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Lista de obras de Shu Ye

A Novel Role of Matrix Metalloproteinase-8 in Macrophage Differentiation and Polarization

artículo científico publicado en 2015

A blood pressure-associated variant of the SLC39A8 gene influences cellular cadmium accumulation and toxicity

artículo científico publicado en 2016

A role of matrix metalloproteinase-8 in atherosclerosis

artículo científico publicado en 2009

A simple high-performance liquid chromatography (HPLC) method for the measurement of pyridoxal-5-phosphate and 4-pyridoxic acid in human plasma

artículo científico publicado en 2014

A study of mitochondrial DNA mutations in peripheral lymphocytes in an aging cohort

artículo científico publicado en 2003

ADAM33 expression in atherosclerotic lesions and relationship of ADAM33 gene variation with atherosclerosis

article

ADAMTS7 cleavage and vascular smooth muscle cell migration is affected by a coronary-artery-disease-associated variant

artículo científico publicado en 2013

ADAMTS7: a promising new therapeutic target in coronary heart disease

artículo científico publicado en 2013

Advanced glycation end-product of low density lipoprotein activates the toll-like 4 receptor pathway implications for diabetic atherosclerosis

artículo científico publicado en 2008

Allele specific amplification by tetra-primer PCR.

artículo científico publicado en 1992

Allele-specific regulation of matrix metalloproteinase-12 gene activity is associated with coronary artery luminal dimensions in diabetic patients with manifest coronary artery disease

article

Allele-specific regulation of matrix metalloproteinase-3 gene by transcription factor NFkappaB

artículo científico publicado en 2010

Allelic association and functional studies of promoter polymorphism in the leukotriene C4 synthase gene (LTC4S) in asthma

artículo científico publicado en 2003

An efficient procedure for genotyping single nucleotide polymorphisms.

artículo científico publicado en 2001

An important role of matrix metalloproteinase-8 in angiogenesis in vitro and in vivo

artículo científico publicado en 2013

Analysis of circulating cholesterol levels as a mediator of an association between ABO blood group and coronary heart disease

artículo científico publicado en 2014

Angiotensin II type I receptor gene polymorphism: anthropometric and metabolic syndrome traits

artículo científico publicado en 2005

Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis

artículo científico publicado en 2013

Association of MMP8 gene variation with an increased risk of malignant melanoma

artículo científico publicado en 2011

Association of MicroRNAs and YRNAs With Platelet Function

artículo científico publicado en 2015

Association of the lymphotoxin-alpha gene Thr26Asn polymorphism with severity of coronary atherosclerosis.

artículo científico publicado en 2005

Association of variation at the ABO locus with circulating levels of soluble intercellular adhesion molecule-1, soluble P-selectin, and soluble E-selectin: a meta-analysis

artículo científico publicado en 2011

CYP2A6, MAOA, DBH, DRD4, and 5HT2A genotypes, smoking behaviour and cotinine levels in 1518 UK adolescents

artículo científico publicado en 2005

Chromobox Protein Homolog 3 Is Essential for Stem Cell Differentiation to Smooth Muscles In Vitro and in Embryonic Arteriogenesis

artículo científico publicado en 2011

Chromosome 1p13 genetic variants antagonize the risk of myocardial infarction associated with high ApoB serum levels

artículo científico publicado en 2012

Comment on: "A promoter polymorphism (rs17222919, -1316T/G) of ALOX5AP is associated with intracerebral hemorrhage in Korean population" by Hwan Kim D. et al. [Prostaglandins Leukot. Essent. Fatty Acids 85 (2011) 115-120].

artículo científico publicado en 2012

Common variant on chromosome 9p21 predicts severity of coronary artery disease

scientific article published on 01 March 2011

Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration

artículo científico publicado en 2011

Complement factor H Y402H gene polymorphism in coronary artery disease and atherosclerosis

artículo científico publicado en 2006

Coronary artery disease-related genetic variant on chromosome 10q11 is associated with carotid intima-media thickness and atherosclerosis

artículo científico publicado en 2010

Coronary-Heart-Disease-Associated Genetic Variant at the COL4A1/COL4A2 Locus Affects COL4A1/COL4A2 Expression, Vascular Cell Survival, Atherosclerotic Plaque Stability and Risk of Myocardial Infarction

artículo científico publicado en 2016

Detecting polymorphisms in MMP genes

artículo científico publicado en 2001

Detection of mutations and DNA polymorphisms in genes involved in cardiovascular diseases by polymerase chain reaction-single-strand conformation polymorphism analysis

artículo científico publicado en 1999

Difference in Leukocyte Composition between Women before and after Menopausal Age, and Distinct Sexual Dimorphism.

