Lipidomic and metabolomic characterization of a genetically modified mouse model of the early stages of human type 1 diabetes pathogenesis-Reference-Cited by-同舟云学术

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Lipidomic and metabolomic characterization of a genetically modified mouse model of the early stages of human type 1 diabetes pathogenesis

Published:2015-11-17 Issue:1 Volume:12 Page:
ISSN:1573-3882
Container-title:Metabolomics
language:en
Short-container-title:Metabolomics

Author:

Overgaard Anne Julie,Weir Jacquelyn M.,De Souza David Peter,Tull Dedreia,Haase Claus,Meikle Peter J.,Pociot Flemming

Funder

Juvenile Diabetes Research Foundation International

Sundhed og Sygdom, Det Frie Forskningsråd

National Health & Medical Research Council of Australia

OIS Program of the Victorian Government

Publisher

Springer Science and Business Media LLC

Subject

Clinical Biochemistry,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://link.springer.com/content/pdf/10.1007/s11306-015-0889-1.pdf

Reference36 articles.

1. American Diabetes Association (ADA). (2013). Economic costs of diabetes in the U.S. in 2012. Diabetes Care, 36, 1033–1046.

2. Bennett, S. R. M., Carbone, F. R., Karamalis, F., Flavell, R. A., Miller, J. F. A. P., & Heath, W. R. (1998). Help for cytotoxic-T-cell responses is mediated by CD40 signalling. Nature, 393(6684), 478–480.

3. Bligh, E. G., & Dyer, W. J. (1959). A rapid method of total lipid extraction and purification. Canadian Journal of Biochemistry and Physiology, 37(8), 911–917.

4. Boslem, E., Meikle, P. J., & Biden, T. J. (2012). Roles of ceramide and sphingolipids in pancreatic β-cell function and dysfunction. Islets, 4(3), 177–187.

5. Carneiro, A. B., Iaciura, B. M. F., Nohara, L. L., Lopes, C. D., Veas, E. M. C., Mariano, V. S., et al. (2013). Lysophosphatidylcholine triggers TLR2- and TLR4-mediated signaling pathways but counteracts LPS-induced NO synthesis in peritoneal macrophages by inhibiting NF-κB translocation and MAPK/ERK phosphorylation. PLoS ONE, 8(9), e76233.

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