(Q34576832)

3 August 2017

Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction (English)

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3 August 2017

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myocardial infarction

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Toshihiro Tanaka

13

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Kouichi Ozaki

object named as

Kouichi Ozaki

2

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Satoshi Saito

11

object named as

Satoshi Saito

1 reference

3 August 2017

6

Atsushi Takahashi

1 reference

3 August 2017

Nobuaki Ishii

1

1 reference

3 August 2017

Hiroshi Sato

3

1 reference

3 August 2017

Hiroya Mizuno

4

1 reference

3 August 2017

Susumu Saito

5

1 reference

3 August 2017

Yoshinari Miyamoto

7

1 reference

3 August 2017

Shiro Ikegawa

8

1 reference

3 August 2017

Naoyuki Kamatani

9

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3 August 2017

Masatsugu Hori

10

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3 August 2017

Yusuke Nakamura

12

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3 August 2017

26 October 2006

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Journal of Human Genetics

3 August 2017

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3 August 2017

51

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3 August 2017

1087-1099

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3 August 2017

12

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https://scigraph.springernature.com/pub.10.1007/s10038-006-0070-9

3 August 2017

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cites work

Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome

1 reference

12 December 2020

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

1 reference

12 December 2020

Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis

1 reference

12 December 2020

A single-nucleotide deletion leads to rapid degradation of TAP-1 mRNA in a melanoma cell line.

1 reference

12 December 2020

The new genomics: global views of biology

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12 December 2020

The future of genetic studies of complex human diseases

1 reference

12 December 2020

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

1 reference

12 December 2020

A strategy for probing the function of noncoding RNAs finds a repressor of NFAT

1 reference

12 December 2020

Haploview: analysis and visualization of LD and haplotype maps

1 reference

12 December 2020

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

1 reference

12 December 2020

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

12 December 2020

Thrombospondin-4 and its variants: expression and differential effects on endothelial cells

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12 December 2020

Identification of 187 single nucleotide polymorphisms (SNPs) among 41 candidate genes for ischemic heart disease in the Japanese population

1 reference

12 December 2020

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

1 reference

12 December 2020

Variations on a theme: cataloging human DNA sequence variation

1 reference

12 December 2020

siRNA and miRNA: an insight into RISCs

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12 December 2020

Cardiovascular disease burden increases, NIH funding decreases

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12 December 2020

A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome

1 reference

12 December 2020

A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population

1 reference

12 December 2020

The transcriptional landscape of the mammalian genome

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12 December 2020

The structural H19 gene is required for transgene imprinting

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12 December 2020

Genetics of atherosclerosis

1 reference

12 December 2020

A rapid micropreparation technique for extraction of DNA-binding proteins from limiting numbers of mammalian cells

1 reference

12 December 2020

Shattuck lecture--cardiovascular medicine at the turn of the millennium: triumphs, concerns, and opportunities.

1 reference

12 December 2020

Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction

1 reference

12 December 2020

A catalogue of splice junction sequences

1 reference

12 December 2020

Catalog of 258 single-nucleotide polymorphisms (SNPs) in genes encoding three organic anion transporters, three organic anion-transporting polypeptides, and three NADH:ubiquinone oxidoreductase flavoproteins

1 reference

12 December 2020

Databases on transcriptional regulation: TRANSFAC, TRRD and COMPEL

1 reference

12 December 2020

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

1 reference

12 December 2020

Association between a single-nucleotide polymorphism in the promoter of the human interleukin-3 gene and rheumatoid arthritis in Japanese patients, and maximum-likelihood estimation of combinatorial effect that two genetic loci have on susceptibilit

1 reference

12 December 2020

Basic local alignment search tool

1 reference

12 December 2020

The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke

1 reference

12 December 2020

Hoxa 11 structure, extensive antisense transcription, and function in male and female fertility

1 reference

12 December 2020

Prediction of the risk of myocardial infarction from polymorphisms in candidate genes

1 reference

12 December 2020

10.1007/S10038-006-0070-9

Identifiers

DOI

1 reference

3 August 2017

1 reference