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1
المؤلفون: Ceren Acar, Harun Evrengul, Deniz Seleci, Asuman Kaftan, Seyhan Tanriverdi, Halil Tanriverdi, Omur Kuru, Hatice Mergen
المصدر: Heart and Vessels. 22:1-8
مصطلحات موضوعية: Carotid Artery Diseases, Male, angiocardiography, AT1R A/C1166 polymorphism, Adult, Aged, Alleles, Carotid Artery Diseases/*genetics/*physiopathology, Coronary Angiography, Coronary Vessels/*physiopathology, Female, Humans, Middle Aged, Peptidyl-Dipeptidase A/*genetics, Polymorphism, Genetic/*physiology, Regional Blood Flow, Renin-Angiotensin System, Tunica Intima/pathology, Tunica Media/pathology, Intima-media thickness, correlation analysis, genotype, Renin-angiotensin gene system, image display, Coronary artery disease, cardiovascular disease, Carotid atherosclerosis, coronary artery blood flow, renin angiotensin aldosterone system, Myocardial infarction, Common carotid artery, statistical significance, clinical article, biology, adult, pathogenesis, artery intima, allele, article, vascular disease, Coronary Vessels, transducer, ACEI/D polymorphism, aged, female, medicine.anatomical_structure, priority journal, risk factor, Cardiology, Tunica Media, Cardiology and Cardiovascular Medicine, coronary artery disease, gene insertion, TIMI, medicine.medical_specialty, regulatory mechanism, angiotensin 1 receptor, dipeptidyl carboxypeptidase, common carotid artery, Peptidyl-Dipeptidase A, artery media, Internal medicine, medicine.artery, medicine, inheritance, controlled study, human, cardiovascular diseases, artery wall, Polymorphism, Genetic, Slow coronary flow, carotid artery, gene deletion, business.industry, disease association, echography, Angiotensin-converting enzyme, medicine.disease, Angiotensin II, thickness, Coronary arteries, enzyme polymorphism, biology.protein, Gene polymorphism, atherosclerosis, Tunica Intima, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7d718dcd247dbc8ffed8d0c8678ed4eTest
https://doi.org/10.1007/s00380-006-0925-1Test -
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المؤلفون: Gang Xu, Dong Li, Tong Liu, Michael Shehata, Panagiotis Korantzopoulos, Xunzhang Wang, Guangping Li
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Peptidyl-Dipeptidase A, Bioinformatics, Peptidyl-Dipeptidase A/*genetics, Renin-Angiotensin System, INDEL Mutation, Risk Factors, Physiology (medical), Internal medicine, Atrial Fibrillation, Medicine, Insertion deletion, Humans, Polymorphism, Genetic/genetics, Aged, Polymorphism, Genetic, biology, business.industry, Case-control study, Angiotensin-converting enzyme, Atrial fibrillation, Atrial Fibrillation/epidemiology/*genetics/physiopathology, Middle Aged, medicine.disease, Clinical trial, INDEL Mutation/*genetics, Endocrinology, Meta-analysis, Case-Control Studies, biology.protein, Dominant model, Female, Gene polymorphism, Renin-Angiotensin System/physiology, Cardiology and Cardiovascular Medicine, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cb34bb3b79e1ba9ba3bf6720e1ebaffTest
http://olympias.lib.uoi.gr/jspui/handle/123456789/23675Test -
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المؤلفون: John Chalmers, Cock M. van Duijn, Roberto Ferrari, Stephen MacMahon, Jacqueline C. M. Witteman, Toshiharu Ninomiya, Michel E. Bertrand, Maarten L. Simoons, Claudio Ceconi, A.H. Jan Danser, François Cambien, Aaron Isaacs, Kim Fox, Willem J. Remme, André G. Uitterlinden, Jasper J. Brugts, Moniek P.M. de Maat, Stephen B. Harrap, Eric Boersma, K. Martijn Akkerhuis
المساهمون: Cardiology, Epidemiology, Hematology, Internal Medicine
المصدر: Journal of Hypertension, 29(3), 509-19. LIPPINCOTT WILLIAMS & WILKINS
