adenosine monophosphate and Genetic Predisposition
adenosine monophosphate has been researched along with Genetic Predisposition in 10 studies
Research
Studies (10)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (20.00) | 18.2507 |
2000's | 3 (30.00) | 29.6817 |
2010's | 4 (40.00) | 24.3611 |
2020's | 1 (10.00) | 2.80 |
Authors
Authors | Studies |
---|---|
Eilenberger, J; Fischer, M; Haas, N; Hauck, F; Hermann, M; Huebner, J; Jakob, A; Kappler, M; Kim-Hellmuth, S; Klein, C; Ley-Zaporozhan, J; von Both, U | 1 |
Gray, A; Hardie, DG; Padbury, J; Phornphutkul, C; Shaw, S; Tseng, YT; Uzun, A; Xu, Y | 1 |
Butcher, SE; Cui, Q; Montemayor, EJ; Nomura, Y; Roston, D | 1 |
Chepurko, E; Covarrubias, R; Cowan, PJ; Dwyer, KM; Gumina, RJ; Huttinger, R; Huttinger, ZM; Novitskaya, T; Reynolds, A; Robson, SC; Stanfill, K; Wheeler, DG | 1 |
Chen, BC; Duley, JA; Khoo, TB; McGown, IN; Ngu, LH; Pitt, J; Thong, MK; Yunus, ZM | 1 |
Tiainen, M; Udd, L; Vaahtomeri, K | 1 |
Arbustini, E; Pasotti, M; Repetto, A; Tavazzi, L | 1 |
Covar, RA | 1 |
Feldman, AM; McNamara, DM; Wagner, DR | 1 |
DeNofrio, D; Holmes, EW; Loh, E; Mahoney, PD; Rebbeck, TR; Swain, JL | 1 |
Reviews
2 review(s) available for adenosine monophosphate and Genetic Predisposition
Article | Year |
---|---|
Genetic predisposition to heart failure.
Topics: Adenosine Monophosphate; Atrial Natriuretic Factor; Cardiomyopathy, Dilated; Carrier Proteins; Consanguinity; Cytokines; Cytoskeletal Proteins; Effect Modifier, Epidemiologic; Endothelins; Gene Pool; Genetic Predisposition to Disease; Genetic Variation; Growth Substances; Heart Failure; Humans; Matrix Metalloproteinases; Models, Genetic; Molecular Epidemiology; Muscle Proteins; Nitric Oxide; Oxidative Stress; Phenotype; Polymorphism, Genetic; Receptors, Adrenergic; Renin-Angiotensin System | 2004 |
Bronchoprovocation testing in asthma.
Topics: Adenosine Monophosphate; Anti-Inflammatory Agents; Asthma; Biomarkers; Bronchial Hyperreactivity; Bronchial Provocation Tests; Genetic Predisposition to Disease; Humans | 2007 |
Other Studies
8 other study(ies) available for adenosine monophosphate and Genetic Predisposition
Article | Year |
---|---|
SARS-CoV-2 Triggering Severe Acute Respiratory Distress Syndrome and Secondary Hemophagocytic Lymphohistiocytosis in a 3-Year-Old Child With Down Syndrome.
Topics: Adenosine Monophosphate; Alanine; Antiviral Agents; Child, Preschool; COVID-19; COVID-19 Drug Treatment; COVID-19 Testing; Critical Care; Down Syndrome; Genetic Predisposition to Disease; Glucocorticoids; Humans; Immunoglobulins, Intravenous; Lymphohistiocytosis, Hemophagocytic; Male; Prednisolone; SARS-CoV-2; Systemic Inflammatory Response Syndrome | 2021 |
A novel, de novo mutation in the
Topics: Adenosine Monophosphate; AMP-Activated Protein Kinases; Cardiomyopathy, Hypertrophic; Carrier Proteins; Case-Control Studies; DNA Mutational Analysis; Enzyme Activation; Fibroblasts; Genetic Predisposition to Disease; HEK293 Cells; Humans; Infant, Newborn; Intracellular Signaling Peptides and Proteins; Models, Molecular; Mutation, Missense; Myocytes, Cardiac; Phenformin; Phenotype; Phosphoproteins; Phosphorylation; Protein Conformation; Protein Kinase Inhibitors; Ribosomal Protein S6 Kinases, 70-kDa; Signal Transduction; Sirolimus; Structure-Activity Relationship; TOR Serine-Threonine Kinases; Transfection | 2017 |
Structural and mechanistic basis for preferential deadenylation of U6 snRNA by Usb1.
