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Research 271–300 of 1000+
- Serum Ferritin and Vitamin D in Female Hair Loss: Do They Play a Role?
- Role of -catenin in Epidermal Stem Cell Expansion, Lineage Selection, and Cancer
- Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing
- Apoptosis and cutaneous biology
- Safety Profile of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors: A Disproportionality Analysis of FDA Adverse Event Reporting System
- Does prostaglandin D<sub>2</sub> hold the cure to male pattern baldness?
- Cyclosporin A-induced hair growth in mice is associated with inhibition of calcineurin-dependent activation of NFAT in follicular keratinocytes
- AGD1, a class 1 ARF‐GAP, acts in common signaling pathways with phosphoinositide metabolism and the actin cytoskeleton in controlling Arabidopsis root hair polarity
- How to diagnose a lipodystrophy syndrome
- Disruption of the hedgehog signaling pathway contributes to the hair follicle cycling deficiency in Vdr knockout mice
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Dermal White Adipose Tissue: A Newly Recognized Layer of Skin Innate Defense
- Nonclassic Congenital Adrenal Hyperplasia
- Epidermal abnormalities and increased malignancy of skin tumors in human epidermal keratin 8‐expressing transgenic mice
- Wnt signaling: the good and the bad
- Module-based complexity formation: periodic patterning in feathers and hairs
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Roles of tumor suppressors in regulating tumor-associated inflammation
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations
- Regulatory T cells in inflammatory skin disease: from mice to humans
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Transient mitochondrial DNA double strand breaks in mice cause accelerated aging phenotypes in a ROS-dependent but p53/p21-independent manner
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Congenital hair loss disorders: Rare, but not too rare
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- Network-Based Drug Repositioning: Approaches, Resources, and Research Directions
- GLI2-specific Transcriptional Activation of the Bone Morphogenetic Protein/Activin Antagonist Follistatin in Human Epidermal Cells