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Research 61–90 of 1000+
- Size Polymorphisms in the Human Ultrahigh Sulfur Hair Keratin-Associated Protein 4, KAP4, Gene Family
- Mediator 1 ablation induces enamel-to-hair lineage conversion through enhancer dynamics
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- The role of Glucosylceramides in Keratinocyte Differentiation and Epidermal Barrier Function
- Loss of ERBB2 and ERBB3 Receptors Impacts Epidermal Differentiation in Mice
- Birt-Hogg-Dube Syndrome with a Novel Mutation in the <i>FLCN</i> Gene
- A novel 22-bp InDel within <i>FGF7</i> gene is significantly associated with growth traits in goat
- ROBO4 deletion ameliorates PAF-mediated skin inflammation via regulating the mRNA translation efficiency of LPCAT1/LPCAT2 and the expression of PAF receptor
- Pseudo Pemphigus Phenotypes in Mice with Inactivated Desmoglein 3
- Loss of Stem Cells Correlates with Premature Aging in Animal Study, Penn Researchers Find
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in <i>FoxD1</i>-lineage mesenchymal cells leads to congenital truncal alopecia
- Melatonin promotes hair regeneration by modulating the Wnt/β‐catenin signalling pathway
- CD169+ Skin Macrophages Function as a Specialized Subpopulation in Promoting Psoriasis-like Skin Disease in Mice
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Motoneuron-Specific PTEN Deletion in Mice Induces Neuronal Hypertrophy and Also Regeneration after Facial Nerve Injury
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Lymphatic vessels interact dynamically with the hair follicle stem cell niche during skin regeneration <i>in vivo</i>
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in FoxD1-lineage mesenchymal cells leads to congenital truncal alopecia
- 186 Dissecting the role of the common neurotrophin receptor CD271 in the skin: generation and characterization of a novel mouse model with keratinocyte-specific conditional deletion
- 855 Targeted deletion of crif1 in mouse skin epidermis impairs skin homeostasis
- Regulation of a hair follicle keratin intermediate filament gene promoter
- The ITGB6 gene: its role in experimental and clinical biology
- Combination of Transcriptomics and Proteomics Reveals Differentially Expressed Genes and Proteins in the Skin of EDAR Gene-Targeted and Wildtype Cashmere Goats
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Spatial Gene Profiling in the Ischemic Heart
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice