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Shong Lau

Researcher at Lund University

Publications -  9
Citations -  738

Shong Lau is an academic researcher from Lund University. The author has contributed to research in topics: Reprogramming & Induced pluripotent stem cell. The author has an hindex of 6, co-authored 6 publications receiving 599 citations.

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Generation of induced neurons via direct conversion in vivo.

TL;DR: It is shown that transplanted human fibroblasts and human astrocytes, which are engineered to express inducible forms of neural reprogramming genes, convert into neurons when reprograming genes are activated after transplantation.
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In Vivo Reprogramming of Striatal NG2 Glia into Functional Neurons that Integrate into Local Host Circuitry

TL;DR: An adeno-associated virus-based reporter system that allows selective GFP labeling of reprogrammed neurons is developed that allows mapping of 3D circuitry integration into local and distal brain regions and shows that the newly reprogramed neurons are integrated into host brain.
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REST suppression mediates neural conversion of adult human fibroblasts via microRNA-dependent and -independent pathways

TL;DR: An optimized one‐step method to efficiently reprogram dermal fibroblasts from elderly individuals using a single‐vector system is developed and it is demonstrated that it is possible to obtain iNs of high yield and purity from aged individuals with a range of familial and sporadic neurodegenerative disorders including Parkinson's, Huntington's, as well as Alzheimer's disease.
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Highly efficient generation of induced neurons from human fibroblasts that survive transplantation into the adult rat brain.

TL;DR: A protocol for highly efficient generation of functional iNs from fetal human fibroblasts is presented and the ability of these converted human iNs (hiNs) to survive transplantation and maintain their phenotype in the adult rat brain is demonstrated.
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Direct Neural Conversion from Human Fibroblasts Using Self-Regulating and Nonintegrating Viral Vectors

TL;DR: An improved system for direct neural conversion of human fibroblasts that can be combined with integrase-deficient vectors, providing a nonintegrative and self-regulated conversion system that rids problems associated with the integration of viral transgenes into the host genome.