(Q37864570)

24 August 2017

1 reference

title

Genetic mechanisms mediating atherosclerosis susceptibility at the chromosome 9p21 locus (English)

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24 August 2017

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Michael S Cunnington

1

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PubMed ID

21487702

24 August 2017

Bernard Keavney

series ordinal

2

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24 August 2017

1 June 2011

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Current Atherosclerosis Reports

24 August 2017

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24 August 2017

13

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24 August 2017

3

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24 August 2017

193-201

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https://scigraph.springernature.com/pub.10.1007/s11883-011-0178-z

24 August 2017

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cites work

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A common variant on chromosome 9p21 affects the risk of myocardial infarction

21 January 2018

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A common allele on chromosome 9 associated with coronary heart disease

21 January 2018

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21 January 2018

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Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

21 January 2018

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A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese

21 January 2018

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Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility

21 January 2018

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The 9p21 myocardial infarction risk allele increases risk of peripheral artery disease in older people

21 January 2018

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Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke

21 January 2018

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Association between 9p21 genomic markers and heart disease: a meta-analysis

21 January 2018

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Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes.

21 January 2018

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Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective study

21 January 2018

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ANRIL expression is associated with atherosclerosis risk at chromosome 9p21.

21 January 2018

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Gene dosage of the common variant 9p21 predicts severity of coronary artery disease.

21 January 2018

1 reference

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Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease

21 January 2018

1 reference

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Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease.

21 January 2018

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Genetic variation at the 9p21 locus predicts angiographic coronary artery disease prevalence but not extent and has clinical utility.

21 January 2018

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Validation of the association of genetic variants on chromosome 9p21 and 1q41 with myocardial infarction in a Japanese population

21 January 2018

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Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease

21 January 2018

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The regulation of INK4/ARF in cancer and aging

21 January 2018

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21 January 2018

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21 January 2018

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p15INK4B is a potential effector of TGF-beta-induced cell cycle arrest

21 January 2018

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Smad expression in human atherosclerotic lesions: evidence for impaired TGF-beta/Smad signaling in smooth muscle cells of fibrofatty lesions

21 January 2018

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Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men.

21 January 2018

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INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis

21 January 2018

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Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression

21 January 2018

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Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus.

21 January 2018

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Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants

21 January 2018

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Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family: identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF.

21 January 2018

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21 January 2018

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Long non-coding RNAs: insights into functions

21 January 2018

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The Polycomb group proteins bind throughout the INK4A-ARF locus and are disassociated in senescent cells

21 January 2018

1 reference

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Expression of the p16INK4a tumor suppressor versus other INK4 family members during mouse development and aging.

21 January 2018

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Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice

21 January 2018

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p19(ARF) deficiency reduces macrophage and vascular smooth muscle cell apoptosis and aggravates atherosclerosis

21 January 2018

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Epigenetic silencing of tumour suppressor gene p15 by its antisense RNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-011-0178-Z

Molecular interplay of the noncoding RNA ANRIL and methylated histone H3 lysine 27 by polycomb CBX7 in transcriptional silencing of INK4a

21 January 2018

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A common variant of CDKN2A (p16) predisposes to breast cancer

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11883-011-0178-Z

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-011-0178-Z

The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease

21 January 2018

1 reference

12 December 2020

Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations

1 reference

12 December 2020

Methylthioadenosine phosphorylase, a gene frequently codeleted with p16(cdkN2a/ARF), acts as a tumor suppressor in a breast cancer cell line

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12 December 2020

9p21 is a shared susceptibility locus strongly for coronary artery disease and weakly for ischemic stroke in Chinese Han population

1 reference

12 December 2020

Expression of Chr9p21 genes CDKN2B (p15(INK4b)), CDKN2A (p16(INK4a), p14(ARF)) and MTAP in human atherosclerotic plaque.

1 reference

12 December 2020

10.1007/S11883-011-0178-Z

Identifiers

DOI

1 reference

24 August 2017

1 reference

PubMed ID

21487702