Topics: Adenosine; Adenosine Monophosphate; Base Sequence; Crystallography, X-Ray; Genetic Predisposition to Disease; Humans; Models, Molecular; Mutation; Neutropenia; Nucleic Acid Conformation; Phosphoric Diester Hydrolases; Protein Binding; Protein Conformation; RNA, Small Nuclear; Skin Abnormalities; Substrate Specificity; Uridine | 2018 |
Role of the CD39/CD73 Purinergic Pathway in Modulating Arterial Thrombosis in Mice.
Topics: 5'-Nucleotidase; Adenosine; Adenosine Diphosphate; Adenosine Monophosphate; Adenosine Triphosphate; Animals; Antigens, CD; Apyrase; Arterial Occlusive Diseases; Blood Coagulation; Bone Marrow Transplantation; Chlorides; Disease Models, Animal; Endothelial Cells; Ferric Compounds; Genetic Predisposition to Disease; HEK293 Cells; Humans; Hydrolysis; Mice, Inbred C57BL; Mice, Knockout; Mice, Transgenic; Monocytes; Phenotype; Platelet Activation; Thrombosis; Time Factors; Transfection | 2016 |
Adenylosuccinate lyase deficiency in a Malaysian patient, with novel adenylosuccinate lyase gene mutations.
Topics: Adenosine; Adenosine Monophosphate; Adenylosuccinate Lyase; Aminoimidazole Carboxamide; Autistic Disorder; Biomarkers; Child Development; Chromatography, High Pressure Liquid; DNA Mutational Analysis; Genetic Predisposition to Disease; Genetic Testing; Heterozygote; Humans; Infant; Infant, Newborn; Malaysia; Male; Mutation; Myoclonus; Phenotype; Predictive Value of Tests; Psychomotor Disorders; Psychomotor Performance; Purine-Pyrimidine Metabolism, Inborn Errors; Ribonucleosides; Seizures; Spectrometry, Mass, Electrospray Ionization; Tandem Mass Spectrometry | 2010 |
[A surprising link between the tumor suppressor gene and regulation of metabolism].
Topics: Adenosine Monophosphate; Animals; Blood Glucose; Enzyme Activation; Genes, Tumor Suppressor; Genetic Predisposition to Disease; Humans; Intestinal Neoplasms; Peutz-Jeghers Syndrome; Saccharomyces cerevisiae; Species Specificity | 2004 |
AMPD1 gene mutation in congestive heart failure: new insights into the pathobiology of disease progression.
Topics: Adenosine; Adenosine Monophosphate; Alleles; AMP Deaminase; Cardiomyopathy, Dilated; Disease Progression; Energy Metabolism; Genetic Predisposition to Disease; Genotype; Heart Failure; Humans; Myocardium; Receptors, Purinergic P1 | 1999 |
Common variant in AMPD1 gene predicts improved clinical outcome in patients with heart failure.
Topics: Adenosine Monophosphate; Aged; Alleles; AMP Deaminase; Angiotensin-Converting Enzyme Inhibitors; Cardiomyopathy, Dilated; Coronary Disease; Digoxin; Disease Progression; Diuretics; DNA Mutational Analysis; Energy Metabolism; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Heart Failure; Hemodynamics; Humans; Male; Middle Aged; Myocardium; Oxygen Consumption; Phenotype; Proportional Hazards Models; Survival Analysis; Treatment Outcome | 1999 |