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Megakaryoblastic leukemia factor-1 gene in the susceptibility to coronary artery disease.
- Published in:
- Human Genetics, 2009, v. 126, n. 4, p. 539, doi. 10.1007/s00439-009-0698-6
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- Article
Mitochondrial haplogroup N9b is protective against myocardial infarction in Japanese males.
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- Human Genetics, 2007, v. 120, n. 6, p. 827, doi. 10.1007/s00439-006-0269-z
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- Article
Identification of 12 novel loci that confer susceptibility to early-onset dyslipidemia.
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- International Journal of Molecular Medicine, 2019, v. 43, n. 1, p. 57, doi. 10.3892/ijmm.2018.3943
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- Article
Identification of 13 novel susceptibility loci for early-onset myocardial infarction, hypertension, or chronic kidney disease.
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- International Journal of Molecular Medicine, 2018, v. 42, n. 5, p. 2415, doi. 10.3892/ijmm.2018.3852
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- Article
Identification of novel hyper- or hypomethylated CpG sites and genes associated with atherosclerotic plaque using an epigenome-wide association study.
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- International Journal of Molecular Medicine, 2018, v. 41, n. 5, p. 2724, doi. 10.3892/ijmm.2018.3453
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- Article
Identification of six polymorphisms as novel susceptibility loci for ischemic or hemorrhagic stroke by exome-wide association studies.
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- International Journal of Molecular Medicine, 2017, v. 39, n. 6, p. 1477, doi. 10.3892/ijmm.2017.2972
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- Article
Identification of EGFLAM, SPATC1L and RNASE13 as novel susceptibility loci for aortic aneurysm in Japanese individuals by exome-wide association studies.
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- International Journal of Molecular Medicine, 2017, v. 39, n. 5, p. 1091, doi. 10.3892/ijmm.2017.2927
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- Article
Association of six genetic variants with myocardial infarction.
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- International Journal of Molecular Medicine, 2015, v. 35, n. 5, p. 1451, doi. 10.3892/ijmm.2015.2115
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- Article
Association of genetic variants with dyslipidemia and chronic kidney disease in a longitudinal population-based genetic epidemiological study.
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- International Journal of Molecular Medicine, 2015, v. 35, n. 5, p. 1290, doi. 10.3892/ijmm.2015.2152
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- Article
Association of genetic variants with hypertension in a longitudinal population-based genetic epidemiological study.
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- International Journal of Molecular Medicine, 2015, v. 35, n. 5, p. 1189, doi. 10.3892/ijmm.2015.2151
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- Publication type:
- Article
Identification of hypo- and hypermethylated genes related to atherosclerosis by a genome-wide analysis of DNA methylation.
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- International Journal of Molecular Medicine, 2014, v. 33, n. 5, p. 1355, doi. 10.3892/ijmm.2014.1692
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- Publication type:
- Article
Multivariate meta-analysis of the association of G-protein beta 3 gene ( GNB3) haplotypes with cardiovascular phenotypes.
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- Molecular Biology Reports, 2014, v. 41, n. 5, p. 3113, doi. 10.1007/s11033-014-3171-0
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- Article
Association of polymorphisms of the androgen receptor and klotho genes with bone mineral density in Japanese women.
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- Journal of Molecular Medicine, 2005, v. 83, n. 1, p. 50, doi. 10.1007/s00109-004-0578-4
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- Article
Lack of association of polymorphisms of the lymphotoxin a gene with myocardial infarction in Japanese.
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- Journal of Molecular Medicine, 2004, v. 82, n. 7, p. 477
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- Article
Association of a polymorphism of the phospholipase D<sub>2</sub> gene with the prevalence of colorectal cancer.
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- Journal of Molecular Medicine, 2003, v. 81, n. 2, p. 126, doi. 10.1007/s00109-002-0411-x
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- Article
Association of polymorphisms of the estrogen receptor α gene with bone mineral density of the femoral neck in elderly Japanese women.
