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1دورية أكاديمية
المساهمون: Sung Kyu Ha, Ha, Sung Kyu
المصدر: T201404602.pdf
مصطلحات موضوعية: Angiotensin II Type 1 Receptor Blockers/therapeutic use, Angiotensin-Converting Enzyme Inhibitors/therapeutic use, Animals, Diabetic Nephropathies/drug therapy, Diabetic Nephropathies/enzymology, Diabetic Nephropathies/genetics, Disease Progression, Genetic Predisposition to Disease, Humans, Kidney Failure, Chronic/drug therapy, Chronic/enzymology, Chronic/genetics, Peptidyl-Dipeptidase A/genetics, Phenotype, Polymorphism, Genetic, Proteinuria/drug therapy, Proteinuria/enzymology, Proteinuria/genetics, Renin-Angiotensin System/drug effects, Renin-Angiotensin System/genetics, Risk Factors, Treatment Outcome
وصف الملف: application/pdf
العلاقة: JOURNAL OF DIABETES RESEARCH; J01378; OAK-2014-02707; https://ir.ymlib.yonsei.ac.kr/handle/22282913/138440Test; T201404602; JOURNAL OF DIABETES RESEARCH, Vol.2014 : 846068, 2014
الإتاحة: https://doi.org/10.1155/2014/846068Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/138440Test -
2
المؤلفون: Catalina Santiago, Félix Gómez-Gallego, Marta Gonzalez-Freire, Carlos A. Muniesa, Alejandro Lucia, M. Fernández del Valle, Carl Foster, Margarita Pérez
المصدر: International Journal of Sports Medicine. 30:66-72
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Genotype, Peptidyl-Dipeptidase A/*Genetics, Ace genotype, Peak power output, Physical Therapy, Sports Therapy and Rehabilitation, Peptidyl-Dipeptidase A, Biology, Fisiología humana, Respiratory compensation, Physical Endurance/*Genetics, Pulmonary Ventilation/Physiology, Atleta, Internal medicine, medicine, Humans, Actinin, Orthopedics and Sports Medicine, Gross efficiency, Gene, Analysis of Variance, Bicycling, Deporte, Respiratory Function Tests, Phenotype, Endocrinology, Physical Endurance, Exercise Test, Physical therapy, Analysis of variance, Pulmonary Ventilation, human activities
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ce293dfc17acd560fff18570bee4e91Test
https://doi.org/10.1055/s-2008-1038677Test -
3دورية أكاديمية
المؤلفون: Vardy, Emma R L C, Brown, Kristelle, Stopford, Cheryl L, Thompson, Jennifer C, Richardson, Anna M, Neary, David, Kalsheker, Noor, Morgan, Kevin, Mann, David M, Snowden, Julie S
المصدر: Vardy , E R L C , Brown , K , Stopford , C L , Thompson , J C , Richardson , A M , Neary , D , Kalsheker , N , Morgan , K , Mann , D M & Snowden , J S 2012 , ' Cognitive phenotypes in Alzheimer's disease and genetic variants in ACE and IDE ' , Neurobiology of Aging , vol. 33 , no. 7 , pp. 1486.e1-1486.e2 . https://doi.org/10.1016/j.neurobiolaging.2010.11.003Test , https://doi.org/10.1016/j.neurobiolaging.2010.11.003Test
مصطلحات موضوعية: Alzheimer Disease/diagnosis, Cognition Disorders/diagnosis, Female, Genetic Predisposition to Disease/genetics, Genetic Variation/genetics, Humans, Insulysin/genetics, Male, Peptidyl-Dipeptidase A/genetics, Phenotype
الإتاحة: https://doi.org/10.1016/j.neurobiolaging.2010.11.003Test
https://research.manchester.ac.uk/en/publications/6fb64a9d-4563-452a-a29f-abbe2f77c511Test -
4دورية أكاديمية
المؤلفون: González-Freire, Marta, Santiago Dorrego, Catalina, Gómez Gallego, Félix, Pérez Ruiz, Margarita, Foster, Carl, Arenas, Joaquín, Lucía Mulas, Alejandro
مصطلحات موضوعية: Genetic Predisposition To Disease/*Genetics, Glycogen Storage Disease Type V/*Genetics, Mutation/*Genetics, Myostatin/*Genetics, Amp Deaminase/Genetics, Dna Mutational Analysis, Exercise Tolerance/Genetics, Female, Genetic Variation/Genetics, Genotype, Glycogen/Metabolism, Glycogen Storage Disease Type V/Metabolism, Glycogen Storage Disease Type V/Physiopathology, Heterozygote, Humans, Muscle Weakness/Genetics, Muscle, Skeletal/Metabolism, Skeletal/Physiopathology, Peptidyl-Dipeptidase A/Genetics, Phenotype, Respiratory Insufficiency/Genetics, Enfermedad nutricional, Deporte, Tratamiento médico
العلاقة: González-Freire, M., Santiago-Dorrego, C., Gómez-Gallego, F., Pérez-Ruiz, M., Foster, C., Arenas, J., & Lucía-Mulas, A. (2009). Does the K153R variant of the myostatin gene influence the clinical presentation of women with McArdle disease? Neuromuscular Disorders, 19(3), 220-222.; http://hdl.handle.net/11268/1120Test
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5دورية أكاديمية
المؤلفون: Gómez Gallego, Félix, Santiago Dorrego, Catalina, González-Freire, Marta, Muniesa Ferrero, Carlos Alberto, Fernández del Valle, María, Pérez Ruiz, Margarita, Foster, Carl, Lucía Mulas, Alejandro
مصطلحات موضوعية: Bicycling, Peptidyl-Dipeptidase A/*Genetics, Physical Endurance/*Genetics, Analysis of Variance, Exercise Test, Genotype, Humans, Male, Phenotype, Pulmonary Ventilation/Physiology, Respiratory Function Tests, Atleta, Fisiología humana, Deporte
العلاقة: Gómez-Gallego, F., Santiago-Dorrego, C., González-Freire, M., Muniesa-Ferrero, C. A., Fernández, V., Pérez-Ruiz, M., ., & Lucía-Mulas, A. (2009). Endurance performance: genes or gene combinations? International Journal of Sports Medicine, 30(1), 66-72.; http://hdl.handle.net/11268/468Test
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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 -
7دورية أكاديمية
المؤلفون: Pernod, G., Bosson, J.L., Golshayan, D., Barro, C., Alloatti, S., Turc-Baron, C., Quarello, F., Jeantet, A., Von Albertini, B., Forêt, M., Lauren, G., Cordonnier, D., Piccoli, G., Wauters, J.P.
المصدر: Journal of Nephrology, vol. 17, no. 1, pp. 66-75
مصطلحات موضوعية: Adult, Aged, 80 and over, Cardiovascular Diseases/etiology, Cardiovascular Diseases/genetics, Cohort Studies, Female, Genotype, Haptoglobins/genetics, Homocysteine/blood, Humans, Kidney Failure, Chronic/complications, Lipids/blood, Male, Middle Aged, Peptidyl-Dipeptidase A/genetics, Phenotype, Plasminogen Activator Inhibitor 1/genetics, Polymorphism, Genetic, Renal Dialysis/adverse effects, Risk Factors
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/15151261; info:eu-repo/semantics/altIdentifier/pissn/1121-8428; https://serval.unil.ch/notice/serval:BIB_BC365247C8EETest