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Research 991–1000 of 1000+
- 376 Tsc2 disruption in mesenchymal progenitors regulates hair follicles and TGF beta signaling
- 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
- Comparative Study of Some Potential Paracrine Factors Produced by Normal and Androgenetic Alopecia Hair Follicles
- CD4+CD25+FoxP3+ Regulatory Tregs inhibit fibrocyte recruitment and fibrosis via suppression of FGF-9 production in the TGF-β1 exposed murine lung
- 165 Single-cell RNA sequencing analysis unveils highly active yet diminished CD14+CD16- circulating monocytes, independent of alopecia areata severity
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Keratinocyte-Expressed Podoplanin is Dispensable for Multi-Step Skin Carcinogenesis
- Loss of TET2 Tips the Scales Toward Tumorigenesis