The association between the angiotensin I converting enzyme gene polymorphism and cardiovascular disease

Molecular genetics of myotonic dystrophy.

Trends in cardiovascular medicine·2011

Metabolic and diagnostic significance of creatine kinase isoenzymes.

Trends in cardiovascular medicine·2011

Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in mice.

Human molecular genetics·2009

Myotonic dystrophy protein kinase domains mediate localization, oligomerization, novel catalytic activity, and autoinhibition.

Biochemistry·2000

Phospholemman is a substrate for myotonic dystrophy protein kinase.

The Journal of biological chemistry·2000

Myocardial-directed overexpression of the human beta(1)-adrenergic receptor in transgenic mice.

Journal of molecular and cellular cardiology·2000

The perforation triad as a recognition-and-response pattern for balloon- or stent-related Ellis II-III coronary artery perforation during percutaneous coronary intervention.

Coronary artery disease·2026

Radiation burden in chronic total occlusion percutaneous coronary intervention is driven more by lesion complexity and planned strategy than by the target vessel.

Coronary artery disease·2026

Combined triglyceride-glucose index and systemic inflammation for long-term risk stratification in major adverse cardiovascular events: a 10-year prospective study.

Coronary artery disease·2026

Deconditioning in coronary artery disease: an underrecognized problem with contemporary clinical relevance.

Coronary artery disease·2026

Intracoronary supersaturated oxygen therapy after primary percutaneous coronary intervention in ST-segment elevation myocardial infarction: a systematic review and meta-analysis.

Coronary artery disease·2026

Management of multivessel disease in patients with ST-segment elevation myocardial infarction: questioning routine immediate complete revascularization in all patients.

Coronary artery disease·2026

Regulation of the histone H3K36 methyltransferase Set2 by the histone chaperone Spt6.

Nucleic acids research·2026

The clinical utility of exome sequencing for risk stratification in celiac disease.

Journal of human immunity·2026

Expanding the KBG syndrome phenotype through 2D facial morphometry, clinical and molecular characterization.

Biomedical reports·2026

Non-invasive embryo assessment: Cell-free DNA-based genetic testing and amino acid metabolomics in relation to morphology: A case-control study.

International journal of reproductive biomedicine·2026

Symposium report- epigenetic inheritance: impact for biology and society 27-29 August 2025, Zurich, Switzerland.

Environmental epigenetics·2026

Severity-stratified gut microbiome dysbiosis and systemic neuroinflammation in acute traumatic brain injury: a metagenomic and cytokine profiling study.

Frontiers in microbiology·2026

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The association between the angiotensin I converting enzyme gene polymorphism and cardiovascular disease

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Molecular genetics of myotonic dystrophy.

Metabolic and diagnostic significance of creatine kinase isoenzymes.

Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in mice.

Myotonic dystrophy protein kinase domains mediate localization, oligomerization, novel catalytic activity, and autoinhibition.

Phospholemman is a substrate for myotonic dystrophy protein kinase.

Myocardial-directed overexpression of the human beta(1)-adrenergic receptor in transgenic mice.

The perforation triad as a recognition-and-response pattern for balloon- or stent-related Ellis II-III coronary artery perforation during percutaneous coronary intervention.

Radiation burden in chronic total occlusion percutaneous coronary intervention is driven more by lesion complexity and planned strategy than by the target vessel.

Combined triglyceride-glucose index and systemic inflammation for long-term risk stratification in major adverse cardiovascular events: a 10-year prospective study.

Deconditioning in coronary artery disease: an underrecognized problem with contemporary clinical relevance.

Intracoronary supersaturated oxygen therapy after primary percutaneous coronary intervention in ST-segment elevation myocardial infarction: a systematic review and meta-analysis.

Management of multivessel disease in patients with ST-segment elevation myocardial infarction: questioning routine immediate complete revascularization in all patients.

Regulation of the histone H3K36 methyltransferase Set2 by the histone chaperone Spt6.

The clinical utility of exome sequencing for risk stratification in celiac disease.

Expanding the KBG syndrome phenotype through 2D facial morphometry, clinical and molecular characterization.

Non-invasive embryo assessment: Cell-free DNA-based genetic testing and amino acid metabolomics in relation to morphology: A case-control study.

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The association between the angiotensin I converting enzyme gene polymorphism and cardiovascular disease

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