Jingting Li
University of California, San Diego
42 Papers
164 Citations
Jingting Li is an academic researcher from University of California, San Diego. The author has contributed to research in topics: Stem cell & Biology. The author has an hindex of 18, co-authored 36 publications. Previous affiliations of Jingting Li include West Virginia University & Wuhan University.
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Papers
Molecular mechanism of hepatic stellate cell activation and antifibrotic therapeutic strategies.
TL;DR: The latest advances in the understanding of the mechanisms of HSC activation and possible antifibrotic therapeutic strategies are summarized.
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A review of decellularized stem cell matrix: a novel cell expansion system for cartilage tissue engineering.
TL;DR: Key parameters in an in vivo stem cell niche are introduced and recent work on DSCM for its rejuvenating or reprograming effect on various adult stem cells and chondrocytes is focused on.
SLUG is required for SOX9 stabilization and functions to promote cancer stem cells and metastasis in human lung carcinoma
Sudjit Luanpitpong,Jingting Li,Amruta Manke,Kathleen M. Brundage,Emily Ellis,Sarah L. McLaughlin,Paweorn Angsutararux,Nawin Chanthra,Maria A. Voronkova,Yi Charlie Chen,Liying Wang,Pithi Chanvorachote,Ming Pei,Surapol Issaragrisil,Yon Rojanasakul +14 more
TL;DR: A novel mechanistic insight is provided into the regulation of CSCs via SLUG-SOX9 regulatory axis, which represents a potential novel target for CSC therapy that may overcome cancer chemoresistance and relapse.
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Increasing the Efficacy of Stem Cell Therapy via Triple-Function Inorganic Nanoparticles.
Fang Chen,Eric Zhao,Ghanim Hableel,Tao Hu,Taeho Kim,Jingting Li,Natalia I. Gonzalez-Pech,David J. Cheng,Jeanne E. Lemaster,Yijun Xie,Vicki H. Grassian,George L. Sen,Jesse V. Jokerst +12 more
TL;DR: In vivo rodent studies show that labeling stem cells with this nanoparticle increased the efficacy of stem cell therapy in a ligation/reperfusion model and improves stem cell survival via the sustained release of pro-survival agents.
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Modulation of in vitro microenvironment facilitates synovium-derived stem cell-based nucleus pulposus tissue regeneration.
TL;DR: The in vitro microenvironment can be modulated by low oxygen and tissue-specific cell-based DECM to facilitate SDSC-based NP tissue regeneration.
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