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Research 151–180 of 1000+
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- m6A Methylation Analysis Reveals Networks and Key Genes Underlying the Coarse and Fine Wool Traits in a Full-sib Merino Family
- Generation of iPS-derived model cells for the analysis of hair development
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Molecular stratification of the human fetal vaginal epithelium by spatial transcriptome analysis
- Expression of Plectin-1 and Trichohyalin in Human Tongue Cancer Cells
- Lentiviral Arrays for Live-cell Dynamic Monitoring of Gene and Pathway Activity During Stem Cell Differentiation
- Intradermal Injection of Bleomycin Shows Preliminary Evidence of Dermal Fibrosis in a Mouse Model
- Effect of Sun exposure-induced ferroptosis mechanisms on pathology and potential biological processes of primary melanoma by microarray data analysis
- Combining multiomics to analyze the molecular mechanism of hair follicle cycle change in cashmere goats from Inner Mongolia
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Cellular response of keratinocytes to the entry and accumulation of nanoplastic particles
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Effects of oxytocin receptor agonists on hair growth promotion
- 854 CCL5 affects the hair-inductive capacity of three-dimensional (3D)-cultured dermal papilla cells
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Adverse effects of the 5-alpha-reductase inhibitor finasteride on Daphnia magna: Endocrine system and lipid metabolism disruption
- Androgenic Alopecia: Cross-Talk Between Cell Signal Transduction Pathways
- Knockdown of FOXA2 Impairs Hair-Inductive Activity of Cultured Human Follicular Keratinocytes
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- High-confidence cancer patient stratification through multiomics investigation of DNA repair disorders
- 14-3-3σ Is Required for Club Hair Retention
- Decoding the role of <i>OsPRX83</i> in enhancing osmotic stress tolerance in rice through ABA-dependent pathways and ROS scavenging
- The mesenchymal component of hair follicle neogenesis: background, methods and molecular characterization
- Follicular dermal papilla structures by organization of epithelial and mesenchymal cells in interfacial polyelectrolyte complex fibers
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Induction of Skin-Derived Precursor Cells from Human Induced Pluripotent Stem Cells
- Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis