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

المؤلفون: Ceylan Ayada, Ümran Toru, Sebahat Turgut, Osman Genç, Günfer Turgut, Server Sahin, A. Yerlikaya

مصطلحات موضوعية: Gene Frequency, Genetic Association Studies, Genetic Predisposition to Disease, Humans, INDEL Mutation/*genetics, Peptidyl-Dipeptidase A/*genetics, Pulmonary Disease, Chronic Obstructive/*genetics/pathology, Renin-Angiotensin System/*genetics, Risk Factors, Turkey, genomic DNA, genetic association, genotype, polymerase chain reaction, genetic risk, Gastroenterology, Turkey (republic), Turkish population, Renin-Angiotensin System, Pulmonary Disease, Chronic Obstructive, INDEL Mutation, renin angiotensin aldosterone system, Genotype, genetic variability, genetic polymorphism, genetics, pathophysiology, COPD, education.field_of_study, clinical article, biology, Chronic obstructive pulmonary disease, allele, General Medicine, risk factor, Renin angiotensin system, blood sampling, Angiotensin converting enzyme, medicine.medical_specialty, Population, dipeptidyl carboxypeptidase, DNA determination, Peptidyl-Dipeptidase A, Article, Internal medicine, geographic distribution, medicine, Genetic predisposition, ACE protein, human, heterozygosity, controlled study, human, education, Molecular Biology, Allele frequency, gene identification, business.industry, population genetics, Angiotensin-converting enzyme, ACE gene, medicine.disease, DNA isolation, Endocrinology, gene function, biology.protein, gene expression, Turk (people), pathology, homozygosity, business, genetic predisposition, chronic obstructive lung disease, Blood sampling

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f6d6032137ce50699698c4d9415dcd5Test
https://hdl.handle.net/20.500.12438/4548Test

المؤلفون: Ioanna Bouba, Athina Tatsioni, Charilaos Kostoulas, Ioannis Georgiou, Sotirios Maranis, Sotirios Giannopoulos, Athanassios P. Kyritsis, Sofia Markoula

المصدر: Journal of the Renin-Angiotensin-Aldosterone System, Vol 12 (2011)

مصطلحات موضوعية: Male, medicine.medical_specialty, Medicine (General), Stroke/complications/*enzymology/*genetics, Myocardial Ischemia, Peptidyl-Dipeptidase A, Peptidyl-Dipeptidase A/*genetics, Endocrinology, R5-920, Gene Frequency, Polymorphism (computer science), Internal medicine, Ischaemic stroke, Genotype, Internal Medicine, medicine, Humans, Medical history, Genetic Predisposition to Disease, Allele, Gene, Stroke, Myocardial Ischemia/*complications/*enzymology/genetics, Sex Characteristics, biology, business.industry, Hypertension/complications/enzymology/genetics, Angiotensin-converting enzyme, Middle Aged, medicine.disease, Atherosclerosis, Atherosclerosis/complications/enzymology/genetics, Gene Frequency/genetics, Case-Control Studies, Hypertension, biology.protein, Female, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80823a56726a80349926c0dc85832263Test
https://pubmed.ncbi.nlm.nih.gov/21421656Test

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

المؤلفون: Raziye Akcılar, Ceylan Ayada, Sebahat Turgut, Fulya Akin, Günfer Turgut

مصطلحات موضوعية: Male, systolic blood pressure, genetic association, genotype, Angiotensinogen, cholesterol blood level, Blood Pressure, insulin blood level, low density lipoprotein cholesterol, chemistry.chemical_compound, Gene Frequency, INDEL Mutation, high density lipoprotein cholesterol, insulin resistance, Genotype, genetic polymorphism, Receptor, clinical article, biology, adult, article, General Medicine, Middle Aged, growth hormone blood level, female, Female, triacylglycerol, Acromegaly/enzymology/*genetics/physiopathology, Adult, Angiotensinogen/*genetics, Blood Pressure/genetics, Case-Control Studies, Gene Frequency/genetics, Genetic Predisposition to Disease, Humans, INDEL Mutation/*genetics, Peptidyl-Dipeptidase A/*genetics, Polymorphism, Single Nucleotide/*genetics, Receptor, Angiotensin, Type 1/*genetics, Angiotensin converting enzyme, medicine.medical_specialty, insulin, hypertension, angiotensin 1 receptor, dipeptidyl carboxypeptidase, AT1-receptor, Peptidyl-Dipeptidase A, gene frequency, Polymorphism, Single Nucleotide, Receptor, Angiotensin, Type 1, protein denaturation, male, Internal medicine, Acromegaly, Genetics, medicine, controlled study, human, Polymorphism, Molecular Biology, Angiotensin II receptor type 1, Triglyceride, diastolic blood pressure, Angiotensin-converting enzyme, medicine.disease, triacylglycerol blood level, Angiotensin II, somatomedin C, body mass, Endocrinology, Blood pressure, glucose blood level, chemistry, biology.protein, homozygosity

