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Research 121–150 of 1000+
- Regulatory pathway analysis of coat color genes in Mongolian horses
- 3,4,5-Tri-O-Caffeoylquinic Acid Promoted Hair Pigmentation Through β-Catenin and Its Target Genes
- Deciphering gene regulatory programs in mouse embryonic skin through single-cell multiomics analysis
- Neural Wiskott-Aldrich syndrome protein modulates Wnt signaling and is required for hair follicle cycling in mice
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Runx Family Genes in Tissue Stem Cell Dynamics
- Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat (Capra hircus)
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Facial Appearance and Markers of Cardiometabolic Risk in Healthy Adult Men
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- Epigenetic regulation and factors that influence the effect of iPSCs-derived neural stem/progenitor cells (NS/PCs) in the treatment of spinal cord injury
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- JMJD3 and NF-κB-dependent activation of Notch1 gene is required for keratinocyte migration during skin wound healing
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics
- Loss of ‘Epidermal Melanin Unit’ Integrity in Human Skin During Melanoma-Genesis
- Diversity of Adult Stem Cell Niches in the Dermal Compartment of Skin
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- 皮膚組織の再生に向けた皮膚由来幹細胞に関する研究
- Follikelhormone
- The human keratins: biology and pathology
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- 854 CCL5 affects the hair-inductive capacity of three-dimensional (3D)-cultured dermal papilla cells
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- Considerations in genetic counseling of transgender patients: Cultural competencies and altered disease risk profiles
- Multimodal imaging of hair follicle bulge-derived stem cells in a mouse model of traumatic brain injury
- Characterization of Primary Cilia and Intraflagellar Transport 20 in the Epidermis
- Prospect of Stem Cell Conditioned Medium in Regenerative Medicine