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Ni Li

Researcher at Matsumoto Dental University

Publications -  8
Citations -  67

Ni Li is an academic researcher from Matsumoto Dental University. The author has contributed to research in topics: Mesenchymal stem cell & Spheroid. The author has an hindex of 3, co-authored 5 publications receiving 39 citations.

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Enhanced bone regeneration capability of chitosan sponge coated with TiO2 nanoparticles

TL;DR: Chitosan hybridized with titanium dioxide nanoparticles improves its bone regeneration capability and results in significantly improved sponge robustness, biomineralization, and bone regeneration capabilities, as indicated by DMP1 and OCN gene upregulation in chitosAn-50% nanoTiO2 sample.
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Spontaneously Formed Spheroids from Mouse Compact Bone-Derived Cells Retain Highly Potent Stem Cells with Enhanced Differentiation Capability

TL;DR: Spontaneously formed spheroids expressed stem cell markers and showed enhanced osteogenic and neurogenic differentiation capabilities than cells from the conventional monolayer culture, which supports the superior stemness.
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Characterization of spontaneous spheroids from oral mucosa-derived cells and their direct comparison with spheroids from skin-derived cells

TL;DR: Both spheroid-forming cell types had the ability to differentiate into neural and Schwann cells after neurogenic induction, although significantly higher MAP 2, MBP, Nestin, and Nurr1 gene expression was noted in the cells from oral mucosa-derived spheroids.
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Cryopreserved Spontaneous Spheroids from Compact Bone-Derived Mesenchymal Stromal Cells for Bone Tissue Engineering

TL;DR: In this paper, the effect of cryopreservation on viability, stemness, and osteogenic differentiation capability of spontaneous mesenchymal stromal cells (CB-MSC) was investigated.
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Tooth transplantation with a β-tricalcium phosphate scaffold accelerates bone formation and periodontal tissue regeneration.

TL;DR: This study showed accelerated bone formation and periodontal tissue regeneration when tooth transplantation was performed with a β-TCP scaffold and BM-MNCs may accelerate bone maturation, while the effect on bone formation was limited.