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: 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: 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: Ayfer Atalay, Günfer Turgut, Erol Ömer Atalay, Sebahat Turgut

مصطلحات موضوعية: Male, genomic DNA, genetic association, Turkey, polymerase chain reaction, Behcet's disease, Polymerase Chain Reaction, law.invention, Gene Frequency, law, Medicine, Polymerase chain reaction, comparative study, chemistry.chemical_classification, clinical article, biology, Behçet's disease, Behcet Syndrome, allele, article, General Medicine, chromosome 17, Chromosome 17 (human), Angiotensin-converting enzyme I/D polymorphism, female, Female, Angiotensin-converting enzyme, gene insertion, intron, dipeptidyl carboxypeptidase, DNA determination, gene frequency, Peptidyl-Dipeptidase A, Humans, Behcet Syndrome/etiology/*genetics, Chromosomes, Human, Pair 17, Peptidyl-Dipeptidase A/*genetics, Polymorphism, Genetic, controlled study, human, polymorphism, Gene, Allele frequency, gene location, business.industry, gene deletion, Intron, medicine.disease, Molecular biology, angiotensin-converting enzyme, angiotensin-converting enzyme I/D, stomatognathic diseases, Enzyme, chemistry, DNA polymorphism, biology.protein, business, Behcet disease

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f86a7e16b5235f85c769c36fa1141c9Test
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/4838Test