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Research 481–510 of 1000+
- The role of multiomics in revealing the mechanism of skin repair and regeneration
- Deep skin fibroblast-mediated macrophage recruitment supports acute wound healing
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- A pig model exploring the postnatal hair follicle cycle
- Mechanistic synergy of hair growth promotion by the Avicennia marina extract and its active constituent (avicequinone C) in dermal papilla cells isolated from androgenic alopecia patients
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Insights into male androgenetic alopecia using comparative transcriptome profiling: hypoxia-inducible factor-1 and Wnt/β-catenin signalling pathways
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- The Roles of EDA2R in Ageing and Disease
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen
- PCSK9: From Nature’s Loss to Patient’s Gain
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- An <i>mTurq2-Col4a1</i> mouse model allows for live visualization of mammalian basement membrane development
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Molecular stratification of the human fetal vaginal epithelium by spatial transcriptome analysis
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Identification of Key Pathways and Genes Related to the Development of Hair Follicle Cycle in Cashmere Goats
- Epigenetic Effects of Gender-Affirming Hormone Treatment: A Pilot Study of the ESR2 Promoter’s Methylation in AFAB People
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- Transcription factor-based transdifferentiation of human embryonic to trophoblast stem cells
- Characters of KRT80 and its roles in neoplasms diseases
- Potential Involvement of miR-144 in the Regulation of Hair Follicle Development and Cycle Through Interaction with Lhx2
- Whitaker syndrome: A case report of autoimmune polyendocrine syndrome type 1 with dilated cardiomyopathy
- FOXN1 deficient nude severe combined immunodeficiency
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- Genetic Variants and Protective Immunity against SARS-CoV-2
- Role of Extracellular Vesicles as Mediators of Cell Communication and Novel Biomarkers in Sepsis