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Research 541–570 of 1000+
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Ptch2 is a Potential Regulator of Mesenchymal Stem Cells
- Tissue Regeneration, Stem Cells, and Wound Healing
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- CRISPR/Cas9-mediated<i>VDR</i>knockout plays an essential role in the growth of dermal papilla cells through enhanced relative genes
- Cyclin D3 deficiency inhibits skin tumor development, but does not affect normal keratinocyte proliferation
- Autophagy Controls the Protein Composition of Hair Shafts
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Machine learning driven multi-omics analysis of the genetic mechanisms behind the double-coat fleece formation in Hetian sheep
- Chronic circadian misalignment is a risk factor for hair growth impairment
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- Synopsis: 2005 Annual Meeting of the American Society of Andrology
- Malicious Mites—Sarcoptes scabiei in Raccoon Dogs (Nyctereutes procyonoides) in Schleswig-Holstein, Germany
- MITF E318K naevus phenotype: the modifying role of MC1R Red Hair Variants
- Poxvirus and Toxoplasma gondii co-infection in a free-ranging Paraguayan hairy dwarf porcupine (Coendou spinosus), Brazil
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Ligand-Independent Vitamin D Receptor Actions Essential for Keratinocyte Homeostasis in the Skin
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- Diseases of Honeybee (Apis mellifera)
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Author response: Loss of Dnmt3a and Dnmt3b does not affect epidermal homeostasis but promotes squamous transformation through PPAR-γ
- Decision letter: Loss of Dnmt3a and Dnmt3b does not affect epidermal homeostasis but promotes squamous transformation through PPAR-γ
- Single-Nucleus and Bulk RNA Sequencing Reveals the Involvement of Natural Killer and CD8+ T Cells in the Progression of Androgenetic Alopecia
- The Impact of Sulforaphane on Sex-Specific Conditions and Hormone Balance: A Comprehensive Review
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Role of the soluble epoxide hydrolase in the hair follicle stem cell homeostasis and hair growth
- Author response: Spatiotemporal dynamics of PIEZO1 localization controls keratinocyte migration during wound healing