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: Alejandro Lucia, Juan C. Rubio, Jonatan R. Ruiz, Luis Serratosa, M. A. Martín, R. Furrer, Francisco Morate, Joaquín Arenas, Félix Gómez-Gallego, Marta Gonzalez-Freire, Catalina Santiago, Zoraida Verde, P. Juffer

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adolescent, Genotype, Peptidyl-Dipeptidase A/*Genetics, Physical Therapy, Sports Therapy and Rehabilitation, Muscle Strength/Physiology, Athletic Performance, Peptidyl-Dipeptidase A, Genética humana, Muscle mass, AMP Deaminase, Running, Young Adult, Gene Frequency, Statistical significance, Atleta, Soccer, Medicine, Myostatin/*Genetics, Humans, Running/Physiology, Orthopedics and Sports Medicine, Muscle Strength, Allele frequency, Athletic Performance/Physiology, Alleles, Amp Deaminase/*Genetics, Polymorphism, Genetic, biology, business.industry, Athletes, Myostatin, Deporte, biology.organism_classification, Physical Endurance/Physiology, Physical Endurance, Physical therapy, business, human activities, Soccer/*Physiology, Demography

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05c732444447192820476c0adea16446Test
https://hdl.handle.net/11268/161Test

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: Vural Kucukatay, Günfer Turgut, Melek Bor-Kucukatay, Gülten Emmungil, Sebahat Turgut

مصطلحات موضوعية: erythrocyte deformability, Male, genetic association, angiotensin II, high risk patient, chemistry.chemical_compound, Gene Frequency, cardiovascular disease, renin angiotensin aldosterone system, Genotype, blood vessel tone, blood rheology, allele, article, General Medicine, chromosome 17, female, Female, Angiotensin-converting enzyme, gene insertion, cardiovascular risk, Adult, medicine.medical_specialty, intron, prevalence, dipeptidyl carboxypeptidase, Bradykinin, Biology, Peptidyl-Dipeptidase A, volunteer, General Biochemistry, Genetics and Molecular Biology, Internal medicine, Erythrocyte Deformability, Renin–angiotensin system, medicine, Humans, controlled study, human, Allele, Polymorphism, Allele frequency, Polymorphism, Genetic, gene deletion, Molecular biology, Angiotensin II, Endocrinology, chemistry, DNA polymorphism, Hemorheology, biology.protein, Erythrocyte Deformability/*genetics, Peptidyl-Dipeptidase A/*genetics, plasma viscosity, angiotensin I, bradykinin, erythrocyte aggregation

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33368362d328c164cd20e4faaacb7a20Test
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/4675Test

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

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