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Research 721–750 of 1000+
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- A novel actor in skin biology: the mineralocorticoid receptor
- A novel 22-bp InDel within <i>FGF7</i> gene is significantly associated with growth traits in goat
- Novel PLCL nanofibrous/keratin hydrogel bilayer wound dressing for skin wound repair
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Polyamine-controlled proliferation and protein biosynthesis are independent determinants of hair follicle stem cell fate
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- 1049 Novel strategy to promote hair follicle growth and stem cell activation in human male scalp skin: Targeting prolactin receptor with ABS-201
- Novel tissue mechanics-guided cellular flows drive the formation of feather follicles
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Novel delivery strategy: finasteride-loaded solid lipid nanoparticles for improved androgenetic alopecia therapy
- Evaluation of neutrophil to lymphocyte ratio, platelet to lymphocyte ratio, mean platelet volume, CRP and ESR with disease severity in patients with alopecia areata
- A Novel Nutraceutical Gummy for Hair Regrowth in Women: A Case Series
- 573 Discovery of JW0061, a novel GFRA1 agonist, as a hair regeneration stimulant via WNT signaling activation in dermal papilla cells
- 1344 Novel human 3D skin model for skin aging research
- 328 The transcription factor CEBPB is a novel hub gene and multi-functional disease driver in Psoriatic skin inflammation
- 600 Evaluation of anti-hairloss shampoo through in vitro activity in human hair follicule dermal papilla cells and sensorial study
- 034 Characterization of novel TMEM173 mutation causing a lupus- and SAVI-like phenotype, modified by polymorphisms in TMEM173 and IFIH1
- 602 Sox13 is a novel marker for hair follicle development and differentiation
- BJD Snippet
- A Novel Role of IL-17+ Cell Subsets in Ross River Virus-Induced Arthritic Disease
- Obtenção e caracterização das células-tronco do folículo piloso de fetos caninos
- Scratching the surface of skin development
- Signaling Involved in Hair Follicle Morphogenesis and Development
- Biomaterials Functionalized with MSC Secreted Extracellular Vesicles and Soluble Factors for Tissue Regeneration
- Hair follicle differentiation and regulation.
- Epigenetic control of adult stem cell function
- Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion
- Molecular biology of hair morphogenesis: Development and cycling