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Research 61–90 of 864
- 321 Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in FoxD1-lineage mesenchymal cells leads to congenital truncal alopecia
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- Gene expression of FOXA1 and CCL2 in different phenotypes of infertile women with polycystic ovarian syndrome
- Transcriptomics sequencing reveals Qu-shi-yu-fa Decoction promotes hair cycle and keratinization by upregulating FOXN1 and TGM3 to treat androgenetic alopecia
- Qu-Shi-Yu-Fa Decoction Promotes Hair Cycle and Keratinization by Upregulating Foxn1 and Tgm3 to Treat Androgenetic Alopecia
- Dermal white adipose tissue development and metabolism: The role of transcription factor Foxn1
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Over-, ectopic-expression of FoxN1 at early life adversely influences lymphopoiesis (HEM3P.280)
- FoxN1 in K14 promoter-driven epithelium is required for generation and maintenance of 3D-thymus medulla and preventing nude phenotype in the skin (36.33)
- Transcription factor FOXC1 positively regulates SFRP1 expression in androgenetic alopecia
- First use of thymus transplantation therapy for FOXN1 deficiency (nude/SCID): a report of 2 cases
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- MiR-325-3p functions as a suppressor miRNA and inhibits the proliferation and metastasis of glioma through targeting FOXM1
- Inhibition of Bmp signaling affects growth and differentiation in the anagen hair follicle
- `Cyclic alopecia' in<i>Msx2</i>mutants: defects in hair cycling and hair shaft differentiation
- Molecular biology of hair morphogenesis: Development and cycling
- Linking diet to acne metabolomics, inflammation, and comedogenesis: an update
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Skin expression of mammalian target of rapamycin and forkhead box transcription factor O1, and serum insulin‐like growth factor‐1 in patients with acne vulgaris and their relationship with diet
- Learning from nudity: lessons from the nude phenotype
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- Phospholipase C‐δ1 is an essential molecule downstream of <i>Foxnl,</i> the gene responsible for the nude mutation, in normal hair development
- Aging, alopecia, and stem cells
- The nude gene and the skin
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- Gsdma3 is required for hair follicle differentiation in mice
- Formation of regulator/target gene relationships during evolution
- Case Series: Gene Expression Analysis in Canine Vogt-Koyanagi-Harada/Uveodermatologic Syndrome and Vitiligo Reveals Conserved Immunopathogenesis Pathways Between Dog and Human Autoimmune Pigmentary Disorders
- miR-150 regulates endothelial progenitor cell differentiation via Akt and promotes thrombus resolution