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Jan Ure

Researcher at University of Edinburgh

Publications -  14
Citations -  4281

Jan Ure is an academic researcher from University of Edinburgh. The author has contributed to research in topics: Haematopoiesis & Embryonic stem cell. The author has an hindex of 12, co-authored 13 publications receiving 4135 citations. Previous affiliations of Jan Ure include JDRF.

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Altered immune responses in mice lacking inducible nitric oxide synthase

TL;DR: The infected mutant mice developed a significantly stronger Thl type of immune response than the wild-type or heterozygous mice, and showed reduced nonspecific inflammatory response to carrageenin, and were resistant to lipopolysaccharide-induced mortality.
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The tetrodotoxin-resistant sodium channel SNS has a specialized function in pain pathways

TL;DR: Data show that SNS is involved in pain pathways and suggest that blockade of SNS expression or function may produce analgesia without side effects, and show that TTX-resistant sodium channel α subunit is encoded by the sns gene.
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HLA-A2.1–restricted Education and Cytolytic Activity of CD8+ T Lymphocytes from β2 Microglobulin (β2m) HLA-A2.1 Monochain Transgenic H-2Db β2m Double Knockout Mice

TL;DR: Three different HLA-A2.1 monochains were engineered in which either the human or mouse β2-microglobulin (β2m) is covalently linked to the NH2 terminus of the heavy chain by a 15– amino acid long peptide, and the selected HHD construct was introduced by transgenesis in H-2Db/− β2m−/− double knockout mice.
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Endoglin, an Ancillary TGFβ Receptor, Is Required for Extraembryonic Angiogenesis and Plays a Key Role in Heart Development

TL;DR: The phenotype of derived mice that carry a targeted nonsense mutation in the endoglin gene is remarkably similar to that of the T GFbeta1 and the TGFbeta receptor II knockout mice, indicating that endogslin is needed in vivo for TGF beta1 signaling during extraembryonic vascular development.
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Quantitative developmental anatomy of definitive haematopoietic stem cells/long-term repopulating units (HSC/RUs): role of the aorta-gonad-mesonephros (AGM) region and the yolk sac in colonisation of the mouse embryonic liver

TL;DR: The estimates indicate that the cumulative activity of the AGM region and the yolk sac is sufficient to provide the day 12 liver with a large number of definitive HSC/RUs, suggesting that the large pool of Definitive HSCs in day 12 foetal liver is formed predominantly by recruiting 'ready-to-use' definitive H SCs from extra-hepatic sources.