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Research 31–60 of 428
- Regulation and Role of GLI1 in Cutaneous Squamous Cell Carcinoma Pathogenesis
- Regeneration of fat cells from myofibroblasts during wound healing
- Targeting of Smoothened for therapeutic gain
- The chemokine SDF-1/CXCL12 regulates the migration of melanocyte progenitors in mouse hair follicles
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Parsing patterns: Emerging roles of tissue self-organization in health and disease
- S100A6 Protein—Expression and Function in Norm and Pathology
- Mommy — where do tumors come from?
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- Genome-Wide Identification and Characterization of the Wnt Gene Family in Donkey (Equus asinus): Phylogenetic Analysis and Expression Profiling
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Dual-Action Icariin-Containing Thermosensitive Hydrogel for Wound Macrophage Polarization and Hair-Follicle Neogenesis
- Human epidermal neural crest stem cells as a source of Schwann cells
- CXCL12 inhibits hair growth through CXCR4
- Regeneration of Dermis: Scarring and Cells Involved
- Ca <sup>2+</sup> -mediated protein citrullination regulates proliferation in the regenerating and malignant CNS
- Transforming growth factor-β in stem cells and tissue homeostasis
- A role of melatonin in neuroectodermal‐mesodermal interactions: the hair follicle synthesizes melatonin and expresses functional melatonin receptors
- Laminin-511 is an epithelial message promoting dermal papilla development and function during early hair morphogenesis
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Thiamin Deficiency and Alopecia
- Embolic Stroke as the Initial Manifestation of Systemic Lupus Erythematosus
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Oral Manifestations of Hematologic and Nutritional Diseases
- Inherited Disorders of the Hair
- Locally Synthetized 17-β-Estradiol Reverses Amyloid-β-42-Induced Hippocampal Long-Term Potentiation Deficits
- Schmallenberg virus infection suspected in a calf born to an imported heifer
- Vitamins and their derivatives synergistically promote hair shaft elongation ex vivo via PlGF/VEGFR-1 signalling activation