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Research 421–450 of 1000+
- <i>Hoxc13</i> mutant mice lack external hair
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- Differential Auxin-Transporting Activities of PIN-FORMED Proteins in Arabidopsis Root Hair Cells
- Keratin disorders: from gene to therapy
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Differentiation of Mouse Induced Pluripotent Stem Cells into a Multipotent Keratinocyte Lineage
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Physiologic functions of PP2A: Lessons from genetically modified mice
- Activin Controls Skin Morphogenesis and Wound Repair Predominantly via Stromal Cells and in a Concentration-Dependent Manner via Keratinocytes
- <i>Sept4/</i> ARTS Regulates Stem Cell Apoptosis and Skin Regeneration
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Treatment of MSCs with Wnt1a-conditioned medium activates DP cells and promotes hair follicle regrowth
- AGD1, a class 1 ARF‐GAP, acts in common signaling pathways with phosphoinositide metabolism and the actin cytoskeleton in controlling Arabidopsis root hair polarity
- α3β1-integrin regulates hair follicle but not interfollicular morphogenesis in adult epidermis
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- Prediction of male-pattern baldness from genotypes
- Lymphoid Enhancer-binding Factor-1 (LEF1) Interacts with the DNA-binding Domain of the Vitamin D Receptor
- Human TSC2-null fibroblast-like cells induce hair follicle neogenesis and hamartoma morphogenesis
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Elucidating the roles of three β-glucuronosyltransferases (GLCATs) acting on arabinogalactan-proteins using a CRISPR-Cas9 multiplexing approach in Arabidopsis
- Epidermal Stem Cells Cultured on Collagen-Modified Chitin Membrane Induce In Situ Tissue Regeneration of Full-Thickness Skin Defects in Mice
- Alopecia Areata
- Androgen receptor modulators: a review of recent patents and reports (2012-2018)
- Consequences of steroid-5α-reductase deficiency and inhibition in vertebrates
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Epigenetic regulation in adult stem cells and cancers
- Androgenetic alopecia: combing the hair follicle signaling pathways for new therapeutic targets and more effective treatment options