نتائج البحث - "G Wayne Towers"

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

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

4

Gene–environment and gene–gene interactions of specific MTHFR, MTR and CBS gene variants in relation to homocysteine in black South Africans

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

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

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5

Associations between Common Variants in Iron-Related Genes with Haematological Traits in Populations of African Ancestry

المؤلفون: Jacobien Veenemans, Toshiko Tanaka, Edith J. M. Feskens, Alida Melse-Boonstra, G. Wayne Towers, Wanjiku N. Gichohi-Wainaina, J.L. Harryvan, Hans Verhoef, Mark V. Boekschoten, Elise F. Talsma

المصدر: PLoS ONE
PLoS ONE 11 (2016) 6
PLoS ONE, 11(6)
PLoS ONE, Vol 11, Iss 6, p e0157996 (2016)

مصطلحات موضوعية: 0301 basic medicine, Male, Population genetics, lcsh:Medicine, Genome-wide association study, 030105 genetics & heredity, Pathology and Laboratory Medicine, Biochemistry, Cohort Studies, Voeding, Metabolisme en Genomica, Database and Informatics Methods, Hemoglobins, Gene Frequency, Genotype, Medicine and Health Sciences, Ethnicities, lcsh:Science, Child, Immune Response, Human Nutrition & Health, 2. Zero hunger, Genetics, African Americans, Multidisciplinary, biology, Humane Voeding & Gezondheid, Nutritional Deficiencies, Iron deficiency, Genomics, Population groupings, Genomic Databases, Metabolism and Genomics, Metabolisme en Genomica, Child, Preschool, Nutrition, Metabolism and Genomics, Female, Research Article, Adult, Genotyping, Iron, Immunology, Black People, Single-nucleotide polymorphism, Celbiologie en Immunologie, OS&DAEB, Research and Analysis Methods, Polymorphism, Single Nucleotide, 03 medical and health sciences, Signs and Symptoms, Voeding, Diagnostic Medicine, medicine, Life Science, Humans, Molecular Biology Techniques, Allele frequency, Molecular Biology, VLAG, Nutrition, Global Nutrition, Inflammation, Wereldvoeding, Ferritin, Evolutionary Biology, Population Biology, lcsh:R, Biology and Life Sciences, Proteins, Protein Complexes, Computational Biology, medicine.disease, Genome Analysis, 030104 developmental biology, Biological Databases, Cell Biology and Immunology, Ferritins, biology.protein, Iron Deficiency, lcsh:Q, People and places, Population Genetics, Africans, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45c1ef26f2821ad330fa26c558c86bc5
http://europepmc.org/articles/PMC4917107

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6

CRP Genotypes Predict Increased Risk to Co-Present with Low Vitamin D and Elevated CRP in a Group of Healthy Black South African Women

المؤلفون: G. Wayne Towers, Iolanthé M. Kruger, Cornelie Nienaber-Rousseau, Pieter Hermanus Myburgh

المصدر: International Journal of Environmental Research and Public Health; Volume 15; Issue 1; Pages: 111
International Journal of Environmental Research and Public Health

مصطلحات موضوعية: Health, Toxicology and Mutagenesis, 030204 cardiovascular system & hematology, single nucleotide polymorphisms, 0302 clinical medicine, Genotype, 030212 general & internal medicine, Vitamin D, Tswana, 25(OH)D, biology, Vitamins, Middle Aged, 25-hydroxyvitamin D, calcidiol, Phenotype, Cardiovascular Diseases, Female, SNPs, Adult, Risk, medicine.medical_specialty, Black People, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Article, Nutrigenetics, vitamin D deficiency, C-reactive protein, 03 medical and health sciences, Internal medicine, calciferol, Vitamin D and neurology, Genetic predisposition, medicine, Humans, Genetic Predisposition to Disease, nutrigenetics, Inflammation, business.industry, Public Health, Environmental and Occupational Health, Vitamin D Deficiency, medicine.disease, Cross-Sectional Studies, Blood pressure, Endocrinology, biology.protein, Women's Health, business

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebcc16ef3b564adc92413a09c2d46c80
https://doi.org/10.3390/ijerph15010111

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7

Protective effect against type 2 diabetes mellitus identified within the ACDC gene in a black South African diabetic cohort

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

المصدر: Metabolism. 56:587-592

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

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8

Erratum to: Inter-ethnic differences in genetic variants within the transmembrane protease, serine 6 (TMPRSS6) gene associated with iron status indicators: a systematic review with meta-analyses

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

المساهمون: 12686417 - Towers, Gordon Wayne

المصدر: Genes & Nutrition 10 (2015) 9
Genes & Nutrition 10 (2015)
Genes & Nutrition, 10
Genes and Nutrition, 10, 1, pp. 442
Genes and Nutrition, 10, 442
Genes & Nutrition, 10(9)

مصطلحات موضوعية: racial-differences, TMPRSS6, Nutrition and Disease, medicine.medical_treatment, Endocrinology, Diabetes and Metabolism, Population, united-states, deficiency anemia, Genome-wide association study, Single-nucleotide polymorphism, Biology, serum hepcidin, Serine, transferrin saturation, Voeding en Ziekte, common variants, Genetics, Medicine, Life Science, Allele, education, VLAG, Human Nutrition & Health, Genetic association, Global Nutrition, Wereldvoeding, education.field_of_study, Protease, Transferrin saturation, business.industry, Kazal-type serine protease inhibitor domain, Iron status, caucasian populations, Humane Voeding & Gezondheid, Genetic variants, Transmembrane protein, Minor allele frequency, matriptase-2 tmprss6, Renal disorders Radboud Institute for Molecular Life Sciences [Radboudumc 11], african-americans, Meta-analyses, Systematic review, genome-wide association, Erratum, business, MASP1, Research Paper