Increased de novo lipogenesis and delayed conversion of large VLDL into intermediate density lipoprotein particles contribute to hyperlipidemia in glycogen storage disease type 1a.
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Nonalcoholic fatty liver disease: a comprehensive review of a growing epidemicPathway-selective insulin resistance and metabolic disease: the importance of nutrient fluxGlycogen storage disease type I and G6Pase-β deficiency: etiology and therapyFurther delineation of the phenotype of severe congenital neutropenia type 4 due to mutations in G6PC3.Human fatty liver disease: old questions and new insightsVascular dysfunction in glycogen storage disease type IGlycogen Storage Disease type 1a - a secondary cause for hyperlipidemia: report of five cases.Increased activin bioavailability enhances hepatic insulin sensitivity while inducing hepatic steatosis in male mice.Glycogen storage disease type Ia: linkage of glucose, glycogen, lactic acid, triglyceride, and uric acid metabolismHyperlipidemia in glycogen storage disease type III: effect of age and metabolic control.Liver glucose metabolism in humans.Hepatic mitochondrial dysfunction is a feature of Glycogen Storage Disease Type Ia (GSDIa).Hepatic glucose sensing and integrative pathways in the liver.Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics.Lipids in hepatic glycogen storage diseases: pathophysiology, monitoring of dietary management and future directions.New insight into inter-organ crosstalk contributing to the pathogenesis of non-alcoholic fatty liver disease (NAFLD).Sustained high plasma mannose less sensitive to fluctuating blood glucose in glycogen storage disease type Ia children.Current status of hepatic glycogen storage disease in Japan: clinical manifestations, treatments and long-term outcomes.Flux analysis of inborn errors of metabolism.Signal transducer and activator of transcription 5 plays a crucial role in hepatic lipid metabolism through regulation of CD36 expression.Lack of liver glycogen causes hepatic insulin resistance and steatosis in mice.Adiponectin levels correlate with the severity of hypertriglyceridaemia in glycogen storage disease Ia.Intracellular lipids are an independent cause of liver injury and chronic kidney disease in non alcoholic fatty liver disease-like context
P2860
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P2860
Increased de novo lipogenesis and delayed conversion of large VLDL into intermediate density lipoprotein particles contribute to hyperlipidemia in glycogen storage disease type 1a.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Increased de novo lipogenesis ...... cogen storage disease type 1a.
@en
Increased de novo lipogenesis ...... cogen storage disease type 1a.
@nl
type
label
Increased de novo lipogenesis ...... cogen storage disease type 1a.
@en
Increased de novo lipogenesis ...... cogen storage disease type 1a.
@nl
prefLabel
Increased de novo lipogenesis ...... cogen storage disease type 1a.
@en
Increased de novo lipogenesis ...... cogen storage disease type 1a.
@nl
P2093
P2860
P1433
P1476
Increased de novo lipogenesis ...... cogen storage disease type 1a.
@en
P2093
Berthil H Prinsen
Dirk-Jan Reijngoud
Folkert Kuipers
G Peter A Smit
Jan-Peter Rake
Monique de Sain van Der Velden
Robert H J Bandsma
P2860
P2888
P304
P356
10.1203/PDR.0B013E31816C9013
P407
P577
2008-06-01T00:00:00Z
P5875
P6179
1027570231