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Research 91–120 of 99
- Sebum Free Fatty Acids Enhance the Innate Immune Defense of Human Sebocytes by Upregulating β-Defensin-2 Expression
- Unraveling the web of defense: the crucial role of polysaccharides in immunity
- Mining Therapeutic Efficacy from Treasure Chest of Biodiversity and Chemodiversity: Pharmacophylogeny of Ranunculales Medicinal Plants
- 1H NMR-based lipidomics of rodent fur: species-specific lipid profiles and SCD1 inhibitor-related dermal toxicity
- Recent Progress in Health Benefits of Hederagenin and Its Glycosides
- Phytochemicals With Anti 5-alpha-reductase Activity: A Prospective For Prostate Cancer Treatment
- The Influence of Monosaccharide Composition on the Bioactivity of Medicinal Plant Polysaccharides
- The Influence of Monosaccharide Composition on the Bioactivity of Medicinal Plant Polysaccharides: A Review
- Anti-inflammatory Effects in LPS-treated RAW 264.7 Cells and the Influences on Drug Metabolizing Enzyme Activities by the Traditional Herbal Formulas, Yongdamsagan-Tang and Paljung-san
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Scraggly, a new hair loss mutation on mouse Chromosome 19
- Animal Models of Psoriasis – What Can We Learn from Them?
- 666 Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in follicular dystrophy and primary cicatricial alopecia
- Clinical Snippets
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- The expression of the gene <i>asebia</i> in the laboratory mouse: 3. Sebaceous glands
- Glycerol Regulates Stratum Corneum Hydration in Sebaceous Gland Deficient (Asebia) Mice
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Roles of GasderminA3 in Catagen–Telogen Transition During Hair Cycling
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Fertility and Sterility Vol 101 No 4, April 2014
- Adipocyte Lineage Cells Contribute to the Skin Stem Cell Niche to Drive Hair Cycling
- Lichen Planopilaris
- Cicatricial (Scarring) Alopecias