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Research 751–780 of 1000+
- How the leopard gets its spots: a transmembrane peptidase specifies feline pigmentation patterns
- Mitochondrial dysfunction in metabolic syndrome and inflammatory skin disease
- Tackling underrepresentation to aid understanding of Parkinson’s disease: Progress and further opportunities
- Stem Cell Use to Treat Dermatological Disorders
- Hair loss in women
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- BMP-FGF Signaling Axis Mediates Wnt-Induced Epidermal Stratification in Developing Mammalian Skin
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- LncRNA H19 Overexpression Activates Wnt Signaling to Maintain the Hair Follicle Regeneration Potential of Dermal Papilla Cells
- Comprehensive Program Planning for the Integration of 21st Century Learning Center After-School Programs with Regular Day Programs and Community Partners.
- The probable destructive mechanisms behind COVID-19 on male reproduction system and fertility
- P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- Physical and mechanical cues affecting biomaterial-mediated plasmid DNA delivery: insights into non-viral delivery systems
- Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Preliminary study on microR-148a and microR-10a in dermal papilla cells of Hu sheep
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Single-Cell Sequencing Reveals Differential Cell Types in Skin Tissues of Liaoning Cashmere Goats and Key Genes Related Potentially to the Fineness of Cashmere Fiber
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Telomere dysfunction impairs epidermal stem cell specification and differentiation by disrupting BMP/pSmad/P63 signaling
- Assessing protein sequencing in human single hair shafts of decreasing lengths
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- CD34 defines melanocyte stem cell subpopulations with distinct regenerative properties