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Research 601–630 of 1000+
- Roles of p38- and c-jun NH2-terminal kinase-mediated pathways in 2-methoxyestradiol-induced p53 induction and apoptosis
- Epidermal Wnt/β-catenin signaling regulates adipocyte differentiation via secretion of adipogenic factors
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Comparative Transcriptome Analysis of Fetal Skin Reveals Key Genes Related to Hair Follicle Morphogenesis in Cashmere Goats
- Care of the transgender patient: the role of the gynecologist
- Free Testosterone: Pumping up the Tires or Ending the Free Ride?
- Bone Morphogenetic Protein Signaling Regulates Postnatal Hair Follicle Differentiation and Cycling
- Microporous Dermal-Like Electrospun Scaffolds Promote Accelerated Skin Regeneration
- Brg1 Governs a Positive Feedback Circuit in the Hair Follicle for Tissue Regeneration and Repair
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- C/EBPα and C/EBPβ Are Required for Sebocyte Differentiation and Stratified Squamous Differentiation in Adult Mouse Skin
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Neural Wiskott-Aldrich syndrome protein modulates Wnt signaling and is required for hair follicle cycling in mice
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia
- High-throughput sequencing of hair follicle development-related micrornas in cashmere goat at various fetal periods
- Experimental Modulation of the Differentiated Phenotype of Keratinocytes from Epidermis and Hair Follicle Outer Root Sheath and Matrix Cells
- Síndrome do ovário policístico: abordagem dermatológica
- Suppression of Wnt/β-catenin signaling by EGF receptor is required for hair follicle development
- Integrative Analysis of Methylome and Transcriptome Reveals the Regulatory Mechanisms of Hair Follicle Morphogenesis in Cashmere Goat
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- A case of recalcitrant pediatric Vogt-Koyanagi-Harada disease successfully controlled with adalimumab
- New developments in the treatment of systemic lupus erythematosus
- Hair tourniquet syndrome in an infant
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Phenotypic modulation of human hair matrix cells (trichocytes) by environmental influence in vitro and in vivo.
- Development and validation of an UPLC method for determination of content uniformity in low-dose solid drugs products using the design space approach
- <i>Pseudomonas aeruginosa</i> heme metabolites biliverdin IXβ and IXδ are integral to lifestyle adaptations associated with chronic infection