Zobrazeno 1 - 10
of 306
pro vyhledávání: '"combined lipase deficiency"'
Publikováno v:
Science, 1983 Jul 01. 221(4606), 167-169.
Externí odkaz:
https://www.jstor.org/stable/1691582
Autor:
Péterfy, Miklós1,2 mpeterfy@ucla.edu, Ben-Zeev, Osnat1,2, Mao, Hui Z.1,2,3, Weissglas-Volkov, Daphna4, Aouizerat, Bradley E.5,6, Pullinger, Clive R.5,7, Frost, Philip H.8, Kane, John P.7,8,9, Malloy, Mary J.7,8,10, Reue, Karen2,4, Pajukanta, Päivi4, Doolittle, Mark H.1,2 markdool@ucla.edu
Publikováno v:
Nature Genetics. Dec2007, Vol. 39 Issue 12, p1483-1487. 5p. 5 Graphs.
Publikováno v:
Journal of Lipid Research, Vol 42, Iss 11, Pp 1858-1864 (2001)
Combined lipase deficiency (cld) is a recessively inherited disorder in mice associated with a deficiency of LPL and hepatic lipase (HL) activity. LPL is synthesized in cld tissues but is retained in the endoplasmic reticulum (ER), whereas mouse HL (
Externí odkaz:
https://doaj.org/article/4d21f1ef6db94e49a865f24be8a9a70a
Publikováno v:
In Journal of Lipid Research November 2001 42(11):1858-1864
Publikováno v:
Journal of Lipid Research, Vol 31, Iss 10, Pp 1845-1852 (1990)
Combined lipase deficiency (cld) is a genetic abnormality in mice resulting in the production of enzymatically inactive lipoprotein lipase (LPL). After suckling, these mice have markedly elevated levels of circulating triglyceride. An alteration of L
Externí odkaz:
https://doaj.org/article/8ed9470d9b744d35bc107d6fd5814c2c
Autor:
John P. Kane, Bradley E. Aouizerat, Miklós Péterfy, Daphna Weissglas-Volkov, Päivi Pajukanta, Mary J. Malloy, Osnat Ben-Zeev, Clive R. Pullinger, Karen Reue, Hui Z. Mao, Mark H. Doolittle, Philip H. Frost
Publikováno v:
Nature genetics. 39(12)
Hypertriglyceridemia is a hallmark of many disorders, including metabolic syndrome, diabetes, atherosclerosis and obesity. A well-known cause is the deficiency of lipoprotein lipase (LPL), a key enzyme in plasma triglyceride hydrolysis. Mice carrying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::599623906cbbb7b18cc82a42cdc7a3c9
https://pubmed.ncbi.nlm.nih.gov/18046326
https://pubmed.ncbi.nlm.nih.gov/18046326
Publikováno v:
Journal of Lipid Research, Vol 31, Iss 10, Pp 1845-1852 (1990)
Combined lipase deficiency (cld) is a genetic abnormality in mice resulting in the production of enzymatically inactive lipoprotein lipase (LPL). After suckling, these mice have markedly elevated levels of circulating triglyceride. An alteration of L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86c7753f862ca110aa18029c3d36862b
http://www.sciencedirect.com/science/article/pii/S0022227520423284
http://www.sciencedirect.com/science/article/pii/S0022227520423284
Publikováno v:
Journal of Biological Chemistry. 265:17960-17966
Newborn combined lipase-deficient (cld) mice have severe hypertriglyceridemia associated with a marked decrease of lipoprotein lipase (LPL) and hepatic lipase (HL) activities. Since the cld mutation and lipase genes reside on separate chromosomes, co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f339b5f295bdf6bb80d60d3bf4749f96
https://doi.org/10.1016/s0021-9258(18)38257-7
https://doi.org/10.1016/s0021-9258(18)38257-7
Publikováno v:
Chemistry and physics of lipids. 93(1-2)
Lipoprotein lipase (LPL) and hepatic lipase (HL), which act on plasma lipoproteins, belong to the same gene family as pancreatic lipase. LPL is synthesized in heart, muscle and adipose tissue, while HL is synthesized primarily in liver. LPL is also s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f97b88c2af53504806caa552723ecb94
https://pubmed.ncbi.nlm.nih.gov/9720257
https://pubmed.ncbi.nlm.nih.gov/9720257
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