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Jun Cai

Researcher at University of Louisville

Publications -  71
Citations -  3421

Jun Cai is an academic researcher from University of Louisville. The author has contributed to research in topics: Oligodendrocyte & OLIG2. The author has an hindex of 29, co-authored 65 publications receiving 2939 citations. Previous affiliations of Jun Cai include Wenzhou Medical College & Jilin University.

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Journal ArticleDOI

Control of oligodendrocyte differentiation by the Nkx2.2 homeodomain transcription factor.

TL;DR: The results strongly suggest that Nkx2.2 regulates the differentiation and/or maturation, but not the initial specification, of oligodendrocyte progenitors, and that overproduction of Nk X.2 protein in fibroblast cells can induce gene expression from the proteolipid protein promoter.
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Generation of Oligodendrocyte Precursor Cells from Mouse Dorsal Spinal Cord Independent of Nkx6 Regulation and Shh Signaling

TL;DR: In this study, in vivo evidence for a late phase of Olig gene expression independent of Nkx6 and Shh gene activities is provided and a brief second wave of oligodendrogenesis in the dorsal spinal cord is revealed.
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Dual origin of spinal oligodendrocyte progenitors and evidence for the cooperative role of Olig2 and Nkx2.2 in the control of oligodendrocyte differentiation.

TL;DR: The co-expression of Nkx2.2 and Olig2 in OLPs is tightly associated with myelin gene expression in the normal and PDGFA(-/-) embryos, suggesting a cooperative role of these transcription factors in the control of oligodendrocyte differentiation.
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Current approaches to enhance CNS delivery of drugs across the brain barriers.

TL;DR: The current approaches to open or facilitate penetration across brain barriers for enhanced drug delivery to the CNS are reviewed, and the associated mechanisms and problems are discussed.
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Induction of oligodendrocyte differentiation by Olig2 and Sox10 : Evidence for reciprocal interactions and dosage-dependent mechanisms

TL;DR: Evidence is presented that the control of oligodendrocyte differentiation by Olig2, Sox10 and Nkx2.2 is a dosage-dependent developmental process and can be affected by both haploinsufficiency and over-dosage.