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Research 61–90 of 119
- Transcriptomic Analysis Reveals Candidate Ligand-Receptor Pairs and Signaling Networks Mediating Intercellular Communication between Hair Matrix Cells and Dermal Papilla Cells from Cashmere Goats
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Orchestration of tissue‐scale mechanics and fate decisions by polarity signalling
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Integrated Meta-Analysis of Scalp Transcriptomics and Serum Proteomics Defines Alopecia Areata Subtypes and Core Disease Pathways
- Environmental Air Pollutants Affecting Skin Functions with Systemic Implications
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Role of skin enzymes in metabolism of topical drugs
- Biology and Genetics of Hair
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Congenital hair loss disorders: Rare, but not too rare
- The role of hair follicles and Edar signalling in cutaneous wound healing
- Mechanical forces in skin disorders
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Molecular Genetics of Alopecias
- 196 The endocannabinoid tone regulates human sebocyte biology
- 194 An underlying mechanism of hair loss in acrodermatitis enteropathica
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Learning from nudity: lessons from the nude phenotype
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Oral cyclosporin does not arrest progression of androgenetic alopecia
- Genetics of Structural Hair Disorders
- Complex Hair Cycle Domain Patterns and Regenerative Hair Waves in Living Rodents