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Research 961–990 of 1000+
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- Loss of keratin 10 is accompanied by increased sebocyte proliferation and differentiation
- Epigenetics and Other Autoimmune Skin Diseases
- The effect of proteolytic enzymes on hair follicles of transgenic mice expressing the lac Z-protein in cells of the bulge region
- Fecal Microbiota and Metabolites Predict Metabolic Health Features Across Various Dietary Patterns
- Dysregulation of Grainyhead-like 3 expression causes widespread developmental defects
- 855 Targeted deletion of crif1 in mouse skin epidermis impairs skin homeostasis
- Research Snippets
- In vivo Alteration of the Keratin 17 Gene in Hair Follicles by Oligonucleotide-directed Gene Targeting
- Molecular Mechanisms Regulating Hair Follicle Development
- Expression of Hypothalamic–Pituitary–Thyroid Axis RelatedGenes in the Human Skin
- Deciphering the Mesodermal Potency of Porcine Skin-Derived Progenitors (SKP) by Microarray Analysis
- DNA Microarray and Bioinformatic Analysis Reveals the Potential of Whale Oil in Enhancing Hair Growth in a C57BL/6 Mice Dorsal Skin Model
- Identification of key pathways and genes that regulate cashmere development in cashmere goats mediated by exogenous melatonin
- Seasonal Gene Expression Profile Responsible For Hair Follicle Development In Angora Goats
- Identification of N6-Methyladenosine-Related Factors and the Prediction of the Regulatory Mechanism of Hair Follicle Development in Rex and Hycole Rabbits
- Seasonal Gene Expression Profile Responsible for Hair Follicle Development in Angora Goats
- 723 DNA dioxygenases Tet2/3 regulate gene promoter accessibility and three-dimensional chromatin topology in lineage-specific loci to control hair growth
- The pattern recognition receptor toll-like receptor 3 regulates skin barrier homeostasis
- SFRP2/DPP4 and FMO1/LSP1 Define Major Fibroblast Populations in Human Skin
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Keratin disorders: from gene to therapy
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- What causes hidradenitis suppurativa ?—15 years after
- Thyrotropin-releasing hormone and oestrogen differentially regulate prolactin and prolactin receptor expression in female human skin and hair follicles <i>in vitro</i>
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Identification of genes and proteins associated with anagen wool growth
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Human umbilical cord mesenchymal stem cell treatment alleviates symptoms in an atopic dermatitis-like mouse model
- Characteristics of Malassezia furfur at various pH and effects of Malassezia lipids on skin cells