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Lyle Armstrong

Researcher at Newcastle University

Publications -  142
Citations -  8502

Lyle Armstrong is an academic researcher from Newcastle University. The author has contributed to research in topics: Induced pluripotent stem cell & Embryonic stem cell. The author has an hindex of 39, co-authored 135 publications receiving 7449 citations. Previous affiliations of Lyle Armstrong include Centre for Life & BioMérieux.

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Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage

Katherine Amps, +124 more
- 27 Nov 2011 - 
TL;DR: Of these genes, BCL2L1 is a strong candidate for driving culture adaptation of ES cells, and single-nucleotide polymorphism analysis revealed that they included representatives of most major ethnic groups.
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Ethical and Safety Issues of Stem Cell-Based Therapy.

TL;DR: An overview of the most important ethical issues in stem cell therapy is provided, as a contribution to the controversial debate about their clinical usage in regenerative and transplantation medicine.
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The role of PI3K/AKT, MAPK/ERK and NFκβ signalling in the maintenance of human embryonic stem cell pluripotency and viability highlighted by transcriptional profiling and functional analysis

TL;DR: Bioinformatic analysis of expression changes observed when these cells were induced to differentiate as embryoid bodies suggested that quite a few of the downregulated genes were components of signal transduction networks and implicated components of the PI3K/AKT kinase, MAPK/ERK and NFkappabeta pathways and confirmed that these components are decreased upon differentiation.
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Downregulation of NANOG induces differentiation of human embryonic stem cells to extraembryonic lineages.

TL;DR: The findings suggest that NANOG acts as a gatekeeper of pluripotency in human embryonic stem and carcinoma cells by preventing their differentiation to extraembryonic endoderm and trophectoderm lineages.
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Efficient Hematopoietic Differentiation of Human Embryonic Stem Cells on Stromal Cells Derived from Hematopoietic Niches

TL;DR: Investigation of coculture with monolayers of cells derived from mouse AGM and fetal liver, or with stromal cell lines derived from these tissues, found that under such conditions hESC-derived differentiating cells formed early hematopoietic progenitors, with a peak at day 18-21 of differentiation that corresponded to the highest CD34 expression.