Journal of Hypertension, 29(3), 509-519. Lippincott Williams & Wilkinsمصطلحات موضوعية: Receptors, Cell Surface/genetics, Male, ACE inhibitors, Physiology, Angiotensinogen, Angiotensin-Converting Enzyme Inhibitors, Blood Pressure, Gastroenterology, Plasma renin activity, polymorphism, chemistry.chemical_compound, Receptors, Perindopril, Prorenin Receptor, pharmacogenetics, Hypertension/drug therapy, gene, hypertension, PERGENE, PROGRESS, renin-angiotensin-aldosterone system, Single Nucleotide, Middle Aged, Female, Cardiology and Cardiovascular Medicine, medicine.drug, medicine.medical_specialty, Receptors, Cell Surface, Angiotensin-Converting Enzyme Inhibitors/pharmacology, Peptidyl-Dipeptidase A/genetics, Peptidyl-Dipeptidase A, Polymorphism, Single Nucleotide, Blood Pressure/drug effects, Internal medicine, Internal Medicine, medicine, Humans, Aged, Cell Surface/genetics, business.industry, Vascular disease, Aliskiren, medicine.disease, Blood pressure, Endocrinology, chemistry, Haplotypes, ACE inhibitor, Gene polymorphism, Angiotensinogen/genetics, business, Pharmacogenetics
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30d6ed0683feb6ebb5ea000e9d5162f8Test
http://hdl.handle.net/11392/1735104Test -
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المؤلفون: Carl Foster, Joaquín Arenas, Alejandro Lucia, Félix Gómez-Gallego, Margarita Pérez, Catalina Santiago, Marta Gonzalez-Freire
مصطلحات موضوعية: DNA Mutational Analysis, Respiratory Insufficiency/Genetics, Myostatin, Disease, AMP Deaminase, Tratamiento médico, Genotype, Glycogen/Metabolism, Actinin, Genetics (clinical), Exercise Tolerance, Muscle Weakness, Exercise Tolerance/Genetics, biology, Muscle, Skeletal/Physiopathology, Genetic Variation/Genetics, Deporte, Dna Mutational Analysis, Phenotype, Neurology, Peptidyl-Dipeptidase A/Genetics, Female, medicine.symptom, Respiratory Insufficiency, Glycogen storage disease type V, Glycogen, Adult, Glycogen Storage Disease Type V/Physiopathology, medicine.medical_specialty, Heterozygote, Adolescent, Genetic Predisposition To Disease/*Genetics, Peptidyl-Dipeptidase A, Internal medicine, Genetic variation, Glycogen Storage Disease Type V/*Genetics, medicine, Myostatin/*Genetics, Humans, Genetic Predisposition to Disease, Muscle, Skeletal, Enfermedad nutricional, Muscle Weakness/Genetics, Aged, Muscle weakness, Genetic Variation, Cardiorespiratory fitness, Heterozygote advantage, medicine.disease, Endocrinology, Muscle, Skeletal/Metabolism, Amp Deaminase/Genetics, Pediatrics, Perinatology and Child Health, Mutation, biology.protein, Glycogen Storage Disease Type V, Neurology (clinical), Glycogen Storage Disease Type V/Metabolism, Mutation/*Genetics
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::539c42aa69b9ade0cc7de6f61a11a30dTest
https://hdl.handle.net/11268/1120Test -
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المؤلفون: Antonis Vylliotis, Vasilis Ragos, Christos Yapijakis, Stavros Vassiliou, Sofia Spyridonidou, E. Vorris, Efstratios Patsouris, Emeka Nkenke, Christos Tsigris, Eleftherios Vairaktaris, Spyridoula Derka, Friedrich Wilhelm Neukam
مصطلحات موضوعية: Adult, Male, Risk, medicine.medical_specialty, Mouth Neoplasms/*genetics, Genotype, Polymorphism, Genetic, Peptidyl-Dipeptidase A, medicine.disease_cause, Thrombophilia, Peptidyl-Dipeptidase A/*genetics, INDEL Mutation, Gene Frequency, Internal medicine, Germany, Renin–angiotensin system, medicine, Humans, Radiology, Nuclear Medicine and imaging, Genetic Predisposition to Disease, Family history, Allele, Allele frequency, Aged, Aged, 80 and over, biology, Greece, business.industry, Angiotensin-converting enzyme, Hematology, General Medicine, Odds ratio, Middle Aged, medicine.disease, Endocrinology, Oncology, Case-Control Studies, biology.protein, Carcinoma, Squamous Cell, Disease Progression, Mouth Neoplasms, Female, Carcinogenesis, business, Carcinoma, Squamous Cell/*genetics
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45e7cab25fd8dab521ea25e1718af2d4Test
http://olympias.lib.uoi.gr/jspui/handle/123456789/23667Test