artículo científico publicado en 2016

Differences in matrix metalloproteinase-1 and matrix metalloproteinase-12 transcript levels among carotid atherosclerotic plaques with different histopathological characteristics

artículo científico publicado en 2004

Different effects of angiotensin II and angiotensin-(1-7) on vascular smooth muscle cell proliferation and migration

artículo científico publicado en 2010

Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect

artículo científico publicado en 2006

Effect of a coronary-heart-disease-associated variant of ADAMTS7 on endothelial cell angiogenesis

artículo científico publicado en 2020

Effect of the peroxisome proliferator activated receptor-gamma gene Pro12Ala variant on body mass index: a meta-analysis

artículo científico publicado en 2003

Effect of the stromelysin-1 promoter on efficacy of pravastatin in coronary atherosclerosis and restenosis

artículo científico publicado en 1999

Effects of polymorphisms in endothelial nitric oxide synthase and folate metabolizing genes on the concentration of serum nitrate, folate, and plasma total homocysteine after folic acid supplementation: a double-blind crossover study

artículo científico publicado en 2014

Eicosapentaenoic acid (EPA) from highly concentrated n-3 fatty acid ethyl esters is incorporated into advanced atherosclerotic plaques and higher plaque EPA is associated with decreased plaque inflammation and increased stability.

artículo científico publicado en 2010

Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus

scientific article published on 09 March 2022

European Atherosclerosis Research Study: genotype at the fibrinogen locus (G-455-A beta-gene) is associated with differences in plasma fibrinogen levels in young men and women from different regions in Europe. Evidence for gender-genotype-environmen

scientific article published on 01 January 1995

Evolutionary path to the heart

artículo científico publicado en 2005

FURIN Expression in Vascular Endothelial Cells Is Modulated by a Coronary Artery Disease-Associated Genetic Variant and Influences Monocyte Transendothelial Migration

artículo científico publicado en 2020

Functional Impact of Heterogeneous Nuclear Ribonucleoprotein A2/B1 in Smooth Muscle Differentiation from Stem Cells and Embryonic Arteriogenesis ⬇️

artículo científico publicado el 5 de diciembre de 2011

Functional analyses of coronary artery disease associated variation on chromosome 9p21 in vascular smooth muscle cells

artículo científico publicado en 2012

Functional involvements of heterogeneous nuclear ribonucleoprotein A1 in smooth muscle differentiation from stem cells in vitro and in vivo

artículo científico publicado en 2013

Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients

artículo científico publicado en 2007

Functional role of matrix metalloproteinase-8 in stem/progenitor cell migration and their recruitment into atherosclerotic lesions

artículo científico publicado en 2012

Genetic Assessment of Potential Long-Term On-Target Side Effects of PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9) Inhibitors

scientific article published on 01 January 2019

Genetic Variation at the ADAMTS7 Locus is Associated With Reduced Severity of Coronary Artery Disease

artículo científico publicado en 2017

Genetic and Pharmacologic Inhibition of the Neutrophil Elastase Inhibits Experimental Atherosclerosis

artículo científico publicado en 2018

Genetic determinants of coronary heart disease: new discoveries and insights from genome-wide association studies ⬇️

artículo científico publicado el 26 de julio de 2011

Genetic polymorphisms in the endotoxin receptor may influence platelet count as part of the acute phase response in critically ill children

article

Genetic variation at the matrix metalloproteinase-9 locus on chromosome 20q12.2-13.1

article published in 1999

Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults: Implications for Primary Prevention

artículo científico publicado en 2018

Genotypic Effect of the −565C>T Polymorphism in the ABCA1 Gene Promoter on ABCA1 Expression and Severity of Atherosclerosis

article

HHIPL1, a Gene at the 14q32 Coronary Artery Disease Locus, Positively Regulates Hedgehog Signaling and Promotes Atherosclerosis

scientific article published on 05 June 2019

Haplotype Effect of the Matrix Metalloproteinase-1 Gene on Risk of Myocardial Infarction

article

Haplotype effects on matrix metalloproteinase-1 gene promoter activity in cancer cells

artículo científico publicado en 2007

Haplotypic analysis of the MMP-9 gene in relation to coronary artery disease

artículo científico publicado en 2003

Human stromelysin gene promoter activity is modulated by transcription factor ZBP-89

artículo científico publicado en 1999

Increased NBCn1 expression, Na+/HCO3- co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension

artículo científico publicado en 2017

Independent effects of the -219 G>T and epsilon 2/ epsilon 3/ epsilon 4 polymorphisms in the apolipoprotein E gene on coronary artery disease: the Southampton Atherosclerosis Study

artículo científico publicado en 2003

Influence of a Coronary Artery Disease-Associated Genetic Variant on FURIN Expression and Effect of Furin on Macrophage Behavior.

artículo científico publicado en 2018

Influence of matrix metalloproteinase genotype on cardiovascular disease susceptibility and outcome.

artículo científico publicado en 2005

Influence of matrix metalloproteinase-12 on fibrinogen level

artículo científico publicado en 2011

Influences of matrix metalloproteinase-3 gene variation on extent of coronary atherosclerosis and risk of myocardial infarction.

artículo científico publicado en 2003

Insulin-like growth factor-I genotype and birthweight

scientific article published in The Lancet

Invasiveness of cutaneous malignant melanoma is influenced by matrix metalloproteinase 1 gene polymorphism.

artículo científico publicado en 2001

JCAD Gene at the 10p11 Coronary Artery Disease Locus Regulates Hippo Signaling in Endothelial Cells.

