المؤلفون: Dorine W. Swinkels, Wanjiku N. Gichohi-Wainaina, Edith J. M. Feskens, G. Wayne Towers, Alida Melse-Boonstra, Michael B. Zimmermann

المصدر: Journal of Nutrition, 145, 945-953
The Journal of Nutrition 145 (2015) 5
Journal of Nutrition, 145, 5, pp. 945-953
The Journal of Nutrition, 145(5), 945-953

مصطلحات موضوعية: Nutrition and Disease, Medicine (miscellaneous), Cohort Studies, South Africa, Voeding en Ziekte, Genotype, Prospective Studies, hfe, Human Nutrition & Health, risk, Aged, 80 and over, chemistry.chemical_classification, Genetics, Nutrition and Dietetics, Anemia, Iron-Deficiency, biology, saturation, Serine Endopeptidases, Humane Voeding & Gezondheid, Transferrin, Middle Aged, Female, women, transferrin g277s mutation, Adult, medicine.medical_specialty, deficiency anemia, Black People, Nutritional Status, Single-nucleotide polymorphism, Transferrin receptor, Polymorphism, Single Nucleotide, serum hepcidin, Internal medicine, Receptors, Transferrin, medicine, Humans, Genetic Predisposition to Disease, Allele, Alleles, Genetic Association Studies, Adaptor Proteins, Signal Transducing, Aged, VLAG, Soluble transferrin receptor, Global Nutrition, Wereldvoeding, disease, Tumor Necrosis Factor-alpha, Haplotype, Histocompatibility Antigens Class II, Membrane Proteins, Minor allele frequency, Renal disorders Radboud Institute for Molecular Life Sciences [Radboudumc 11], Endocrinology, Solubility, chemistry, biology.protein, polymorphisms, tumor-necrosis-factor

وصف الملف: application/pdf; application/octet-stream

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d98d9b816fe9a911bb045f560129562d
https://doi.org/10.3945/jn.114.209148

المؤلفون: Alida Melse-Boonstra, Suria Ellis, G. Wayne Towers, Sarah J. Moss, Cornelie Nienaber-Rousseau

المساهمون: 12632449 - Nienaber-Rousseau, Cornelie, 10188908 - Ellis, Susanna Maria, 10210407 - Moss, Sarah Johanna, 12686417 - Towers, Gordon Wayne

المصدر: Gene, 530(1), 113-118
Gene 530 (2013) 1

مصطلحات موضوعية: Male, coronary-artery-disease, high prevalence, Homocysteine, cardiovascular-disease, Cystathionine beta-synthase, chemistry.chemical_compound, South Africa, tHcy, hyperhomocysteinemia, risk-factors, Genetics, High prevalence, biology, General Medicine, Middle Aged, Medical research, Phosphotransferases (Alcohol Group Acceptor), Female, Health department, Adult, Genotype, Hyperhomocysteinemia, Cystathionine beta-Synthase, Single-nucleotide polymorphism, urbanization, Population health, vascular-disease, Polymorphism, Single Nucleotide, beta-synthase gene, Humans, Genetic Predisposition to Disease, Gene, Genetic Association Studies, Methylenetetrahydrofolate Reductase (NADPH2), VLAG, methionine synthase, Global Nutrition, Wereldvoeding, business.industry, Epistasis, Genetic, methylenetetrahydrofolate reductase, heart-disease, Biotechnology, chemistry, Methylenetetrahydrofolate reductase, biology.protein, Gene-Environment Interaction, business, plasma homocysteine

وصف الملف: application/octet-stream; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21dbf534ab4221027b48b901714920c4
https://doi.org/10.1016/j.gene.2013.07.065

المؤلفون: Peter Schwarz, G. Wayne Towers, Antonel Olckers, Paul Rheeder, Annelize van der Merwe, Aletta E. Schutte

المصدر: Metabolism. 56:587-592

مصطلحات موضوعية: Adult, Blood Glucose, Male, medicine.medical_specialty, Endocrinology, Diabetes and Metabolism, Population, Black People, Single-nucleotide polymorphism, Type 2 diabetes, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Body Mass Index, Cohort Studies, South Africa, Endocrinology, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Promoter Regions, Genetic, education, Genetics, education.field_of_study, Adiponectin, Waist-Hip Ratio, Genetic heterogeneity, business.industry, ACDC, Haplotype, Type 2 Diabetes Mellitus, DNA, Middle Aged, medicine.disease, Diabetes Mellitus, Type 2, Haplotypes, Female, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecc4337d70937df51f70dcd5b0305e38
https://doi.org/10.1016/j.metabol.2006.10.004

المؤلفون: Annelize van der Merwe, G. Wayne Towers, Chris F. Retief, Antonel Olckers, Engela Honey, Clara-Maria Schutte

المصدر: Neuromuscular disorders : NMD. 22(8)

مصطلحات موضوعية: Male, Pathology, medicine.medical_specialty, Heterozygote, Population, Compound heterozygosity, Deoxyribonuclease EcoRI, South Africa, Atrophy, medicine, Facioscapulohumeral muscular dystrophy, Humans, Muscular dystrophy, education, Deoxyribonucleases, Type II Site-Specific, Genetics (clinical), Genetics, education.field_of_study, business.industry, Facial weakness, Autosomal dominant trait, Middle Aged, medicine.disease, Muscular Dystrophy, Facioscapulohumeral, Pedigree, Chromosome 4, Neurology, Haplotypes, Pediatrics, Perinatology and Child Health, Neurology (clinical), medicine.symptom, Chromosomes, Human, Pair 4, business, Gene Deletion

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55e48224f4fce57fe9c9161234dac92f
https://pubmed.ncbi.nlm.nih.gov/22652079