(Q34283448)

English

Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia: intrafamilial association study in an eight-generation hyperlipidemic kindred

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scholarly article

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Europe PubMed Central

PubMed publication ID

1 August 2017

Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia: intrafamilial association study in an eight-generation hyperlipidemic kindred (English)

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Europe PubMed Central

PubMed publication ID

1 August 2017

hypercholesterolemia

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inferred from title

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familial hypercholesterolemia

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Soluble epoxide hydrolase

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13

object named as

Paul N Hopkins

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1 August 2017

12

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Steven C Hunt

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PubMed publication ID

1 August 2017

author name string

Keiko Sato

1

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1 August 2017

Mitsuru Emi

2

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1 August 2017

Yoichi Ezura

3

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1 August 2017

Yuko Fujita

4

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1 August 2017

Daisuke Takada

5

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1 August 2017

Tomoaki Ishigami

6

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1 August 2017

Satoshi Umemura

7

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1 August 2017

Yunpei Xin

8

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1 August 2017

Lily L Wu

9

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1 August 2017

Stacey Larrinaga-Shum

10

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1 August 2017

Susan H Stephenson

11

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1 August 2017

publication date

13 December 2003

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1 August 2017

Journal of Human Genetics

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1 August 2017

49

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1 August 2017

1

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1 August 2017

29-34

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1 August 2017

Clinical variant of Tangier disease in Japan: mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage disequilibrium and haplotype analysis among eight novel single-nucleotide polymorphisms in the human tissue-type plasminogen activator (t-PA) gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development of genetic hypotheses in essential hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A high-throughput SNP typing system for genome-wide association studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Eicosapentaenoic acid reduces hepatic synthesis and secretion of triacylglycerol by decreasing the activity of acyl-coenzyme A:1,2-diacylglycerol acyltransferase

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the gene for lipoprotein lipase. A cause for low HDL cholesterol levels in individuals heterozygous for familial hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of common missense changes in ELAC2 ( HPC2) with prostate cancer in a Japanese case-control series

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of 779 genetic variations in eight genes encoding members of the ATP-binding cassette, subfamily C (ABCC/MRP/CFTR

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Head-to-head juxtaposition of Fas-associated phosphatase-1 (FAP-1) and c-Jun NH2-terminal kinase 3 (JNK3) genes: genomic structure and seven polymorphisms of the FAP-1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional antagonism between CCAAT/Enhancer binding protein-alpha and peroxisome proliferator-activated receptor-gamma on the leptin promoter

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SNP alleles in human disease and evolution

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interaction between the LDL-receptor gene bearing a novel mutation and a variant in the apolipoprotein A-II promoter: molecular study in a 1135-member familial hypercholesterolemia kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Similar to oleic acid, eicosapentaenoic acid stimulates apolipoprotein B secretion by inhibiting its intracellular degradation in Hep G2 cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common mutation in the lipoprotein lipase gene (N291S) alters the lipoprotein phenotype and risk for cardiovascular disease in patients with familial hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Significance of hypertriglyceridemia in the occurrence of ischemic heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

N-3 fatty acids stimulate intracellular degradation of apoprotein B in rat hepatocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PPARγ Is Required for the Differentiation of Adipose Tissue In Vivo and In Vitro

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipoproteins and cardiovascular risk-from genetics to CHD prevention

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A functional polymorphism in the promoter region of the microsomal triglyceride transfer protein (MTP -493G/T) influences lipoprotein phenotype in familial hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical characteristics of double heterozygotes with familial hypercholesterolemia and cholesteryl ester transfer protein deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalog of 77 single-nucleotide polymorphisms (SNPs) in the carbohydrate sulfotransferase 1 (CHST1) and carbohydrate sulfotransferase 3 (CHST3) genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monogenic dyslipidemias: window on determinants of plasma lipoprotein metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Eight novel mutations and functional impairments of the LDL receptor in familial hypercholesterolemia in the north of Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of three genetic loci in a pedigree with multiple lipoprotein phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development of coronary heart disease in familial hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/14673705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-003-0103-6

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

ResearchGate publication ID

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