asparagine has been researched along with Arteriosclerosis, Coronary in 9 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (11.11) | 18.7374 |
1990's | 2 (22.22) | 18.2507 |
2000's | 3 (33.33) | 29.6817 |
2010's | 3 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Marian, AJ | 1 |
Fernandez, C; Melander, O; Ottosson, F; Smith, E | 1 |
Chang, KL; Chang, PC; Chang, TT; Chang, YL; Chen, KB; Chen, KC; Chen, YC | 1 |
Dedoussis, G; Deltas, C; Kasparian, C; Lamnissou, K; Nastos, P; Nikolakis, D; Pantazopoulos, N; Vasilakou, M; Votteas, V | 1 |
BLUMBERGER, KJ; NIEPER, HA | 1 |
Hannah, BL; Misenheimer, TM; Mosher, DF; Pranghofer, MM | 1 |
Kyriakou, T; Laxton, R; Pearce, E; Ye, S | 1 |
Cavanna, J; Galton, DJ; Gross, W; Marz, W; Shine, B; Winkelman, BR; Zhang, Q | 1 |
Abildgaard, S; Jensen, G; Nordestgaard, BG; Steffensen, R; Tybjaerg-Hansen, A; Wittrup, HH | 1 |
9 other study(ies) available for asparagine and Arteriosclerosis, Coronary
Article | Year |
---|---|
Non-syndromic cardiac progeria in a patient with the rare pathogenic p.Asp300Asn variant in the LMNA gene.
Topics: Adult; Amino Acid Sequence; Asparagine; Aspartic Acid; Base Sequence; Coronary Artery Disease; Echocardiography; Electrocardiography; Fatal Outcome; Female; Humans; Lamin Type A; Mutation, Missense; Myocardial Infarction; Pedigree; Progeria; Sequence Homology, Amino Acid | 2017 |
Altered Asparagine and Glutamate Homeostasis Precede Coronary Artery Disease and Type 2 Diabetes.
Topics: Aged; Aged, 80 and over; Asparagine; Case-Control Studies; Coronary Artery Disease; Diabetes Mellitus, Type 2; Diabetic Angiopathies; Female; Follow-Up Studies; Glutamic Acid; Homeostasis; Humans; Male; Middle Aged; Prodromal Symptoms | 2018 |
In Silico Investigation of Traditional Chinese Medicine for Potential Lead Compounds as SPG7 Inhibitors against Coronary Artery Disease.
Topics: Asparagine; ATPases Associated with Diverse Cellular Activities; Binding Sites; Computer Simulation; Coronary Artery Disease; Crystallography, X-Ray; Drugs, Chinese Herbal; Enzyme Inhibitors; Humans; Metalloendopeptidases; Molecular Docking Simulation; Molecular Dynamics Simulation; Molecular Structure; Mutation; Quinazolinones; Structure-Activity Relationship | 2016 |
Lack of association between endothelial nitric oxide synthase gene polymorphisms and risk of premature coronary artery disease in the Greek population.
Topics: Adult; Age Factors; Aged; Alleles; Asparagine; Case-Control Studies; Coronary Artery Disease; Endothelium, Vascular; Exons; Female; Glutamine; Greece; Humans; Introns; Male; Middle Aged; Minisatellite Repeats; Myocardial Infarction; Nitric Oxide; Nitric Oxide Synthase; Nitric Oxide Synthase Type III; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Risk Factors | 2008 |
[Experimental basis and clinical use of electrolyte carrier compounds. I. Metabolic activity of Mg- and K-asparaginate, especially in coronary insufficiency].
Topics: Asparagine; Biochemical Phenomena; Coronary Artery Disease; Electrolytes; Heart Failure; Humans; Magnesium; Potassium | 1961 |
A polymorphism in thrombospondin-1 associated with familial premature coronary artery disease alters Ca2+ binding.
Topics: Amino Acid Motifs; Amino Acid Sequence; Asparagine; Binding Sites; Calcium; Coronary Artery Disease; Humans; In Vitro Techniques; Kinetics; Molecular Sequence Data; Peptide Fragments; Polymorphism, Single Nucleotide; Recombinant Proteins; Serine; Thrombospondin 1 | 2004 |
Association of the lymphotoxin-alpha gene Thr26Asn polymorphism with severity of coronary atherosclerosis.
Topics: Asparagine; Cohort Studies; Coronary Artery Disease; Female; Humans; Lymphotoxin-alpha; Male; Polymorphism, Genetic; Sex Factors; Threonine | 2005 |
Common genetic variants of lipoprotein lipase that relate to lipid transport in patients with premature coronary artery disease.
Topics: Asparagine; Aspartic Acid; Coronary Artery Disease; Genetic Variation; Humans; Lipid Metabolism; Lipoprotein Lipase; Lipoproteins; Middle Aged; Point Mutation; Serine | 1995 |
Heterozygous lipoprotein lipase deficiency: frequency in the general population, effect on plasma lipid levels, and risk of ischemic heart disease.
Topics: Adult; Aged; Aged, 80 and over; Apolipoprotein A-I; Asparagine; Cholesterol, HDL; Coronary Artery Disease; Female; Gene Frequency; Glutamic Acid; Glycine; Heterozygote; Humans; Isoleucine; Lipids; Lipoprotein Lipase; Male; Middle Aged; Phenotype; Point Mutation; Risk Factors; Serine; Triglycerides | 1997 |