Review
- 5α-Reductase Inhibitory Potential of <i>Hibiscus rosa sinensis</i>: Effective for the Management of Alopecia