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Research 31–60 of 866
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Hydroxychloroquine modulates the progression of experimentally induced benign prostatic hyperplasia in rats via targeting EGFR/ERK/STAT3 and AR/FOXO1/TRAIL pathways: computational and in vivo studies
- Cutaneous gain-of-function mutation of LRIG3 leads to alopecia by upregulation of ERBB, PI3K/AKT, NOTCH1 signaling pathways
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- 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)
- Molecular biology of hair morphogenesis: Development and cycling
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Molecular Genetics of Alopecias
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Woolly Antics between the Sheaths
- A missense mutation in Lama3 causes androgen alopecia
- Foxp1 Regulates the Proliferation of Hair Follicle Stem Cells in Response to Oxidative Stress during Hair Cycling
- Dermal white adipose tissue development and metabolism: The role of transcription factor Foxn1
- Linking diet to acne metabolomics, inflammation, and comedogenesis: an update
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- The Genetics of Human Skin Disease
- Consequences of steroid-5α-reductase deficiency and inhibition in vertebrates
- Somatic Mutations in Normal Tissues: New Perspectives on Early Carcinogenesis
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness