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Research 31–60 of 865
- Inhibition of Bmp signaling affects growth and differentiation in the anagen hair follicle
- Gsdma3 is required for hair follicle differentiation in mice
- <i>FOXN1</i> Duplication and Congenital Hypertrichosis
- FOXN1 deficient nude severe combined immunodeficiency
- FOXN1 Is Critical for Onycholemmal Terminal Differentiation in Nude (Foxn1nu) Mice
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Knockdown of miR-361-5p promotes the induced activation of SHF-stem cells through FOXM1 mediated Wnt/β-catenin pathway in cashmere goats
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- Di-Genic Inheritance in Genodermatoses: Insights from Two Consanguineous Cases in a Reference Lebanese Center within the Middle East and North Africa (MENA) Region
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in FoxD1-lineage mesenchymal cells leads to congenital truncal alopecia
- 1438 KLF4 maintains hair follicle stem cell quiescence
- Screened of long non-coding RNA related to wool development and fineness in Gansu alpine fine-wool sheep
- miR-150 regulates endothelial progenitor cell differentiation via Akt and promotes thrombus resolution
- Dermal white adipose tissue development and metabolism: The role of transcription factor Foxn1
- Genetically separable determinants of hair keratin gene expression
- Genome-wide p63-Target Gene Analyses Reveal TAp63/NRF2-Dependent Oxidative Stress Responses
- MiR-325-3p functions as a suppressor miRNA and inhibits the proliferation and metastasis of glioma through targeting FOXM1
- Aging, alopecia, and stem cells
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in <i>FoxD1</i>-lineage mesenchymal cells leads to congenital truncal alopecia
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- Melatonin-Mediated Circadian Rhythm Signaling Exhibits Bidirectional Regulatory Effects on the State of Hair Follicle Stem Cells
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis.
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response