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1
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 -
2
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 -
3
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 -
4
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 -
5
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