(Q36504914)

14 August 2017

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title

Inflammation as a risk factor for myocardial infarction (English)

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14 August 2017

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Toshihiro Tanaka

1

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Kouichi Ozaki

object named as

Kouichi Ozaki

series ordinal

2

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publication date

13 June 2006

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14 August 2017

10

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Journal of Human Genetics

inferred from page(s)

published in

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14 August 2017

51

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14 August 2017

7

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14 August 2017

595-604

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https://scigraph.springernature.com/pub.10.1007/s10038-006-0411-8

14 August 2017

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cites work

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Cytokine-stimulated human vascular smooth muscle cells synthesize a complement of enzymes required for extracellular matrix digestion

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Tumor necrosis factor, tumor necrosis factor receptors type 1 and 2, lymphotoxin-alpha, and HLA-DRB1 gene polymorphisms in human T-cell lymphotropic virus type I associated myelopathy

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Site of intimal rupture or erosion of thrombosed coronary atherosclerotic plaques is characterized by an inflammatory process irrespective of the dominant plaque morphology

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Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro

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Insulin recruits GLUT4 from distinct compartments via distinct traffic pathways with differential microtubule dependence in rat adipocytes

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Cardiovascular disease burden increases, NIH funding decreases

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Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

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Lack of association of polymorphisms of the lymphotoxin alpha gene with myocardial infarction in Japanese

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Mast cells in rupture-prone areas of human coronary atheromas produce and store TNF-alpha

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Association analysis between polymorphisms of the lymphotoxin-alpha gene and myocardial infarction in a Japanese population

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Loss of lymphotoxin-alpha but not tumor necrosis factor-alpha reduces atherosclerosis in mice

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Isolation and expression of a gene encoding L-14-II, a new human soluble lactose-binding lectin

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Influence of TNF gene polymorphism and HLA-DRB1 haplotype in Japanese patients with chronic liver disease caused by HCV.

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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

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Genetic susceptibility to death from coronary heart disease in a study of twins

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A generic protein purification method for protein complex characterization and proteome exploration

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Accumulation of activated mast cells in the shoulder region of human coronary atheroma, the predilection site of atheromatous rupture

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12 December 2020

10.1007/S10038-006-0411-8

Identifiers

DOI

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14 August 2017

1 reference

PubMed ID

16770523