artículo científico publicado en 2018

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

artículo científico publicado en 2011

Late life metabolic syndrome, early growth, and common polymorphism in the growth hormone and placental lactogen gene cluster

artículo científico publicado en 2004

Matrix metalloproteinase-8 promotes vascular smooth muscle cell proliferation and neointima formation.

artículo científico publicado en 2013

Matrix metalloproteinases: implication in vascular matrix remodelling during atherogenesis.

artículo científico publicado en 1998

Microarray analysis of peroxisome proliferator-activated receptor-gamma induced changes in gene expression in macrophages.

artículo científico publicado en 2003

Mutation scanning by meltMADGE: validations using BRCA1 and LDLR, and demonstration of the potential to identify severe, moderate, silent, rare, and paucimorphic mutations in the general population

artículo científico publicado en 2005

Myopia and polymorphisms in genes for matrix metalloproteinases.

artículo científico publicado en 2009

PCR designer for restriction analysis of various types of sequence mutation

artículo científico publicado en 2002

PIRA PCR designer for restriction analysis of single nucleotide polymorphisms

artículo científico publicado en 2001

PLA2G7 genotype, lipoprotein-associated phospholipase A2 activity, and coronary heart disease risk in 10 494 cases and 15 624 controls of European Ancestry

artículo científico publicado en 2010

Plasma MMP1 and MMP8 expression in breast cancer: protective role of MMP8 against lymph node metastasis

artículo científico publicado en 2008

Plasma MMP1, MMP8 and MMP13 expression in breast cancer: protective role of MMP8 against lymph node metastasis

artículo científico publicado en 2008

Polymorphism in the promoter region of the apolipoprotein AI gene associated with differences in apolipoprotein AI levels: the European Atherosclerosis Research Study

artículo científico publicado en 1994

Polymorphisms in matrix metalloproteinase-1, -3, -9, and -12 genes in relation to subarachnoid hemorrhage

artículo científico publicado en 2001

Promoter polymorphism influences the effect of dexamethasone on transcriptional activation of the LTC4 synthase gene

artículo científico publicado en 2003

Propofol Suppresses Proinflammatory Cytokine Production by Increasing ABCA1 Expression via Mediation by the Long Noncoding RNA LOC286367

scientific article published on 17 December 2018

Putative targeting of matrix metalloproteinase-8 in atherosclerosis

artículo científico publicado en 2014

Rapid genotype analysis of the matrix metalloproteinase-1 gene 1G/2G polymorphism that is associated with risk of cancer

scientific article published on 01 May 2000

Rapid genotype analysis of the stromelysin gene 5A/6A polymorphism

artículo científico publicado en 2000

SDF1 gene variation is associated with circulating SDF1alpha level and endothelial progenitor cell number: the Bruneck Study

artículo científico publicado en 2008

Single nucleotide polymorphism genotyping in MMP genes: the 5' nuclease assay

artículo científico publicado en 2010

Single nucleotide polymorphism on chromosome 9p21 and endothelial progenitor cells in a general population cohort.

artículo científico publicado en 2009

Sp1-dependent activation of HDAC7 is required for platelet-derived growth factor-BB-induced smooth muscle cell differentiation from stem cells.

artículo científico publicado en 2010

Statins inhibit toll-like receptor 4-mediated lipopolysaccharide signaling and cytokine expression

artículo científico publicado en 2008

Subcutaneous Injection of Nitroglycerin at the Radial Artery Puncture Site Reduces the Risk of Early Radial Artery Occlusion After Transradial Coronary Catheterization: A Randomized, Placebo-Controlled Clinical Trial

scientific article published on 01 July 2018

TLR4 Asp299Gly polymorphism is not associated with coronary artery stenosis

artículo científico publicado en 2003

The 4G/5G genetic polymorphism in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene is associated with differences in plasma PAI-1 activity but not with risk of myocardial infarction in the ECTIM study. Etude CasTemoins de I'nfarctu

artículo científico publicado en 1995

The biological impact of blood pressure-associated genetic variants in the natriuretic peptide receptor C gene on human vascular smooth muscle.

artículo científico publicado en 2017

The genetics of epigenetics: is there a link with cardiovascular disease

scientific article published on 01 January 2011

The role of the LncRNA-FA2H-2-MLKL pathway in atherosclerosis by regulation of autophagy flux and inflammation through mTOR-dependent signaling

scientific article published on 25 January 2019

Toll-like receptors, their ligands, and atherosclerosis.

artículo científico publicado en 2011

Transmission disequilibrium test of stromelysin-1 gene variation in relation to Crohn's disease

artículo científico publicado en 2004

Upregulated sirtuin 1 by miRNA-34a is required for smooth muscle cell differentiation from pluripotent stem cells

scientific journal article

VEGF polymorphisms and severity of atherosclerosis.

artículo científico publicado en 2005

Variation in the matrix metalloproteinase-1 gene and risk of coronary heart disease

scientific article published on 01 September 2003

Variation in the matrix metalloproteinase-3, -7, -12 and -13 genes is associated with functional status in rheumatoid arthritis

article

Variation in the toll-like receptor 4 gene and susceptibility to myocardial infarction

artículo científico publicado en 2005

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