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Elizabeth Di Lullo

Researcher at University of California, San Francisco

Publications -  15
Citations -  3812

Elizabeth Di Lullo is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Viral entry & Induced pluripotent stem cell. The author has an hindex of 14, co-authored 15 publications receiving 2677 citations. Previous affiliations of Elizabeth Di Lullo include PSL Research University.

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The use of brain organoids to investigate neural development and disease

TL;DR: Recent advances in stem cell technologies that enable the generation of human brain organoids from pluripotent stem cells (PSCs) promise to profoundly change understanding of the development of the human brain and enable a detailed study of the pathogenesis of inherited and acquired brain diseases.
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Expression Analysis Highlights AXL as a Candidate Zika Virus Entry Receptor in Neural Stem Cells

TL;DR: Examining the expression of receptors implicated in cell entry of several enveloped viruses including ZIKV across diverse cell types in the developing brain found that the candidate viral entry receptor AXL is highly expressed by human radial glial cells, astrocytes, endothelial cells, and microglia in developing human cortex and by progenitor cells in developing retina.
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Single-cell profiling of human gliomas reveals macrophage ontogeny as a basis for regional differences in macrophage activation in the tumor microenvironment

TL;DR: It is concluded that blood-derived TAMs significantly infiltrate pre-treatment gliomas, to a degree that varies by glioma subtype and tumor compartment, and a novel signature that distinguishes TAMs by ontogeny in humangliomas is presented.
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Human iPSC-Derived Cerebral Organoids Model Cellular Features of Lissencephaly and Reveal Prolonged Mitosis of Outer Radial Glia.

TL;DR: Cerebral organoids derived from control and MDS-induced pluripotent stem cells (iPSCs) are analyzed and a mitotic defect in outer radial glia is identified, a progenitor subtype that is largely absent from lissencephalic rodents but critical for human neocortical expansion.