Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humans

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"Triglyceride (TG) metabolism is crucial for whole body and local energy homeostasis and accumulating evidence suggests an independent association between plasma TG concentration and increased atherosclerosis risk. We previously generated a mouse insertional mutation lpd (lipid defect) whose phenotype included elevated plasma TG and hepatic steatosis. Using shotgun sequencing (∼500 kb) and bioinformatics, we have now identified a novel lipase gene lpdl (lpd lipase) within the lpd locus, and demonstrate the genetic disruption of exon 10 of lpdl in the lpd mutant locus." (as cited in abstract)
Date created

2003-05-13
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Article (Published)
DOI

https://doi.org/10.7939/r3-edd3-8p09
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Attribution 4.0 International

Language
- English
Citation for previous publication
- Wen, X. Y., Hegele, R. A., Wang, J., Wang, D. Y., Cheung, J., Wilson, M., Yahyapour, M., Bai, Y., Zhuang, L., Skaug, J., Young, T. K., Connelly, P. W., Koop, B. F., Tsui, L. C., & Stewart, A. K. (2003). Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humans. Human Molecular Genetics, 12(10), 1131-1142. https://doi.org/10.1093/hmg/ddg124
Source

<https://academic.oup.com/hmg/article/12/10/1131/641761>
Link to related item

<https://v2.sherpa.ac.uk/id/publication/335>