USF1 and dyslipidemias: converging evidence for a functional intronic variant (Q46632174)

23 December 2017

title

USF1 and dyslipidemias: converging evidence for a functional intronic variant (English)

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23 December 2017

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5

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23 December 2017

Janna Saarela

Janna Saarela

4

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Marja-Riitta Taskinen

Marja-Riitta Taskinen

7

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Leena Peltonen-Palotie

8

Leena Peltonen

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23 December 2017

Päivi Pajukanta

6

Päivi Pajukanta

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23 December 2017

Jussi Naukkarinen

1

Jussi Naukkarinen

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23 December 2017

author name string

Massimiliano Gentile

2

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23 December 2017

Aino Soro-Paavonen

3

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23 December 2017

publication date

2 August 2005

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23 December 2017

number of pages

11

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published in

Human Molecular Genetics

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23 December 2017

volume

14

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23 December 2017

issue

17

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23 December 2017

page(s)

2595-2605

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23 December 2017

Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).

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Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II.

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Insulin-mediated down-regulation of apolipoprotein A5 gene expression through the phosphatidylinositol 3-kinase pathway: role of upstream stimulatory factor

30 October 2021

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Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families

30 October 2021

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Linkage of a candidate gene locus to familial combined hyperlipidemia: lecithin:cholesterol acyltransferase on 16q.

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ATP-binding cassette transporter A1 and cholesterol trafficking

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Overexpression of apolipoprotein E in transgenic mice: marked reduction in plasma lipoproteins except high density lipoprotein and resistance against diet-induced hypercholesterolemia

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Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

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Structure, sequence, and chromosome 19 localization of human USF2 and its rearrangement in a patient with multicystic renal dysplasia

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PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

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Immunochemical characterization and transacting properties of upstream stimulatory factor isoforms

30 October 2021

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Induction of Atherosclerosis by Human Chylomicron Remnants: A Hypothesis

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Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

30 October 2021

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Impaired recycling of apolipoprotein E4 is associated with intracellular cholesterol accumulation.

30 October 2021

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Essential role in vivo of upstream stimulatory factors for a normal dietary response of the fatty acid synthase gene in the liver

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Cloning of human acetyl-CoA carboxylase cDNA

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Essential role of vascular endothelial growth factor in angiotensin II-induced vascular inflammation and remodeling.

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Lipoprotein lipase enhances the binding of chylomicrons to low density lipoprotein receptor-related protein

30 October 2021

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Coronary artery disease risk in familial combined hyperlipidemia and familial hypertriglyceridemia: a case-control comparison from the National Heart, Lung, and Blood Institute Family Heart Study

30 October 2021

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Family study of serum lipids and lipoproteins in coronary heart-disease

30 October 2021

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Use and abuse of HOMA modeling

30 October 2021

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Molecular variation of the human angiotensinogen core promoter element located between the TATA box and transcription initiation site affects its transcriptional activity

30 October 2021

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Familial combined hyperlipidaemia linked to the apolipoprotein AI–CIII–AIV gene cluster on chromosome 11q23q–q24

30 October 2021

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Identification of a non-canonical E-box motif as a regulatory element in the proximal promoter region of the apolipoprotein E gene

30 October 2021

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The role of apolipoprotein E genetic variants in lipoprotein disorders

30 October 2021

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Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

30 October 2021

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30 October 2021

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Molecular mechanisms of type III hyperlipoproteinemia: The contribution of the carboxy-terminal domain of ApoE can account for the dyslipidemia that is associated with the E2/E2 phenotype

30 October 2021

1 reference

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Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia

30 October 2021

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https://opencitations.net/index/coci/api/v1/references/10.1093/HMG/DDI294

Spontaneous hypercholesterolemia and arterial lesions in mice lacking apolipoprotein E

30 October 2021

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1093/HMG/DDI294

Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels

30 October 2021

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1093/HMG/DDI294

In VivoRegulation of the Activity of the Two Promoters of the Rat Acetyl Coenzyme-A Carboxylase Gene*

30 October 2021

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1093/HMG/DDI294

Upstream stimulatory factor proteins are major components of the glucose response complex of the L-type pyruvate kinase gene promoter

30 October 2021

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1093/HMG/DDI294

30 October 2021

Identifiers

DOI

10.1093/HMG/DDI294

1 reference

23 December 2017

PubMed ID

16076849

1 reference

23 December 2017