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- Journal of Molecular Medicine, 2002, v. 80, n. 7, p. 452, doi. 10.1007/s00109-002-0348-0
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- Article
Association of the C<sup>–509</sup>→T polymorphism, alone or in combination with the T<sup>869</sup>→C polymorphism, of the transforming growth factor-β<sub>1</sub> gene with bone mineral density and genetic susceptibility to osteoporosis in Japanese women
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- Journal of Molecular Medicine, 2001, v. 79, n. 2/3, p. 149, doi. 10.1007/s001090100190
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- Article
Genetic risk score based on the lifetime prevalence of femoral fracture in 924 consecutive autopsies of Japanese males.
- Published in:
- 2016
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- Publication type:
- journal article
A missense single nucleotide polymorphism, V114I of the Werner syndrome gene, is associated with risk of osteoporosis and femoral fracture in the Japanese population.
- Published in:
- 2015
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- Publication type:
- journal article
ADRB2 and LEPR Gene Polymorphisms: Synergistic Effects on the Risk of Obesity in Japanese.
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- Obesity (19307381), 2011, v. 19, n. 7, p. 1523, doi. 10.1038/oby.2010.322
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- Article
Association of a polymorphism of the interleukin 6 receptor gene with chronic kidney disease in Japanese individuals.
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- Nephrology, 2015, v. 20, n. 4, p. 273, doi. 10.1111/nep.12381
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- Article
Association of a genetic variant of BTN2A1 with chronic kidney disease in Japanese individuals.
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- Nephrology, 2011, v. 16, n. 7, p. 642, doi. 10.1111/j.1440-1797.2011.01470.x
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- Publication type:
- Article
Prostaglandin E<sub>2</sub> Induces Expression of Receptor Activator of Nuclear Factor-κB Ligand/Osteoprotegrin Ligand on Pre-B Cells: Implications for Accelerated Osteoclastogenesis in Estrogen Deficiency.
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- Journal of Bone & Mineral Research, 2000, v. 15, n. 7, p. 1321, doi. 10.1359/jbmr.2000.15.7.1321
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- Article
Association of Transforming Growth Factor β1 Genotype with Therapeutic Response to Active Vitamin D for Postmenopausal Osteoporosis.
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- Journal of Bone & Mineral Research, 2000, v. 15, n. 3, p. 415, doi. 10.1359/jbmr.2000.15.3.415
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- Article
Immunological Characterization of Circulating Osteoprotegerin/Osteoclastogenesis Inhibitory Factor: Increased Serum Concentrations in Postmenopausal Women with Osteoporosis.
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- Journal of Bone & Mineral Research, 1999, v. 14, n. 4, p. 518, doi. 10.1359/jbmr.1999.14.4.518
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- Publication type:
- Article
Association of a Polymorphism of the Transforming Growth Factor-β1 Gene with Genetic Susceptibility to Osteoporosis in Postmenopausal Japanese Women.
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- Journal of Bone & Mineral Research, 1998, v. 13, n. 10, p. 1569, doi. 10.1359/jbmr.1998.13.10.1569
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- Publication type:
- Article
Interaction Between Nitric Oxide Synthase and Cyclooxygenase Pathways in Osteoblastic MC3T3-E1 Cells.
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- Journal of Bone & Mineral Research, 1997, v. 12, n. 11, p. 1789, doi. 10.1359/jbmr.1997.12.11.1789
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- Publication type:
- Article
Association of Polymorphisms of Interleukin-6, Osteocalcin, and Vitamin D Receptor Genes, Alone or in Combination, with Bone Mineral Density in Community Dwelling Japanese Women and Men.
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- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 7, p. 3372, doi. 10.1210/jc.2002-021449
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- Article
Privacy-preserving genome-wide association studies on cloud environment using fully homomorphic encryption.
- Published in:
- 2015
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- Publication type:
- journal article
Phenotypic Variation of Familial Hypertrophic Cardiomyopathy Caused by the Phe[sup 110] →Ile Mutation in Cardiac Troponin T.
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- Cardiology, 2000, v. 93, n. 3, p. 155, doi. 10.1159/000007020
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- Article
Brain Natriuretic Peptide Is a Sensitive Indicator of Impaired Left-Ventricular Function in Elderly Patients with Cardiovascular Disease.
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- Cardiology, 1997, v. 88, n. 5, p. 401, doi. 10.1159/000177368
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- Publication type:
- Article
Association of a Deletion Polymorphism of the Angiotensin-Converting Enzyme Gene with Left-Ventricular Hypertrophy in Japanese Women with Essential Hypertension; Multicenter Study of 1,919 Subjects.
