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glycerol and Hyperlipidemia, Familial Combined

glycerol has been researched along with Hyperlipidemia, Familial Combined in 2 studies

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Hyperlipidemia, Familial Combined: A type of familial lipid metabolism disorder characterized by a variable pattern of elevated plasma CHOLESTEROL and/or TRIGLYCERIDES. Multiple genes on different chromosomes may be involved, such as the major late transcription factor (UPSTREAM STIMULATORY FACTORS) on CHROMOSOME 1.

Research Excerpts

ExcerptRelevanceReference
"The pathophysiology of familial combined hyperlipidemia (FCHL) is unknown, but altered lipid turnover in peripheral tissues as well as hepatic overproduction of apolipoprotein B have been suggested as possible causes."1.29Impaired activation of adipocyte lipolysis in familial combined hyperlipidemia. ( Angelin, B; Arner, P; Eriksson, M; Reynisdottir, S, 1995)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Eurlings, PM1
van der Kallen, CJ1
Vermeulen, VM1
de Bruin, TW1
Reynisdottir, S1
Eriksson, M1
Angelin, B1
Arner, P1

Other Studies

2 other studies available for glycerol and Hyperlipidemia, Familial Combined

ArticleYear
Variants in the PPARgamma gene affect fatty acid and glycerol metabolism in familial combined hyperlipidemia.
    Molecular genetics and metabolism, 2003, Volume: 80, Issue:3

    Topics: Adult; Case-Control Studies; Fatty Acids; Female; Gene Frequency; Genetic Variation; Glycerol; Human

2003
Impaired activation of adipocyte lipolysis in familial combined hyperlipidemia.
    The Journal of clinical investigation, 1995, Volume: 95, Issue:5

    Topics: Adipocytes; Adipose Tissue; Adrenergic Agents; Adult; Apolipoproteins; Blood Glucose; Cells, Culture

1995