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Georgina H. Cornish

Researcher at Francis Crick Institute

Publications -  33
Citations -  1889

Georgina H. Cornish is an academic researcher from Francis Crick Institute. The author has contributed to research in topics: T cell & Cytotoxic T cell. The author has an hindex of 13, co-authored 32 publications receiving 1458 citations. Previous affiliations of Georgina H. Cornish include Imperial College London & King's College London.

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Phosphatidylinositol-3-OH kinase and nutrient-sensing mTOR pathways control T lymphocyte trafficking.

TL;DR: PI(3)K-mTOR nutrient-sensing pathways also determined expression of the chemokine receptor CCR7 and regulated lymphocyte trafficking in vivo, showing that lymphocytes use PI( 3)K and mTOR to match metabolism and trafficking.
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Differential regulation of T-cell growth by IL-2 and IL-15.

TL;DR: The present results show that cytokines that are equivalent mitogens can have different potency in terms of regulating protein synthesis and cell growth.
Posted ContentDOI

Pre-existing and de novo humoral immunity to SARS-CoV-2 in humans

TL;DR: The presence of pre-existing humoral immunity in uninfected and unexposed humans to the new coronavirus is demonstrated and identified as SARS-CoV-2 S-reactive antibodies, which were readily detectable by a sensitive flow cytometry-based method in SARS/COVID-19-uninfected individuals and were particularly prevalent in children and adolescents.
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Expression of transcription factor AML-2 (RUNX3, CBF(alpha)-3) is induced by Epstein-Barr virus EBNA-2 and correlates with the B-cell activation phenotype.

TL;DR: The AML genes are the first example of cell transcription factors whose expression correlates with the latency I/III phenotype, and analysis of a panel of B-cell lines indicated that AML-2 expression is normally predominant in EBV latency III, whereasAML-1 is associated withEBV latency I or EBV-negative cells.