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2e76bb23295505227da5da7e4e11c32Test
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/6129Test

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 & Wilkins

مصطلحات 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

المؤلفون: Aydin Guclu, Mehmet Bastemir, Günfer Turgut, Uğur Karasu, Fulya Akin, Raziye Kursunluoglu, Sebahat Turgut

مصطلحات موضوعية: Blood Glucose, Male, obesity, genetic association, Turkey, genotype, polymerase chain reaction, Blood Pressure, Overweight, Turkey (republic), Body Mass Index, Gene Frequency, Polymorphism (computer science), insulin resistance, middle aged, Genotype, genetic polymorphism, Insulin, genetics, Metabolic Syndrome, biology, non insulin dependent diabetes mellitus, adult, Metabolic Syndrome X, Adipose Tissue/anatomy & histology, Adult, Blood Glucose/metabolism, Blood Pressure/physiology, Diabetes Mellitus, Type 2/genetics, Female, Gene Frequency/genetics, Humans, Insulin/blood, Insulin Resistance/*genetics, Lipids/blood, Metabolic Syndrome/genetics, Middle Aged, Obesity/*genetics, Overweight/*genetics, Peptidyl-Dipeptidase A/*genetics, Polymorphism, Genetic/*genetics, Uric Acid/blood, Waist Circumference/genetics, allele, article, General Medicine, waist circumference, Lipids, adipose tissue, female, Adipose Tissue, priority journal, Waist Circumference, medicine.symptom, gene insertion, medicine.medical_specialty, Turkish population, dipeptidyl carboxypeptidase, Peptidyl-Dipeptidase A, histology, Insulin resistance, uric acid, lipid, blood, Internal medicine, ACE protein, human, Genetics, medicine, controlled study, Obesity, human, Molecular Biology, gene identification, Polymorphism, Genetic, gene deletion, Angiotensin-converting enzyme, Cell Biology, medicine.disease, major clinical study, body mass, Uric Acid, glucose blood level, Endocrinology, Diabetes Mellitus, Type 2, physiology, biology.protein, Gene polymorphism, Insulin Resistance, population research, metabolism

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd5d97db37271abd0791af41c80fd648Test

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

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

المؤلفون: Ilhan Oztop, Canan Kelten, Serkan Degirmencioglu, Ergun Erdem, Raziye Kursunluoglu, Günfer Turgut, Sebahat Turgut, Arzu Yaren

المصدر: Europe PubMed Central

مصطلحات موضوعية: medicine.medical_specialty, cancer patient, gene overexpression, genotype, polymerase chain reaction, dipeptidyl carboxypeptidase, Angiotensin-Converting Enzyme Inhibitors, Breast Neoplasms, Peptidyl-Dipeptidase A, Biology, Prognostic factors, medical record, Gastroenterology, General Biochemistry, Genetics and Molecular Biology, law.invention, Breast cancer, breast cancer, law, blood, Internal medicine, Genotype, medicine, Humans, In patient, controlled study, human, Alleles, Angiotensin-Converting Enzyme Inhibitors/pharmacology, Breast Neoplasms/*genetics/mortality/pathology, Female, Peptidyl-Dipeptidase A/*genetics, Polymorphism, Genetic, Prognosis, Allele, Lymph node, Gene, Polymerase chain reaction, Angiotensin-converting enzyyme gene polymorphism, gene deletion, article, General Medicine, medicine.disease, major clinical study, Endocrinology, medicine.anatomical_structure, female, Hormone receptor, DNA polymorphism, epidermal growth factor receptor 2, gene insertion

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c294161b5f541b2237f863959195f605Test
https://doi.org/10.2310/6650.2007.00006Test