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- Cardiology, 1997, v. 88, n. 4, p. 309, doi. 10.1159/000177351
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- Article
Association of a--1997G→T Polymorphism of the Collagen Iα1 Gene with Bone Mineral Density in Postmenopausal Japanese Women.
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- Human Biology, 2005, v. 77, n. 1, p. 27, doi. 10.1353/hub.2005.0035
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- Article
Identification of 26 novel loci that confer susceptibility to early-onset coronary artery disease in a Japanese population.
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- Biomedical Reports, 2018, v. 9, n. 5, p. 383, doi. 10.3892/br.2018.1152
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- Article
Six novel susceptibility loci for coronary artery disease and cerebral infarction identified by longitudinal exome-wide association studies in a Japanese population.
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- Biomedical Reports, 2018, v. 9, n. 2, p. 123, doi. 10.3892/br.2018.1109
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- Article
Identification of four genes as novel susceptibility loci for early-onset type 2 diabetes mellitus, metabolic syndrome, or hyperuricemia.
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- Biomedical Reports, 2018, v. 9, n. 1, p. 21, doi. 10.3892/br.2018.1105
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- Article
Identification of nine genes as novel susceptibility loci for early-onset ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage.
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- Biomedical Reports, 2018, v. 9, n. 1, p. 8, doi. 10.3892/br.2018.1104
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- Article
Association of smoking with prevalence of common diseases and metabolic abnormalities in community-dwelling Japanese individuals.
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- Biomedical Reports, 2017, v. 7, n. 5, p. 429, doi. 10.3892/br.2017.991
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- Article
Association of renal function with clinical parameters and conditions in a longitudinal population-based epidemiological study.
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- Biomedical Reports, 2017, v. 6, n. 2, p. 242, doi. 10.3892/br.2016.831
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- Article
Association of genetic variants with atrial fibrillation.
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- Biomedical Reports, 2016, v. 4, n. 2, p. 178, doi. 10.3892/br.2015.551
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- Article
Age-related changes in clinical parameters and their associations with common complex diseases.
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- Biomedical Reports, 2015, v. 3, n. 6, p. 767, doi. 10.3892/br.2015.505
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- Article
Association of FURIN and ZPR1 polymorphisms with metabolic syndrome.
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- Biomedical Reports, 2015, v. 3, n. 5, p. 641, doi. 10.3892/br.2015.484
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- Article
Association of FURIN and ZPR1 polymorphisms with metabolic syndrome.
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- Biomedical Reports, 2015, p. 641, doi. 10.3892/br.2015.484
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- Article
Association of TOMM40 and SLC22A4 polymorphisms with ischemic stroke.
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- Biomedical Reports, 2015, v. 3, n. 4, p. 491, doi. 10.3892/br.2015.457
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- Article
Association of genetic variants with coronary artery disease and ischemic stroke in a longitudinal population-based genetic epidemiological study.
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- Biomedical Reports, 2015, v. 3, n. 3, p. 413, doi. 10.3892/br.2015.440
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- Article
Association of genetic variants of the a-kinase 1 gene with type 2 diabetes mellitus in a longitudinal population-based genetic epidemiological study.
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- Biomedical Reports, 2015, v. 3, n. 3, p. 347, doi. 10.3892/br.2015.439
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- Article
Association of a transcription factor 21 gene polymorphism with hypertension.
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- Biomedical Reports, 2015, v. 3, n. 1, p. 118, doi. 10.3892/br.2014.371
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- Article
Association of a genetic variant of the ZPR1 zinc finger gene with type 2 diabetes mellitus.
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- Biomedical Reports, 2015, v. 3, n. 1, p. 88, doi. 10.3892/br.2014.379
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- Article
Association of a butyrophilin, subfamily 2, member A1 gene polymorphism with hypertension.
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- Biomedical Reports, 2014, v. 2, n. 6, p. 818, doi. 10.3892/br.2014.340
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- Article
Association of genetic variants of the α-kinase 1 gene with myocardial infarction in community-dwelling individuals.
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- Biomedical Reports, 2014, v. 2, n. 1, p. 127, doi. 10.3892/br.2013.190
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- Article